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Naomi Kondo
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171
Orii, Tadao
102
Fukao, Toshiyuki
91
Suzuki, Yasuyuki
87
Shimozawa, Nobuyuki
87
Kaneko, Hideo
57
Kato, Zenichiro
53
Tomatsu, Shunji
49
Inoue, Ryosuke
46
Kasahara, Kimiko
44
Fukutomi, Osamu
44
Teramoto, Takahide
43
Sukegawa, Kazuko
34
Agata, H
32
Shinoda, Shinji
31
Matsui, Eiko
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All Publications
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2009: Kato Zenichiro; Yamagishi Atsushi; Nakamura Mitsuhiro; Kondo Naomi
Theophylline-associated status epilepticus in an infant: pharmacokinetics and the risk of suppository use.
World journal of pediatrics : WJP 2009;5(4):316-8.
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2009: Funato Michinori; Kato Hiroki; Sasai Hideo; Kubota Kazuo; Ozeki Michio; Kato Zenichiro; Kaneko Hideo; Fukao Toshiyuki; Kondo Naomi
Diffuse large B-cell lymphoma presenting with osteolytic lesions in the bilateral femur.
European journal of haematology 2009;83(5):502.
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2009: Kato Zenichiro; Okuda Miho; Okumura Yu; Arai Takahiro; Teramoto Takahide; Nishimura Masaaki; Kaneko Hideo; Kondo Naomi
Oral administration of the thyrotropin-releasing hormone (TRH) analogue, taltireline hydrate, in spinal muscular atrophy.
Journal of child neurology 2009;24(8):1010-2.
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2009: Funato Michinori; Fukao Toshiyuki; Sasai Hideo; Hori Tomohiro; Terazawa Daisuke; Ozeki Michio; Orii Kenji; Teramoto Takahide; Kaneko Hideo; Kondo Naomi
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.
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2009: Kaneko Hideo; Suzuki Hiroko; Kondo Naomi
[IgA subclass and IgA deficiency]
Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology 2009;32(3):142-8.
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2009: Ohnishi Hidenori; Tochio Hidehito; Kato Zenichiro; Orii Kenji E; Li Ailian; Kimura Takeshi; Hiroaki Hidekazu; Kondo Naomi; Shirakawa Masahiro
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.
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2009: Suzuki Hiroko; Kaneko Hideo; Fukao Toshiyuki; Jin Rong; Kawamoto Norio; Asano Tsutomu; Matsui Eiko; Kasahara Kimiko; Kondo Naomi
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.
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2009: Morimoto Masahiro; Matsui Eiko; Kawamoto Norio; Sakurai Satomi; Kaneko Hideo; Fukao Toshiyuki; Iwasa Shinichi; Shiraki Makoto; Kasahara Kimiko; Kondo Naomi
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.
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2009: Teramoto Takahide; Fukao Toshiyuki; Hirayama Kouichiro; Asano Tsutomu; Aoki Yusuke; Kondo Naomi
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.
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2009: Kuratsubo Izumi; Suzuki Yasuyuki; Orii Koji O; Kato Tomomi; Orii Tadao; Kondo Naomi
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.
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2009: Frappart Pierre-Olivier; Lee Youngsoo; Russell Helen R; Chalhoub Nader; Wang Yong-Dong; Orii Kenji E; Zhao Jingfeng; Kondo Naomi; Baker Suzanne J; McKinnon Peter J
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.
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2008: Kimura Takeshi; Kato Zenichiro; Ohnishi Hidenori; Tochio Hidehito; Shirakawa Masahiro; Kondo Naomi
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.
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2008: Arai Takahiro; Kaneko Hideo; Ohnishi Hidenori; Matsui Eiko; Fukao Toshiyuki; Kawamoto Norio; Kasahara Kimiko; Kondo Naomi
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.
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2008: Kondo Masashi; Kaneko Hideo; Fukao Toshiyuki; Suzuki Kiyotaka; Sakaguchi Heima; Shinoda Shinji; Kato Zenichiro; Matsui Eiko; Teramoto Takahide; Nakano Taku; Kondo Naomi
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.
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2008: Kondo Naomi; Hirayama Koichiro; Matsui Eiko; Teramoto Takahide; Kaneko Hideo; Fukao Toshiyuki; Orii Kenji; Kawamoto Minako; Funato Michinori; Ohnishi Hidenori; Kawamoto Norio; Morita Hideyuki; Kimura Takeshi; Nada Masatoshi; Tokumi Tetsuji; Hori Tomohiro; Watanabe Rinko
[QOL questionnaire for pediatric patients with bronchial asthma and their parents or caregivers. Preparation and evaluation of the short form version 2008 (Gifu)]
Arerugi = [Allergy] 2008;57(8):1022-33.
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2008: Fukao Toshiyuki; Boneh Avihu; Aoki Yusuke; Kondo Naomi
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.
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2008: Kuratsubo Izumi; Suzuki Yasuyuki; Shimozawa Nobuyuki; Kondo Naomi
Parents of childhood X-linked adrenoleukodystrophy: high risk for depression and neurosis.
Brain & development 2008;30(7):477-82.
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2008: Orii Kenji E; Fukao Toshiyuki; Song Xiang-Qian; Mitchell Grant A; Kondo Naomi
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.
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2008: Matsukuma Eiji; Kato Zenichiro; Orii Koji; Asano Takahiko; Orii Kenji; Matsui Eiko; Kaneko Hideo; Kondo Naomi
Acute mumps cerebellitis with abnormal findings in MRI diffusion-weighted images.
European journal of pediatrics 2008;167(7):829-30.
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2008: Funato Michinori; Kaneko Hideo; Ozeki Michio; Kanda Kaori; Fukao Toshiyuki; Kondo Naomi
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.
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2008: Taneichi Hiromichi; Kanegane Hirokazu; Sira Mostafa Mohamed; Futatani Takeshi; Agematsu Kazunaga; Sako Masahiro; Kaneko Hideo; Kondo Naomi; Kaisho Tsuneyasu; Miyawaki Toshio
Toll-like receptor signaling is impaired in dendritic cells from patients with X-linked agammaglobulinemia.
Clinical immunology (Orlando, Fla.) 2008;126(2):148-54.
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2008: Jin Rong; Kaneko Hideo; Suzuki Hiroko; Arai Takahiro; Teramoto Takahide; Fukao Toshiyuki; Kondo Naomi
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.
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2008: Bai Chunying; Matsui Eiko; Ohnishi Hidenori; Kimata Kaori; Kasahara Kimiko; Kaneko Hideo; Kato Zenichiro; Fukao Toshiyuki; Kondo Naomi
A novel polymorphism, E254K, in the 5-lipoxygenase gene associated with bronchial asthma.
International journal of molecular medicine 2008;21(2):139-44.
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2008: Kondo M; Fukao T; Omoya K; Kawamoto N; Aoki M; Teramoto T; Kaneko H; Kondo N
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.
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2007: Fukao Toshiyuki; Zhang Gaixiu; Rolland Marie-Odile; Zabot Marie-Therese; Guffon Nathalie; Aoki Yusuke; Kondo Naomi
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.
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2007: Funato Michinori; Kaneko Hideo; Ozeki Michio; Suzuki Hiroko; Orii Kenji; Teramoto Takahide; Fukao Toshiyuki; Kondo Naomi
A positive Donath-Landsteiner test in paroxysmal cold haemoglobinuria.
European journal of haematology 2007;79(5):462.
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2007: Fukao Toshiyuki; Kursula Petri; Owen Elizabeth Patricia; Kondo Naomi
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.
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2007: Montaño A M; Sukegawa K; Kato Z; Carrozzo R; Di Natale P; Christensen E; Orii K O; Orii T; Kondo N; Tomatsu S
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.
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2007: Ozeki Michio; Funato Michinori; Kanda Kaori; Ito Masahumi; Teramoto Takahide; Kaneko Hideo; Fukao Toshiyuki; Kondo Naomi
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.
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2007: Aoyama Yumi; Asai Kanako; Hioki Kana; Funato Michinori; Kondo Naomi; Kitajima Yasuo
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.
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2007: Fukao Toshiyuki; Zhang Gaixiu; Aoki Yusuke; Arai Takahiro; Teramoto Takahide; Kaneko Hideo; Sugie Hideo; Kondo Naomi
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.
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2007: Funato Michinori; Kaneko Hideo; Matsui Eiko; Teramoto Takahide; Kato Zenichiro; Fukao Toshiyuki; Okusu Kiyofumi; Kondo Naomi
Refractory osteomyelitis caused by bacille Calmette-Guérin vaccination: a case report.
Diagnostic microbiology and infectious disease 2007;59(1):89-91.
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2007: Aoki Minako; Fukao Toshiyuki; Kaneko Hideo; Mizunaga Shingo; Mitsuyama Junichi; Sawamura Haruki; Seishima Mitsuru; Kondo Naomi
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.
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2007: Kato Zenichiro; Nakamura Mitsuhiro; Funato Michinori; Kuwabara Hideaki; Kondo Naomi
Accidental etizolam ingestion in a child.
Pediatric emergency care 2007;23(7):472-3.
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2007: Yamada Keitaro; Fukao Toshiyuki; Suzuki Hiroko; Inoue Ryosuke; Kondo Tomio; Kondo Naomi
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.
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2007: Kato Tomomi; Kato Zenichiro; Kuratsubo Izumi; Ota Tetsuo; Orii Tadao; Kondo Naomi; Suzuki Yasuyuki
Evaluation of ADL in patients with Hunter disease using FIM score.
Brain & development 2007;29(5):298-305.
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2007: Kondo Naomi; Shinoda Shinji; Kaneko Hideo
[The pathophysiology of food allergy]
Arerugi = [Allergy] 2007;56(5):439-43.
