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Naomi Kondo

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Tomohiro Hori; Toshiyuki Fukao; Cary O Harding; Keiko Murase; Naomi Sakaguchi; Naomi Kondo
Molecular basis of two-exon skipping (exons 12 and 13) by c.1248+5g>a in OXCT1 gene: study on intermediates of OXCT1 transcripts in fibroblasts.
Michinori Funato; Naomi Kondo
[New knowledge of Li-Fraumeni syndrome].
Kazuo Kubota; Eiko Matsui; Kana Murase; Hidenori Ohnishi; Mariko Seishima; Takahide Teramoto; Hideo Kaneko; Hiroyuki Kanoh; Zenichiro Kato; Naomi Kondo
In vitro analysis of the functional effects of an NLRP3 G809S variant with the co-existence of MEFV haplotype variants in atypical autoinflammatory syndrome.

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All Publications

2013: Tomohiro Hori; Toshiyuki Fukao; Cary O Harding; Keiko Murase; Naomi Sakaguchi; Naomi Kondo
Molecular basis of two-exon skipping (exons 12 and 13) by c.1248+5g>a in OXCT1 gene: study on intermediates of OXCT1 transcripts in fibroblasts.
Human mutation 2013;34(3):473-80.
2013: Michinori Funato; Naomi Kondo
[New knowledge of Li-Fraumeni syndrome].
Gan to kagaku ryoho. Cancer & chemotherapy 2013;40(2):148-53.
2013: Kazuo Kubota; Eiko Matsui; Kana Murase; Hidenori Ohnishi; Mariko Seishima; Takahide Teramoto; Hideo Kaneko; Hiroyuki Kanoh; Zenichiro Kato; Naomi Kondo
In vitro analysis of the functional effects of an NLRP3 G809S variant with the co-existence of MEFV haplotype variants in atypical autoinflammatory syndrome.
Journal of clinical immunology 2013;33(2):325-34.
2013: Zenichiro Kato; Takahiko Asano; Michinori Funato; Hideo Sasai; Naomi Kondo
Acute cerebellitis associated with rotavirus infection.
World journal of pediatrics : WJP 2013;9(1):87-9.
2013: Michio Ozeki; Hidenori Ohnishi; Eiichi Azuma; Akihiro Fujino; Toshiyuki Fukao; Masahiro Hirayama; Kaori Kanda; Zenichiro Kato; Norio Kawamoto; Naomi Kondo
Propranolol as an alternative treatment option for pediatric lymphatic malformation.
The Tohoku journal of experimental medicine 2013;229(1):61-6.
2013: Norio Kawamoto; Naomi Kondo; Hidenori Ohnishi; Jack L Strominger
The role of dendritic cells in the generation of CD4(+) CD25(HI) Foxp3(+) T cells induced by amino acid copolymers.
International immunology 2013;25(1):53-65.
2012: Naomi Kondo; Eiko Matsui; Hidenori Ohnishi; Zenichiro Kato; Norio Kawamoto; Takahide Teramoto; Manami Ooga
[To get a cure for childfood asthma -a new strategy -therapy on two wheels-].
Arerugī = [Allergy] 2012;61(12):1736-43.
2012: Takahide Teramoto; Hiroshi Yonezawa; Hidenori Ohnishi; Kazuaki Sakai; Junichi Azuma; Toshiyuki Fukao; Hideo Kaneko; Zenichiro Kato; Naomi Kondo; Eiko Matsui; Sankei Nishima
Repeated-dose pharmacokinetics of inhaled ciclesonide (CIC-HFA) in Japanese children with bronchial asthma: a phase I study.
Allergology international : official journal of the Japanese Society of Allergology 2012;61(4):619-24.
2012: Tomohiro Hori; Hideo Kaneko; Toshiyuki Fukao; Yoshinobu Hirose; Takafumi Naiki; Osamu Ohara; Hidenori Ohnishi; Mariko Seishima; Takahide Teramoto; Kohji Tsubouchi; Naomi Kondo
Autosomal-dominant chronic mucocutaneous candidiasis with STAT1-mutation can be complicated with chronic active hepatitis and hypothyroidism.
Journal of clinical immunology 2012;32(6):1213-20.
2012: Masatoshi Nada; Hidenori Ohnishi; Masahiro Shirakawa; Hidehito Tochio; Naotaka Tsutsumi; Takahiro Yamamoto; Yuji O Kamatari; Zenichiro Kato; Takeshi Kimura; Kazuo Kubota; Naomi Kondo
Molecular analysis of the binding mode of Toll/interleukin-1 receptor (TIR) domain proteins during TLR2 signaling.
Molecular immunology 2012;52(3-4):108-16.
2012: Naomi Kondo
[Long-term management of child asthma].
Arerugī = [Allergy] 2012;61(6):771-84.
2012: Kentaro Omoya; Toshiaki Taga; Yasushi Uchida; Seiichiro Yoshioka; Yoshinori Aoki; Hideki Deguchi; Zenichiro Kato; Yasuhiro Naiki; Naomi Kondo
Sweet's syndrome in a neonate with non-B54 types of human leukocyte antigen.
World journal of pediatrics : WJP 2012;8(2):181-4.
2012: Hidenori Ohnishi; Mariko Seishima; Takahide Teramoto; Kazuo Kubota; Ryuta Nishikomori; Hiroaki Iwata; Hideo Kaneko; Zenichiro Kato; Takeshi Kimura; Naomi Kondo
Characterization of NLRP3 variants in Japanese cryopyrin-associated periodic syndrome patients.
Journal of clinical immunology 2012;32(2):221-9.
2012: Hideyuki Morita; Hidenori Ohnishi; Takahide Teramoto; Takahiro Yamamoto; Toshiyuki Fukao; Hideo Kaneko; Kimiko Kasahara; Zenichiro Kato; Kazuo Kubota; Eiko Matsui; Naomi Kondo
Structural property of soybean protein P34 and specific IgE response to recombinant P34 in patients with soybean allergy.
International journal of molecular medicine 2012;29(2):153-8.
2012: Hidenori Ohnishi; Tomonori Suzuki; Hideo Kaneko; Zenichiro Kato; Kazuo Kubota; Rie Miyata; Touichiro Nose; Naomi Kondo
A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome.
The Journal of allergy and clinical immunology 2012;129(2):578-80.
2012: Toshiyuki Fukao; Antti M Haapalainen; Yuki Hasegawa; Mari Imamura; Naomi Kuwada; Shinsuke Maruyama; Toshihiro Ohura; Mitsuo Toyoshima; Rik K Wierenga; Seiji Yamaguchi; Isao Yuasa; Naomi Kondo
Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass Spectrometry.
JIMD reports 2012;3():107-15.
2012: Hidenori Ohnishi; Masahiro Shirakawa; Hidehito Tochio; Richard W Wong; Takahiro Yamamoto; Tatsuyoshi Funasaka; Zenichiro Kato; Norio Kawamoto; Takeshi Kimura; Kazuo Kubota; Hiroshi Nakano; Naomi Kondo
TRAM is involved in IL-18 signaling and functions as a sorting adaptor for MyD88.
PloS one 2012;7(6):e38423.
2012: Norio Kawamoto; T Kimura; Masashi Kondo; Y Aoki; T Arai; C Bai; Toshiyuki Fukao; K Hirayama; Shinichi Iwasa; Hideo Kaneko; Kimiko Kasahara; M Kawamoto; Eiko Matsui; Eiji Matsukuma; M Morimoto; H Morita; M Nada; Kentaro Omoya; Satomi Sakurai; Mitsuru Seishima; Makoto Shiraki; Hiroko Suzuki; Masao Takemura; Takahide Teramoto; T Tokumi; G Zhang; Naomi Kondo
Risk factors for infantile atopic dermatitis and recurrent wheezing.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2012;22(2):116-25.
2012: Hiroki Kato; Zenichiro Kato; Naomi Kondo; Takahide Teramoto; Masayuki Kanematsu; Hiroaki Hoshi
Computed tomographic findings of Kawasaki disease with cervical lymphadenopathy.
Journal of computer assisted tomography 2012;36(1):138-42.
2011: Hiroki Kato; Zenichiro Kato; Naomi Kondo; Takahide Teramoto; Yoshinobu Hirose; Masayuki Kanematsu; Hiroaki Hoshi
MR imaging findings of cervical lymphadenopathy in patients with Kikuchi disease.
European journal of radiology 2011;80(3):e576-81.
2011: Michinori Funato; Tomohiro Hori; Hideo Kaneko; Kazuo Kubota; Kenji Orii; Michio Ozeki; Hideo Sasai; Daisuke Terazawa; Toshiyuki Fukao; Naomi Kondo
Successful treatment of pediatric immune thrombocytopenic purpura associated with ulcerative colitis.
Pediatrics international : official journal of the Japan Pediatric Society 2011;53(5):771-3.
2011: Michinori Funato; Kaori Kanda; Hideo Kaneko; Zenichiro Kato; Kazuo Kubota; Kenji Orii; Michio Ozeki; Toshiyuki Fukao; Naomi Kondo
Pediatric acute lymphoblastic leukemia mimicking Henoch-Schönlein purpura.
Pediatrics international : official journal of the Japan Pediatric Society 2011;53(5):766-8.
2011: Michinori Funato; Hideo Kaneko; Zenichiro Kato; Kazuo Kubota; Kiyofumi Ohkusu; Hidenori Ohnishi; Hideo Sasai; Toshiyuki Fukao; Naomi Kondo
Refractory chronic pleurisy caused by Helicobacter equorum-like bacterium in a patient with X-linked agammaglobulinemia.
Journal of clinical microbiology 2011;49(9):3432-5.
2011: Zenichiro Kato; Naomi Kondo; Kei Miyamoto; Hideyuki Morita; Hiroki Kato; Takahide Teramoto; Katsuji Shimizu
Selective pontine hypoplasia: a possible common feature in 5p monosomy syndrome.
Brain & development 2011;33(8):702-3.
2011: Hiroki Kato; Zenichiro Kato; Masahiro Morimoto; Kenji E Orii; Masayuki Kanematsu; Naomi Kondo
Apparition of iodinated contrast agents in twin neonatal gastrointestinal tracts after maternal contrast-enhanced computed tomography.
Japanese journal of radiology 2011;29(7):521-3.
2011: Tomoyoshi Terada; Toshibumi Shimokawa; Seiichi Era; Naomi Kondo; Koichi Murayama; Satoshi Nunomura; Chisei Ra
FcεRI-induced mast cell cytokine production critically involves an aspartic acid residue (D234) in the C-terminal intracellular domain of the FcεRIβ chain.
Biochemical and biophysical research communications 2011;410(4):744-8.
2011: Hideo Kaneko; Toshiyuki Fukao; Kimiko Kasahara; Taketo Yamada; Naomi Kondo
Augmented cell death with Bloom syndrome helicase deficiency.
Molecular medicine reports 2011;4(4):607-9.
2011: Yang An; Hidenori Ohnishi; Eiko Matsui; Michinori Funato; Zenichiro Kato; Takahide Teramoto; Hideo Kaneko; Takeshi Kimura; Kazuo Kubota; Kimiko Kasahara; Naomi Kondo
Genetic variations in MyD88 adaptor-like are associated with atopic dermatitis.
International journal of molecular medicine 2011;27(6):795-801.
2011: Toshiyuki Fukao; Jörn Oliver Sass; Petri Kursula; Eva Thimm; Udo Wendel; Can Ficicioglu; Kamel Monastiri; Nathalie Guffon; Ivo Barić; Marie-Therese Zabot; Naomi Kondo
Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency.
Biochimica et biophysica acta 2011;1812(5):619-24.
2011: Zenichiro Kato; Tomoko Manabe; Takahide Teramoto; Naomi Kondo
Adenovirus infection mimics the cerebellitis caused by rotavirus infection.
European journal of pediatrics 2011;170(3):405-6.
2011: Yasushi Uchida; Hideyuki Morita; Shinya Adachi; Tsutomu Asano; Toshiaki Taga; Naomi Kondo
Bacterial meningitis and septicemia of neonate due to Lactococcus lactis.
Pediatrics international : official journal of the Japan Pediatric Society 2011;53(1):119-20.
2010: Zenichiro Kato; Masahiro Morimoto; Kenji E Orii; Tomomi Kato; Naomi Kondo
Developmental changes of radiological findings in Fukuyama-type congenital muscular dystrophy.
Pediatric radiology 2010;40 Suppl 1():S127-9.
2010: Yusuke Aoki; Toshiyuki Fukao; Gaixiu Zhang; Hidenori Ohnishi; Naomi Kondo
Mutation in the Q28SDD31SD site, but not in the two SQ sites of the survival of motor neuron protein, affects its foci formation.
International journal of molecular medicine 2010;26(5):667-71.
2010: Zenichiro Kato; Joel N H Stern; Hironori K Nakamura; Naoyuki Miyashita; Kazuo Kuwata; Naomi Kondo; Jack L Strominger
The autoimmune TCR-Ob.2F3 can bind to MBP85-99/HLA-DR2 having an unconventional mode as in TCR-Ob.1A12.
Molecular immunology 2010;48(1-3):314-20.
2010: Hidenori Ohnishi; Hidehito Tochio; Zenichiro Kato; Takeshi Kimura; Hidekazu Hiroaki; Naomi Kondo; Masahiro Shirakawa
1H, 13C, and 15N resonance assignment of the TIR domain of human MyD88.
Biomolecular NMR assignments 2010;4(2):123-5.
2010: Naomi Kondo; Eiko Matsui; Hideo Kaneko; Zenichiro Kato; Makiko Orito
[Allergic disorders].
Nihon rinsho. Japanese journal of clinical medicine 2010;68 Suppl 8():388-96.
2010: Toshiyuki Fukao; Reiko Horikawa; Yasuhiro Naiki; Toju Tanaka; Masaki Takayanagi; Seiji Yamaguchi; Naomi Kondo
A novel mutation (c.951C>T) in an exonic splicing enhancer results in exon 10 skipping in the human mitochondrial acetoacetyl-CoA thiolase gene.
Molecular genetics and metabolism 2010;100(4):339-44.
2010: Tomohiro Hori; Toshiyuki Fukao; Hironori Kobayashi; Takahide Teramoto; Masaki Takayanagi; Yuki Hasegawa; Tetsuhiko Yasuno; Seiji Yamaguchi; Naomi Kondo
Carnitine palmitoyltransferase 2 deficiency: the time-course of blood and urinary acylcarnitine levels during initial L-carnitine supplementation.
The Tohoku journal of experimental medicine 2010;221(3):191-5.
2010: Makiko Suzuki; Hidehiko Fujii; Hidetsugu Fujigaki; Shinji Shinoda; Kanako Takahashi; Kuniaki Saito; Hisayasu Wada; Masumi Kimoto; Naomi Kondo; Mitsuru Seishima
Lipocalin-type prostaglandin D synthase and egg white cystatin react with IgE antibodies from children with egg allergy.
Allergology international : official journal of the Japanese Society of Allergology 2010;59(2):175-83.
2010: Michio Ozeki; Michinori Funato; Takahide Teramoto; Naoyuki Ohe; Takahiko Asano; Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo
Reversible cerebrospinal fluid edema and porencephalic cyst, a rare complication of ventricular catheter.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2010;17(5):658-61.
2010: Toshiyuki Fukao; Hoan Thi Nguyen; Nhan Thu Nguyen; Dung Chi Vu; Ngoc Thi Bich Can; Anh Thi Van Pham; Khanh Ngoc Nguyen; Hironori Kobayashi; Yuki Hasegawa; Thao Phuong Bui; Kary E Niezen-Koning; Ronald J A Wanders; Tom de Koning; Liem Thanh Nguyen; Seiji Yamaguchi; Naomi Kondo
A common mutation, R208X, identified in Vietnamese patients with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency.
Molecular genetics and metabolism 2010;100(1):37-41.
2010: Toshiyuki Fukao; Gaixiu Zhang; Naoki Matsuo; Naomi Kondo
CpG islands around exon 1 in the succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene are hypomethylated even in human and mouse hepatic tissues where SCOT gene expression is completely suppressed.
Molecular medicine reports 2010;3(2):355-9.
2010: Zenichiro Kato; Wataru Morimoto; Takeshi Kimura; Akihiro Matsushima; Naomi Kondo
Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
Birth defects research. Part A, Clinical and molecular teratology 2010;88(2):132-5.
2010: Michio Ozeki; Shinji Kunishima; Kimiko Kasahara; Michinori Funato; Takahide Teramoto; Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo
A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimers.
Thrombosis research 2010;125(2):e17-22.
2010: Hideo Kaneko; Takahide Teramoto; Masashi Kondo; H Morita; H Ohnishi; K Orii; Eiko Matsui; Naomi Kondo
Efficacy of the slow dose-up method for specific oral tolerance induction in children with cow's milk allergy: comparison with reported protocols.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2010;20(6):538-9.
2010: Naomi Kondo; Eiko Matsui; Akane Nishimura; Hideo Kaneko
Pharmacogenetics of asthma in children.
Allergy, asthma & immunology research 2010;2(1):14-9.
2009: Naomi Kondo
[Kindly medicine for the allergic patients and the Earth].
Arerugī = [Allergy] 2009;58(12):1581-90.
