鈴木洋一 (Yoichi Suzuki) - マイポータル - researchmap

基本情報

所属: 千葉大学医学部大学院医学研究院千葉大学

学位: 博士・甲(東北)

J-GLOBAL ID: 200901084151066884
researchmap会員ID: 1000004075

外部リンク: http://www.m.chiba-u.ac.jp/class/pubheal/

MISC

49

An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway. (共著)

J Hum Genet; PMID: 16432636 2006年
Evaluation of clinical usefulness of second-generation HCV core antigen assay: comparison with COBAS AMPLICOR HCV MONITOR assay version 2.0. (共著)

Liver Int; PMID: 16343063 25(6) 1136-1141 2005年12月
Functional haplotypes of IL-12B are associated with childhood atopic asthma. (共著)

J Allergy Clin Immunol; PMID: 16210052 116(4) 789-795 2005年10月
Mutations in the holocarboxylase synthetase gene HLCS. (共著)

Hum Mutat; PMID: 16134170 26(4) 285-290 2005年10月
Fas polymorphisms influence susceptibility to autoimmune hepatitis. (共著)

Am J Gastroenterol; PMID: 15929764 100(6) 1322-1329 2005年6月
Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. (共著)

NIIHORI Tetsuya, OHASHI Hirofumi, KUROSAWA Kenji, KONDOH Tatsuro, ISHIKIRIYAMA Satoshi, KAWAME Hiroshi, KAMASAKI Hotaka, YAMANAKA Tsutomu, TAKADA Fumio

J Hum Genet; PMID: 15834506 50(4) 192-202 2005年
Germline mutations in HRAS proto-oncogene cause Costello syndrome. (共著)

AOKI Yoko, NIIHORI Tetsuya, KAWAME Hiroshi, KUROSAWA Kenji, OHASHI Hirofumi, TANAKA Yukichi, FILOCAMO Mirella, KATO Kumi, KATO Kumi, SUZUKI Yoichi …

Nat Genet; PMID: 16170316 37(10) 1038-1040 2005年
Association of the hCLCA1 gene with childhood and adult asthma. (共著)

Genes Immun; PMID: 15318163 5(7) 540-547 2004年11月
Artificial neural network approach for selection of susceptible single nucleotide polymorphisms and construction of prediction model on childhood allergic asthma. (共著)

BMC Bioinformatics; PMID: 15339344 5 120-122 2004年9月
Mutation analysis of the MMAA and MMAB genes in Japanese patients with vitamin B(12)-responsive methylmalonic acidemia: identification of a prevalent MMAA mutation. (共著)

Mol Genet Metab; PMID: 15308131 82(4) 329-333 2004年8月
Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia. (共著)

Mol Genet Metab; PMID: 15059621 81(4) 335-342 2004年4月
Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118R. (共著)

Mol Genet Metab; PMID: 15059622 81(4) 343-346 2004年4月
Linkage and association of childhood asthma with the chromosome 12 genes. (共著)

SHAO C, TAMARI M, ENDO H, MORIKAWA T, MORIKAWA M, MIYABAYASHI S, CHIBA Y, KARAHASHI M, SAITO S

J Hum Genet; PMID: 14767694 49(3) 115-122 2004年
Wild-type phenylalanine hydroxylase activity is enhanced by tetrahydrobiopterin supplementation in vivo: an implication for therapeutic basis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency. (共著)

KURE S

Mol Genet Metab; PMID: 15464429 83 150-156 2004年
Significant association between nonsyndromic oral clefts and arylhydrocarbon receptor nuclear translocator (ARNT). (共著)

Am J Med Genet; PMID: 15368494 130A 40-44 2004年
Association between nonsyndromic cleft lip with or without cleft palate and the glutamic acid decarboxylase 67 gene in the Japanese population. (共著)

Am J Med Genet; PMID: 15103710 127A 11-16 2004年
Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma. (共著)

J Hum Genet; PMID: 15179560 49 370-375 2004年
Variations in the C3, C3a receptor, and C5 genes affect susceptibility to bronchial asthma. (共著)

Hum Genet 115 160-166 2004年
Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects. (共著)

Mol Genet Metab ; PMID: 12855220 79(3) 160-166 2003年7月
遺伝性疾患の種類と分子遺伝病態学 (遺伝子医学別冊「これだけは知っておきたい遺伝子医学の基礎知識」)

メディカルドゥ 2003年

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所属学協会

12