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2007: Haapalainen Antti M; Meriläinen Gitte; Pirilä Päivi L; Kondo Naomi; Fukao Toshiyuki; Wierenga Rik K
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.
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2007: Sakurai Satomi; Fukao Toshiyuki; Haapalainen Antti M; Zhang Gaixiu; Yamada Keitaro; Lilliu Franco; Yano Shoji; Robinson Peter; Gibson Michael K; Wanders Ronald J A; Mitchell Grant A; Wierenga Rik K; Kondo Naomi
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.
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2007: Yamada Keitaro; Fukao Toshiyuki; Zhang Gaixiu; Sakurai Satomi; Ruiter Jos P N; Wanders Ronald J A; Kondo Naomi
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.
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2007: Kondo Naomi
[Influence of genes and environment on allergic disorders]
Arerugi = [Allergy] 2007;56(2):94-100.
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2007: Kato Zenichiro; Yamagishi Atsushi; Kondo Naomi
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.
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2006: Sukegawa-Hayasaka K; Kato Z; Nakamura H; Tomatsu S; Fukao T; Kuwata K; Orii T; Kondo N
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.
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2006: Zhang Gaixiu; Fukao Toshiyuki; Sakurai Satomi; Yamada Keitaro; Michael Gibson K; Kondo Naomi
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.
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2006: Fukao Toshiyuki; Sakurai Satomi; Rolland Marie-Odile; Zabot Marie-Therese; Schulze Andreas; Yamada Keitaro; Kondo Naomi
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.
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2006: Kato Tomomi; Isogai Koji; Orii Koji; Kuratsubo Izumi; Kondo Naomi; Orii Tadao; Suzuki Yasuyuki
Portal hypertension in a patient with Hunter disease.
Journal of inherited metabolic disease 2006;29(5):686.
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2006: Teramoto Takahide; Fukao Toshiyuki; Tomita Yoshiko; Terauchi Yoshiaki; Hosoi Kaori; Matsui Eiko; Aoki Minako; Kondo Naomi; Mikawa Haruki
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.
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2006: Kondo Naomi; Katsunuma Toshio; Odajima Yasuhei; Morikawa Akihiro
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.
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2006: Kondo Naomi; Fukuda Kazuhito
[Ataxia-telangiectasia]
Nippon rinsho. Japanese journal of clinical medicine 2006;Suppl 3():114-8.
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2006: Kaneko Hideo; Matsui Eiko; Asano Tsutomu; Kato Zenichiro; Teramoto Takahide; Aoki Minako; Kawamoto Norio; Lian Li Ai; Kasahara Kimiko; Kondo Naomi
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.
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2006: Horikoshi Hiroko; Kato Zenichiro; Masuno Mitsuo; Asano Takahiko; Nagase Tomoko; Yamagishi Yuka; Kozawa Ryo; Arai Takahiro; Aoki Minako; Teramoto Takahide; Omoya Kentaro; Matsumoto Naomichi; Kurotaki Naohiro; Shimokawa Osamu; Kurosawa Kenji; Kondo Naomi
Neuroradiologic findings in Sotos syndrome.
Journal of child neurology 2006;21(7):614-8.
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2006: Kaneko Hideo; Isogai Koji; Kondo Masashi; Hosoi Kaori; Asano Tsutomu; Funato Michinori; Kondo Naomi
Autologous peripheral blood stem cell transplantation in a patient with relapsed pleuropulmonary blastoma.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2006;28(6):383-5.
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2006: Orii Kenji E; Lee Youngsoo; Kondo Naomi; McKinnon Peter J
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.
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2006: Funato Michinori; Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Suzuki Yasuyuki; Imamura Yoshihiko; Matsumoto Tadashi; Tsukamoto Toshiro; Kojidani Tomoko; Osumi Takashi; Fukao Toshiyuki; Kondo Naomi
Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies.
Brain & development 2006;28(5):287-92.
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2006: Kaneko Hideo; Matsui Eiko; Shinoda Shinnji; Kawamoto Norio; Nakamura Yosikazu; Uehara Ritei; Matsuura Nobuo; Morita Masatoshi; Tada Hiroshi; Kondo Naomi
Effects of dioxins on the quantitative levels of immune components in infants.
Toxicology and industrial health 2006;22(3):131-6.
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2006: Matsukuma Eiji; Kato Zenichiro; Omoya Kentaro; Hashimoto Kazuyuki; Li Ailian; Yamamoto Yutaka; Ohnishi Hidenori; Hiranuma Hidenori; Komine Hisakazu; Kondo Naomi
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.
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2006: Kawamoto Norio; Kaneko Hideo; Takemura Masao; Seishima Mitsuru; Sakurai Satomi; Fukao Toshiyuki; Kasahara Kimiko; Iwasa Shinichi; Kondo Naomi
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.
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2006: Kato Zenichiro; Asano Takahiko; Kondo Naomi
Inosiplex affects the spectra of proton magnetic resonance spectroscopy in subacute sclerosing panencephalitis.
Journal of child neurology 2006;21(2):177-8.
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2005: Kondo Naomi; Nagaya Soichiro; Kuwabara Manami; Matsui Eiko
[Genetic testing and gene-based testing forAllergic disorders]
Nippon rinsho. Japanese journal of clinical medicine 2005;63 Suppl 12():232-9.
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2005: Kato Zenichiro; Tsubouchi Kohji; Kondo Naomi
Molluscum contagiosum prevents progression of staphylococcal scalded skin syndrome.
European journal of pediatrics 2005;164(12):768-9.
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2005: Yoshikawa Kaori; Matsui Eiko; Kaneko Hideo; Fukao Toshiyuki; Inoue Ryosuke; Teramoto Takahide; Shinoda Shinji; Fukutomi Osamu; Aoki Minako; Kasahara Kimiko; Kondo Naomi
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.
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2005: Orii Koji O; Grubb Jeffrey H; Vogler Carole; Levy Beth; Tan Yun; Markova Kamelia; Davidson Beverly L; Mao Q; Orii Tadao; Kondo Naomi; Sly William S
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.
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2005: Hashimoto Kazuyuki; Kato Zenichiro; Nagase Tomoko; Shimozawa Nobuyuki; Kuwata Kazuo; Omoya Kentaro; Li Ailian; Matsukuma Eiji; Yamamoto Yutaka; Ohnishi Hidenori; Tochio Hidehito; Shirakawa Masahiro; Suzuki Yasuyuki; Wanders Ronald J A; Kondo Naomi
Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder.
Pediatric research 2005;58(2):263-9.
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2005: Kondo Masashi; Fukao Toshiyuki; Teramoto Takahide; Kaneko Hideo; Takahashi Yukitoshi; Okamoto Hiroyuki; Kondo Naomi
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.
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2005: Kaneko H; Kawamoto N; Asano T; Mabuchi Y; Horikoshi H; Teramoto T; Matsui E; Kondo M; Fukao T; Kasahara K; Kondo N
Leaky phenotype of X-linked agammaglobulinaemia in a Japanese family.
Clinical and experimental immunology 2005;140(3):520-3.
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2005: Kondo Naomi; Kaneko Hideo; Kuwabara Manami
[Classification of immunodeficiency diseases]
Nippon rinsho. Japanese journal of clinical medicine 2005;63 Suppl 5():548-58.
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2005: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Funato Michinori; Kondo Naomi; Suzuki Yasuyuki
Molecular and neurologic findings of peroxisome biogenesis disorders.
Journal of child neurology 2005;20(4):326-9.
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2005: Kursula Petri; Sikkilä Herkko; Fukao Toshiyuki; Kondo Naomi; Wierenga Rik K
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.
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2005: Kato Tomomi; Kato Zenichiro; Kuratsubo Izumi; Tanaka Noboru; Ishigami Tabito; Kajihara Jun-Ichi; Sukegawa-Hayasaka Kazuko; Orii Koji; Isogai Koji; Fukao Toshiyuki; Shimozawa Nobuyuki; Orii Tadao; Kondo Naomi; Suzuki Yasuyuki
Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II.
Journal of human genetics 2005;50(8):395-402.
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2005: Kondo M; Suzuki K; Inoue R; Sakaguchi H; Matsukuma E; Kato Z; Kaneko H; Fukao T; Kondo N
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.
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2004: Fukao Toshiyuki; Shintaku Haruo; Kusubae Ryou; Zhang Gai X; Nakamura Kozue; Kondo Masashi; Kondo Naomi
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.
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2004: Nagao-Watanabe M; Fukao T; Matsui E; Kaneko H; Inoue R; Kawamoto N; Kasahara K; Nagai M; Ichiki Y; Kitajima Y; Kondo N
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.
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2004: Kaneko Hideo; Isogai Kouji; Fukao Toshiyuki; Matsui Eiko; Kasahara Kimiko; Yachie Akihiro; Seki Hidetoshi; Koizumi Shoichi; Arai Masami; Utunomiya Joji; Miki Yoshio; Kondo Naomi
Relatively common mutations of the Bloom syndrome gene in the Japanese population.
International journal of molecular medicine 2004;14(3):439-42.
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2004: Omoya Kentaro; Kato Zenichiro; Matsukuma Eiji; Li Ailian; Hashimoto Kazuyuki; Yamamoto Yutaka; Ohnishi Hidenori; Kondo Naomi
Systematic optimization of active protein expression using GFP as a folding reporter.
Protein expression and purification 2004;36(2):327-32.
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2004: Tomatsu Shunji; Filocamo Mirella; Orii Koji O; Sly William S; Gutierrez Monica A; Nishioka Tatsuo; Serrato Olga Peña; Di Natale Paola; Montaño Adriana Maria; Yamaguchi Seiji; Kondo Naomi; Orii Tadao; Noguchi Akihiko
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.
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2004: Zhang Gai Xiu; Fukao Toshiyuki; Rolland Marie-Odile; Zabot Marie-Therese; Renom Gilles; Touma Elias; Kondo Masashi; Matsuo Naoki; Kondo Naomi
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.