2009: Zenichiro Kato; Kenji E Orii; Masahiro Morimoto; Hideo Sasai; Michinori Funato; Seiko Sawatari; Hideaki Kuwabara; Naomi Kondo
A transient lesion in the corpus callosum during rotavirus infection.
Pediatric neurology 2009;41(6):467-9; author reply 469.
2009: Hidenori Ohnishi; Zenichiro Kato; Takahide Teramoto; Michinori Funato; Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo
[Diagnostic approach for the autoinflammatory syndromes based on the molecular mechanism of innate immunity].
Arerugī = [Allergy] 2009;58(11):1502-12.
2009: Zenichiro Kato; Atsushi Yamagishi; Mitsuhiro Nakamura; Naomi Kondo
Theophylline-associated status epilepticus in an infant: pharmacokinetics and the risk of suppository use.
World journal of pediatrics : WJP 2009;5(4):316-8.
2009: Michinori Funato; Hiroki Kato; Hideo Sasai; Kazuo Kubota; Michio Ozeki; Zenichiro Kato; Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo
Diffuse large B-cell lymphoma presenting with osteolytic lesions in the bilateral femur.
European journal of haematology 2009;83(5):502.
2009: Michio Ozeki; Zenichiro Kato; Hideo Sasai; Kazuo Kubota; Michinori Funato; Kenji Orii; Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo
Congenital inner ear malformations without sensorineural hearing loss in children.
International journal of pediatric otorhinolaryngology 2009;73(10):1484-7.
2009: Zenichiro Kato; Miho Okuda; Yu Okumura; Takahiro Arai; Takahide Teramoto; Masaaki Nishimura; Hideo Kaneko; Naomi Kondo
Oral administration of the thyrotropin-releasing hormone (TRH) analogue, taltireline hydrate, in spinal muscular atrophy.
Journal of child neurology 2009;24(8):1010-2.
2009: Michinori Funato; Toshiyuki Fukao; Hideo Sasai; Tomohiro Hori; Daisuke Terazawa; Michio Ozeki; Kenji Orii; Takahide Teramoto; Hideo Kaneko; Naomi Kondo
Translocation (1;10)(p34;p15) in infant acute myeloid leukemia with extramedullary infiltration in multiple sites.
Cancer genetics and cytogenetics 2009;192(2):86-9.
2009: Hidenori Ohnishi; Hidehito Tochio; Zenichiro Kato; Kenji E Orii; Ailian Li; Takeshi Kimura; Hidekazu Hiroaki; Naomi Kondo; Masahiro Shirakawa
Structural basis for the multiple interactions of the MyD88 TIR domain in TLR4 signaling.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(25):10260-5.
2009: Hideo Kaneko; Hiroko Suzuki; Naomi Kondo
[IgA subclass and IgA deficiency].
Nihon Rinshō Men'eki Gakkai kaishi = Japanese journal of clinical immunology 2009;32(3):142-8.
2009: Hiroko Suzuki; Hideo Kaneko; Toshiyuki Fukao; Rong Jin; Norio Kawamoto; Tsutomu Asano; Eiko Matsui; Kimiko Kasahara; Naomi Kondo
Various expression patterns of alpha1 and alpha2 genes in IgA deficiency.
Allergology international : official journal of the Japanese Society of Allergology 2009;58(1):111-7.
2009: Masahiro Morimoto; Eiko Matsui; Norio Kawamoto; Satomi Sakurai; Hideo Kaneko; Toshiyuki Fukao; Shinichi Iwasa; Makoto Shiraki; Kimiko Kasahara; Naomi Kondo
Age-related changes of transforming growth factor beta1 in Japanese children.
Allergology international : official journal of the Japanese Society of Allergology 2009;58(1):97-102.
2009: Pierre-Olivier Frappart; youngsoo Lee; Helen R Russell; Nader Chalhoub; Yong-Dong Wang; Kenji E Orii; Jingfeng Zhao; Naomi Kondo; Suzanne J Baker; Peter J McKinnon
Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(6):1880-5.
2009: Takahide Teramoto; Toshiyuki Fukao; Kouichiro Hirayama; Tsutomu Asano; Yusuke Aoki; Naomi Kondo
Escherichia coli O-157-induced hemolytic uremic syndrome: Usefulness of SCWP score for the prediction of neurological complication.
Pediatrics international : official journal of the Japan Pediatric Society 2009;51(1):107-9.
2009: Izumi Kuratsubo; Yasuyuki Suzuki; Koji O Orii; Tomomi Kato; Tadao Orii; Naomi Kondo
Psychological status of patients with mucopolysaccharidosis type II and their parents.
Pediatrics international : official journal of the Japan Pediatric Society 2009;51(1):41-7.
2009: Zenichiro Kato; Mitsuhiro Nakamura; Yuka Yamagishi; Takahide Teramoto; Naomi Kondo
Pediatric thioridazine poisoning as a result of a pharmacy compounding error.
Pediatric reports 2009;1(1):e9.
2009: Toshiyuki Fukao; Masashi Kondo; Takahiro Yamamoto; Kenji E Orii; Naomi Kondo
Comparison of mitochondrial A3243G mutation loads in easily accessible samples from a family with maternally inherited diabetes and deafness.
Molecular medicine reports 2009;2(1):69-72.
2008: Takeshi Kimura; Zenichiro Kato; Hidenori Ohnishi; Hidehito Tochio; Masahiro Shirakawa; Naomi Kondo
Expression, purification and structural analysis of human IL-18 binding protein: a potent therapeutic molecule for allergy.
Allergology international : official journal of the Japanese Society of Allergology 2008;57(4):367-76.
2008: Takahiro Arai; Hideo Kaneko; Hidenori Ohnishi; Eiko Matsui; Toshiyuki Fukao; Norio Kawamoto; Kimiko Kasahara; Naomi Kondo
Hypothermia augments NF-kappaB activity and the production of IL-12 and IFN-gamma.
Allergology international : official journal of the Japanese Society of Allergology 2008;57(4):331-8.
2008: Minako Kawamoto; Eiko Matsui; Hideo Kaneko; Toshiyuki Fukao; Takahide Teramoto; Kimiko Kasahara; Naomi Kondo
IL-10 plays an important role as an immune-modulator in the pathogenesis of atopic diseases.
Molecular medicine reports 2008;1(6):837-42.
2008: Masashi Kondo; Hideo Kaneko; Toshiyuki Fukao; Kiyotaka Suzuki; Heima Sakaguchi; Shinji Shinoda; Zenichiro Kato; Eiko Matsui; Takahide Teramoto; Taku Nakano; Naomi Kondo
The response of bovine beta-lactoglobulin-specific T-cell clones to single amino acid substitution of T-cell core epitope.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2008;19(7):592-8.
2008: Naomi Kondo; Koichiro Hirayama; Eiko Matsui; Takahide Teramoto; Hideo Kaneko; Toshiyuki Fukao; Kenji Orii; Minako Kawamoto; Michinori Funato; Hidenori Ohnishi; Norio Kawamoto; Hideyuki Morita; Takeshi Kimura; Masatoshi Nada; Tetsuji Tokumi; Tomohiro Hori; Rinko Watanabe
[QOL questionnaire for pediatric patients with bronchial asthma and their parents or caregivers. Preparation and evaluation of the short form version 2008 (Gifu)].
Arerugī = [Allergy] 2008;57(8):1022-33.
2008: Toshiyuki Fukao; Avihu Boneh; Yusuke Aoki; Naomi Kondo
A novel single-base substitution (c.1124A>G) that activates a 5-base upstream cryptic splice donor site within exon 11 in the human mitochondrial acetoacetyl-CoA thiolase gene.
Molecular genetics and metabolism 2008;94(4):417-21.
2008: Izumi Kuratsubo; Yasuyuki Suzuki; Nobuyuki Shimozawa; Naomi Kondo
Parents of childhood X-linked adrenoleukodystrophy: high risk for depression and neurosis.
Brain & development 2008;30(7):477-82.
2008: Kenji E Orii; Toshiyuki Fukao; Xiang-Qian Song; Grant A Mitchell; Naomi Kondo
Liver-specific silencing of the human gene encoding succinyl-CoA: 3-ketoacid CoA transferase.
The Tohoku journal of experimental medicine 2008;215(3):227-36.
2008: Eiji Matsukuma; Zenichiro Kato; Koji Orii; Takahiko Asano; Kenji E Orii; Eiko Matsui; Hideo Kaneko; Naomi Kondo
Acute mumps cerebellitis with abnormal findings in MRI diffusion-weighted images.
European journal of pediatrics 2008;167(7):829-30.
2008: Michinori Funato; Hideo Kaneko; Michio Ozeki; Kaori Kanda; Toshiyuki Fukao; Naomi Kondo
Anaphylactoid transfusion reactions associated with a positively charged white-cell reduction filter: a case report.
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2008;38(3):199-201.
2008: Hiroko Suzuki; Hideo Kaneko; Jin Rong; Norio Kawamoto; Tsutomu Asano; Eiko Matsui; Kimiko Kasahara; Toshiyuki Fukao; Naomi Kondo
Induction of α1 and α2 gene expression in selective immunoglobulin A deficiency.
Molecular medicine reports 2008;1(3):395-9.
2008: Hiromichi Taneichi; Hirokazu Kanegane; Mostafa Sira; Takeshi Futatani; Kazunaga Agematsu; Masahiro Sako; Hideo Kaneko; Naomi Kondo; Tsuneyasu Kaisho; Toshio Miyawaki
Toll-like receptor signaling is impaired in dendritic cells from patients with X-linked agammaglobulinemia.
Clinical immunology (Orlando, Fla.) 2008;126(2):148-54.
2008: Rong Jin; Hideo Kaneko; Hiroko Suzuki; Takahiro Arai; Takahide Teramoto; Toshiyuki Fukao; Naomi Kondo
Age-related changes in BAFF and APRIL profiles and upregulation of BAFF and APRIL expression in patients with primary antibody deficiency.
International journal of molecular medicine 2008;21(2):233-8.
2008: Chunying Bai; Eiko Matsui; Hidenori Ohnishi; Kaori Kimata; Kimiko Kasahara; Hideo Kaneko; Zenichiro Kato; Toshiyuki Fukao; Naomi Kondo
A novel polymorphism, E254K, in the 5-lipoxygenase gene associated with bronchial asthma.
International journal of molecular medicine 2008;21(2):139-44.
2008: M Kondo; Toshiyuki Fukao; Kentaro Omoya; Norio Kawamoto; Minako Aoki; Takahide Teramoto; Hideo Kaneko; Naomi Kondo
Protein-losing enteropathy associated with egg allergy in a 5-month-old boy.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2008;18(1):63-6.
2007: Toshiyuki Fukao; Gaixiu Zhang; Marie-Odile Rolland; Marie-Therese Zabot; Nathalie Guffon; Yusuke Aoki; Naomi Kondo
Identification of an Alu-mediated tandem duplication of exons 8 and 9 in a patient with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency.
Molecular genetics and metabolism 2007;92(4):375-8.
2007: Michinori Funato; Hideo Kaneko; Michio Ozeki; Hiroko Suzuki; Kenji E Orii; Takahide Teramoto; Toshiyuki Fukao; Naomi Kondo
A positive Donath-Landsteiner test in paroxysmal cold haemoglobinuria.
European journal of haematology 2007;79(5):462.
2007: Toshiyuki Fukao; Petri Kursula; Elizabeth Patricia Owen; Naomi Kondo
Identification and characterization of a temperature-sensitive R268H mutation in the human succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene.
Molecular genetics and metabolism 2007;92(3):216-21.
2007: Adriana Montaño; Kazuko Sukegawa; Zenichiro Kato; R Carrozzo; Paola Di Natale; E Christensen; Koji O Orii; Tadao Orii; Naomi Kondo; Shunji Tomatsu
Effect of 'attenuated' mutations in mucopolysaccharidosis IVA on molecular phenotypes of N-acetylgalactosamine-6-sulfate sulfatase.
Journal of inherited metabolic disease 2007;30(5):758-67.
2007: Michio Ozeki; Michinori Funato; Kaori Kanda; Masahumi Ito; Takahide Teramoto; Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo
Clinical improvement of diffuse lymphangiomatosis with pegylated interferon alfa-2b therapy: case report and review of the literature.
Pediatric hematology and oncology 2007;24(7):513-24.
2007: YUMI AOYAMA; Kanako Asai; Kana Hioki; Michinori Funato; Naomi Kondo; Yasuo Kitajima
Herpes gestationis in a mother and newborn: immunoclinical perspectives based on a weekly follow-up of the enzyme-linked immunosorbent assay index of a bullous pemphigoid antigen noncollagenous domain.
Archives of dermatology 2007;143(9):1168-72.
2007: Toshiyuki Fukao; Gaixiu Zhang; Yusuke Aoki; Takahiro Arai; Takahide Teramoto; Hideo Kaneko; Hideo Sugie; Naomi Kondo
Identification of Alu-mediated, large deletion-spanning introns 19-26 in PHKA2 in a patient with X-linked liver glycogenosis (hepatic phosphorylase kinase deficiency).
Molecular genetics and metabolism 2007;92(1-2):179-82.
2007: Michinori Funato; Hideo Kaneko; Eiko Matsui; Takahide Teramoto; Zenichiro Kato; Toshiyuki Fukao; Kiyofumi Okusu; Naomi Kondo
Refractory osteomyelitis caused by bacille Calmette-Guérin vaccination: a case report.
Diagnostic microbiology and infectious disease 2007;59(1):89-91.
2007: Minako Aoki; Toshiyuki Fukao; Hideo Kaneko; Shingo Mizunaga; Junichi Mitsuyama; Haruki Sawamura; Mitsuru Seishima; Naomi Kondo
Clinical and bacteriological evaluation of the efficacy of piperacillin in children with pneumonia.
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 2007;13(4):224-9.
2007: Zenichiro Kato; Mitsuhiro Nakamura; Michinori Funato; Hideaki Kuwabara; Naomi Kondo
Accidental etizolam ingestion in a child.
Pediatric emergency care 2007;23(7):472-3.
2007: Keitaro Yamada; Toshiyuki Fukao; Hiroko Suzuki; Ryosuke Inoue; Tomio Kondo; Naomi Kondo
Vitamin K-deficient intracranial hemorrhage as the first symptom of cytomegalovirus hepatitis with cholestasis.
The Tohoku journal of experimental medicine 2007;212(3):335-9.
2007: Tomomi Kato; Zenichiro Kato; Izumi Kuratsubo; Tetsuo Ota; Tadao Orii; Naomi Kondo; Yasuyuki Suzuki
Evaluation of ADL in patients with Hunter disease using FIM score.
Brain & development 2007;29(5):298-305.
2007: Naomi Kondo; Shinji Shinoda; Hideo Kaneko
[The pathophysiology of food allergy].
Arerugī = [Allergy] 2007;56(5):439-43.
2007: Antti M Haapalainen; Gitte Meriläinen; Päivi L Pirilä; Naomi Kondo; Toshiyuki Fukao; Rik K Wierenga
Crystallographic and kinetic studies of human mitochondrial acetoacetyl-CoA thiolase: the importance of potassium and chloride ions for its structure and function.
Biochemistry 2007;46(14):4305-21.
2007: Satomi Sakurai; Toshiyuki Fukao; Antti M Haapalainen; Gaixiu Zhang; Keitaro Yamada; Franco Lilliu; Shoji Yano; Peter Robinson; Michael K Gibson; Ronald J A Wanders; Grant A Mitchell; Rik K Wierenga; Naomi Kondo
Kinetic and expression analyses of seven novel mutations in mitochondrial acetoacetyl-CoA thiolase (T2): identification of a Km mutant and an analysis of the mutational sites in the structure.
Molecular genetics and metabolism 2007;90(4):370-8.
2007: Masashi Kondo; Toshiyuki Fukao; Shinji Shinoda; Norio Kawamoto; Hideo Kaneko; Zenichiro Kato; Eiko Matsui; Takahide Teramoto; Taku Nakano; Naomi Kondo
Lymphocyte Responses to Chymotrypsin- or Trypsin V-Digested beta-Lactoglobulin in Patients with Cow's Milk Allergy.
Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2007;3(1):1-9.
2007: Keitaro Yamada; Toshiyuki Fukao; Gaixiu Zhang; Satomi Sakurai; Jos P N Ruiter; Ronald J A Wanders; Naomi Kondo
Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene.
Molecular genetics and metabolism 2007;90(3):291-7.
2007: Naomi Kondo
[Influence of genes and environment on allergic disorders].
Arerugī = [Allergy] 2007;56(2):94-100.
2007: Zenichiro Kato; Atsushi Yamagishi; Naomi Kondo
Interstitial deletion of 1q42.13-q43 with Duane retraction syndrome.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus 2007;11(1):62-4.
2006: K Sukegawa-Hayasaka; Zenichiro Kato; H Nakamura; Shunji Tomatsu; Toshiyuki Fukao; K Kuwata; Tadao Orii; Naomi Kondo
Effect of Hunter disease (mucopolysaccharidosis type II) mutations on molecular phenotypes of iduronate-2-sulfatase: enzymatic activity, protein processing and structural analysis.
Journal of inherited metabolic disease 2006;29(6):755-61.
2006: Gaixiu Zhang; Toshiyuki Fukao; Satomi Sakurai; Keitaro Yamada; K Michael Gibson; Naomi Kondo
Identification of Alu-mediated, large deletion-spanning exons 2-4 in a patient with mitochondrial acetoacetyl-CoA thiolase deficiency.
