Kimura A - Search Results

1

HLA-DPB1 and NFKBIL1 may confer the susceptibility to chronic thromboembolic pulmonary hypertension in the absence of deep vein thrombosis.

Kominami S, Tanabe N, Ota M, Naruse TK, Katsuyama Y, Nakanishi N, Tomoike H, Sakuma M, Shirato K, Takahashi M, Shibata H, Yasunami M, Chen Z, Kasahara Y, Tatsumi K, Kuriyama T, Kimura A. Kominami S, et al. Among authors: kimura a. J Hum Genet. 2009 Feb;54(2):108-14. doi: 10.1038/jhg.2008.15. Epub 2009 Jan 23. J Hum Genet. 2009. PMID: 19165231

2

Titin mutations as the molecular basis for dilated cardiomyopathy.

Itoh-Satoh M, Hayashi T, Nishi H, Koga Y, Arimura T, Koyanagi T, Takahashi M, Hohda S, Ueda K, Nouchi T, Hiroe M, Marumo F, Imaizumi T, Yasunami M, Kimura A. Itoh-Satoh M, et al. Among authors: kimura a. Biochem Biophys Res Commun. 2002 Feb 22;291(2):385-93. doi: 10.1006/bbrc.2002.6448. Biochem Biophys Res Commun. 2002. PMID: 11846417

3

Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritis.

Okamoto K, Makino S, Yoshikawa Y, Takaki A, Nagatsuka Y, Ota M, Tamiya G, Kimura A, Bahram S, Inoko H. Okamoto K, et al. Among authors: kimura a. Am J Hum Genet. 2003 Feb;72(2):303-12. doi: 10.1086/346067. Epub 2002 Dec 31. Am J Hum Genet. 2003. PMID: 12509789 Free PMC article.

4

Association study of CD14 polymorphism with myocardial infarction in a Japanese population.

Hohda S, Kimura A, Sasaoka T, Hayashi T, Ueda K, Yasunami M, Okabe M, Fukuta N, Kurosawa T, Izumi T. Hohda S, et al. Among authors: kimura a. Jpn Heart J. 2003 Sep;44(5):613-22. doi: 10.1536/jhj.44.613. Jpn Heart J. 2003. PMID: 14587643 Free article.

5

A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.

Arimura T, Hayashi T, Terada H, Lee SY, Zhou Q, Takahashi M, Ueda K, Nouchi T, Hohda S, Shibutani M, Hirose M, Chen J, Park JE, Yasunami M, Hayashi H, Kimura A. Arimura T, et al. Among authors: kimura a. J Biol Chem. 2004 Feb 20;279(8):6746-52. doi: 10.1074/jbc.M311849200. Epub 2003 Dec 3. J Biol Chem. 2004. PMID: 14660611 Free article.

6

Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy.

Hayashi T, Arimura T, Ueda K, Shibata H, Hohda S, Takahashi M, Hori H, Koga Y, Oka N, Imaizumi T, Yasunami M, Kimura A. Hayashi T, et al. Among authors: kimura a. Biochem Biophys Res Commun. 2004 Jan 2;313(1):178-84. doi: 10.1016/j.bbrc.2003.11.101. Biochem Biophys Res Commun. 2004. PMID: 14672715

7

The role of a common TNNT2 polymorphism in cardiac hypertrophy.

Komamura K, Iwai N, Kokame K, Yasumura Y, Kim J, Yamagishi M, Morisaki T, Kimura A, Tomoike H, Kitakaze M, Miyatake K. Komamura K, et al. Among authors: kimura a. J Hum Genet. 2004;49(3):129-133. doi: 10.1007/s10038-003-0121-4. Epub 2004 Feb 24. J Hum Genet. 2004. PMID: 14986170

8

Clinical and genetic characteristics of GAD-antibody positive patients initially diagnosed as having type 2 diabetes.

Hamaguchi K, Kimura A, Kusuda Y, Yamashita T, Yasunami M, Takahasi M, Abe N, Yoshimatsu H. Hamaguchi K, et al. Among authors: kimura a. Diabetes Res Clin Pract. 2004 Nov;66(2):163-71. doi: 10.1016/j.diabres.2004.02.019. Diabetes Res Clin Pract. 2004. PMID: 15533584

9

HLA-B polymorphism in Japanese HIV-1-infected long-term surviving hemophiliacs.

Munkanta M, Terunuma H, Takahashi M, Hanabusa H, Miura T, Ikeda S, Sakai M, Fujii T, Takahashi Y, Oka S, Matsuda J, Ishikawa M, Taki M, Takashima Y, Mimaya J, Ito M, Kimura A, Yasunami M. Munkanta M, et al. Among authors: kimura a. Viral Immunol. 2005;18(3):500-5. doi: 10.1089/vim.2005.18.500. Viral Immunol. 2005. PMID: 16212528

10

A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.

Noguchi Y, Yashima T, Hatanaka A, Uzawa M, Yasunami M, Kimura A, Kitamura K. Noguchi Y, et al. Among authors: kimura a. Acta Otolaryngol. 2005 Nov;125(11):1189-94. doi: 10.1080/00016480510044232. Acta Otolaryngol. 2005. PMID: 16353398

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