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2004: Tomatsu Shunji; Orii Koji O; Bi Y; Gutierrez Monica A; Nishioka Tatsuo; Yamaguchi Seiji; Kondo Naomi; Orii Tadao; Noguchi Akihiko; Sly William S
General implications for CpG hot spot mutations: methylation patterns of the human iduronate-2-sulfatase gene locus.
Human mutation 2004;23(6):590-8.
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2004: Shimozawa Nobuyuki; Tsukamoto Toshiro; Nagase Tomoko; Takemoto Yasuhiko; Koyama Naoki; Suzuki Yasuyuki; Komori Masayuki; Osumi Takashi; Jeannette Gootjes; Wanders Ronald J A; Kondo Naomi
Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene.
Human mutation 2004;23(6):552-8.
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2004: Kaneko Hideo; Kondo Naomi
Clinical features of Bloom syndrome and function of the causative gene, BLM helicase.
Expert review of molecular diagnostics 2004;4(3):393-401.
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2004: Asano T; Kaneko H; Terada T; Kasahara Y; Fukao T; Kasahara K; Kondo N
Molecular analysis of B-cell differentiation in selective or partial IgA deficiency.
Clinical and experimental immunology 2004;136(2):284-90.
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2004: Yamamoto Yutaka; Kato Zenichiro; Matsukuma Eiji; Li Ailian; Omoya Kentaro; Hashimoto Kazuyuki; Ohnishi Hidenori; Kondo Naomi
Generation of highly stable IL-18 based on a ligand-receptor complex structure.
Biochemical and biophysical research communications 2004;317(1):181-6.
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2004: Tomatsu Shunji; Okamura Kazuo; Taketani Takeshi; Orii Koji O; Nishioka Tatsuo; Gutierrez Monica A; Velez-Castrillon Susana; Fachel Abgela A; Grubb Jeffrey H; Cooper Alan; Thornley Margaret; Wraith Ed; Barrera Luis A; Giugliani Roberto; Schwartz Ida V; Frenking Gudrun Schulze; Beck Michael; Kircher Susanne G; Paschke Eduard; Yamaguchi Seiji; Ullrich Kurt; Isogai Koji; Suzuki Yasuyuki; Orii Tadao; Kondo Naomi; Creer Michael; Noguchi Akihiko
Development and testing of new screening method for keratan sulfate in mucopolysaccharidosis IVA.
Pediatric research 2004;55(4):592-7.
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2004: Nagase Tomoko; Shimozawa Nobuyuki; Takemoto Yasuhiko; Suzuki Yasuyuki; Komori Masayuki; Kondo Naomi
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.
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2004: Kondo N; Matsui E; Kaneko H; Aoki M; Kato Z; Fukao T; Kasahara K; Morimoto N
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.
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2004: Fukao Toshiyuki; Chen Philip; Ren Jun; Kaneko Hideo; Zhang Gai Xiu; Kondo Masahi; Yamamoto Ken-Ichi; Furuichi Yasuhiro; Takeda Shunichi; Kondo Naomi; Lavin Martin F
Disruption of the BLM gene in ATM-null DT40 cells does not exacerbate either phenotype.
Oncogene 2004;23(8):1498-506.
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2004: Kaneko Hideo; Fukao Toshiyuki; Kondo Naomi
The function of RecQ helicase gene family (especially BLM) in DNA recombination and joining.
Advances in biophysics 2004;38():45-64.
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2003: Terada T; Kaneko H; Fukao T; Teramoto T; Asano T; Li A L; Kasahara K; Kondo N
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.
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2003: Tomatsu Shunji; Orii Koji O; Vogler Carole; Nakayama Jun; Levy Beth; Grubb Jeffrey H; Gutierrez Monica A; Shim Soomin; Yamaguchi Seiji; Nishioka Tatsuo; Montano Adriana Maria; Noguchi Akihiko; Orii Tadao; Kondo Naomi; Sly William S
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.
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2003: Li Ailian; Kato Zenichiro; Ohnishi Hidenori; Hashimoto Kazuyuki; Matsukuma Eiji; Omoya Kentaro; Yamamoto Yutaka; Kondo Naomi
Optimized gene synthesis and high expression of human interleukin-18.
Protein expression and purification 2003;32(1):110-8.
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2003: Kato Zenichiro; Jee JunGoo; Shikano Hiroaki; Mishima Masaki; Ohki Izuru; Ohnishi Hidenori; Li Ailian; Hashimoto Kazuyuki; Matsukuma Eiji; Omoya Kentaro; Yamamoto Yutaka; Yoneda Teruyo; Hara Takane; Kondo Naomi; Shirakawa Masahiro
The structure and binding mode of interleukin-18.
Nature structural biology 2003;10(11):966-71.
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2003: Kato Zenichiro; Kozawa Ryo; Teramoto Takahide; Hashimoto Kazuyuki; Shinoda Shinji; Kondo Naomi
Acute cerebellitis in primary human herpesvirus-6 infection.
European journal of pediatrics 2003;162(11):801-3.
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2003: Kasahara Yukiko; Kaneko Hideo; Fukao Toshiyuki; Terada Tomoyoshi; Asano Tsutomu; Kasahara Kimiko; Kondo Naomi
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.
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2003: Takemoto Yasuhiko; Suzuki Yasuyuki; Horibe Ryoko; Shimozawa Nobuyuki; Wanders Ronald J A; Kondo Naomi
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.
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2003: Matsumoto Naomi; Tamura Shigehiko; Furuki Satomi; Miyata Non; Moser Ann; Shimozawa Nobuyuki; Moser Hugo W; Suzuki Yasuyuki; Kondo Naomi; Fujiki Yukio
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.
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2003: Aoki Minako; Matsui Eiko; Kaneko Hideo; Inoue Ryosuke; Fukao Toshiyuki; Watanabe Mizuho; Teramoto Takahide; Kato Zenichiro; Suzuki Kiyotaka; Suzuki Yasuyuki; Kasahara Kimiko; Kondo Naomi
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.
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2003: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Ohura Toshihiro; Suzuki Yasuyuki; Kondo Naomi
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.
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2003: Montaño Adriana Maria; Kaitila Ilkka; Sukegawa Kazuko; Tomatsu Shunji; Kato Zenichiro; Nakamura Haruki; Fukuda Seiji; Orii Tadao; Kondo Naomi
Mucopolysaccharidosis IVA: characterization of a common mutation found in Finnish patients with attenuated phenotype.
Human genetics 2003;113(2):162-9.
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2003: Fukao Toshiyuki; Matsuo Naoki; Zhang Gai Xiu; Urasawa Rintaro; Kubo Tetsuo; Kohno Yoshinori; Kondo Naomi
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.
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2003: Tomatsu Shunji; Orii Koji O; Vogler Carole; Grubb Jeffrey H; Snella Elizabeth M; Gutierrez Monica; Dieter Tatiana; Holden Christopher C; Sukegawa Kazuko; Orii Tadao; Kondo Naomi; Sly William S
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.
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2003: Kato Zenichiro; Kozawa Ryo; Hashimoto Kazuyuki; Kondo Naomi
Transient lesion in the splenium of the corpus callosum in acute cerebellitis.
Journal of child neurology 2003;18(4):291-2.
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2003: Teramoto Takahide; Kaneko Hideo; Funato Michinori; Sawa Hirofumi; Nagashima Kazuo; Hirose Yoshinobu; Kondo Naomi
Progressive multifocal leukoencephalopathy in a patient with X-linked agammaglobulinemia.
Scandinavian journal of infectious diseases 2003;35(11-12):909-10.
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2003: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Suzuki Yasuyuki; Kondo Naomi
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: Fukao T; Zhang G X; Sakura N; Kubo T; Yamaga H; Hazama A; Kohno Y; Matsuo N; Kondo M; Yamaguchi S; Shigematsu Y; Kondo N
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.
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2002: Tomatsu Shunji; Orii Koji O; Vogler Carole; Grubb Jeffrey H; Snella Elizabeth M; Gutierrez Monica A; Dieter Tatiana; Sukegawa Kazuko; Orii Tadao; Kondo Naomi; Sly William S
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.
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2002: Kato Zenichiro; Saito Kyoko; Yamada Michiko; Asano Takahiko; Kondo Naomi
Proton magnetic resonance spectroscopy in a case of subacute sclerosing panencephalitis.
Journal of child neurology 2002;17(10):788-90.
-
2002: Suzuki K; Inoue R; Sakaguchi H; Aoki M; Kato Z; Kaneko H; Matsushita S; Kondo N
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.
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2002: Beamish Heather; Kedar Padmini; Kaneko Hideo; Chen Philip; Fukao Toshiyuki; Peng Cheng; Beresten Sergei; Gueven Nuri; Purdie David; Lees-Miller Susan; Ellis Nathan; Kondo Naomi; Lavin Martin F
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.
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2002: Morimoto Wataru; Kaneko Hideo; Isogai Kouji; Kasahara Kimiko; Kondo Naomi
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: Orii Kenji E; Kato Zenichiro; Osamu Fukutomi; Funato Michinori; Kubodera Uniko; Inoue Ryosuke; Shimozawa Nobuyuki; Kondo Naomi
Changes of autonomic nervous system function in patients with breath-holding spells treated with iron.
Journal of child neurology 2002;17(5):337-40.
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2002: Kondo Naomi; Teramoto Takahide; Inoue Ryosuke; Fukutomi Osamu; Matsui Eiko; Shinoda Shinji; Watanabe Mizuho; Sakaguchi Heima; Aoki Minako; Morimoto Wataru; Suzuki Kiyotaka; Ohnishi Hidenori; Takemoto Yasuhiko; Tanaka Yoko; Asano Tsutomu; Yoshikawa Kaori; Nagase Tomoko; Hashimoto Kazuyuki; Fujita Yukiko; Yamamoto Yutaka; Ri Airen; Hirayama Khoichirou
[Evaluation before and after pranlukast administration with the QOL questionnaire (revised version 2001) for pediatric patients with bronchial asthma and their parents or caregivers]
Arerugi = [Allergy] 2002;51(5):421-9.