Molecular genetics and metabolism 2006;89(3):222-6.
2006: Toshiyuki Fukao; Satomi Sakurai; Marie-Odile Rolland; Marie-Therese Zabot; Andreas Schulze; Keitaro Yamada; Naomi Kondo
A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency.
Molecular genetics and metabolism 2006;89(3):280-2.
2006: Tomomi Kato; Koji Isogai; Koji O Orii; Izumi Kuratsubo; Naomi Kondo; Tadao Orii; Yasuyuki Suzuki
Portal hypertension in a patient with Hunter disease.
Journal of inherited metabolic disease 2006;29(5):686.
2006: Naomi Kondo; Kazuhito Fukuda
[Ataxia-telangiectasia].
Nihon rinsho. Japanese journal of clinical medicine 2006;Suppl 3():114-8.
2006: Takahide Teramoto; Toshiyuki Fukao; Yoshiko Tomita; Yoshiaki Terauchi; Kaori Hosoi; Eiko Matsui; Minako Aoki; Naomi Kondo; Haruki Mikawa
Pharmacokinetics of beclomethasone dipropionate in an hydrofluoroalkane-134a propellant system in Japanese children with bronchial asthma.
Allergology international : official journal of the Japanese Society of Allergology 2006;55(3):317-20.
2006: Naomi Kondo; Toshio Katsunuma; Yasuhei Odajima; Akihiro Morikawa
A randomized open-label comparative study of montelukast versus theophylline added to inhaled corticosteroid in asthmatic children.
Allergology international : official journal of the Japanese Society of Allergology 2006;55(3):287-93.
2006: Hideo Kaneko; Eiko Matsui; Tsutomu Asano; Zenichiro Kato; Takahide Teramoto; Minako Aoki; Norio Kawamoto; Li Ai Lian; Kimiko Kasahara; Naomi Kondo
Suppression of IFN-gamma production in atopic group at the acute phase of RSV infection.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2006;17(5):370-5.
2006: Hiroko Horikoshi; Zenichiro Kato; Mitsuo Masuno; Takahiko Asano; Tomoko Nagase; Yuka Yamagishi; Ryo Kozawa; Takahiro Arai; Minako Aoki; Takahide Teramoto; Kentaro Omoya; Naomichi Matsumoto; Naohiro Kurotaki; Osamu Shimokawa; Kenji Kurosawa; Naomi Kondo
Neuroradiologic findings in Sotos syndrome.
Journal of child neurology 2006;21(7):614-8.
2006: Kenji E Orii; youngsoo Lee; Naomi Kondo; Peter J McKinnon
Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(26):10017-22.
2006: Hideo Kaneko; Koji Isogai; Masashi Kondo; Kaori Hosoi; Tsutomu Asano; Michinori Funato; Naomi Kondo
Autologous peripheral blood stem cell transplantation in a patient with relapsed pleuropulmonary blastoma.
Journal of pediatric hematology/oncology 2006;28(6):383-5.
2006: Michinori Funato; Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Yasuyuki Suzuki; Yoshihiko Imamura; Tadashi Matsumoto; Toshiro Tsukamoto; Tomoko Kojidani; Takashi Osumi; Toshiyuki Fukao; Naomi Kondo
Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies.
Brain & development 2006;28(5):287-92.
2006: Hideo Kaneko; Eiko Matsui; Shinnji Shinoda; Norio Kawamoto; Yosikazu Nakamura; Ritei Uehara; Nobuo Matsuura; Masatoshi Morita; Hiroshi Tada; Naomi Kondo
Effects of dioxins on the quantitative levels of immune components in infants.
Toxicology and industrial health 2006;22(3):131-6.
2006: Eiji Matsukuma; Zenichiro Kato; Kentaro Omoya; Kazuyuki Hashimoto; Ailian Li; Yutaka Yamamoto; Hidenori Ohnishi; Hidenori Hiranuma; Hisakazu Komine; Naomi Kondo
Development of fluorescence-linked immunosorbent assay for high throughput screening of interferon-gamma.
Allergology international : official journal of the Japanese Society of Allergology 2006;55(1):49-54.
2006: Norio Kawamoto; Hideo Kaneko; Masao Takemura; Mitsuru Seishima; Satomi Sakurai; Toshiyuki Fukao; Kimiko Kasahara; Shinichi Iwasa; Naomi Kondo
Age-related changes in intracellular cytokine profiles and Th2 dominance in allergic children.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2006;17(2):125-33.
2006: Zenichiro Kato; Takahiko Asano; Naomi Kondo
Inosiplex affects the spectra of proton magnetic resonance spectroscopy in subacute sclerosing panencephalitis.
Journal of child neurology 2006;21(2):177-8.
2005: Naomi Kondo; Soichiro Nagaya; Manami Kuwabara; Eiko Matsui
[Genetic testing and gene-based testing forAllergic disorders].
Nihon rinsho. Japanese journal of clinical medicine 2005;63 Suppl 12():232-9.
2005: Zenichiro Kato; Kohji Tsubouchi; Naomi Kondo
Molluscum contagiosum prevents progression of staphylococcal scalded skin syndrome.
European journal of pediatrics 2005;164(12):768-9.
2005: Kaori Yoshikawa; Eiko Matsui; Hideo Kaneko; Toshiyuki Fukao; Ryosuke Inoue; Takahide Teramoto; Shinji Shinoda; Osamu Fukutomi; Minako Aoki; Kimiko Kasahara; Naomi Kondo
A novel single-nucleotide substitution, Glu 4 Lys, in the leukotriene C4 synthase gene associated with allergic diseases.
International journal of molecular medicine 2005;16(5):827-31.
2005: Koji O Orii; Jeffrey H Grubb; Carole Vogler; Beth Levy; Yun Tan; Kamelia Markova; Beverly L Davidson; Q Mao; Tadao Orii; Naomi Kondo; William S Sly
Defining the pathway for Tat-mediated delivery of beta-glucuronidase in cultured cells and MPS VII mice.
Molecular therapy : the journal of the American Society of Gene Therapy 2005;12(2):345-52.
2005: Kazuyuki Hashimoto; Zenichiro Kato; Tomoko Nagase; Nobuyuki Shimozawa; Kazuo Kuwata; Kentaro Omoya; Ailian Li; Eiji Matsukuma; Yutaka Yamamoto; Hidenori Ohnishi; Hidehito Tochio; Masahiro Shirakawa; Yasuyuki Suzuki; Ronald J A Wanders; Naomi Kondo
Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder.
Pediatric research 2005;58(2):263-9.
2005: Masashi Kondo; Toshiyuki Fukao; Takahide Teramoto; Hideo Kaneko; Yukitoshi Takahashi; Hiroyuki Okamoto; Naomi Kondo
A common variable immunodeficient patient who developed acute disseminated encephalomyelitis followed by the Lennox-Gastaut syndrome.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2005;16(4):357-60.
2005: Hideo Kaneko; Norio Kawamoto; Tsutomu Asano; Y Mabuchi; H Horikoshi; Takahide Teramoto; Eiko Matsui; M Kondo; Toshiyuki Fukao; Kimiko Kasahara; Naomi Kondo
Leaky phenotype of X-linked agammaglobulinaemia in a Japanese family.
Clinical and experimental immunology 2005;140(3):520-3.
2005: Naomi Kondo; Hideo Kaneko; Manami Kuwabara
[Classification of immunodeficiency diseases].
Nihon rinsho. Japanese journal of clinical medicine 2005;63 Suppl 5():548-58.
2005: Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Michinori Funato; Naomi Kondo; Yasuyuki Suzuki
Molecular and neurologic findings of peroxisome biogenesis disorders.
Journal of child neurology 2005;20(4):326-9.
2005: Petri Kursula; Herkko Sikkilä; Toshiyuki Fukao; Naomi Kondo; Rik K Wierenga
High resolution crystal structures of human cytosolic thiolase (CT): a comparison of the active sites of human CT, bacterial thiolase, and bacterial KAS I.
Journal of molecular biology 2005;347(1):189-201.
2005: Tomomi Kato; Zenichiro Kato; Izumi Kuratsubo; Noboru Tanaka; Tabito Ishigami; Jun-Ichi Kajihara; Kazuko Sukegawa-Hayasaka; Koji O Orii; Koji Isogai; Toshiyuki Fukao; Nobuyuki Shimozawa; Tadao Orii; Naomi Kondo; Yasuyuki Suzuki
Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II.
Journal of human genetics 2005;50(8):395-402.
2005: M Kondo; K Suzuki; Ryosuke Inoue; H Sakaguchi; Eiji Matsukuma; Zenichiro Kato; Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo
Characterization of T-cell clones specific to ovomucoid from patients with egg-white allergy.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2005;15(2):107-11.
2004: Toshiyuki Fukao; Haruo Shintaku; Ryou Kusubae; Gai Xiu Zhang; Kozue Nakamura; Masashi Kondo; Naomi Kondo
Patients homozygous for the T435N mutation of succinyl-CoA:3-ketoacid CoA Transferase (SCOT) do not show permanent ketosis.
Pediatric research 2004;56(6):858-63.
2004: M Nagao-Watanabe; Toshiyuki Fukao; Eiko Matsui; Hideo Kaneko; R Inoue; Norio Kawamoto; Kimiko Kasahara; M Nagai; Y Ichiki; Y Kitajima; Naomi Kondo
Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case.
Clinical genetics 2004;66(3):236-8.
2004: Hideo Kaneko; Koji Isogai; Toshiyuki Fukao; Eiko Matsui; Kimiko Kasahara; Akihiro Yachie; Hidetoshi Seki; Shoichi Koizumi; Masami Arai; Joji Utunomiya; Yoshio Miki; Naomi Kondo
Relatively common mutations of the Bloom syndrome gene in the Japanese population.
International journal of molecular medicine 2004;14(3):439-42.
2004: Kentaro Omoya; Zenichiro Kato; Eiji Matsukuma; Ailian Li; Kazuyuki Hashimoto; Yutaka Yamamoto; Hidenori Ohnishi; Naomi Kondo
Systematic optimization of active protein expression using GFP as a folding reporter.
Protein expression and purification 2004;36(2):327-32.
2004: Shunji Tomatsu; Mirella Filocamo; Koji O Orii; William S Sly; Monica A Gutierrez; Tatsuo Nishioka; Olga Peña Serrato; Paola Di Natale; Adriana Montaño; Seiji Yamaguchi; Naomi Kondo; Tadao Orii; Akihiko Noguchi
Mucopolysaccharidosis IVA (Morquio A): identification of novel common mutations in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene in Italian patients.
Human mutation 2004;24(2):187-8.
2004: Gai Xiu Zhang; Toshiyuki Fukao; Marie-Odile Rolland; Marie-Therese Zabot; Gilles Renom; Elias Touma; Masashi Kondo; Naoki Matsuo; Naomi Kondo
Mitochondrial acetoacetyl-CoA thiolase (T2) deficiency: T2-deficient patients with "mild" mutation(s) were previously misinterpreted as normal by the coupled assay with tiglyl-CoA.
Pediatric research 2004;56(1):60-4.
2004: Shunji Tomatsu; Koji O Orii; Y Bi; Monica A Gutierrez; Tatsuo Nishioka; Seiji Yamaguchi; Naomi Kondo; Tadao Orii; Akihiko Noguchi; William S Sly
General implications for CpG hot spot mutations: methylation patterns of the human iduronate-2-sulfatase gene locus.
Human mutation 2004;23(6):590-8.
2004: Nobuyuki Shimozawa; Toshiro Tsukamoto; Tomoko Nagase; Yasuhiko Takemoto; Naoki Koyama; Yasuyuki Suzuki; Masayuki Komori; Takashi Osumi; Gootjes Jeannette; Ronald J A Wanders; Naomi Kondo
Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene.
Human mutation 2004;23(6):552-8.
2004: Hideo Kaneko; Naomi Kondo
Clinical features of Bloom syndrome and function of the causative gene, BLM helicase.
Expert review of molecular diagnostics 2004;4(3):393-401.
2004: T Asano; Hideo Kaneko; T Terada; Y Kasahara; Toshiyuki Fukao; Kimiko Kasahara; Naomi Kondo
Molecular analysis of B-cell differentiation in selective or partial IgA deficiency.
Clinical and experimental immunology 2004;136(2):284-90.
2004: Yutaka Yamamoto; Zenichiro Kato; Eiji Matsukuma; Ailian Li; Kentaro Omoya; Kazuyuki Hashimoto; Hidenori Ohnishi; Naomi Kondo
Generation of highly stable IL-18 based on a ligand-receptor complex structure.
Biochemical and biophysical research communications 2004;317(1):181-6.
2004: Shunji Tomatsu; Kazuo Okamura; Takeshi Taketani; Koji O Orii; Tatsuo Nishioka; Monica A Gutierrez; Susana Velez-Castrillon; Angela Aguirres Fachel; Jeffrey H Grubb; Alan Cooper; Margaret Thornley; Ed Wraith; Luis A Barrera; Roberto Giugliani; Ida V Schwartz; Gudrun Schulze Frenking; Michael Beck; Susanne Kircher; Eduard Paschke; Seiji Yamaguchi; Kurt Ullrich; Koji Isogai; Yasuyuki Suzuki; Tadao Orii; Naomi Kondo; Michael Creer; Akihiko Noguchi
Development and testing of new screening method for keratan sulfate in mucopolysaccharidosis IVA.
Pediatric research 2004;55(4):592-7.
2004: Tomoko Nagase; Nobuyuki Shimozawa; Yasuhiko Takemoto; Yasuyuki Suzuki; Masayuki Komori; Naomi Kondo
Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes.
Biochimica et biophysica acta 2004;1671(1-3):26-33.
2004: Naomi Kondo; Eiko Matsui; Hideo Kaneko; Minako Aoki; Zenichiro Kato; Toshiyuki Fukao; Kimiko Kasahara; N Morimoto
RNA editing of interleukin-12 receptor beta2, 2451 C-to-U (Ala 604 Val) conversion, associated with atopy.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2004;34(3):363-8.
2004: Toshiyuki Fukao; Philip Chen; Jun Ren; Hideo Kaneko; Gai Xiu Zhang; Masahi Kondo; Ken-Ichi Yamamoto; Yasuhiro Furuichi; Shunichi Takeda; Naomi Kondo; Martin F Lavin
Disruption of the BLM gene in ATM-null DT40 cells does not exacerbate either phenotype.
Oncogene 2004;23(8):1498-506.
2004: Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo
The function of RecQ helicase gene family (especially BLM) in DNA recombination and joining.
Advances in biophysics 2004;38():45-64.
2003: Shunji Tomatsu; Koji O Orii; Carole Vogler; Jun Nakayama; Beth Levy; Jeffrey H Grubb; Monica A Gutierrez; Soomin Shim; Seiji Yamaguchi; Tatsuo Nishioka; Adriana Montaño; Akihiko Noguchi; Tadao Orii; Naomi Kondo; William S Sly
Mouse model of N-acetylgalactosamine-6-sulfate sulfatase deficiency (Galns-/-) produced by targeted disruption of the gene defective in Morquio A disease.
Human molecular genetics 2003;12(24):3349-58.
2003: Tomoyoshi Terada; Hideo Kaneko; Toshiyuki Fukao; Takahide Teramoto; T Asano; AL Li; Kimiko Kasahara; Naomi Kondo
Semiquantitative evaluation of mRNAs for the membranous form of immunoglobulin heavy chain is useful for investigating the etiology in CVID.
Scandinavian journal of immunology 2003;58(6):649-54.
2003: Ailian Li; Zenichiro Kato; Hidenori Ohnishi; Kazuyuki Hashimoto; Eiji Matsukuma; Kentaro Omoya; Yutaka Yamamoto; Naomi Kondo
Optimized gene synthesis and high expression of human interleukin-18.
Protein expression and purification 2003;32(1):110-8.
2003: Zenichiro Kato; Jun-Goo Jee; Hiroaki Shikano; Masaki Mishima; ohki izuru; Hidenori Ohnishi; Ailian Li; Kazuyuki Hashimoto; Eiji Matsukuma; Kentaro Omoya; Yutaka Yamamoto; Teruyo Yoneda; Takane Hara; Naomi Kondo; Masahiro Shirakawa
The structure and binding mode of interleukin-18.
Nature structural biology 2003;10(11):966-71.
2003: Zenichiro Kato; Ryo Kozawa; Takahide Teramoto; Kazuyuki Hashimoto; Shinji Shinoda; Naomi Kondo
Acute cerebellitis in primary human herpesvirus-6 infection.
European journal of pediatrics 2003;162(11):801-3.
2003: Yukiko Kasahara; Hideo Kaneko; Toshiyuki Fukao; Tomoyoshi Terada; Tsutomu Asano; Kimiko Kasahara; Naomi Kondo
Hyper-IgM syndrome with putative dominant negative mutation in activation-induced cytidine deaminase.
The Journal of allergy and clinical immunology 2003;112(4):755-60.
2003: Yasuhiko Takemoto; Yasuyuki Suzuki; Ryoko Horibe; Nobuyuki Shimozawa; Ronald J A Wanders; Naomi Kondo
Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders.
Brain & development 2003;25(7):481-7.
2003: Naomi Matsumoto; Shigehiko Tamura; Satomi Furuki; Non Miyata; Ann B Moser; Nobuyuki Shimozawa; Hugo W Moser; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
American journal of human genetics 2003;73(2):233-46.
