宮脇利男 (Toshio Miyawaki) - マイポータル - researchmap

基本情報

所属: 富山大学医学部医学科小児科学教授

学位: 医学博士

J-GLOBAL ID: 200901059119277160
researchmap会員ID: 1000206769

外部リンク: http://www.toyama-mpu.ac.jp/md/pedi/index-j.html

研究キーワード

2

研究分野

1

ライフサイエンス / 胎児医学、小児成育学 /

委員歴

3

MISC

74

S100A12 (EN-RAGE) in monitoring Kawasaki disease.

LANCET 361 : 1270-1272 2003年
Identification of an SH2D1A mutation in a hypogammaglobulinemic male patient with a diagnosis of common variable immunodificiency.

Int J Hematol 78 : 45-47 2003年
Mutational analysis of the WASP Gene in 2 Korean families with Wiskott-Aldrich syndrome.

Int J Hematol 78 : 40-44 2003年
Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function.

Clin Exp Immunol 133 : 115-122 2003年
Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients.

J Hum Genet 48 : 322-326 2003年
Novel Ig alpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia

Y Wang, H Kanegane, O Sanal, Tezcan, I, F Ersoy, T Futatani, T Miyawaki

AMERICAN JOURNAL OF MEDICAL GENETICS 108(4) 333-336 2002年4月
Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations.

J Immunol Method 260 : 195-205 2002年
Non-progressive viral myelitis in X-linked agammaglobulinemia.

Brain Dev-JPN 24 : 109-111 2002年
Bruton's tyrosine kinase regulates B cell antigen receptor-mediated JNK1 response through Rac1 and phospholipase C-g2 activation.

FEBS Lett 13 : 260-262 2002年
Characterization of granulocyte colony-stimulating factor receptor expressed on human lymphocytes.

Brit J Haematol 118 : 296-304 2002年
Identification of mutations of Bruton's tyrosine kinase gene (BTK) in Brazilian patients with X-linked agammagulobulinemia.

Hum Mutat 531 : 195-205 2002年
Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection.

Int Immunol. 14 : 1215-1223 2002年
Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel Genotype-phenotype correlations.

Am. J. Hum. Genet. 71: 724-738 2002年
Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysis

H Kanegane, T Futatani, Y Wang, K Nomura, K Shinozaki, H Matsukura, T Kubota, S Tsukada, T Miyawaki

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 108(6) 1012-1020 2001年12月
SH2D1A mutations in Japanese males with severe Epstein-Barr virus-associated illnesses

R Sumazaki, H Kanegane, M Osaki, T Fukushima, M Tsuchida, H Matsukura, K Shinozaki, H Kimura, A Matsui, T Miyawaki

BLOOD 98(4) 1268-1270 2001年8月
Complete arrest from pro- to pre-B cells in a case of B cell-negative severe combined immunodeficiency (SCID) without recombinase activating gene (RAG) mutations

K Agematsu, H Nagumo, S Hokibara, T Mori, T Wada, A Yachie, H Kanegane, T Miyawaki, K Sugita, H Karasuyama …

CLINICAL AND EXPERIMENTAL IMMUNOLOGY 124(3) 461-464 2001年6月
Maternal germinal mosaicism of X-linked agammaglobulinemia

M Sakamoto, H Kanegane, H Fujii, S Tsukada, T Miyawaki, N Shinomiya

AMERICAN JOURNAL OF MEDICAL GENETICS 99(3) 234-237 2001年3月
Maternal germinal mosaicism of X-linked agammaglobulinemia.

Am J Med genet 99 : 234-237 2001年
Complete arrest from pro- to pre-B cells in a case of B cell-negative severe combined immunodeficiency (SCID) without recombinase activating gene (RAG) mutations.

Clin Exp Immunol 124 : 461-464 2001年
Characterization of mutations, including a novel regulatory defect in the first intron, in Bruton's tyrosine kinase gene from seven Korean X-linked agammaglobulinemia families.

J Immunol 167 : 4038-4045 2001年

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所属学協会

5

共同研究・競争的資金等の研究課題

4