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2002: Kato Zenichiro; Funato Michinori; Orii Kenji E; Saito Kayoko; Kondo Naomi
Spinal muscular atrophy type 1 with anti-acetylcholine receptor antibody.
European journal of pediatrics 2002;161(5):293-4.
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2002: Sakaguchi H; Inoue R; Kaneko H; Watanabe M; Suzuki K; Kato Z; Matsushita S; Kondo N
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.
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2002: Watanabe Mizuho; Kaneko Hideo; Shikano Hiroaki; Aoki Minako; Sakaguchi Heima; Matsui Eiko; Inoue Ryosuke; Kato Zenichiro; Kasahara Kimiko; Fukutomi Osamu; Kondo Tomio; Kondo Naomi
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.
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2002: Fukao Toshiyuki; Nakamura Haruki; Nakamura Kozue; Perez-Cerda Celia; Baldellou Antonio; Barrionuevo Carlos R; Castello Francisco Girona; Kohno Yoshinori; Ugarte Magdalena; Kondo Naomi
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.
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2002: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Suzuki Yasuyuki; Fujiki Yukio; Wanders Ronald J A; Kondo Naomi
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.
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2002: Tomatsu Shunji; Orii Koji O; Islam M Rafiqul; Shah Gul N; Grubb Jeffrey H; Sukegawa Kazuko; Suzuki Yasuyuki; Orii Tadao; Kondo Naomi; Sly William S
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.
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2002: Suzuki Yasuyuki; Iai Mizue; Kamei Atsushi; Tanabe Yuzo; Chida Shoichi; Yamaguchi Seiji; Zhang Zhongyi; Takemoto Yasuhiko; Shimozawa Nobuyuki; Kondo Naomi
Peroxisomal acyl CoA oxidase deficiency.
The Journal of pediatrics 2002;140(1):128-30.
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2002: Kato Zenichiro; Fukutomi Osamu; Kondo Naomi
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.
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2002: Takemoto Yasuhiko; Suzuki Yasuyuki; Tamakoshi Akiko; Onodera Osamu; Tsuji Shoji; Hashimoto Takashi; Shimozawa Nobuyuki; Orii Tadao; Kondo Naomi
Epidemiology of X-linked adrenoleukodystrophy in Japan.
Journal of human genetics 2002;47(11):590-3.
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2002: Kaneko Hideo; Inoue Ryosuke; Teramoto Takahide; Morimoto Wataru; Isogai Kouji; Kasahara Kimiko; Kondo Naomi
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.
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2001: Takahashi Y; Sato T; Goto K; Fujino M; Fujiwara T; Yamaga M; Ito T; Isono H; Kondo N
Optical filters inhibiting television-induced photosensitive seizures.
Neurology 2001;57(10):1767-73.
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2001: Toietta G; Severini G M; Traversari C; Tomatsu S; Sukegawa K; Fukuda S; Kondo N; Tortora P; Bordignon C
Various cells retrovirally transduced with N-acetylgalactosoamine-6-sulfate sulfatase correct Morquio skin fibroblasts in vitro.
Human gene therapy 2001;12(16):2007-16.
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2001: Terada T; Kaneko H; Li A L; Kasahara K; Ibe M; Yokota S; Kondo N
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.
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2001: Suzuki Y; Shimozawa N; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Kondo N
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: Kaneko H; Morimoto W; Fukao T; Kasahara K; Kondo N
Telomerase activity in cell lines and lymphoma originating from Bloom syndrome.
Leukemia & lymphoma 2001;42(4):757-60.
-
2001: Kondo N; Inoue R; Matsui E; Shinoda S; Fukutomi O; Teramoto T; Watanabe M; Sakaguchi H; Aoki M; Hirayama K
[QOL questionnaire version 2001 for pediatric patients with bronchial asthma and their parents or caregivers--preparation and evaluation]
Arerugi = [Allergy] 2001;50(8):667-78.
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2001: Shikano H; Kato Z; Kaneko H; Watanabe M; Inoue R; Kasahara K; Takemura M; Kondo N
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: Kondo N; Matsui E; Kaneko H; Fukao T; Teramoto T; Inoue R; Watanabe M; Aoki M; Kasahara K; Morimoto N
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.
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2001: Inoue R; Matsushita S; Kaneko H; Shinoda S; Sakaguchi H; Nishimura Y; Kondo N
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: Tamura S; Matsumoto N; Imamura A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
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: Takahashi S; Takahashi Y; Kondo N; Orii T
Epileptic seizures and structural abnormalities in a patient with holoprosencephaly.
Brain & development 2001;23(4):264-8.
-
2001: Suzuki Y; Shimozawa N; Imamura A; Fukuda S; Zhang Z; Orii T; Kondo N
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.
Journal of inherited metabolic disease 2001;24(2):151-65.
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2001: Takahashi Y; Sukegawa K; Aoki M; Ito A; Suzuki K; Sakaguchi H; Watanabe M; Isogai K; Mizuno S; Hoshi H; Kuwata K; Tomatsu S; Kato S; Ito T; Kondo N; Orii T
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: Suzuki Y; Imamura A; Shimozawa N; Kondo N
The clinical course of childhood and adolescent adrenoleukodystrophy before and after Lorenzo's oil.
Brain & development 2001;23(1):30-3.
-
2001: Takahashi Y; Ozawa T; Nakamura H; Yamada S; Okamoto H; Yajima S; Goto K; Kondo N
Long-wavelength red light emission from TV and photosensitive siezures.
Acta neurologica Scandinavica 2001;103(2):114-9.
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2001: Nakamura K; Fukao T; Perez-Cerda C; Luque C; Song X Q; Naiki Y; Kohno Y; Ugarte M; Kondo N
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: Fukao T; Scriver C R; Kondo N;
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: Fukao T; Watanabe H; Orii K; Takahashi Y; Hirano A; Kondo T; Yamaguchi S; Aoyama T; Kondo N
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: Terada T; Kaneko H; Fukao T; Tashita H; Li A L; Takemura M; Kondo N
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.
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2001: Kondo N; Matsui E; Kaneko H; Fukao T; Teramoto T; Inoue R; Watanabe M; Kasahara K; Morimoto N
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.
-
2001: Kaneko H; Orii K E; Yamada M; Inoue R; Kondo N
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: Matsumoto N; Tamura S; Moser A; Moser H W; Braverman N; Suzuki Y; Shimozawa N; Kondo N; Fujiki Y
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.
Journal of human genetics 2001;46(5):273-7.
-
2000: Imamura A; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Fujiki Y; Orii T; Osumi T; Wanders R J; Kondo N
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: Ghaedi K; Honsho M; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
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.
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2000: Fujii H; Fukutomi O; Inoue R; Shinoda S; Okammoto H; Teramoto T; Kondo N; Wada H; Saito K; Matsuoka T; Seishima M
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.
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2000: Mizuno S; Takahashi Y; Kato Z; Goto H; Kondo N; Hoshi H
Magnetic resonance spectroscopy of tubers in patients with tuberous sclerosis.
Acta neurologica Scandinavica 2000;102(3):175-8.
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2000: Matsui E; Kaneko H; Teramoto T; Fukao T; Inoue R; Kasahara K; Takemura M; Seishima M; Kondo N
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: Fukao T; Mitchell G A; Song X Q; Nakamura H; Kassovska-Bratinova S; Orii K E; Wraith J E; Besley G; Wanders R J; Niezen-Koning K E; Berry G T; Palmieri M; Kondo N
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: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Ghaedi K; Fujiki Y; Kondo N
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: Suzuki Y; Isogai K; Teramoto T; Tashita H; Shimozawa N; Nishimura M; Asano T; Oda M; Kamei A; Ishiguro H; Kato S; Ohashi T; Kobayashi H; Eto Y; Kondo N
Bone marrow transplantation for the treatment of X-linked adrenoleukodystrophy.
Journal of inherited metabolic disease 2000;23(5):453-8.
-
2000: Kondo N
[Bloom syndrome]
Nippon rinsho. Japanese journal of clinical medicine 2000;58(7):1460-6.
-
2000: Sukegawa K; Nakamura H; Kato Z; Tomatsu S; Montaño A M; Fukao T; Toietta G; Tortora P; Orii T; Kondo N
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: Hayakawa S; Kaneko H; Fukao T; Kasahara K; Matsumoto T; Furuichi Y; Kondo N
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: Tanaka Y; Suzuki Y; Shimozawa N; Nanba E; Kondo N
Congenital myotonic dystrophy: report of paternal transmission.
Brain & development 2000;22(2):132-4.
-
2000: Montaño A M; Yamagishi A; Tomatsu S; Fukuda S; Copeland N G; Orii K E; Isogai K; Yamada N; Kato Z I; Jenkins N A; Gilbert D J; Sukegawa K; Orii T; Kondo N
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: Shimozawa N; Zhang Z; Imamura A; Suzuki Y; Fujiki Y; Tsukamoto T; Osumi T; Aubourg P; Wanders R J; Kondo N
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: Fukao T; Yoshida T; Kaneko H; Song X Q; Tashita H; Teramoto T; Inoue R; Watters D; Lavin M; Kondo N
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: Kondo N; Shinoda S; Fukutomi O; Agata H; Terada T; Shikano H; Montaño A M; Sakaguchi H; Watanabe M; Komiyama K; Yokoyama Y; Morimoto N
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: Imamura A; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Fujiki Y; Orii T; Osumi T; Kondo N
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: Iwata S; Sukegawa K; Kokuryu M; Tomatsu S; Kondo N; Iwasa S; Orii T
Glycosaminoglycans in neonatal urine.