2003: Minako Aoki; Eiko Matsui; Hideo Kaneko; Ryosuke Inoue; Toshiyuki Fukao; Mizuho Watanabe; Takahide Teramoto; Zenichiro Kato; Kiyotaka Suzuki; Yasuyuki Suzuki; Kimiko Kasahara; Naomi Kondo
A novel single-nucleotide substitution, Leu 467 Pro, in the interferon-gamma receptor 1 gene associated with allergic diseases.
International journal of molecular medicine 2003;12(2):185-91.
2003: Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Toshihiro Ohura; Yasuyuki Suzuki; Naomi Kondo
Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation.
American journal of medical genetics. Part A 2003;120A(1):40-3.
2003: Adriana Montaño; Ilkka Kaitila; Kazuko Sukegawa; Shunji Tomatsu; Zenichiro Kato; Haruki Nakamura; Seiji Fukuda; Tadao Orii; Naomi Kondo
Mucopolysaccharidosis IVA: characterization of a common mutation found in Finnish patients with attenuated phenotype.
Human genetics 2003;113(2):162-9.
2003: Toshiyuki Fukao; Naoki Matsuo; Gai Xiu Zhang; Rintaro Urasawa; Tetsuo Kubo; Yoshinori Kohno; Naomi Kondo
Single base substitutions at the initiator codon in the mitochondrial acetoacetyl-CoA thiolase (ACAT1/T2) gene result in production of varying amounts of wild-type T2 polypeptide.
Human mutation 2003;21(6):587-92.
2003: Shunji Tomatsu; Koji O Orii; Carole Vogler; Jeffrey H Grubb; Elizabeth Snella; Monica Gutierrez; Tatiana Dieter; Christopher C Holden; Kazuko Sukegawa; Tadao Orii; Naomi Kondo; William S Sly
Production of MPS VII mouse (Gus(tm(hE540A x mE536A)Sly)) doubly tolerant to human and mouse beta-glucuronidase.
Human molecular genetics 2003;12(9):961-73.
2003: Zenichiro Kato; Ryo Kozawa; Kazuyuki Hashimoto; Naomi Kondo
Transient lesion in the splenium of the corpus callosum in acute cerebellitis.
Journal of child neurology 2003;18(4):291-2.
2003: Takahide Teramoto; Hideo Kaneko; Michinori Funato; Hirofumi Sawa; Kazuo Nagashima; Yoshinobu Hirose; Naomi Kondo
Progressive multifocal leukoencephalopathy in a patient with X-linked agammaglobulinemia.
Scandinavian journal of infectious diseases 2003;35(11-12):909-10.
2003: Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Yasuyuki Suzuki; Naomi Kondo
Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.
Advances in experimental medicine and biology 2003;544():71.
2003: Toshiyuki Fukao; Gai Xiu Zhang; N Sakura; T Kubo; H Yamaga; A Hazama; Yoshinori Kohno; N Matsuo; M Kondo; Seiji Yamaguchi; Y Shigematsu; Naomi Kondo
The mitochondrial acetoacetyl-CoA thiolase (T2) deficiency in Japanese patients: urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T2-deficient patients with some residual T2 activity.
Journal of inherited metabolic disease 2003;26(5):423-31.
2002: Shunji Tomatsu; Koji O Orii; Carole Vogler; Jeffrey H Grubb; Elizabeth Snella; Monica A Gutierrez; Tatiana Dieter; Kazuko Sukegawa; Tadao Orii; Naomi Kondo; William S Sly
Missense models [Gustm(E536A)Sly, Gustm(E536Q)Sly, and Gustm(L175F)Sly] of murine mucopolysaccharidosis type VII produced by targeted mutagenesis.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(23):14982-7.
2002: Zenichiro Kato; Kyoko Saito; Michiko Yamada; Takahiko Asano; Naomi Kondo
Proton magnetic resonance spectroscopy in a case of subacute sclerosing panencephalitis.
Journal of child neurology 2002;17(10):788-90.
2002: Heather Beamish; Padmini Kedar; Hideo Kaneko; Philip Chen; Toshiyuki Fukao; Cheng Peng; Sergei Beresten; Nuri Gueven; David Purdie; Susan Lees-Miller; Nathan Ellis; Naomi Kondo; Martin F Lavin
Functional link between BLM defective in Bloom's syndrome and the ataxia-telangiectasia-mutated protein, ATM.
The Journal of biological chemistry 2002;277(34):30515-23.
2002: K Suzuki; Ryosuke Inoue; H Sakaguchi; Minako Aoki; Zenichiro Kato; Hideo Kaneko; S Matsushita; Naomi Kondo
The correlation between ovomucoid-derived peptides, human leucocyte antigen class II molecules and T cell receptor-complementarity determining region 3 compositions in patients with egg-white allergy.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2002;32(8):1223-30.
2002: Wataru Morimoto; Hideo Kaneko; Koji Isogai; Kimiko Kasahara; Naomi Kondo
Expression of BLM (the causative gene for Bloom syndrome) and screening of Bloom syndrome.
International journal of molecular medicine 2002;10(1):95-9.
2002: Kenji E Orii; Zenichiro Kato; Fukutomi Osamu; Michinori Funato; Uniko Kubodera; Ryosuke Inoue; Nobuyuki Shimozawa; Naomi Kondo
Changes of autonomic nervous system function in patients with breath-holding spells treated with iron.
Journal of child neurology 2002;17(5):337-40.
2002: Naomi Kondo; Takahide Teramoto; Ryosuke Inoue; Osamu Fukutomi; Eiko Matsui; Shinji Shinoda; Mizuho Watanabe; Heima Sakaguchi; Minako Aoki; Wataru Morimoto; Kiyotaka Suzuki; Hidenori Ohnishi; Yasuhiko Takemoto; Yoko Tanaka; Tsutomu Asano; Kaori Yoshikawa; Tomoko Nagase; Kazuyuki Hashimoto; Yukiko Fujita; Yutaka Yamamoto; Airen Ri; Khoichirou Hirayama
[Evaluation before and after pranlukast administration with the QOL questionnaire (revised version 2001) for pediatric patients with bronchial asthma and their parents or caregivers].
Arerugī = [Allergy] 2002;51(5):421-9.
2002: Zenichiro Kato; Michinori Funato; Kenji E Orii; Kayoko Saito; Naomi Kondo
Spinal muscular atrophy type 1 with anti-acetylcholine receptor antibody.
European journal of pediatrics 2002;161(5):293-4.
2002: H Sakaguchi; Ryosuke Inoue; Hideo Kaneko; Mizuho Watanabe; K Suzuki; Zenichiro Kato; S Matsushita; Naomi Kondo
Interaction among human leucocyte antigen-peptide-T cell receptor complexes in cow's milk allergy: the significance of human leucocyte antigen and T cell receptor-complementarity determining region 3 loops.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2002;32(5):762-70.
2002: Mizuho Watanabe; Hideo Kaneko; Hiroaki Shikano; Minako Aoki; Heima Sakaguchi; Eiko Matsui; Ryosuke Inoue; Zenichiro Kato; Kimiko Kasahara; Osamu Fukutomi; Tomio Kondo; Naomi Kondo
Predominant expression of 950delCAG of IL-18R alpha chain cDNA is associated with reduced IFN-gamma production and high serum IgE levels in atopic Japanese children.
The Journal of allergy and clinical immunology 2002;109(4):669-75.
2002: Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Yasuyuki Suzuki; Yukio Fujiki; Ronald J A Wanders; Naomi Kondo
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.
Biochemical and biophysical research communications 2002;292(1):109-12.
2002: Toshiyuki Fukao; Haruki Nakamura; Kozue Nakamura; Celia Perez-Cerda; Antonio Baldellou; Carlos R Barrionuevo; Francisco Girona Castello; Yoshinori Kohno; Magdalena Ugarte; Naomi Kondo
Characterization of six mutations in five Spanish patients with mitochondrial acetoacetyl-CoA thiolase deficiency: effects of amino acid substitutions on tertiary structure.
Molecular genetics and metabolism 2002;75(3):235-43.
2002: Shunji Tomatsu; Koji O Orii; M Rafiq Islam; Gul N Shah; Jeffrey H Grubb; Kazuko Sukegawa; Yasuyuki Suzuki; Tadao Orii; Naomi Kondo; William S Sly
Methylation patterns of the human beta-glucuronidase gene locus: boundaries of methylation and general implications for frequent point mutations at CpG dinucleotides.
Genomics 2002;79(3):363-75.
2002: Zenichiro Kato; Osamu Fukutomi; Naomi Kondo
Intrinsic factors for unbound theophylline.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2002;12(3):217-9.
2002: Yasuhiko Takemoto; Yasuyuki Suzuki; Akiko Tamakoshi; Osamu Onodera; Shoji Tsuji; Takashi Hashimoto; Nobuyuki Shimozawa; Tadao Orii; Naomi Kondo
Epidemiology of X-linked adrenoleukodystrophy in Japan.
Journal of human genetics 2002;47(11):590-3.
2002: Hideo Kaneko; Ryosuke Inoue; Takahide Teramoto; Wataru Morimoto; Koji Isogai; Kimiko Kasahara; Naomi Kondo
Detection of the genes induced in activated lymphocytes by modified differential display.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2002;12(2):86-90.
2002: Yasuyuki Suzuki; Mizue Iai; Atsushi Kamei; Yuzo Tanabe; Shoichi Chida; Seiji Yamaguchi; Zhongyi Zhang; Yasuhiko Takemoto; Nobuyuki Shimozawa; Naomi Kondo
Peroxisomal acyl CoA oxidase deficiency.
The Journal of pediatrics 2002;140(1):128-30.
2001: Yukitoshi Takahashi; T Sato; K Goto; M Fujino; T Fujiwara; M Yamaga; T Ito; Hideo Isono; Naomi Kondo
Optical filters inhibiting television-induced photosensitive seizures.
Neurology 2001;57(10):1767-73.
2001: Gabriele Toietta; Giovanni Maria Severini; Catia Traversari; Shunji Tomatsu; Kazuko Sukegawa; Seiji Fukuda; Naomi Kondo; paolo tortora; Claudio Bordignon
Various cells retrovirally transduced with N-acetylgalactosoamine-6-sulfate sulfatase correct Morquio skin fibroblasts in vitro.
Human gene therapy 2001;12(16):2007-16.
2001: Tomoyoshi Terada; Hideo Kaneko; AL Li; Kimiko Kasahara; M Ibe; S Yokota; Naomi Kondo
Analysis of Ig subclass deficiency: First reported case of IgG2, IgG4, and IgA deficiency caused by deletion of C alpha 1, psi C gamma, C gamma 2, C gamma 4, and C epsilon in a Mongoloid patient.
The Journal of allergy and clinical immunology 2001;108(4):602-6.
2001: Yasuyuki Suzuki; Nobuyuki Shimozawa; Tadao Orii; Toshiro Tsukamoto; Takashi Osumi; Yukio Fujiki; Naomi Kondo
Genetic and molecular bases of peroxisome biogenesis disorders.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(5):372-6.
2001: Hideo Kaneko; Wataru Morimoto; Toshiyuki Fukao; Kimiko Kasahara; Naomi Kondo
Telomerase activity in cell lines and lymphoma originating from Bloom syndrome.
Leukemia & lymphoma 2001;42(4):757-60.
2001: Naomi Kondo; Ryosuke Inoue; Eiko Matsui; Shinji Shinoda; Osamu Fukutomi; Takahide Teramoto; Mizuho Watanabe; Heima Sakaguchi; Minako Aoki; Khoichirou Hirayama
[QOL questionnaire version 2001 for pediatric patients with bronchial asthma and their parents or caregivers--preparation and evaluation].
Arerugī = [Allergy] 2001;50(8):667-78.
2001: Hiroaki Shikano; Zenichiro Kato; Hideo Kaneko; Mizuho Watanabe; Ryosuke Inoue; Kimiko Kasahara; M Takemura; Naomi Kondo
IFN-gamma production in response to IL-18 or IL-12 stimulation by peripheral blood mononuclear cells of atopic patients.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2001;31(8):1263-70.
2001: Naomi Kondo; Eiko Matsui; Hideo Kaneko; Toshiyuki Fukao; Takahide Teramoto; Ryosuke Inoue; Mizuho Watanabe; Minako Aoki; Kimiko Kasahara; N Morimoto
Atopy and mutations of IL-12 receptor beta 2 chain gene.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2001;31(8):1189-93.
2001: Shigehiko Tamura; Naomi Matsumoto; A Imamura; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
The Biochemical journal 2001;357(Pt 2):417-26.
2001: Ryosuke Inoue; S Matsushita; Hideo Kaneko; S Shinoda; H Sakaguchi; Y Nishimura; Naomi Kondo
Identification of beta-lactoglobulin-derived peptides and class II HLA molecules recognized by T cells from patients with milk allergy.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2001;31(7):1126-34.
2001: S Takahashi; Yukitoshi Takahashi; Naomi Kondo; Tadao Orii
Epileptic seizures and structural abnormalities in a patient with holoprosencephaly.
Brain & development 2001;23(4):264-8.
2001: Yasuyuki Suzuki; Nobuyuki Shimozawa; A Imamura; Seiji Fukuda; Zhongyi Zhang; Tadao Orii; Naomi Kondo
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.
Journal of inherited metabolic disease 2001;24(2):151-65.
2001: Yukitoshi Takahashi; Kazuko Sukegawa; M Aoki; A Ito; K Suzuki; H Sakaguchi; M Watanabe; Koji Isogai; S Mizuno; Hiroaki Hoshi; Kazuo Kuwata; Shunji Tomatsu; S Kato; T Ito; Naomi Kondo; Tadao Orii
Evaluation of accumulated mucopolysaccharides in the brain of patients with mucopolysaccharidoses by (1)H-magnetic resonance spectroscopy before and after bone marrow transplantation.
Pediatric research 2001;49(3):349-55.
2001: Yasuyuki Suzuki; A Imamura; Nobuyuki Shimozawa; Naomi Kondo
The clinical course of childhood and adolescent adrenoleukodystrophy before and after Lorenzo's oil.
Brain & development 2001;23(1):30-3.
2001: Yukitoshi Takahashi; T Ozawa; H Nakamura; S Yamada; H Okamoto; S Yajima; K Goto; Naomi Kondo
Long-wavelength red light emission from TV and photosensitive siezures.
Acta neurologica Scandinavica 2001;103(2):114-9.
2001: Kozue Nakamura; Toshiyuki Fukao; Celia Perez-Cerda; C Luque; XQ Song; Y Naiki; Yoshinori Kohno; Magdalena Ugarte; Naomi Kondo
A novel single-base substitution (380C>T) that activates a 5-base downstream cryptic splice-acceptor site within exon 5 in almost all transcripts in the human mitochondrial acetoacetyl-CoA thiolase gene.
Molecular genetics and metabolism 2001;72(2):115-21.
2001: Toshiyuki Fukao; C R Scriver; Naomi Kondo
The clinical phenotype and outcome of mitochondrial acetoacetyl-CoA thiolase deficiency (beta-ketothiolase or T2 deficiency) in 26 enzymatically proved and mutation-defined patients.
Molecular genetics and metabolism 2001;72(2):109-14.
2001: Toshiyuki Fukao; H Watanabe; KO Orii; Yukitoshi Takahashi; A Hirano; T Kondo; Seiji Yamaguchi; Toshifumi Aoyama; Naomi Kondo
Myopathic form of very-long chain acyl-coa dehydrogenase deficiency: evidence for temperature-sensitive mild mutations in both mutant alleles in a Japanese girl.
Pediatric research 2001;49(2):227-31.
2001: Tomoyoshi Terada; Hideo Kaneko; Toshiyuki Fukao; H Tashita; AL Li; M Takemura; Naomi Kondo
Fate of the mutated IgG2 heavy chain: lack of expression of mutated membrane-bound IgG2 on the B cell surface in selective IgG2 deficiency.
International immunology 2001;13(2):249-56.
2001: Hideo Kaneko; K E Orii; M Yamada; Ryosuke Inoue; Naomi Kondo
Long-term duration of reduced serum complement level following burn injury.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2001;11(4):303-4.
2001: Naomi Matsumoto; Shigehiko Tamura; Ann B Moser; Hugo W Moser; N Braverman; Yasuyuki Suzuki; Nobuyuki Shimozawa; Naomi Kondo; Yukio Fujiki
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.
Journal of human genetics 2001;46(5):273-7.
2001: Naomi Kondo; Eiko Matsui; Hideo Kaneko; Toshiyuki Fukao; Takahide Teramoto; Ryosuke Inoue; Mizuho Watanabe; Kimiko Kasahara; N Morimoto
Reduced interferon-gamma production and mutations of the interleukin-12 receptor beta(2) chain gene in atopic subjects.
International archives of allergy and immunology 2001;124(1-3):117-20.
2000: A Imamura; Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; Toshiro Tsukamoto; Yukio Fujiki; Tadao Orii; Takashi Osumi; Ronald J A Wanders; Naomi Kondo
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1.
Pediatric research 2000;48(4):541-5.
2000: Kamran Ghaedi; Masanori Honsho; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.
American journal of human genetics 2000;67(4):976-81.
