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Naomi Kondo

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Kato Zenichiro; Yamagishi Atsushi; Nakamura Mitsuhiro; Kondo Naomi
Theophylline-associated status epilepticus in an infant: pharmacokinetics and the risk of suppository use.
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.
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.

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All Publications

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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
2007: Kondo Naomi; Shinoda Shinji; Kaneko Hideo
[The pathophysiology of food allergy]
Arerugi = [Allergy] 2007;56(5):439-43.
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.
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.
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.
2007: Kondo Naomi
[Influence of genes and environment on allergic disorders]
Arerugi = [Allergy] 2007;56(2):94-100.
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.
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.
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.
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.
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.
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.
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.
2006: Kondo Naomi; Fukuda Kazuhito
[Ataxia-telangiectasia]
Nippon rinsho. Japanese journal of clinical medicine 2006;Suppl 3():114-8.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
2005: Kondo Naomi; Kaneko Hideo; Kuwabara Manami
[Classification of immunodeficiency diseases]
Nippon rinsho. Japanese journal of clinical medicine 2005;63 Suppl 5():548-58.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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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