Archives of disease in childhood. Fetal and neonatal edition 2000;82(1):F78.
-
2000: Kaneko H; Kondo N
[IgA-IgM deficiency]
Ryoikibetsu shokogun shirizu 2000;(32):96-8.
-
2000: Matsui E; Kondo N
[Hermans syndrome]
Ryoikibetsu shokogun shirizu 2000;(32):53-5.
-
2000: Kaneko H; Kondo N
[Good syndrome, immunodeficiency with thymoma]
Ryoikibetsu shokogun shirizu 2000;(32):49-52.
-
2000: Kondo N
[Common variable immunodeficiency(CVID)]
Ryoikibetsu shokogun shirizu 2000;(32):46-8.
-
2000: Kato Z; Kondo N
[Seckel syndrome]
Ryoikibetsu shokogun shirizu 2000;(32):276-8.
-
2000: Kondo N
[Bloom syndrome]
Ryoikibetsu shokogun shirizu 2000;(32):261-4.
-
2000: Kondo N
[Ataxia-telangiectasia(AT), Louis-Bar syndrome]
Ryoikibetsu shokogun shirizu 2000;(32):131-4.
-
2000: Kaneko H; Fukao T; Inoue R; Kasahara K; Matsui E; Kondo N
Long-term study of a female hyper-IgM immunodeficiency.
Experimental and clinical immunogenetics 2000;17(4):173-8.
-
2000: Suzuki Y; Shimozawa N; Imamura A; Kondo N
[Peroxisomal disorders]
Ryoikibetsu shokogun shirizu 2000;(29 Pt 4):452-9.
-
2000: Watanabe H; Orii K E; Fukao T; Song X Q; Aoyama T; IJlst L; Ruiter J; Wanders R J; Kondo N
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.
-
1999: Kondo N
[Analysis of atopic gene]
Nippon rinsho. Japanese journal of clinical medicine 1999;57 Suppl():750-5.
-
1999: Kondo N; Suzuki Y; Shimozawa N; Takahashi Y; Fukao T
[Genetics of neurologic disorders in children]
Nippon rinsho. Japanese journal of clinical medicine 1999;57 Suppl():700-6.
-
1999: Matsui E; Kaneko H; Fukao T; Teramoto T; Inoue R; Watanabe M; Kasahara K; Kondo N
Mutations of the IL-12 receptor beta2 chain gene in atopic subjects.
Biochemical and biophysical research communications 1999;266(2):551-5.
-
1999: Inoue R; Fukao T; Kato Y; Teramoto T; Utsumi M; Kondo N
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: Kaneko H; Matsui E; Fukao T; Kasahara K; Morimoto W; Kondo N
Expression of the BLM gene in human haematopoietic cells.
Clinical and experimental immunology 1999;118(2):285-9.
-
1999: Shimozawa N; Imamura A; Zhang Z; Suzuki Y; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Wanders R J; Besley G; Kondo N
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: Fukao T; Kaneko H; Birrell G; Gatei M; Tashita H; Yoshida T; Cross S; Kedar P; Watters D; Khana K K; Misko I; Kondo N; Lavin M F
ATM is upregulated during the mitogenic response in peripheral blood mononuclear cells.
Blood 1999;94(6):1998-2006.
-
1999: Toyama R; Mukai S; Itagaki A; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Wanders R J; Fujiki Y
Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.
Human molecular genetics 1999;8(9):1673-81.
-
1999: Shimozawa N; Zhang Z; Suzuki Y; Imamura A; Tsukamoto T; Osumi T; Fujiki Y; Orii T; Barth P G; Wanders R J; Kondo N
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.
Biochemical and biophysical research communications 1999;262(2):504-8.
-
1999: Agata H; Kawakami N; Kondo N; Hayashi T; Fukutomi O; Shimizu H; Orii T
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: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Toyama R; Mukai S; Fujiki Y; Tsukamoto T; Osumi T; Orii T; Wanders R J; Kondo N
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: Kondo N; Fukao T; Hirayama K; Sakamoto T; Torii S
[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]
Arerugi = [Allergy] 1999;48(5):533-45.
-
1999: Ghaedi K; Kawai A; Okumoto K; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
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: Ghaedi K; Itagaki A; Toyama R; Tamura S; Matsumura T; Kawai A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
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: Suzuki Y; Shimozawa N; Imamura A; Zhang Z; Kondo N
[Newly identified peroxisomal disorders]
No to shinkei = Brain and nerve 1999;51(4):295-302.
-
1999: Orii K E; Orii K O; Souri M; Orii T; Kondo N; Hashimoto T; Aoyama T
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: Matsuzono Y; Kinoshita N; Tamura S; Shimozawa N; Hamasaki M; Ghaedi K; Wanders R J; Suzuki Y; Kondo N; Fujiki Y
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: Zhang Z; Suzuki Y; Shimozawa N; Fukuda S; Imamura A; Tsukamoto T; Osumi T; Fujiki Y; Orii T; Wanders R J; Barth P G; Moser H W; Paton B C; Besley G T; Kondo N
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: Suzuki Y; Zhang Z; Shimozawa N; Muro M; Shono H; Toda S; Miyahara S; Hashimoto T; Usuda N; Ito M; Takashima S; Kondo N
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: Shimozawa N; Suzuki Y; Zhang Z; Miura K; Matsumoto A; Nagaya M; Castillo-Taucher S; Kondo N
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: Kasai T; Ohguchi K; Nakashima S; Ito Y; Naganawa T; Kondo N; Nozawa Y
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: Honsho M; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
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: Imamura A; Tamura S; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Orii T; Kondo N; Osumi T; Fujiki Y
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.
Human molecular genetics 1998;7(13):2089-94.
-
1998: Kondo N; Kobayashi Y; Shinoda S; Takenaka R; Teramoto T; Kaneko H; Fukao T; Matsui E; Kasahara K; Yokoyama Y
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: Yamada Y; Inoue R; Fukao T; Kaneko H; Isogai K; Fukuda S; Shimozawa N; Suzuki Y; Kondo N; Azuma E; Sakurai M
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: Kinoshita N; Ghaedi K; Shimozawa N; Wanders R J; Matsuzono Y; Imanaka T; Okumoto K; Suzuki Y; Kondo N; Fujiki Y
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: Okumoto K; Itoh R; Shimozawa N; Suzuki Y; Tamura S; Kondo N; Fujiki Y
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
Human molecular genetics 1998;7(9):1399-405.
-
1998: Kondo N; Fukao T; Kaneko H; Teramoto T; Tashita H; Inoue R
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: Okumoto K; Shimozawa N; Kawai A; Tamura S; Tsukamoto T; Osumi T; Moser H; Wanders R J; Suzuki Y; Kondo N; Fujiki Y
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: Kato Z; Fukutomi O; Kondo N
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: Tamura S; Okumoto K; Toyama R; Shimozawa N; Tsukamoto T; Suzuki Y; Osumi T; Kondo N; Fujiki Y
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: Yamada Y; Kato K; Sukegawa K; Tomatsu S; Fukuda S; Emura S; Kojima S; Matsuyama T; Sly W S; Kondo N; Orii T
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: Sukegawa K; Matsuzaki T; Fukuda S; Masuno M; Fukao T; Kokuryu M; Iwata S; Tomatsu S; Orii T; Kondo N
Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation.
Clinical genetics 1998;53(2):96-101.
-
1998: Isogai K; Sukegawa K; Tomatsu S; Fukao T; Song X Q; Yamada Y; Fukuda S; Orii T; Kondo N
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: Fukuda S; Suzuki Y; Shimozawa N; Zhang Z; Orii T; Aoyama T; Hashimoto T; Kondo N
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: Kaneko H; Ariyasu T; Inoue R; Fukao T; Kasahara K; Teramoto T; Matsui E; Hayakawa S; Kondo N
Expression of Pax5 gene in human haematopoietic cells and tissues: comparison with immunodeficient donors.
Clinical and experimental immunology 1998;111(2):339-44.
-
1998: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Tsukamoto T; Osumi T; Tateishi K; Okumoto K; Fujiki Y; Orii T; Barth P G; Wanders R J; Kondo N
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: Tashita H; Fukao T; Kaneko H; Teramoto T; Inoue R; Kasahara K; Kondo N
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: Teramoto T; Fukao T; Tashita H; Inoue R; Kaneko H; Takemura M; Kondo N
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: Fukao T; Song X Q; Yoshida T; Tashita H; Kaneko H; Teramoto T; Inoue R; Katamura K; Mayumi M; Hiratani M; Taniguchi N; Arai J; Wakiguchi H; Bar-Shira A; Shiloh Y; Kondo N
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: Fukao T; Nakamura H; Song X Q; Nakamura K; Orii K E; Kohno Y; Kano M; Yamaguchi S; Hashimoto T; Orii T; Kondo N
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: Song X Q; Fukao T; Watanabe H; Shintaku H; Hirayama K; Kassovska-Bratinova S; Kondo N; Mitchell G A
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: Fukao T; Kaneko H; Kondo N
[Ataxia-telangiectasia]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):618-21.
-
1998: Sukegawa K; Tomatsu S; Kondo N; Orii T
[Mucopolysaccharidosis type VII (Sly disease)]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):449-52.
-
1998: Sukegawa K; Tomatsu S; Kondo N; Orii T
[Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome)]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):446-8.
-
1998: Sukegawa K; Tomatsu S; Kondo N; Orii T
[Mucopolysaccharidosis type IV (Morquio syndrome, beta-galactosidase deficiency)]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):442-5.
-
1998: Sukegawa K; Tomatsu S; Kondo N; Orii T
[Mucopolysaccharidosis type III (Sanfilippo syndrome)]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):439-41.