2000: H Fujii; Osamu Fukutomi; Ryosuke Inoue; Shinji Shinoda; H Okammoto; Takahide Teramoto; Naomi Kondo; H Wada; K Saito; T Matsuoka; M Seishima
Autonomic regulation after exercise evidenced by spectral analysis of heart rate variability in asthmatic children.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 2000;85(3):233-7.
2000: S Mizuno; Yukitoshi Takahashi; Zenichiro Kato; H Goto; Naomi Kondo; H Hoshi
Magnetic resonance spectroscopy of tubers in patients with tuberous sclerosis.
Acta neurologica Scandinavica 2000;102(3):175-8.
2000: Eiko Matsui; Hideo Kaneko; Takahide Teramoto; Toshiyuki Fukao; Ryosuke Inoue; Kimiko Kasahara; M Takemura; M Seishima; Naomi Kondo
Reduced IFNgamma production in response to IL-12 stimulation and/or reduced IL-12 production in atopic patients.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2000;30(9):1250-6.
2000: Toshiyuki Fukao; Grant A Mitchell; XQ Song; Haruki Nakamura; S Kassovska-Bratinova; KE Orii; James Wraith; G T N Besley; Ronald J A Wanders; K E Niezen-Koning; Gerard T Berry; M Palmieri; Naomi Kondo
Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations.
Genomics 2000;68(2):144-51.
2000: Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; A Imamura; K Ghaedi; Yukio Fujiki; Naomi Kondo
Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures.
Human molecular genetics 2000;9(13):1995-9.
2000: Yasuyuki Suzuki; Koji Isogai; Takahide Teramoto; H Tashita; Nobuyuki Shimozawa; M Nishimura; T Asano; M Oda; A Kamei; H Ishiguro; S Kato; T Ohashi; H Kobayashi; Y Eto; Naomi Kondo
Bone marrow transplantation for the treatment of X-linked adrenoleukodystrophy.
Journal of inherited metabolic disease 2000;23(5):453-8.
2000: Naomi Kondo
[Bloom syndrome].
Nihon rinsho. Japanese journal of clinical medicine 2000;58(7):1460-6.
2000: Kazuko Sukegawa; Haruki Nakamura; Zenichiro Kato; Shunji Tomatsu; Adriana Montaño; T Fukao; Gabriele Toietta; paolo tortora; Tadao Orii; Naomi Kondo
Biochemical and structural analysis of missense mutations in N-acetylgalactosamine-6-sulfate sulfatase causing mucopolysaccharidosis IVA phenotypes.
Human molecular genetics 2000;9(9):1283-90.
2000: S Hayakawa; Hideo Kaneko; Toshiyuki Fukao; Kimiko Kasahara; T Matsumoto; Y Furuichi; Naomi Kondo
Characterization of the nuclear localization signal in the DNA helicase responsible for Bloom syndrome.
International journal of molecular medicine 2000;5(5):477-84.
2000: Adriana Montaño; A Yamagishi; Shunji Tomatsu; Seiji Fukuda; N G Copeland; K E Orii; Koji Isogai; N Yamada; Zenichiro Kato; N A Jenkins; D J Gilbert; Kazuko Sukegawa; Tadao Orii; Naomi Kondo
The mouse N-acetylgalactosamine-6-sulfate sulfatase (Galns) gene: cDNA isolation, genomic characterization, chromosomal assignment and analysis of the 5'-flanking region.
Biochimica et biophysica acta 2000;1500(3):323-34.
2000: Y Tanaka; Yasuyuki Suzuki; Nobuyuki Shimozawa; E Nanba; Naomi Kondo
Congenital myotonic dystrophy: report of paternal transmission.
Brain & development 2000;22(2):132-4.
2000: Nobuyuki Shimozawa; Zhongyi Zhang; A Imamura; Yasuyuki Suzuki; Yukio Fujiki; Toshiro Tsukamoto; Takashi Osumi; P Aubourg; Ronald J A Wanders; Naomi Kondo
Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient.
Biochemical and biophysical research communications 2000;268(1):31-5.
2000: Hideo Kaneko; Naomi Kondo
[IgA-IgM deficiency].
Ryōikibetsu shōkōgun shirīzu 2000;(32):96-8.
2000: Eiko Matsui; Naomi Kondo
[Hermans syndrome].
Ryōikibetsu shōkōgun shirīzu 2000;(32):53-5.
2000: Hideo Kaneko; Naomi Kondo
[Good syndrome, immunodeficiency with thymoma].
Ryōikibetsu shōkōgun shirīzu 2000;(32):49-52.
2000: Naomi Kondo
[Common variable immunodeficiency(CVID)].
Ryōikibetsu shōkōgun shirīzu 2000;(32):46-8.
2000: Z Kato; Naomi Kondo
[Seckel syndrome].
Ryōikibetsu shōkōgun shirīzu 2000;(32):276-8.
2000: Naomi Kondo
[Bloom syndrome].
Ryōikibetsu shōkōgun shirīzu 2000;(32):261-4.
2000: Naomi Kondo
[Ataxia-telangiectasia(AT), Louis-Bar syndrome].
Ryōikibetsu shōkōgun shirīzu 2000;(32):131-4.
2000: Hideo Kaneko; Toshiyuki Fukao; Ryosuke Inoue; Kimiko Kasahara; Eiko Matsui; Naomi Kondo
Long-term study of a female hyper-IgM immunodeficiency.
Experimental and clinical immunogenetics 2000;17(4):173-8.
2000: Yasuyuki Suzuki; Nobuyuki Shimozawa; A Imamura; Naomi Kondo
[Peroxisomal disorders].
Ryōikibetsu shōkōgun shirīzu 2000;(29 Pt 4):452-9.
2000: H Watanabe; KE Orii; Toshiyuki Fukao; XQ Song; Toshifumi Aoyama; Lodewijk IJlst; J Ruiter; Ronald J A Wanders; Naomi Kondo
Molecular basis of very long chain acyl-CoA dehydrogenase deficiency in three Israeli patients: identification of a complex mutant allele with P65L and K247Q mutations, the former being an exonic mutation causing exon 3 skipping.
Human mutation 2000;15(5):430-8.
2000: Toshiyuki Fukao; T Yoshida; Hideo Kaneko; XQ Song; H Tashita; Takahide Teramoto; Ryosuke Inoue; Dianne Watters; Martin Lavin; Naomi Kondo
Immunoblot analysis for laboratory diagnosis of ataxia-telangiectasia: use of Epstein-Barr virus-transformed or phytohemagglutinin-stimulated lymphoblasts for detection of ATM protein.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2000;10(1):36-40.
2000: Naomi Kondo; Shinji Shinoda; Osamu Fukutomi; H Agata; T Terada; Hiroaki Shikano; Adriana Montaño; Heima Sakaguchi; Mizuho Watanabe; K Komiyama; Y Yokoyama; N Morimoto
Eosinophils are neither migrated nor activated in the skin lesions of atopic dermatitis in infants.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 2000;10(1):11-3.
2000: A Imamura; Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; Toshiro Tsukamoto; Yukio Fujiki; Tadao Orii; Takashi Osumi; Naomi Kondo
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.
Brain & development 2000;22(1):8-12.
2000: S Iwata; Kazuko Sukegawa; M Kokuryu; Shunji Tomatsu; Naomi Kondo; S Iwasa; Tadao Orii
Glycosaminoglycans in neonatal urine.
Archives of disease in childhood. Fetal and neonatal edition 2000;82(1):F78.
1999: Eiko Matsui; Hideo Kaneko; Toshiyuki Fukao; Takahide Teramoto; Ryosuke Inoue; Mizuho Watanabe; Kimiko Kasahara; Naomi Kondo
Mutations of the IL-12 receptor beta2 chain gene in atopic subjects.
Biochemical and biophysical research communications 1999;266(2):551-5.
1999: Naomi Kondo
[Analysis of atopic gene].
Nihon rinsho. Japanese journal of clinical medicine 1999;57 Suppl():750-5.
1999: Naomi Kondo; Yasuyuki Suzuki; Nobuyuki Shimozawa; Yoshito Takahashi; Toshiyuki Fukao
[Genetics of neurologic disorders in children].
Nihon rinsho. Japanese journal of clinical medicine 1999;57 Suppl():700-6.
1999: Ryosuke Inoue; Toshiyuki Fukao; Y Kato; Takahide Teramoto; M Utsumi; Naomi Kondo
Time-course study of the levels of urinary leukotriene E4, serum thromboxane B2 and serum eosinophil cationic protein in spontaneous asthma attacks in five children.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1999;9(6):361-6.
1999: Hideo Kaneko; Eiko Matsui; Toshiyuki Fukao; Kimiko Kasahara; Wataru Morimoto; Naomi Kondo
Expression of the BLM gene in human haematopoietic cells.
Clinical and experimental immunology 1999;118(2):285-9.
1999: Nobuyuki Shimozawa; A Imamura; Zhongyi Zhang; Yasuyuki Suzuki; Tadao Orii; Toshiro Tsukamoto; Takashi Osumi; Yukio Fujiki; Ronald J A Wanders; G T N Besley; Naomi Kondo
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.
Journal of medical genetics 1999;36(10):779-81.
1999: Toshiyuki Fukao; Hideo Kaneko; Geoff W Birrell; Magtouf Gatei; H Tashita; T Yoshida; S Cross; Padmini Kedar; Dianne Watters; K K Khana; Ihor Misko; Naomi Kondo; Martin F Lavin
ATM is upregulated during the mitogenic response in peripheral blood mononuclear cells.
Blood 1999;94(6):1998-2006.
1999: R Toyama; Satoru Mukai; A Itagaki; Shigehiko Tamura; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Ronald J A Wanders; Yukio Fujiki
Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.
Human molecular genetics 1999;8(9):1673-81.
1999: Nobuyuki Shimozawa; Zhongyi Zhang; Yasuyuki Suzuki; A Imamura; Toshiro Tsukamoto; Takashi Osumi; Yukio Fujiki; Tadao Orii; PG Barth; Ronald J A Wanders; Naomi Kondo
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.
Biochemical and biophysical research communications 1999;262(2):504-8.
1999: H Agata; N Kawakami; Naomi Kondo; T Hayashi; Osamu Fukutomi; H Shimizu; T Orii
Differences of genetic effects for the development of allergic diseases in two cities of Japan.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 1999;82(6):586-90.
1999: Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; A Imamura; R Toyama; Satoru Mukai; Yukio Fujiki; Toshiro Tsukamoto; Takashi Osumi; Tadao Orii; Ronald J A Wanders; Naomi Kondo
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
Human molecular genetics 1999;8(6):1077-83.
1999: Naomi Kondo; T Fukao; Khoichirou Hirayama; T Sakamoto; S Torii
[Development and evaluation of parent-related quality of life questionnaires for asthmatic children and their parents or caregivers--evaluation of treatment process with sustained-release theophylline dry syrup].
Arerugī = [Allergy] 1999;48(5):533-45.
1999: Kamran Ghaedi; A Kawai; Kanji Okumoto; Shigehiko Tamura; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein.
Experimental cell research 1999;248(2):489-97.
1999: Kamran Ghaedi; A Itagaki; R Toyama; Shigehiko Tamura; Tsuyoshi Matsumura; A Kawai; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals.
Experimental cell research 1999;248(2):482-8.
1999: Yasuyuki Suzuki; Nobuyuki Shimozawa; A Imamura; Zhongyi Zhang; Naomi Kondo
[Newly identified peroxisomal disorders].
Nō to shinkei = Brain and nerve 1999;51(4):295-302.
1999: K E Orii; K O Orii; M Souri; Tadao Orii; Naomi Kondo; Takao Hashimoto; Toshifumi Aoyama
Genes for the human mitochondrial trifunctional protein alpha- and beta-subunits are divergently transcribed from a common promoter region.
The Journal of biological chemistry 1999;274(12):8077-84.
1999: Yuji Matsuzono; Naohiko Kinoshita; Shigehiko Tamura; Nobuyuki Shimozawa; M Hamasaki; Kamran Ghaedi; Ronald J A Wanders; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(5):2116-21.
1999: Zhongyi Zhang; Yasuyuki Suzuki; Nobuyuki Shimozawa; Seiji Fukuda; A Imamura; Toshiro Tsukamoto; Takashi Osumi; Yukio Fujiki; Tadao Orii; Ronald J A Wanders; PG Barth; H W Moser; B C Paton; G T N Besley; Naomi Kondo
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.
Human mutation 1999;13(6):487-96.
1999: Yasuyuki Suzuki; Zhongyi Zhang; Nobuyuki Shimozawa; Masami Muro; Hideaki Shono; S Toda; S Miyahara; Takao Hashimoto; N Usuda; M Ito; S Takashima; Naomi Kondo
Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency.
Journal of human genetics 1999;44(3):143-7.
1999: Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; K Miura; A Matsumoto; M Nagaya; S Castillo-Taucher; Naomi Kondo
A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata.
Journal of human genetics 1999;44(2):123-5.
1998: T Kasai; Kenji Ohguchi; Shigeru Nakashima; Y Ito; Takashi Naganawa; Naomi Kondo; Yoshinori Nozawa
Increased activity of oleate-dependent type phospholipase D during actinomycin D-induced apoptosis in Jurkat T cells.
Journal of immunology (Baltimore, Md. : 1950) 1998;161(12):6469-74.
1998: Masanori Honsho; Shigehiko Tamura; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
American journal of human genetics 1998;63(6):1622-30.
1998: A Imamura; S Tamura; Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; Toshiro Tsukamoto; Tadao Orii; Naomi Kondo; Takashi Osumi; Yukio Fujiki
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.
Human molecular genetics 1998;7(13):2089-94.
1998: Naomi Kondo; Y Kobayashi; S Shinoda; R Takenaka; Takahide Teramoto; Hideo Kaneko; Toshiyuki Fukao; Eiko Matsui; Kimiko Kasahara; Y Yokoyama
Reduced interferon gamma production by antigen-stimulated cord blood mononuclear cells is a risk factor of allergic disorders--6-year follow-up study.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 1998;28(11):1340-4.
1998: Naohiko Kinoshita; Kamran Ghaedi; Nobuyuki Shimozawa; Ronald J A Wanders; Yuji Matsuzono; T Imanaka; Kanji Okumoto; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.
The Journal of biological chemistry 1998;273(37):24122-30.
1998: Y Yamada; Ryosuke Inoue; Toshiyuki Fukao; Hideo Kaneko; Koji Isogai; S Fukuda; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Eiichi Azuma; M Sakurai
Ataxia telangiectasia associated with B-cell lymphoma: the effect of a half-dose of the drugs administered according to the acute lymphoblastic leukemia standard risk protocol.
Pediatric hematology and oncology 1998;15(5):425-9.
1998: Kanji Okumoto; Ryota Itoh; Nobuyuki Shimozawa; Yasuyuki Suzuki; Shigehiko Tamura; Naomi Kondo; Yukio Fujiki
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
Human molecular genetics 1998;7(9):1399-405.
1998: Naomi Kondo; Toshiyuki Fukao; Hideo Kaneko; Takahide Teramoto; H Tashita; Ryosuke Inoue
DNase I hypersensitive sites in human I epsilon region of immunoglobulin heavy chain genes abnormally induced by interleukin-4 in B-lymphocytes of atopic patients with high levels of serum IgE.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1998;8(4):234-8.
1998: Kanji Okumoto; Nobuyuki Shimozawa; A Kawai; Shigehiko Tamura; Toshiro Tsukamoto; Takashi Osumi; H Moser; Ronald J A Wanders; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.
Molecular and cellular biology 1998;18(7):4324-36.
1998: Zenichiro Kato; Osamu Fukutomi; Naomi Kondo
Developmental changes of unbound theophylline.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 1998;80(6):517.
1998: Shigehiko Tamura; Kanji Okumoto; R Toyama; Nobuyuki Shimozawa; Toshiro Tsukamoto; Yasuyuki Suzuki; Takashi Osumi; Naomi Kondo; Yukio Fujiki
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(8):4350-5.
1998: Y Yamada; Kanefusa Kato; Kazuko Sukegawa; Shunji Tomatsu; S Fukuda; S Emura; S Kojima; T Matsuyama; W S Sly; Naomi Kondo; Tadao Orii
Treatment of MPS VII (Sly disease) by allogeneic BMT in a female with homozygous A619V mutation.
Bone marrow transplantation 1998;21(6):629-34.
1998: Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; A Imamura; Toshiro Tsukamoto; Takashi Osumi; K Tateishi; Kanji Okumoto; Yukio Fujiki; Tadao Orii; PG Barth; Ronald J A Wanders; Naomi Kondo
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.
Biochemical and biophysical research communications 1998;243(2):368-71.
1998: Kazuko Sukegawa; T Matsuzaki; Seiji Fukuda; M Masuno; Toshiyuki Fukao; M Kokuryu; S Iwata; Shunji Tomatsu; Tadao Orii; Naomi Kondo
Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation.
Clinical genetics 1998;53(2):96-101.
1998: Koji Isogai; Kazuko Sukegawa; Shunji Tomatsu; Toshiyuki Fukao; XQ Song; Y Yamada; Seiji Fukuda; Tadao Orii; Naomi Kondo
Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease).
Journal of inherited metabolic disease 1998;21(1):60-70.
1998: Seiji Fukuda; Yasuyuki Suzuki; Nobuyuki Shimozawa; Zhongyi Zhang; Tadao Orii; Toshifumi Aoyama; Takao Hashimoto; Naomi Kondo
Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase cDNA.