-
1998: Sukegawa K; Tomatsu S; Kondo N; Orii T
[Mucopolysaccharidosis type II (Hunter syndrome)]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):435-8.
-
1998: Sukegawa K; Tomatsu S; Kondo N; Orii T
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):431-4.
-
1998: Yamada N; Fukuda S; Tomatsu S; Muller V; Hopwood J J; Nelson J; Kato Z; Yamagishi A; Sukegawa K; Kondo N; Orii T
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: Fukao T; Tashita H; Teramoto T; Inoue R; Kaneko H; Komiyama K; Bar-Shira A; Gilad S; Shiloh Y; Nishimura M; Kondo N
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: Shimozawa N; Suzuki Y; Tomatsu S; Nakamura H; Kono T; Takada H; Tsukamoto T; Fujiki Y; Orii T; Kondo N
A novel mutation, R125X in peroxisome assembly factor-1 responsible for Zellweger syndrome.
Human mutation 1998;Suppl 1():S134-6.
-
1998: Tomatsu S; Fukuda S; Cooper A; Wraith J E; Yamagishi A; Kato Z; Yamada N; Isogai K; Sukegawa K; Suzuki Y; Shimozawa N; Kondo N; Orii T
Fifteen polymorphisms in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene: diagnostic implications in Morquio disease.
Human mutation 1998;Suppl 1():S42-6.
-
1997: Suzuki Y; Lee K; Shimozawa N; Orii T; Kondo N
Biochemical and immunocytochemical properties of peroxisomes and mitochondria in bovine chromaffin cells.
Cell structure and function 1997;22(6):615-9.
-
1997: Kaneko H; Inoue R; Fukao T; Kasahara K; Tashita H; Teramoto T; Kondo N
Two Japanese siblings with Bloom syndrome gene mutation and B-cell lymphoma.
Leukemia & lymphoma 1997;27(5-6):539-42.
-
1997: Kaneko H; Orii K O; Matsui E; Shimozawa N; Fukao T; Matsumoto T; Shimamoto A; Furuichi Y; Hayakawa S; Kasahara K; Kondo N
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: Kato Z; Fukuda S; Tomatsu S; Vega H; Yasunaga T; Yamagishi A; Yamada N; Valencia A; Barrera L A; Sukegawa K; Orii T; Kondo N
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: Suzuki Y; Jiang L L; Souri M; Miyazawa S; Fukuda S; Zhang Z; Une M; Shimozawa N; Kondo N; Orii T; Hashimoto T
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: Fukao T; Song X Q; Mitchell G A; Yamaguchi S; Sukegawa K; Orii T; Kondo N
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: Iwata S; Sukegawa K; Sasaki T; Kokuryu M; Yamasita S; Noma A; Iwasa S; Kondo N; Orii T
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: Tateishi K; Okumoto K; Shimozawa N; Tsukamoto T; Osumi T; Suzuki Y; Kondo N; Okano I; Fujiki Y
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: Orii K E; Aoyama T; Wakui K; Fukushima Y; Miyajima H; Yamaguchi S; Orii T; Kondo N; Hashimoto T
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: Kondo N; Shinbara M; Inoue R; Fukao T; Kaneko H; Teramoto T; Tashita H
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: Orii K O; Aoyama T; Saito-Ohara F; Ikeuchi T; Orii T; Kondo N; Hashimoto T
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: Fukuda S; Yamada N; Tomatsu S; Sukegawa K; Montaño A M; Hopwood J J; Muller V; Orii T; Kondo N
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: Imamura A; Suzuki Y; Song X Q; Fukao T; Uchiyama A; Shimozawa N; Kamijo K; Hashimoto T; Orii T; Kondo N
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: Fukuda S; Yamada Y; Nishimura M; Isogai K; Terada T; Iwata M; Shimozawa N; Suzuki Y; Kondo N
Marinesco-Sjögren syndrome associated with acute myeloblastic leukemia.
Clinical genetics 1997;51(4):278-80.
-
1997: Song X Q; Fukao T; Mitchell G A; Kassovska-Bratinova S; Ugarte M; Wanders R J; Hirayama K; Shintaku H; Churchill P; Watanabe H; Orii T; Kondo N
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: Kondo N; Fukutomi O; Agata H; Yokoyama Y
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: Takahashi Y; Suzuki Y; Kumazaki K; Tanabe Y; Akaboshi S; Miura K; Shimozawa N; Kondo N; Nishiguchi T; Terada K; Orii T
Epilepsy in peroxisomal diseases.
Epilepsia 1997;38(2):182-8.
-
1997: Agata H; Kondo N; Fukutomi O; Takemura M; Tashita H; Kobayashi Y; Shinoda S; Nishida T; Shinbara M; Orii T
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: Kondo N; Inoue R; Kasahara K; Fukao T; Kaneko H; Tashita H; Teramoto T
Reduced expression of the interferon-gamma messenger RNA in IgG2 deficiency.
Scandinavian journal of immunology 1997;45(2):227-30.
-
1997: Shinoda S; Agata H; Fukutomi O; Kondo N
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: Tomatsu S; Fukuda S; Cooper A; Wraith J E; Ferreira P; Di Natale P; Tortora P; Fujimoto A; Kato Z; Yamada N; Isogai K; Yamagishi A; Sukegawa K; Suzuki Y; Shimozawa N; Kondo N; Sly W S; Orii T
Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene.
Human mutation 1997;10(5):368-75.
-
1997: Sukegawa K; Song X Q; Masuno M; Fukao T; Shimozawa N; Fukuda S; Isogai K; Nishio H; Matsuo M; Tomatsu S; Kondo N; Orii T
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: Orii K O; Saito-Ohara F; Ikeuchi T; Orii T; Kondo N; Aoyama T; Hashimoto T
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: Fukao T; Song X Q; Yamaguchi S; Kondo N; Orii T; Matthieu J M; Bachmann C; Hashimoto T
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: Suzuki Y; Shimozawa N; Takahashi Y; Imamura A; Kondo N; Orii T
Peroxisomal disorders: clinical aspects.
Annals of the New York Academy of Sciences 1996;804():442-9.
-
1996: Kaneko H; Inoue R; Yamada Y; Sukegawa K; Fukao T; Tashita H; Teramoto T; Kasahara K; Takami T; Kondo N
Microsatellite instability in B-cell lymphoma originating from Bloom syndrome.
International journal of cancer. Journal international du cancer 1996;69(6):480-3.
-
1996: Fukuda S; Shimozawa N; Suzuki Y; Zhang Z; Tomatsu S; Tsukamoto T; Hashiguchi N; Osumi T; Masuno M; Imaizumi K; Kuroki Y; Fujiki Y; Orii T; Kondo N
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: Inoue K; Suzuki Y; Yajima S; Shimozawa N; Tomatsu S; Orii T; Kondo N
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: Uchiyama A; Aoyama T; Kamijo K; Uchida Y; Kondo N; Orii T; Hashimoto T
Molecular cloning of cDNA encoding rat very long-chain acyl-CoA synthetase.
The Journal of biological chemistry 1996;271(48):30360-5.
-
1996: Fukao T; Kodama A; Aoyanagi N; Tsukino R; Uemura S; Song X Q; Watanebe H; Kuhara T; Matsumoto I; Orii T; Kondo N
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.
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1996: Fukao T; Sakai S; Shimozawa N; Kuwahara T; Kano M; Goto E; Nakashima Y; Katagiri-Kawade M; Ichihashi H; Masuno M; Orii T; Kondo N
Life-threatening cardiac involvement throughout life in a case of Costello syndrome.
Clinical genetics 1996;50(4):244-7.
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1996: Suzuki Y; Shimozawa N; Imamura A; Fukuda Y; Ichihashi H; Orii T; Kondo N
Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defect.
Acta paediatrica Japonica; Overseas edition 1996;38(5):520-3.
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1996: Kato Z; Kato T; Kondo N; Orii T
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.
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1996: Kassovska-Bratinova S; Fukao T; Song X Q; Duncan A M; Chen H S; Robert M F; Pérez-Cerdá C; Ugarte M; Chartrand C; Vobecky S; Kondo N; Mitchell G A
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.
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1996: Fukao T; Kaneko H; Teramoto T; Tashita H; Kondo N
Association between Fc epsilon RI beta and atopic disorder in Japanese population?
Lancet 1996;348(9024):407.
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1996: Shinbara M; Kondo N; Agata H; Fukutomi O; Kuwabara N; Kobayashi Y; Miura M; Orii T
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.
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1996: Fukao T; Song X Q; Yamaguchi S; Hashimoto T; Orii T; Kondo N
Immunotitration analysis of cytosolic acetoacetyl-coenzyme A thiolase activity in human fibroblasts.
Pediatric research 1996;39(6):1055-8.
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1996: Fukao T; Song X Q; Watanabe H; Hirayama K; Sakazaki H; Shintaku H; Imanaka M; Orii T; Kondo N
Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiency.
Prenatal diagnosis 1996;16(5):471-4.
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1996: Shimozawa N; Suzuki Y; Tomatsu S; Tsukamoto T; Osumi T; Fujiki Y; Kamijo K; Hashimoto T; Kondo N; Orii T
Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.
Pediatric research 1996;39(5):812-5.
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1996: Tomatsu S; Fukuda S; Yamagishi A; Cooper A; Wraith J F; Hori T; Kato Z; Yamada N; Isogai K; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orii T
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.
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1996: Suzuki Y; Shimozawa N; Yajima S; Inoue K; Orii T; Kondo N
Incidence of peroxisomal disorders in Japan.
The Japanese journal of human genetics 1996;41(1):167-75.
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1996: Uchida Y; Kondo N; Orii T; Hashimoto T
Purification and properties of rat liver peroxisomal very-long-chain acyl-CoA synthetase.
Journal of biochemistry 1996;119(3):565-71.