Journal of inherited metabolic disease 1998;21(1):23-8.
1998: Hideo Kaneko; T Ariyasu; Ryosuke Inoue; Toshiyuki Fukao; Kimiko Kasahara; Takahide Teramoto; Eiko Matsui; S Hayakawa; Naomi Kondo
Expression of Pax5 gene in human haematopoietic cells and tissues: comparison with immunodeficient donors.
Clinical and experimental immunology 1998;111(2):339-44.
1998: H Tashita; Toshiyuki Fukao; Hideo Kaneko; Takahide Teramoto; Ryosuke Inoue; Kimiko Kasahara; Naomi Kondo
Molecular basis of selective IgG2 deficiency. The mutated membrane-bound form of gamma2 heavy chain caused complete IGG2 deficiency in two Japanese siblings.
The Journal of clinical investigation 1998;101(3):677-81.
1998: Toshiyuki Fukao; XQ Song; T Yoshida; H Tashita; Hideo Kaneko; Takahide Teramoto; Ryosuke Inoue; K Katamura; M Mayumi; M Hiratani; N Taniguchi; J Arai; H Wakiguchi; Anat Bar-Shira; Yosef Shiloh; Naomi Kondo
Ataxia-telangiectasia in the Japanese population: identification of R1917X, W2491R, R2909G, IVS33+2T-->A, and 7883del5, the latter two being relatively common mutations.
Human mutation 1998;12(5):338-43.
1998: Toshiyuki Fukao; Haruki Nakamura; XQ Song; Kozue Nakamura; KE Orii; Yoshinori Kohno; M Kano; Seiji Yamaguchi; Takao Hashimoto; Tadao Orii; Naomi Kondo
Characterization of N93S, I312T, and A333P missense mutations in two Japanese families with mitochondrial acetoacetyl-CoA thiolase deficiency.
Human mutation 1998;12(4):245-54.
1998: XQ Song; Toshiyuki Fukao; H Watanabe; H Shintaku; K Hirayama; S Kassovska-Bratinova; Naomi Kondo; Grant A Mitchell
Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: two pathogenic mutations, V133E and C456F, in Japanese siblings.
Human mutation 1998;12(2):83-8.
1998: Toshiyuki Fukao; Hideo Kaneko; Naomi Kondo
[Ataxia-telangiectasia].
Ryōikibetsu shōkōgun shirīzu 1998;(19 Pt 2):618-21.
1998: Kazuko Sukegawa; Shunji Tomatsu; Naomi Kondo; Tadao Orii
[Mucopolysaccharidosis type VII (Sly disease)].
Ryōikibetsu shōkōgun shirīzu 1998;(19 Pt 2):449-52.
1998: Kazuko Sukegawa; Shunji Tomatsu; Naomi Kondo; Tadao Orii
[Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome)].
Ryōikibetsu shōkōgun shirīzu 1998;(19 Pt 2):446-8.
1998: Kazuko Sukegawa; Shunji Tomatsu; Naomi Kondo; Tadao Orii
[Mucopolysaccharidosis type IV (Morquio syndrome, beta-galactosidase deficiency)].
Ryōikibetsu shōkōgun shirīzu 1998;(19 Pt 2):442-5.
1998: Kazuko Sukegawa; Shunji Tomatsu; Naomi Kondo; Tadao Orii
[Mucopolysaccharidosis type III (Sanfilippo syndrome)].
Ryōikibetsu shōkōgun shirīzu 1998;(19 Pt 2):439-41.
1998: Kazuko Sukegawa; Shunji Tomatsu; Naomi Kondo; Tadao Orii
[Mucopolysaccharidosis type II (Hunter syndrome)].
Ryōikibetsu shōkōgun shirīzu 1998;(19 Pt 2):435-8.
1998: Kazuko Sukegawa; Shunji Tomatsu; Naomi Kondo; Tadao Orii
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)].
Ryōikibetsu shōkōgun shirīzu 1998;(19 Pt 2):431-4.
1998: Takahide Teramoto; Toshiyuki Fukao; H Tashita; Ryosuke Inoue; Hideo Kaneko; M Takemura; Naomi Kondo
Serum IgE level is negatively correlated with the ability of peripheral mononuclear cells to produce interferon gamma (IFNgamma): evidence of reduced expression of IFNgamma mRNA in atopic patients.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 1998;28(1):74-82.
1998: N Yamada; Seiji Fukuda; Shunji Tomatsu; V Muller; J J Hopwood; J Nelson; Zenichiro Kato; A Yamagishi; Kazuko Sukegawa; Naomi Kondo; Tadao Orii
Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotype.
Human mutation 1998;11(3):202-8.
1998: Toshiyuki Fukao; H Tashita; Takahide Teramoto; Ryosuke Inoue; Hideo Kaneko; K Komiyama; Anat Bar-Shira; Susan Gilad; Yosef Shiloh; M Nishimura; Naomi Kondo
Novel exonic mutation (5319 G to A) resulting in two aberrantly spliced transcripts of the ATM gene in a Japanese patient with ataxia-telangiectasia.
Human mutation 1998;Suppl 1():S223-5.
1998: Nobuyuki Shimozawa; Yasuyuki Suzuki; Shunji Tomatsu; Haruki Nakamura; T Kono; H Takada; Toshiro Tsukamoto; Yukio Fujiki; Tadao Orii; Naomi Kondo
A novel mutation, R125X in peroxisome assembly factor-1 responsible for Zellweger syndrome.
Human mutation 1998;Suppl 1():S134-6.
1998: Shunji Tomatsu; Seiji Fukuda; A Cooper; James Wraith; A Yamagishi; Zenichiro Kato; N Yamada; Koji Isogai; Kazuko Sukegawa; Yasuyuki Suzuki; Nobuyuki Shimozawa; Naomi Kondo; Tadao Orii
Fifteen polymorphisms in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene: diagnostic implications in Morquio disease.
Human mutation 1998;Suppl 1():S42-6.
1997: Yasuyuki Suzuki; Ken Lee; Nobuyuki Shimozawa; Tadao Orii; Naomi Kondo
Biochemical and immunocytochemical properties of peroxisomes and mitochondria in bovine chromaffin cells.
Cell structure and function 1997;22(6):615-9.
1997: Hideo Kaneko; K O Orii; Eiko Matsui; Nobuyuki Shimozawa; Toshiyuki Fukao; T Matsumoto; A Shimamoto; Y Furuichi; S Hayakawa; Kimiko Kasahara; Naomi Kondo
BLM (the causative gene of Bloom syndrome) protein translocation into the nucleus by a nuclear localization signal.
Biochemical and biophysical research communications 1997;240(2):348-53.
1997: Hideo Kaneko; Ryosuke Inoue; Toshiyuki Fukao; Kimiko Kasahara; H Tashita; Takahide Teramoto; Naomi Kondo
Two Japanese siblings with Bloom syndrome gene mutation and B-cell lymphoma.
Leukemia & lymphoma 1997;27(5-6):539-42.
1997: Zenichiro Kato; Seiji Fukuda; Shunji Tomatsu; H Vega; T Yasunaga; A Yamagishi; N Yamada; A Valencia; Luis A Barrera; Kazuko Sukegawa; Tadao Orii; Naomi Kondo
A novel common missense mutation G301C in the N-acetylgalactosamine-6-sulfate sulfatase gene in mucopolysaccharidosis IVA.
Human genetics 1997;101(1):97-101.
1997: Yasuyuki Suzuki; LL Jiang; M Souri; S Miyazawa; Seiji Fukuda; Zhongyi Zhang; M Une; Nobuyuki Shimozawa; Naomi Kondo; Tadao Orii; Takao Hashimoto
D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.
American journal of human genetics 1997;61(5):1153-62.
1997: Toshiyuki Fukao; XQ Song; Grant A Mitchell; Seiji Yamaguchi; Kazuko Sukegawa; Tadao Orii; Naomi Kondo
Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases.
Pediatric research 1997;42(4):498-502.
1997: S Iwata; Kazuko Sukegawa; T Sasaki; M Kokuryu; S Yamasita; A Noma; S Iwasa; Naomi Kondo; Tadao Orii
Mass screening test for mucopolysaccharidoses using the 1,9-dimethylmethylene blue method: positive interference from paper diapers.
Clinica chimica acta; international journal of clinical chemistry 1997;264(2):245-50.
1997: K Tateishi; Kanji Okumoto; Nobuyuki Shimozawa; Toshiro Tsukamoto; Takashi Osumi; Yasuyuki Suzuki; Naomi Kondo; I Okano; Yukio Fujiki
Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.
European journal of cell biology 1997;73(4):352-9.
1997: K E Orii; T Aoyama; K Wakui; Y Fukushima; H Miyajima; S Yamaguchi; Tadao Orii; Naomi Kondo; T Hashimoto
Genomic and mutational analysis of the mitochondrial trifunctional protein beta-subunit (HADHB) gene in patients with trifunctional protein deficiency.
Human molecular genetics 1997;6(8):1215-24.
1997: Naomi Kondo; M Shinbara; Ryosuke Inoue; Toshiyuki Fukao; Hideo Kaneko; Takahide Teramoto; H Tashita
Inhibition of interferon-gamma production from lymphocytes stimulated with food antigens by a beta 2-agonist, procaterol, in patients with food-sensitive atopic dermatitis.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1997;7(4):225-8.
1997: KO Orii; Toshifumi Aoyama; F Saito-Ohara; T Ikeuchi; T Orii; Naomi Kondo; Takao Hashimoto
Molecular characterization of the mouse very-long-chain acyl-CoA dehydrogenase gene.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(7):516-8.
1997: S Fukuda; N Yamada; Shunji Tomatsu; Kazuko Sukegawa; Adriana Montaño; J J Hopwood; V Muller; Tadao Orii; Naomi Kondo
Mucopolysaccharidosis IVA: a novel splice acceptor site mutation in intron 4 of the N-acetylgalactosamine-6-sulfate sulfatase gene in an Afghanistan girl with classical Morquio disease.
The Japanese journal of human genetics 1997;42(2):317-22.
1997: A Imamura; Yasuyuki Suzuki; XQ Song; Toshiyuki Fukao; A Uchiyama; Nobuyuki Shimozawa; K Kamijo; Takao Hashimoto; Tadao Orii; Naomi Kondo
Two novel missense mutations in the ATP-binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patients.
Clinical genetics 1997;51(5):322-5.
1997: XQ Song; Toshiyuki Fukao; Grant A Mitchell; S Kassovska-Bratinova; Magdalena Ugarte; Ronald J A Wanders; K Hirayama; H Shintaku; P Churchill; H Watanabe; Tadao Orii; Naomi Kondo
Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency.
Biochimica et biophysica acta 1997;1360(2):151-6.
1997: S Fukuda; Y Yamada; M Nishimura; Koji Isogai; T Terada; M Iwata; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo
Marinesco-Sjögren syndrome associated with acute myeloblastic leukemia.
Clinical genetics 1997;51(4):278-80.
1997: Naomi Kondo; Osamu Fukutomi; H Agata; Y Yokoyama
Proliferative responses of lymphocytes to food antigens are useful for detection of allergens in nonimmediate types of food allergy.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1997;7(2):122-6.
1997: Yukitoshi Takahashi; Yasuyuki Suzuki; K Kumazaki; Y Tanabe; S Akaboshi; K Miura; Nobuyuki Shimozawa; Naomi Kondo; T Nishiguchi; K Terada; Tadao Orii
Epilepsy in peroxisomal diseases.
Epilepsia 1997;38(2):182-8.
1997: H Agata; Naomi Kondo; Osamu Fukutomi; M Takemura; H Tashita; Y Kobayashi; Shinji Shinoda; T Nishida; M Shinbara; T Orii
Pulmonary hemosiderosis with hypersensitivity to buckwheat.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 1997;78(2):233-7.
1997: Naomi Kondo; Ryosuke Inoue; Kimiko Kasahara; Toshiyuki Fukao; Hideo Kaneko; H Tashita; Takahide Teramoto
Reduced expression of the interferon-gamma messenger RNA in IgG2 deficiency.
Scandinavian journal of immunology 1997;45(2):227-30.
1997: Shinji Shinoda; H Agata; Osamu Fukutomi; Naomi Kondo
Combinations of IgE values and lymphocyte proliferative responses for consideration of the clinical course of infantile hen's-egg-sensitive atopic dermatitis.
International archives of allergy and immunology 1997;112(2):163-8.
1997: Shunji Tomatsu; Seiji Fukuda; A Cooper; James Wraith; P Ferreira; Paola Di Natale; paolo tortora; A Fujimoto; Zenichiro Kato; N Yamada; Koji Isogai; A Yamagishi; Kazuko Sukegawa; Yasuyuki Suzuki; Nobuyuki Shimozawa; Naomi Kondo; W S Sly; Tadao Orii
Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene.
Human mutation 1997;10(5):368-75.
1997: Kazuko Sukegawa; XQ Song; M Masuno; Toshiyuki Fukao; Nobuyuki Shimozawa; Seiji Fukuda; Koji Isogai; H Nishio; M Matsuo; Shunji Tomatsu; Naomi Kondo; Tadao Orii
Hunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele.
Human mutation 1997;10(5):361-7.
1997: KO Orii; F Saito-Ohara; T Ikeuchi; T Orii; Naomi Kondo; Toshifumi Aoyama; Takao Hashimoto
Assignment of the gene for very-long-chain acyl-CoA dehydrogenase (Acadvl) to mouse chromosome band 11B2-B5 by in situ hybridization.
Cytogenetics and cell genetics 1997;78(1):25-6.
1997: Toshiyuki Fukao; XQ Song; Seiji Yamaguchi; Naomi Kondo; Tadao Orii; J M Matthieu; C Bachmann; Takao Hashimoto
Identification of three novel frameshift mutations (83delAT, 754insCT, and 435 + 1G to A) of mitochondrial acetoacetyl-coenzyme A thiolase gene in two Swiss patients with CRM-negative beta-ketothiolase deficiency.
Human mutation 1997;9(3):277-9.
1996: Yasuyuki Suzuki; Nobuyuki Shimozawa; Yukitoshi Takahashi; A Imamura; Naomi Kondo; Tadao Orii
Peroxisomal disorders: clinical aspects.
Annals of the New York Academy of Sciences 1996;804():442-9.
1996: Hideo Kaneko; Ryosuke Inoue; Y Yamada; K Sukegawa; Toshiyuki Fukao; H Tashita; Takahide Teramoto; Kimiko Kasahara; T Takami; Naomi Kondo
Microsatellite instability in B-cell lymphoma originating from Bloom syndrome.
International journal of cancer. Journal international du cancer 1996;69(6):480-3.
1996: Seiji Fukuda; Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; Shunji Tomatsu; T Tsukamoto; N Hashiguchi; Takashi Osumi; Mitsuo Masuno; K Imaizumi; Y Kuroki; Yukio Fujiki; Tadao Orii; Naomi Kondo
Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.
American journal of human genetics 1996;59(6):1210-20.
1996: A Uchiyama; Toshifumi Aoyama; K Kamijo; Y Uchida; Naomi Kondo; Tadao Orii; Takao Hashimoto
Molecular cloning of cDNA encoding rat very long-chain acyl-CoA synthetase.
The Journal of biological chemistry 1996;271(48):30360-5.
1996: K Inoue; Yasuyuki Suzuki; S Yajima; Nobuyuki Shimozawa; Shunji Tomatsu; Tadao Orii; Naomi Kondo
Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidation.
Clinical genetics 1996;50(5):348-52.
1996: Toshiyuki Fukao; A Kodama; N Aoyanagi; R Tsukino; S Uemura; XQ Song; H Watanebe; T Kuhara; I Matsumoto; Tadao Orii; Naomi Kondo
Mild form of beta-ketothiolase deficiency (mitochondrial acetoacetyl-CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross-reactive material in EB-transformed lymphocytes.
Clinical genetics 1996;50(4):263-6.
1996: Toshiyuki Fukao; S Sakai; Nobuyuki Shimozawa; T Kuwahara; M Kano; E Goto; Y Nakashima; M Katagiri-Kawade; H Ichihashi; Mitsuo Masuno; Tadao Orii; Naomi Kondo
Life-threatening cardiac involvement throughout life in a case of Costello syndrome.
Clinical genetics 1996;50(4):244-7.
1996: Yasuyuki Suzuki; Nobuyuki Shimozawa; A Imamura; Y Fukuda; H Ichihashi; Tadao Orii; Naomi Kondo
Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defect.
Acta paediatrica Japonica; Overseas edition 1996;38(5):520-3.
1996: Zenichiro Kato; T Kato; Naomi Kondo; Tadao Orii
Interstitial deletion of the short arm of chromosome 10: report of a case and review of the literature.
The Japanese journal of human genetics 1996;41(3):333-8.
1996: S Kassovska-Bratinova; Toshiyuki Fukao; XQ Song; A M Duncan; H S Chen; MF Robert; Celia Pérez-Cerdá; Magdalena Ugarte; C Chartrand; S Vobecky; Naomi Kondo; Grant A Mitchell
Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient.
American journal of human genetics 1996;59(3):519-28.
1996: Toshiyuki Fukao; Hideo Kaneko; T Teramoto; H Tashita; Naomi Kondo
Association between Fc epsilon RI beta and atopic disorder in Japanese population?