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1996: Imamura A; Suzuki Y; Song X Q; Fukao T; Shimozawa N; Orii T; Kondo N
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysis.
Prenatal diagnosis 1996;16(3):259-61.
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1996: Orii K E; Aoyama T; Souri M; Jiang L L; Orii K O; Hayashi S; Yamaguchi S; Kondo N; Orii T; Hashimoto T
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.
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1996: Kaneko H; Katagiri-Kawade M; Motoyoshi F; Tashita H; Teramoto T; Kondo N
Abnormal B cell response of protein kinase C in some common variable immunodeficiency.
Experimental and clinical immunogenetics 1996;13(1):36-42.
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1996: Fukuda S; Tomatsu S; Cooper A; Wraith J E; Kato Z; Yamada N; Isogai K; Sukegawa K; Kondo N; Orii T
Mucopolysaccharidosis IVA (Morquio A): three novel small deletions in the N-acetylgalactosamine-6-sulfate sulfatase gene.
Human mutation 1996;8(2):187-90.
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1996: Fukuda S; Tomatsu S; Masuno M; Ogawa T; Yamagishi A; Rezvi G M; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Imaizumi K; Kuroki Y; Okabe T; Orii T
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.
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1996: Rezvi G M; Tomatsu S; Fukuda S; Yamagishi A; Cooper A; Wraith J E; Iwata H; Kato Z; Yamada N; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Orii T
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.
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1996: Yamagishi A; Tomatsu S; Fukuda S; Uchiyama A; Shimozawa N; Suzuki Y; Kondo N; Sukegawa K; Orii T
Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populations.
Human mutation 1996;7(1):23-9.
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1995: Hayashi T; Kawakami N; Kondo N; Agata H; Fukutomi O; Shimizu H; Orii T
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.
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1995: Orii K O; Aoyama T; Souri M; Orii K E; Kondo N; Orii T; Hashimoto T
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.
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1995: Motoyoshi F; Kondo N; Terasawa S; Orii T
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.
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1995: Kuwabara N; Kondo N; Fukutomi O; Agata H; Orii T
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.
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1995: Kuwabara N; Kondo N; Fukutomi O; Fujii H; Orii T
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.
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1995: Song X Q; Fukao T; Suzuki Y; Imamura A; Uchiyama A; Shimozawa N; Kondo N; Orii T
Identification of a novel frameshift mutation in a Japanese adrenoleukodystrophy patient.
Human molecular genetics 1995;4(6):1093-4.
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1995: Imamura A; Kamei A; Suzuki Y; Kondo N; Orii T; Takashima S
Immunohistochemistry for a bifunctional protein in patients with peroxisomal disorders.
Pediatric neurology 1995;12(4):341-5.
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1995: Iida S; Kondo N; Agata H; Shinoda S; Shinbara M; Nishida T; Fukutomi O; Orii T
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.
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1995: Tomatsu S; Fukuda S; Cooper A; Wraith J E; Uchiyama A; Hori T; Nakashima Y; Yamada N; Sukegawa K; Kondo N
Mucopolysaccharidosis IVA: structural gene alterations identified by Southern blot analysis and identification of racial differences.
Human genetics 1995;95(4):376-81.
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1995: Hori T; Tomatsu S; Nakashima Y; Uchiyama A; Fukuda S; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Horiuchi T
Mucopolysaccharidosis type IVA: common double deletion in the N-acetylgalactosamine-6-sulfatase gene (GALNS).
Genomics 1995;26(3):535-42.
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1995: Ozawa T; Kondo N; Motoyoshi F; Kasahara K; Orii T
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.
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1995: Ogawa T; Tomatsu S; Fukuda S; Yamagishi A; Rezvi G M; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orü T
Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene.
Human molecular genetics 1995;4(3):341-9.
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1995: Nishida T; Kondo N; Agata H; Fukutomi O; Shinoda S; Shinbara M; Orii T
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.
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1995: Lorenzo PR 1st; Kuwabara N; Kondo N; Orii T
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: Inoue R; Kondo N; Kuwabara N; Orii T
Aberrant patterns of immunoglobulin levels in Wiskott-Aldrich syndrome.
Scandinavian journal of immunology 1995;41(2):188-93.
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1995: Inoue R; Kondo N; Kobayashi Y; Fukutomi O; Orii T
IgG2 deficiency associated with defects in production of interferon-gamma; comparison with common variable immunodeficiency.
Scandinavian journal of immunology 1995;41(2):130-4.
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1995: Tomatsu S; Fukuda S; Uchiyama A; Hori T; Nakashima Y; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orii T
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.
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1995: Kondo N; Inoue R; Kasahara K; Kaneko H; Kameyama T; Orii T
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.
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1995: Yamazaki M; Fukutomi O; Kondo N; Orii T
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.
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1995: Yano M; Kondo N; Kato Y; Shinoda S; Inoue R; Orii T
Expression of surrogate light chain in common variable immunodeficiency.
Experimental and clinical immunogenetics 1995;12(1):1-9.
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1995: Tomatsu S; Fukuda S; Cooper A; Wraith J E; Yamada N; Isogai K; Kato Z; Sukegawa K; Kondo N; Suzuki Y
Two new mutations, Q473X and N487S, in a Caucasian patient with mucopolysaccharidosis IVA (Morquio disease).
Human mutation 1995;6(2):195-6.
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1995: Shinbara M; Kondo N; Agata H; Fukutomi O; Nishida T; Kobayashi Y; Orii T
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.
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1994: Agata H; Kondo N; Yomo A; Muraki T; Shinoda S; Fukutomi O; Kato Y; Nishida T; Shinbara M; Orii T
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.
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1994: Kobayashi Y; Kondo N; Shinoda S; Agata H; Fukutomi O; Orii T
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.
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1994: Yamazaki M; Fukutomi O; Kondo N; Kato Z; Nakashima Y; Shinoda S; Agata H; Kondo T; Imaeda N; Orii T
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.
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1994: Asano J; Suzuki Y; Yajima S; Inoue K; Shimozawa N; Kondo N; Murase M; Orii T
Effects of erucic acid therapy on Japanese patients with X-linked adrenoleukodystrophy.
Brain & development 1994;16(6):454-8.
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1994: Kondo N; Takao A; Tomatsu S; Shimozawa N; Suzuki Y; Ogawa T; Iwata H; Orii T
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.
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1994: Fukutomi O; Kondo N; Agata H; Shinoda S; Kuwabara N; Shinbara M; Orii T
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.
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1994: Tomatsu S; Fukuda S; Ogawa T; Kato Z; Isogai K; Kondo N; Suzuki Y; Shimozawa N; Sukegawa K; Orii T
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.
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1994: Kondo N; Kasahara K; Kameyama T; Suzuki Y; Shimozawa N; Tomatsu S; Nakashima Y; Hori T; Yamagishi A; Ogawa T
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.
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1994: Uchiyama A; Tomatsu S; Kondo N; Suzuki Y; Shimozawa N; Fukuda S; Sukegawa K; Taki N; Inamori H; Orii T
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.
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1994: Kondo N; Inoue R; Orii T
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.
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1994: Imamura A; Komori Y; Fukutomi O; Shimozawa N; Suzuki Y; Kondo N; Orii T
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.
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1994: Agata H; Kondo N; Fukutomi O; Hayashi T; Shinoda S; Nishida T; Yomo A; Suzuki Y; Shimozawa N; Tomatsu S
Comparison of allergic diseases and specific IgE antibodies in different parts of Japan.
Annals of allergy 1994;72(5):447-51.
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1994: Inoue Y; Kondo N; Motoyoshi F; Inoue R; Orii T
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: Kato Z; Fukutomi O; Yamazaki M; Kondo N; Imaeda N; Orii T
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.
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1994: Ozawa T; Kondo N; Kato Y; Motoyoshi F; Suzuki Y; Shimozawa N; Kasahara K; Orii T
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.
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1994: Fukutomi O; Kondo N; Agata H; Shinoda S; Kuwabara N; Shinbara M; Inoue R; Orii T
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.
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1994: Nakashima Y; Tomatsu S; Hori T; Fukuda S; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orii T
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.
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1994: Masuno M; Shimozawa N; Suzuki Y; Kondo N; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Imaizumi K; Kuroki Y
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.
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1994: Kondo N; Agata H; Fukutomi O; Kameyama T; Suzuki Y; Shimozawa N; Tomatsu S; Nakashima Y; Hori T; Yamagishi A
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.
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1994: Uchiyama A; Suzuki Y; Song X Q; Fukao T; Imamura A; Tomatsu S; Shimozawa N; Kondo N; Orii T
Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophy.
Biochemical and biophysical research communications 1994;198(2):632-6.
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1994: Suzuki Y; Shimozawa N; Yajima S; Tomatsu S; Kondo N; Nakada Y; Akaboshi S; Lai M; Tanabe Y; Hashimoto T
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.
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1994: Terazawa S; Kondo N; Orii T
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: Kato Z; Asano J; Kato T; Yamaguchi S; Kondo N; Orii T
Thyroid cancer in a case with the Alagille syndrome.
Clinical genetics 1994;45(1):21-4.
-
1994: Suzuki Y; Shimozawa N; Kawabata I; Yajima S; Inoue K; Uchida Y; Izai K; Tomatsu S; Kondo N; Orii T
Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes.
Brain & development 1994;16(1):27-31.
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1994: Watanabe K; Kondo N; Fukutomi O; Takami T; Agata H; Orii T
Characterization of infiltrating CD4+ cells in atopic dermatitis using CD45R and CD29 monoclonal antibodies.
Annals of allergy 1994;72(1):39-44.
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1994: Kato Y; Kondo N; Yano M; Inoue R; Ozawa T; Orii T
Expression of VpreB gene in common variable immunodeficiency.
Experimental and clinical immunogenetics 1994;11(1):53-8.