Lancet 1996;348(9024):407.
1996: M Shinbara; Naomi Kondo; H Agata; Osamu Fukutomi; N Kuwabara; Y Kobayashi; M Miura; Tadao Orii
Interferon-gamma and interleukin-4 production of ovalbumin-stimulated lymphocytes in egg-sensitive children.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 1996;77(1):60-6.
1996: Toshiyuki Fukao; XQ Song; S Yamaguchi; Takao Hashimoto; Tadao Orii; Naomi Kondo
Immunotitration analysis of cytosolic acetoacetyl-coenzyme A thiolase activity in human fibroblasts.
Pediatric research 1996;39(6):1055-8.
1996: Toshiyuki Fukao; XQ Song; H Watanabe; K Hirayama; H Sakazaki; Haruo Shintaku; M Imanaka; Tadao Orii; Naomi Kondo
Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiency.
Prenatal diagnosis 1996;16(5):471-4.
1996: Nobuyuki Shimozawa; Yasuyuki Suzuki; Shunji Tomatsu; T Tsukamoto; Takashi Osumi; Yukio Fujiki; K Kamijo; Takao Hashimoto; Naomi Kondo; Tadao Orii
Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.
Pediatric research 1996;39(5):812-5.
1996: Shunji Tomatsu; Seiji Fukuda; A Yamagishi; A Cooper; J F Wraith; T Hori; Zenichiro Kato; N Yamada; Koji Isogai; Kazuko Sukegawa; Naomi Kondo; Yasuyuki Suzuki; Nobuyuki Shimozawa; Tadao Orii
Mucopolysaccharidosis IVA: four new exonic mutations in patients with N-acetylgalactosamine-6-sulfate sulfatase deficiency.
American journal of human genetics 1996;58(5):950-62.
1996: Yasuyuki Suzuki; Nobuyuki Shimozawa; S Yajima; K Inoue; Tadao Orii; Naomi Kondo
Incidence of peroxisomal disorders in Japan.
The Japanese journal of human genetics 1996;41(1):167-75.
1996: Y Uchida; Naomi Kondo; Tadao Orii; Takao Hashimoto
Purification and properties of rat liver peroxisomal very-long-chain acyl-CoA synthetase.
Journal of biochemistry 1996;119(3):565-71.
1996: A Imamura; Yasuyuki Suzuki; XQ Song; Toshiyuki Fukao; Nobuyuki Shimozawa; Tadao Orii; Naomi Kondo
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysis.
Prenatal diagnosis 1996;16(3):259-61.
1996: K E Orii; Toshifumi Aoyama; M Souri; L L Jiang; Koji Orii; S Hayashi; S Yamaguchi; Naomi Kondo; Tadao Orii; Takao Hashimoto
Formation of the enzyme complex in mitochondria is required for function of trifunctional beta-oxidation protein.
Biochemical and biophysical research communications 1996;219(3):773-7.
1996: Hideo Kaneko; M Katagiri-Kawade; F Motoyoshi; H Tashita; Takahide Teramoto; Naomi Kondo
Abnormal B cell response of protein kinase C in some common variable immunodeficiency.
Experimental and clinical immunogenetics 1996;13(1):36-42.
1996: Seiji Fukuda; Shunji Tomatsu; A Cooper; James Wraith; Zenichiro Kato; N Yamada; Koji Isogai; Kazuko Sukegawa; Naomi Kondo; Tadao Orii
Mucopolysaccharidosis IVA (Morquio A): three novel small deletions in the N-acetylgalactosamine-6-sulfate sulfatase gene.
Human mutation 1996;8(2):187-90.
1996: Seiji Fukuda; Shunji Tomatsu; Mitsuo Masuno; T Ogawa; A Yamagishi; G M Rezvi; Kazuko Sukegawa; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; K Imaizumi; Y Kuroki; T Okabe; Tadao Orii
Mucopolysaccharidosis IVA: submicroscopic deletion of 16q24.3 and a novel R386C mutation of N-acetylgalactosamine-6-sulfate sulfatase gene in a classical Morquio disease.
Human mutation 1996;7(2):123-34.
1996: G M Rezvi; Shunji Tomatsu; Seiji Fukuda; A Yamagishi; A Cooper; James Wraith; H Iwata; Zenichiro Kato; N Yamada; Kazuko Sukegawa; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Tadao Orii
Mucopolysaccharidosis IVA: a comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populations.
Journal of inherited metabolic disease 1996;19(3):301-8.
1996: A Yamagishi; Shunji Tomatsu; Seiji Fukuda; A Uchiyama; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Kazuko Sukegawa; Tadao Orii
Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populations.
Human mutation 1996;7(1):23-9.
1995: Koji Orii; Toshifumi Aoyama; M Souri; K E Orii; Naomi Kondo; Tadao Orii; Takao Hashimoto
Genomic DNA organization of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis.
Biochemical and biophysical research communications 1995;217(3):987-92.
1995: T Hayashi; N Kawakami; Naomi Kondo; H Agata; Osamu Fukutomi; H Shimizu; Tadao Orii
Prevalence of and risk factors for allergic diseases: comparison of two cities in Japan.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 1995;75(6 Pt 1):525-9.
1995: F Motoyoshi; Naomi Kondo; S Terasawa; Tadao Orii
Impaired response to HBcAg in a hepatitis B virus carrier.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1995;5(6):350-3.
1995: N Kuwabara; Naomi Kondo; Osamu Fukutomi; H Agata; Tadao Orii
Relationship between interferon-gamma, interleukin-4 and IgE production of lymphocytes from hen's egg-sensitive patients.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1995;5(4):198-204.
1995: N Kuwabara; Naomi Kondo; Osamu Fukutomi; H Fujii; Tadao Orii
Methylation patterns of I epsilon region in B cells stimulated with interleukin 4 and Epstein-Barr virus in patients with a high level of serum IgE.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 1995;22(3):265-75.
1995: XQ Song; Toshiyuki Fukao; Yasuyuki Suzuki; A Imamura; A Uchiyama; Nobuyuki Shimozawa; Naomi Kondo; Tadao Orii
Identification of a novel frameshift mutation in a Japanese adrenoleukodystrophy patient.
Human molecular genetics 1995;4(6):1093-4.
1995: A Imamura; A Kamei; Yasuyuki Suzuki; Naomi Kondo; Tadao Orii; S Takashima
Immunohistochemistry for a bifunctional protein in patients with peroxisomal disorders.
Pediatric neurology 1995;12(4):341-5.
1995: T Hori; Shunji Tomatsu; Y Nakashima; A Uchiyama; Seiji Fukuda; Kazuko Sukegawa; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; T Horiuchi
Mucopolysaccharidosis type IVA: common double deletion in the N-acetylgalactosamine-6-sulfatase gene (GALNS).
Genomics 1995;26(3):535-42.
1995: S Iida; Naomi Kondo; H Agata; Shinji Shinoda; M Shinbara; T Nishida; Osamu Fukutomi; Tadao Orii
Differences in lymphocyte proliferative responses to food antigens and specific IgE antibodies to foods with age among food-sensitive patients with atopic dermatitis.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 1995;74(4):334-40.
1995: Shunji Tomatsu; Seiji Fukuda; A Cooper; James Wraith; A Uchiyama; T Hori; Y Nakashima; N Yamada; Kazuko Sukegawa; Naomi Kondo
Mucopolysaccharidosis IVA: structural gene alterations identified by Southern blot analysis and identification of racial differences.
Human genetics 1995;95(4):376-81.
1995: T Ozawa; Naomi Kondo; F Motoyoshi; Kimiko Kasahara; Tadao Orii
DNA mutation induced in the sequence upstream of the secreted MYU C-terminal coding sequence by ultraviolet irradiation in the cell line of Bloom's syndrome.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 1995;22(2):163-9.
1995: T Ogawa; Shunji Tomatsu; Seiji Fukuda; A Yamagishi; G M Rezvi; Kazuko Sukegawa; Naomi Kondo; Yasuyuki Suzuki; Nobuyuki Shimozawa; T Orü
Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene.
Human molecular genetics 1995;4(3):341-9.
1995: T Nishida; Naomi Kondo; H Agata; Osamu Fukutomi; Shinji Shinoda; M Shinbara; Tadao Orii
Evaluation of lymphocyte proliferative responses to casein hydrolysate formula in cow's milk-sensitive children: response of peripheral blood mononuclear cells to hydrolysate formula.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1995;5(2):86-90.
1995: N Kuwabara; Naomi Kondo; Tadao Orii
IgE production by B-cells stimulated with interleukin-4 and Epstein-Barr virus in patients with elevated serum IgE levels.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1995;5(2):78-81.
1995: Ryosuke Inoue; Naomi Kondo; N Kuwabara; Tadao Orii
Aberrant patterns of immunoglobulin levels in Wiskott-Aldrich syndrome.
Scandinavian journal of immunology 1995;41(2):188-93.
1995: Ryosuke Inoue; Naomi Kondo; Y Kobayashi; Osamu Fukutomi; Tadao Orii
IgG2 deficiency associated with defects in production of interferon-gamma; comparison with common variable immunodeficiency.
Scandinavian journal of immunology 1995;41(2):130-4.
1995: Shunji Tomatsu; Seiji Fukuda; A Uchiyama; T Hori; Y Nakashima; Kazuko Sukegawa; Naomi Kondo; Yasuyuki Suzuki; Nobuyuki Shimozawa; Tadao Orii
Polymerase chain reaction detection of two novel human N-acetylgalactosamine-6-sulfate sulfatase gene polymorphisms by single-strand conformation polymorphism analysis or by StyI and StuI cleavages.
Human genetics 1995;95(2):243-4.
1995: Naomi Kondo; Ryosuke Inoue; Kimiko Kasahara; Hideo Kaneko; T Kameyama; Tadao Orii
Failure of IgG production due to a defect in the opening of the chromatin structure of I gamma 1 region in a patient with IgG and IgA deficiency.
Clinical and experimental immunology 1995;99(1):21-8.
1995: M Yano; Naomi Kondo; Y Kato; Shinji Shinoda; Ryosuke Inoue; Tadao Orii
Expression of surrogate light chain in common variable immunodeficiency.
Experimental and clinical immunogenetics 1995;12(1):1-9.
1995: Shunji Tomatsu; Seiji Fukuda; A Cooper; James Wraith; N Yamada; Koji Isogai; Zenichiro Kato; Kazuko Sukegawa; Naomi Kondo; Yasuyuki Suzuki
Two new mutations, Q473X and N487S, in a Caucasian patient with mucopolysaccharidosis IVA (Morquio disease).
Human mutation 1995;6(2):195-6.
1995: M Shinbara; Naomi Kondo; H Agata; Osamu Fukutomi; T Nishida; Y Kobayashi; Tadao Orii
T cell proliferation restricted by HLA class II molecules in patients with hen's egg allergy.
Experimental and clinical immunogenetics 1995;12(2):103-10.
1995: M Yamazaki; Osamu Fukutomi; Naomi Kondo; Tadao Orii
Evaluation of theophylline clearance in children with bronchial asthma.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1995;5(1):50-3.
1994: H Agata; Naomi Kondo; A Yomo; T Muraki; Shinji Shinoda; Osamu Fukutomi; Y Kato; T Nishida; M Shinbara; Tadao Orii
Sensitization to sugar cane pollen in Okinawan allergic children.
Asian Pacific journal of allergy and immunology / launched by the Allergy and Immunology Society of Thailand 1994;12(2):151-4.
1994: Y Kobayashi; Naomi Kondo; Shinji Shinoda; H Agata; Osamu Fukutomi; Tadao Orii
Predictive values of cord blood IgE and cord blood lymphocyte responses to food antigens in allergic disorders during infancy.
The Journal of allergy and clinical immunology 1994;94(5):907-16.
1994: M Yamazaki; Osamu Fukutomi; Naomi Kondo; Zenichiro Kato; Y Nakashima; Shinji Shinoda; H Agata; T Kondo; N Imaeda; Tadao Orii
The design of oral sustained-release theophylline dosing after conversion from intravenous to oral therapy.
International journal of clinical pharmacology and therapeutics 1994;32(11):625-31.
1994: J Asano; Yasuyuki Suzuki; S Yajima; K Inoue; Nobuyuki Shimozawa; Naomi Kondo; M Murase; Tadao Orii
Effects of erucic acid therapy on Japanese patients with X-linked adrenoleukodystrophy.
Brain & development 1994;16(6):454-8.
1994: Naomi Kondo; A Takao; S Tomatsu; N Shimozawa; Y Suzuki; T Ogawa; H Iwata; Tadao Orii
Suppression of IgA production by lymphocytes induced by diphenylhydantoin.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1994;4(5):255-7.
1994: Osamu Fukutomi; Naomi Kondo; H Agata; Shinji Shinoda; N Kuwabara; M Shinbara; Tadao Orii
Timing of onset of allergic symptoms as a response to a double-blind, placebo-controlled food challenge in patients with food allergy combined with a radioallergosorbent test and the evaluation of proliferative lymphocyte responses.
International archives of allergy and immunology 1994;104(4):352-7.
1994: Shunji Tomatsu; Seiji Fukuda; T Ogawa; Zenichiro Kato; Koji Isogai; Naomi Kondo; Yasuyuki Suzuki; Nobuyuki Shimozawa; Kazuko Sukegawa; Tadao Orii
A novel splice site mutation in intron 1 of the GALNS gene in a Japanese patient with mucopolysaccharidosis IVA.
Human molecular genetics 1994;3(8):1427-8.
1994: Naomi Kondo; Kimiko Kasahara; T Kameyama; Y Suzuki; N Shimozawa; S Tomatsu; Y Nakashima; T Hori; A Yamagishi; T Ogawa
Intravenous immunoglobulins suppress immunoglobulin productions by suppressing Ca(2+)-dependent signal transduction through Fc gamma receptors in B lymphocytes.
Scandinavian journal of immunology 1994;40(1):37-42.
1994: A Uchiyama; Shunji Tomatsu; Naomi Kondo; Yasuyuki Suzuki; Nobuyuki Shimozawa; Seiji Fukuda; Kazuko Sukegawa; N Taki; H Inamori; Tadao Orii
New Gaucher disease mutations in exon 10: a novel L444R mutation produces a new NciI site the same as L444P.
Human molecular genetics 1994;3(7):1183-4.
1994: Naomi Kondo; Ryosuke Inoue; Tadao Orii
Responses of lymphocytes to Epstein-Barr virus in patients with primary immunodeficiencies.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1994;4(4):182-4.
1994: A Imamura; Y Komori; Osamu Fukutomi; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Tadao Orii
Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy.
Brain & development 1994;16(4):325-8.
1994: H Agata; Naomi Kondo; Osamu Fukutomi; T Hayashi; Shinji Shinoda; T Nishida; A Yomo; Y Suzuki; N Shimozawa; S Tomatsu
Comparison of allergic diseases and specific IgE antibodies in different parts of Japan.
Annals of allergy 1994;72(5):447-51.
1994: Y Inoue; Naomi Kondo; F Motoyoshi; Ryosuke Inoue; Tadao Orii
Interleukin-2 and interferon-gamma production by peripheral blood lymphocytes of patients with common variable immunodeficiency.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1994;4(3):122-5.
1994: Zenichiro Kato; Osamu Fukutomi; M Yamazaki; Naomi Kondo; N Imaeda; Tadao Orii
Prediction of steady-state serum theophylline concentration in children by first-order and zero-order absorption models.
International journal of clinical pharmacology and therapeutics 1994;32(5):231-4.
1994: T Ozawa; Naomi Kondo; Y Kato; F Motoyoshi; Y Suzuki; Nobuyuki Shimozawa; Kimiko Kasahara; Tadao Orii
A wild-type mu s C-terminal gene is expressed in Bloom's syndrome cells.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 1994;21(2):133-9.
1994: Osamu Fukutomi; Naomi Kondo; H Agata; Shinji Shinoda; N Kuwabara; M Shinbara; Ryosuke Inoue; Tadao Orii
Identification of monocyte chemotactic factors in supernatants of ovalbumin-stimulated lymphocytes from patients with atopic dermatitis who are sensitive to hen's egg.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 1994;24(4):359-66.
1994: Y Nakashima; Shunji Tomatsu; T Hori; Seiji Fukuda; Kazuko Sukegawa; Naomi Kondo; Yasuyuki Suzuki; Nobuyuki Shimozawa; Tadao Orii
Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region.
Genomics 1994;20(1):99-104.
1994: Mitsuo Masuno; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Tadao Orii; T Tsukamoto; Takashi Osumi; Yukio Fujiki; K Imaizumi; Y Kuroki
Assignment of the human peroxisome assembly factor-1 gene (PXMP3) responsible for Zellweger syndrome to chromosome 8q21.1 by fluorescence in situ hybridization.
Genomics 1994;20(1):141-2.
1994: Naomi Kondo; H Agata; Osamu Fukutomi; T Kameyama; Y Suzuki; N Shimozawa; S Tomatsu; Y Nakashima; T Hori; A Yamagishi
Effects of the antiallergic drug azelastine hydrochloride on proliferative responses of lymphocytes to food antigens in patients with food-sensitive atopic dermatitis.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1994;4(2):67-70.
1994: A Uchiyama; Yasuyuki Suzuki; XQ Song; Toshiyuki Fukao; A Imamura; Shunji Tomatsu; Nobuyuki Shimozawa; Naomi Kondo; Tadao Orii
Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophy.