-
1994: Miwa Y; Inoue R; Ozawa T; Kondo N; Orii T
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: Tomatsu S; Fukuda S; Uchiyama A; Hori T; Nakashima Y; Kondo N; Suzuki Y; Shimozawa N; Sukegawa K; Orii T
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: Nishida T; Kondo N; Agata H; Fukutomi O; Shinoda S; Suzuki Y; Shimozawa N; Tomatsu S; Orii T
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: Kondo N; Fukutomi O; Shinbara M; Orii T
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.
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1994: Kondo N; Fukutomi O; Kameyama T; Nishida T; Li G P; Agata H; Shinbara M; Shinoda S; Yano M; Orii T
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.
-
1993: Kondo N; Inoue R; Shinoda S; Orii T
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: Takahashi Y; Omiya S; Nakamura Y; Kondo N; Orii T
Urinary oligosaccharide excretion in nephrotic syndrome.
Pediatric research 1993;34(4):429-34.
-
1993: Kondo N; Inoue R; Agata H; Suzuki Y; Shimozawa N; Tomatsu S; Nakashima Y; Yamagishi A; Ogawa T; Orii T
Expression of secreted immunoglobulin heavy chain genes and immunoglobulin-secreting cells in human lymphocytes.
Scandinavian journal of immunology 1993;38(4):320-2.
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1993: Orii T; Tomatsu S; Fukuda S; Sukegawa K; Kondo N
[Mucopolysaccharidosis type VII: characterization of exonic point mutations and molecular heterogeneity]
Nippon rinsho. Japanese journal of clinical medicine 1993;51(9):2330-5.
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1993: Yamada Y; Tomatsu S; Sukegawa K; Suzuki Y; Kondo N; Hopwood J J; Orii T
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: Ozawa T; Kondo N; Motoyoshi F; Kato Y; Orii T
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: Kondo N; Shinoda S; Li G P; Kato Z; Orii T
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: Kato Y; Kondo N; Motoyoshi F; Ozawa T; Agata H; Orii T
Kinetics of hypogammaglobulinemia in patients with common variable immunodeficiency.
Acta paediatrica (Oslo, Norway : 1992) 1993;82(9):739-43.
-
1993: Shinoda S; Kondo N; Fukutomi O; Agata H; Suzuki Y; Shimozawa N; Tomatsu S; Yamada Y; Takemura M; Noma A
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: Kondo N; Inoue R; Nishimura S; Kasahara K; Kameyama T; Miwa Y; Lorenzo P R; Orii T
Defective calcium-dependent signal transduction in T lymphocytes of ataxia-telangiectasia.
Scandinavian journal of immunology 1993;38(1):45-8.
-
1993: Agata H; Kondo N; Fukutomi O; Shinoda S; Nishida T; Orii T
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: Kondo N; Agata H; Fukutomi O; Nishida T; Kameyama T; Fujii H; Hayashi T; Shinbara M; Yamasaki M; Utsumi M
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: Inoue Y; Kondo N; Motoyoshi F; Inoue R; Orii T
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: Agata H; Kondo N; Fukutomi O; Shinoda S; Orii T
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: Kondo N; Fukutomi O; Agata H; Motoyoshi F; Shinoda S; Kobayashi Y; Kuwabara N; Kameyama T; Orii T
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: Agata H; Yomo A; Hanashiro Y; Muraki T; Kondo N; Orii T
Comparison of the MAST chemiluminescent assay system with RAST and skin tests in allergic children.
Annals of allergy 1993;70(2):153-7.
-
1993: Kondo N; Inoue R; Yano M; Hayashi T; Miwa Y; Kasahara K; Yamasaki M; Utsumi M; Shinbara M; Orii T
Defective calcium-dependent signal transduction in B lymphocytes of a certain common variable immunodeficiency.
Experimental and clinical immunogenetics 1993;10(1):16-20.
-
1993: Mushiake K; Motoyoshi F; Kondo N; Orii T
mu-Chain gene expression in common variable immunodeficiency.
Experimental and clinical immunogenetics 1993;10(4):189-94.
-
1993: Kondo N; Takao A; Orii T
Case report: immunoglobulin A deficiency in patients with juvenile rheumatoid arthritis treated with aspirin.
Biotherapy (Dordrecht, Netherlands) 1993;7(1):59-62.
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1993: Kondo N; Takao A; Li G P; Kuwabara N; Fujii H; Orii T
Immunoglobulin secreting cells in lymphocytes of patients with IgA deficiency or hyper-IgA.
Biotherapy (Dordrecht, Netherlands) 1993;6(4):279-82.
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1993: Mushiake K; Motoyoshi F; Kondo N; Shimizu H; Orii T
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.
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1992: Shinoda S; Kondo N; Fukutomi O; Agata H; Orii T
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.
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1992: Mori S; Kondo N; Motoyoshi F; Kaneko H; Inoue Y; Orii T
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.
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1992: Wakazono A; Masuno M; Yamaguchi S; Tsubouchi K; Kondo N; Orii T
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.
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1992: Kondo N; Kobayashi Y; Shinoda S; Kasahara K; Kameyama T; Iwasa S; Orii T
Cord blood lymphocyte responses to food antigens for the prediction of allergic disorders.
Archives of disease in childhood 1992;67(8):1003-7.
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1992: Motoyoshi F; Mori S; Kondo N; Kaneko H; Ozawa T; Kuwabara N; Kato Y; Takemura M; Noma A; Orii T
Common variable immunodeficiency with increased surface IgM-positive double-bearing B cells.
Scandinavian journal of immunology 1992;36(1):21-6.
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1992: Fukutomi O; Kondo N; Agata H; Shinoda S; Shinbara M; Orii T
Abnormal responses of the autonomic nervous system in food-dependent exercise-induced anaphylaxis.
Annals of allergy 1992;68(5):438-45.
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1992: Kondo N; Kasahara K; Shinoda S; Orii T
Accelerated expression of secreted alpha-chain gene in anaphylactoid purpura.
Journal of clinical immunology 1992;12(3):193-6.
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1992: Kondo N; Ozawa T; Kato Y; Motoyoshi F; Kasahara K; Kameyama T; Orii T
Reduced secreted mu mRNA synthesis in selective IgM deficiency of Bloom's syndrome.
Clinical and experimental immunology 1992;88(1):35-40.
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1992: Kondo N; Fukutomi O; Kameyama T; Orii T
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.
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1992: Agata H; Kondo N; Fukutomi O; Shinoda S; Orii T
Interleukin-2 production of lymphocytes in food sensitive atopic dermatitis.
Archives of disease in childhood 1992;67(3):280-4.
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1992: Kondo N; Motoyoshi F; Mori S; Kuwabara N; Orii T; German J
Long-term study of the immunodeficiency of Bloom's syndrome.
Acta paediatrica (Oslo, Norway : 1992) 1992;81(1):86-90.
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1992: Kondo N; Motoyoshi F; Orii T
Asparagine-linked sugar chains of erythrocyte membrane glycoproteins from Wiskott-Aldrich syndrome are not impaired.
Biotherapy (Dordrecht, Netherlands) 1992;4(1):65-7.
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1992: Ozawa T; Motoyoshi F; Kato Y; Kondo N; Orii T
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.
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1992: Kondo N; Ozawa T; Kato Y; Inoue R; Kasahara K; Kameyama T; Orii T
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.
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1992: Kondo N; Motoyoshi F; Orii T
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.
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1992: Kondo N; Shinoda S; Agata H; Nishida T; Miwa Y; Fujii H; Orii T
Lymphocyte responses to food antigens in food sensitive patients with allergic tension-fatigue syndrome.
Biotherapy (Dordrecht, Netherlands) 1992;5(4):281-4.
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1992: Kondo N; Inoue R; Orii T
Various responses of lymphocytes to Epstein-Barr virus in patients with common variable immunodeficiency.
Journal of clinical & laboratory immunology 1992;37(4):183-9.
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1992: Kondo N; Motoyoshi F; Kasahara K; Inoue Y; Mori S; Orii T
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.
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1991: Kaneko H; Kondo N; Motoyoshi F; Mori S; Kobayashi Y; Inoue Y; Orii T
Expression of immunoglobulin genes in common variable immunodeficiency.
Journal of clinical immunology 1991;11(5):262-7.
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1991: Kondo N; Ozawa T; Mushiake K; Motoyoshi F; Kameyama T; Kasahara K; Kaneko H; Yamashina M; Kato Y; Orii T
Suppression of immunoglobulin production of lymphocytes by intravenous immunoglobulin.
Journal of clinical immunology 1991;11(3):152-8.
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1991: Motoyoshi F; Kondo N; Ono H; Orii T
The effect of photosensitive dye platonin on juvenile rheumatoid arthritis.
Biotherapy (Dordrecht, Netherlands) 1991;3(3):241-4.
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1991: Kondo N; Motoyoshi F; Ozawa T; Orii T
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.
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1990: Mori S; Kondo N; Motoyoshi F; Yamaguchi S; Kaneko H; Orii T
Diabetes mellitus in a young man with Bloom's syndrome.
Clinical genetics 1990;38(5):387-90.
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1990: Kaneko H; Kondo N; Motoyoshi F; Mori S; Kobayashi Y; Ozawa T; Orii T
Expression of the alpha-chain gene in heterogeneous IgA immunodeficiency.
Scandinavian journal of immunology 1990;32(5):483-9.
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1990: Yamashina M; Ueda E; Kinoshita T; Takami T; Ojima A; Ono H; Tanaka H; Kondo N; Orii T; Okada N
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.
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1990: Kondo N; Agata H; Fukutomi O; Motoyoshi F; Orii T
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.
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1989: Kondo N; Ko H; Motoyoshi F; Orii T
B cell suppressing and CD8+ T cell enhancing effects of photosensitive dye platonin in humans.
The Journal of rheumatology 1989;16(7):936-9.
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