Biochemical and biophysical research communications 1994;198(2):632-6.
1994: Yasuyuki Suzuki; Nobuyuki Shimozawa; S Yajima; Shunji Tomatsu; Naomi Kondo; Y Nakada; S Akaboshi; M Lai; Y Tanabe; Takao Hashimoto
Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.
American journal of human genetics 1994;54(1):36-43.
1994: S Terazawa; Naomi Kondo; Tadao Orii
Significance of measurement of pre-S2 antigen for the prevention of vertical transmission of hepatitis B virus in infants born to HBsAg carrier mothers.
Acta paediatrica (Oslo, Norway : 1992) 1994;83(1):30-4.
1994: Zenichiro Kato; J Asano; T Kato; S Yamaguchi; Naomi Kondo; Tadao Orii
Thyroid cancer in a case with the Alagille syndrome.
Clinical genetics 1994;45(1):21-4.
1994: Yasuyuki Suzuki; Nobuyuki Shimozawa; I Kawabata; S Yajima; K Inoue; Y Uchida; K Izai; Shunji Tomatsu; Naomi Kondo; Tadao Orii
Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes.
Brain & development 1994;16(1):27-31.
1994: Y Kato; Naomi Kondo; M Yano; Ryosuke Inoue; T Ozawa; Tadao Orii
Expression of VpreB gene in common variable immunodeficiency.
Experimental and clinical immunogenetics 1994;11(1):53-8.
1994: Y Miwa; Ryosuke Inoue; T Ozawa; Naomi Kondo; Tadao Orii
IgG subclass levels and southern analysis of DNA in primary immunodeficiency diseases including IgG subclass deficiency.
Experimental and clinical immunogenetics 1994;11(4):173-81.
1994: Shunji Tomatsu; Seiji Fukuda; A Uchiyama; T Hori; Y Nakashima; Naomi Kondo; Yasuyuki Suzuki; Nobuyuki Shimozawa; Kazuko Sukegawa; Tadao Orii
Molecular analysis by Southern blot for the N-acetylgalactosamine-6-sulphate sulphatase gene causing mucopolysaccharidosis IVA in the Japanese population.
Journal of inherited metabolic disease 1994;17(5):601-5.
1994: T Nishida; Naomi Kondo; H Agata; Osamu Fukutomi; Shinji Shinoda; Y Suzuki; N Shimozawa; S Tomatsu; Tadao Orii
Proliferative responses towards native, heat-denatured and pepsin-treated ovalbumin by peripheral blood mononuclear cells from patients with hen's egg-sensitive atopic dermatitis.
Biotherapy (Dordrecht, Netherlands) 1994;8(1):33-40.
1994: Naomi Kondo; Osamu Fukutomi; M Shinbara; Tadao Orii
Inhibition of interferon-gamma and interleukin-2 production from lymphocytes stimulated with food antigens by an anti-allergic drug, Tranilast, in patients with food-sensitive atopic dermatitis.
Biotherapy (Dordrecht, Netherlands) 1994;8(1):19-22.
1994: Naomi Kondo; Osamu Fukutomi; T Kameyama; T Nishida; G P Li; H Agata; M Shinbara; Shinji Shinoda; M Yano; Tadao Orii
Suppression of proliferative responses of lymphocytes to food antigens by an anti-allergic drug, ketotifen fumarate, in patients with food-sensitive atopic dermatitis.
International archives of allergy and immunology 1994;103(3):234-8.
1994: K Watanabe; Naomi Kondo; Osamu Fukutomi; T Takami; H Agata; Tadao Orii
Characterization of infiltrating CD4+ cells in atopic dermatitis using CD45R and CD29 monoclonal antibodies.
Annals of allergy 1994;72(1):39-44.
1993: Naomi Kondo; Ryosuke Inoue; Shinji Shinoda; Tadao Orii
Immunoglobulin-secreting cells in healthy peripheral blood mononuclear cells.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1993;3(6):330-2.
1993: Yukitoshi Takahashi; S Omiya; Y Nakamura; Naomi Kondo; Tadao Orii
Urinary oligosaccharide excretion in nephrotic syndrome.
Pediatric research 1993;34(4):429-34.
1993: Naomi Kondo; Ryosuke Inoue; H Agata; Y Suzuki; N Shimozawa; S Tomatsu; Y Nakashima; A Yamagishi; T Ogawa; Tadao Orii
Expression of secreted immunoglobulin heavy chain genes and immunoglobulin-secreting cells in human lymphocytes.
Scandinavian journal of immunology 1993;38(4):320-2.
1993: Tadao Orii; Shunji Tomatsu; Seiji Fukuda; Kazuko Sukegawa; Naomi Kondo
[Mucopolysaccharidosis type VII: characterization of exonic point mutations and molecular heterogeneity].
Nihon rinsho. Japanese journal of clinical medicine 1993;51(9):2330-5.
1993: Y Yamada; Shunji Tomatsu; Kazuko Sukegawa; Yasuyuki Suzuki; Naomi Kondo; J J Hopwood; Tadao Orii
Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families.
Human genetics 1993;92(2):110-4.
1993: T Ozawa; Naomi Kondo; F Motoyoshi; Y Kato; Tadao Orii
Preferential damage to IgM production by ultraviolet B in the cells of patients with Bloom's syndrome.
Scandinavian journal of immunology 1993;38(3):225-32.
1993: Naomi Kondo; Shinji Shinoda; G P Li; Zenichiro Kato; Tadao Orii
Immunoglobulin-secreting cells in primary immunodeficiency diseases.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1993;3(5):265-7.
1993: Y Kato; Naomi Kondo; F Motoyoshi; T Ozawa; H Agata; Tadao Orii
Kinetics of hypogammaglobulinemia in patients with common variable immunodeficiency.
Acta paediatrica (Oslo, Norway : 1992) 1993;82(9):739-43.
1993: Shinji Shinoda; Naomi Kondo; Osamu Fukutomi; H Agata; Y Suzuki; N Shimozawa; S Tomatsu; Y Yamada; M Takemura; A Noma
Suppressive effects of elimination diets on T cell responses to ovalbumin in hen's egg-sensitive atopic dermatitis patients.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 1993;23(8):689-95.
1993: Naomi Kondo; Ryosuke Inoue; S Nishimura; Kimiko Kasahara; T Kameyama; Y Miwa; P R Lorenzo; Tadao Orii
Defective calcium-dependent signal transduction in T lymphocytes of ataxia-telangiectasia.
Scandinavian journal of immunology 1993;38(1):45-8.
1993: H Agata; Naomi Kondo; Osamu Fukutomi; Shinji Shinoda; T Nishida; Tadao Orii
Evaluation of lymphocyte proliferative responses to food antigens with regard to age and food-specific IgE antibodies in food-sensitive atopic dermatitis.
Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunología 1993;3(4):174-7.
1993: Naomi Kondo; H Agata; Osamu Fukutomi; T Nishida; T Kameyama; H Fujii; T Hayashi; M Shinbara; M Yamasaki; M Utsumi
Reduced responses of peripheral blood lymphocytes to heat-denatured food antigens in food-sensitive atopic dermatitis.
Annals of allergy 1993;70(6):467-9.
1993: Y Inoue; Naomi Kondo; F Motoyoshi; Ryosuke Inoue; Tadao Orii
Abnormal responses of common variable immunodeficiency patients' B cells to Staphylococcus aureus Cowan I and interleukin-2.
Acta paediatrica (Oslo, Norway : 1992) 1993;82(4):404-7.
1993: H Agata; Naomi Kondo; Osamu Fukutomi; Shinji Shinoda; Tadao Orii
Effect of elimination diets on food-specific IgE antibodies and lymphocyte proliferative responses to food antigens in atopic dermatitis patients exhibiting sensitivity to food allergens.
The Journal of allergy and clinical immunology 1993;91(2):668-79.
1993: Naomi Kondo; Osamu Fukutomi; H Agata; F Motoyoshi; Shinji Shinoda; Y Kobayashi; N Kuwabara; T Kameyama; Tadao Orii
The role of T lymphocytes in patients with food-sensitive atopic dermatitis.
The Journal of allergy and clinical immunology 1993;91(2):658-68.
1993: H Agata; A Yomo; Y Hanashiro; T Muraki; Naomi Kondo; Tadao Orii
Comparison of the MAST chemiluminescent assay system with RAST and skin tests in allergic children.
Annals of allergy 1993;70(2):153-7.
1993: Naomi Kondo; Ryosuke Inoue; M Yano; T Hayashi; Y Miwa; Kimiko Kasahara; M Yamasaki; M Utsumi; M Shinbara; Tadao Orii
Defective calcium-dependent signal transduction in B lymphocytes of a certain common variable immunodeficiency.
Experimental and clinical immunogenetics 1993;10(1):16-20.
1993: K Mushiake; F Motoyoshi; Naomi Kondo; Tadao Orii
mu-Chain gene expression in common variable immunodeficiency.
Experimental and clinical immunogenetics 1993;10(4):189-94.
1993: Naomi Kondo; A Takao; Tadao Orii
Case report: immunoglobulin A deficiency in patients with juvenile rheumatoid arthritis treated with aspirin.
Biotherapy (Dordrecht, Netherlands) 1993;7(1):59-62.
1993: Naomi Kondo; A Takao; G P Li; N Kuwabara; H Fujii; Tadao Orii
Immunoglobulin secreting cells in lymphocytes of patients with IgA deficiency or hyper-IgA.
Biotherapy (Dordrecht, Netherlands) 1993;6(4):279-82.
1993: K Mushiake; F Motoyoshi; Naomi Kondo; H Shimizu; Tadao Orii
Long-term follow up of patients with common variable immunodeficiency treated with intravenous immunoglobulin: reevaluation of intravenous immunoglobulin replacement therapy. IVIG therapy in CVID.
Biotherapy (Dordrecht, Netherlands) 1993;7(2):101-7.
1992: Shinji Shinoda; Naomi Kondo; Osamu Fukutomi; H Agata; Tadao Orii
Proliferative responses of CD4+ T-cell population to ovalbumin in patients with atopic dermatitis who are sensitive to hen eggs.
Acta paediatrica (Oslo, Norway : 1992) 1992;81(11):896-901.
1992: S Mori; Naomi Kondo; F Motoyoshi; Hideo Kaneko; Y Inoue; Tadao Orii
Diversity in DNA rearrangements and in RNA expressions of immunoglobulin gene on common variable immunodeficiency.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 1992;19(5):273-85.
1992: A Wakazono; Mitsuo Masuno; S Yamaguchi; K Tsubouchi; Naomi Kondo; Tadao Orii
Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature.
The Japanese journal of human genetics 1992;37(3):229-34.
1992: Naomi Kondo; Y Kobayashi; Shinji Shinoda; K Kasahara; T Kameyama; S Iwasa; Tadao Orii
Cord blood lymphocyte responses to food antigens for the prediction of allergic disorders.
Archives of disease in childhood 1992;67(8):1003-7.
1992: F Motoyoshi; S Mori; Naomi Kondo; Hideo Kaneko; T Ozawa; N Kuwabara; Y Kato; M Takemura; A Noma; Tadao Orii
Common variable immunodeficiency with increased surface IgM-positive double-bearing B cells.
Scandinavian journal of immunology 1992;36(1):21-6.
1992: Osamu Fukutomi; Naomi Kondo; H Agata; Shinji Shinoda; M Shinbara; Tadao Orii
Abnormal responses of the autonomic nervous system in food-dependent exercise-induced anaphylaxis.
Annals of allergy 1992;68(5):438-45.
1992: Naomi Kondo; Kimiko Kasahara; S Shinoda; Tadao Orii
Accelerated expression of secreted alpha-chain gene in anaphylactoid purpura.
Journal of clinical immunology 1992;12(3):193-6.
1992: Naomi Kondo; T Ozawa; Y Kato; F Motoyoshi; Kimiko Kasahara; T Kameyama; Tadao Orii
Reduced secreted mu mRNA synthesis in selective IgM deficiency of Bloom's syndrome.
Clinical and experimental immunology 1992;88(1):35-40.
1992: Naomi Kondo; Osamu Fukutomi; T Kameyama; Tadao Orii
Inhibition of proliferative responses of lymphocytes to food antigens by an anti-allergic drug, N(3',4'-dimethoxycinnamoyl) anthranilic acid (Tranilast) in children with atopic dermatitis.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 1992;22(4):447-53.
1992: H Agata; Naomi Kondo; Osamu Fukutomi; Shinji Shinoda; Tadao Orii
Interleukin-2 production of lymphocytes in food sensitive atopic dermatitis.
Archives of disease in childhood 1992;67(3):280-4.
1992: Naomi Kondo; F Motoyoshi; S Mori; N Kuwabara; Tadao Orii; J German
Long-term study of the immunodeficiency of Bloom's syndrome.
Acta paediatrica (Oslo, Norway : 1992) 1992;81(1):86-90.
1992: Naomi Kondo; F Motoyoshi; Tadao Orii
Asparagine-linked sugar chains of erythrocyte membrane glycoproteins from Wiskott-Aldrich syndrome are not impaired.
Biotherapy (Dordrecht, Netherlands) 1992;4(1):65-7.
1992: T Ozawa; F Motoyoshi; Y Kato; Naomi Kondo; Tadao Orii
Serum IgG subclass concentrations before and after administration of intravenous immunoglobulin in common variable immunodeficiency.
Journal of clinical & laboratory immunology 1992;38(1):29-39.
1992: Naomi Kondo; T Ozawa; Y Kato; Ryosuke Inoue; Kimiko Kasahara; T Kameyama; Tadao Orii
Evidence for abnormally regulated alternative RNA processing of mu chain gene in B-lymphoblastoid cells from Bloom's syndrome.
Experimental and clinical immunogenetics 1992;9(3):149-53.
1992: Naomi Kondo; F Motoyoshi; Tadao Orii
Asparagine-linked sugar chains of plasma membrane glycoproteins from healthy and common variable immunodeficiency B lymphoblastoid cell lines.
Biotherapy (Dordrecht, Netherlands) 1992;4(4):285-8.
1992: Naomi Kondo; Shinji Shinoda; H Agata; T Nishida; Y Miwa; H Fujii; Tadao Orii
Lymphocyte responses to food antigens in food sensitive patients with allergic tension-fatigue syndrome.
Biotherapy (Dordrecht, Netherlands) 1992;5(4):281-4.
1992: Naomi Kondo; Ryosuke Inoue; Tadao Orii
Various responses of lymphocytes to Epstein-Barr virus in patients with common variable immunodeficiency.
Journal of clinical & laboratory immunology 1992;37(4):183-9.
1992: Naomi Kondo; F Motoyoshi; Kimiko Kasahara; Y Inoue; S Mori; Tadao Orii
Failure of c-myc gene expression in B cells of some patients with common variable immunodeficiencies.
Experimental and clinical immunogenetics 1992;9(2):109-16.
1991: Hideo Kaneko; Naomi Kondo; F Motoyoshi; S Mori; Y Kobayashi; Y Inoue; Tadao Orii
Expression of immunoglobulin genes in common variable immunodeficiency.
Journal of clinical immunology 1991;11(5):262-7.
1991: Naomi Kondo; T Ozawa; K Mushiake; F Motoyoshi; T Kameyama; Kimiko Kasahara; Hideo Kaneko; M Yamashina; Y Kato; Tadao Orii
Suppression of immunoglobulin production of lymphocytes by intravenous immunoglobulin.
Journal of clinical immunology 1991;11(3):152-8.
1991: F Motoyoshi; Naomi Kondo; H Ono; Tadao Orii
The effect of photosensitive dye platonin on juvenile rheumatoid arthritis.
Biotherapy (Dordrecht, Netherlands) 1991;3(3):241-4.
1991: Naomi Kondo; F Motoyoshi; T Ozawa; Tadao Orii
A case report of a 9-year old boy with polyarteritis nodosa in which a combination therapy of corticosteroids and a photosensitive dye platonin was effective.
Biotherapy (Dordrecht, Netherlands) 1991;3(3):261-4.
1990: S Mori; Naomi Kondo; F Motoyoshi; S Yamaguchi; Hideo Kaneko; Tadao Orii
Diabetes mellitus in a young man with Bloom's syndrome.
Clinical genetics 1990;38(5):387-90.
1990: Hideo Kaneko; Naomi Kondo; F Motoyoshi; S Mori; Y Kobayashi; T Ozawa; Tadao Orii
Expression of the alpha-chain gene in heterogeneous IgA immunodeficiency.
Scandinavian journal of immunology 1990;32(5):483-9.
1990: M Yamashina; E Ueda; T Kinoshita; T Takami; A Ojima; H Ono; H Tanaka; Naomi Kondo; Tadao Orii; N Okada
Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria.
The New England journal of medicine 1990;323(17):1184-9.
1990: Naomi Kondo; H Agata; Osamu Fukutomi; F Motoyoshi; Tadao Orii
Lymphocyte responses to food antigens in patients with atopic dermatitis who are sensitive to foods.
The Journal of allergy and clinical immunology 1990;86(2):253-60.
1989: Naomi Kondo; H Ko; F Motoyoshi; Tadao Orii
B cell suppressing and CD8+ T cell enhancing effects of photosensitive dye platonin in humans.
The Journal of rheumatology 1989;16(7):936-9.