Matsubara Y - Search Results

1

Association between nonsyndromic cleft lip with or without cleft palate and the glutamic acid decarboxylase 67 gene in the Japanese population.

Kanno K, Suzuki Y, Yamada A, Aoki Y, Kure S, Matsubara Y. Kanno K, et al. Among authors: matsubara y. Am J Med Genet A. 2004 May 15;127A(1):11-16. doi: 10.1002/ajmg.a.20649. Am J Med Genet A. 2004. PMID: 15103710

2

Lack of evidence for a significant association between nonsyndromic cleft lip with or without cleft palate and the retinoic acid receptor alpha gene in the Japanese population.

Kanno K, Suzuki Y, Yang X, Yamada A, Aoki Y, Kure S, Matsubara Y. Kanno K, et al. Among authors: matsubara y. J Hum Genet. 2002;47(6):269-74. doi: 10.1007/s100380200038. J Hum Genet. 2002. PMID: 12111375

3

Significant association between nonsyndromic oral clefts and arylhydrocarbon receptor nuclear translocator (ARNT).

Kayano S, Suzuki Y, Kanno K, Aoki Y, Kure S, Yamada A, Matsubara Y. Kayano S, et al. Among authors: matsubara y. Am J Med Genet A. 2004 Sep 15;130A(1):40-4. doi: 10.1002/ajmg.a.30023. Am J Med Genet A. 2004. PMID: 15368494

4

Association of the GABRB3 gene with nonsyndromic oral clefts.

Inoue H, Kayano S, Aoki Y, Kure S, Yamada A, Hata A, Matsubara Y, Suzuki Y. Inoue H, et al. Among authors: matsubara y. Cleft Palate Craniofac J. 2008 May;45(3):261-6. doi: 10.1597/06-142. Cleft Palate Craniofac J. 2008. PMID: 18452349

5

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.

Kamada F, Aoki Y, Narisawa A, Abe Y, Komatsuzaki S, Kikuchi A, Kanno J, Niihori T, Ono M, Ishii N, Owada Y, Fujimura M, Mashimo Y, Suzuki Y, Hata A, Tsuchiya S, Tominaga T, Matsubara Y, Kure S. Kamada F, et al. Among authors: matsubara y. J Hum Genet. 2011 Jan;56(1):34-40. doi: 10.1038/jhg.2010.132. Epub 2010 Nov 4. J Hum Genet. 2011. PMID: 21048783

6

Association of the hCLCA1 gene with childhood and adult asthma.

Kamada F, Suzuki Y, Shao C, Tamari M, Hasegawa K, Hirota T, Shimizu M, Takahashi N, Mao XQ, Doi S, Fujiwara H, Miyatake A, Fujita K, Chiba Y, Aoki Y, Kure S, Tamura G, Shirakawa T, Matsubara Y. Kamada F, et al. Among authors: matsubara y. Genes Immun. 2004 Nov;5(7):540-7. doi: 10.1038/sj.gene.6364124. Genes Immun. 2004. PMID: 15318163

7

Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness.

Kudo T, Kure S, Ikeda K, Xia AP, Katori Y, Suzuki M, Kojima K, Ichinohe A, Suzuki Y, Aoki Y, Kobayashi T, Matsubara Y. Kudo T, et al. Among authors: matsubara y. Hum Mol Genet. 2003 May 1;12(9):995-1004. doi: 10.1093/hmg/ddg116. Hum Mol Genet. 2003. PMID: 12700168

8

Detection of single nucleotide substitution by competitive allele-specific short oligonucleotide hybridization (CASSOH) with immunochromatographic strip.

Matsubara Y, Kure S. Matsubara Y, et al. Hum Mutat. 2003 Aug;22(2):166-72. doi: 10.1002/humu.10247. Hum Mutat. 2003. PMID: 12872258

9

Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion.

Kayano S, Kure S, Suzuki Y, Kanno K, Aoki Y, Kondo S, Schutte BC, Murray JC, Yamada A, Matsubara Y. Kayano S, et al. Among authors: matsubara y. J Hum Genet. 2003;48(12):622-628. doi: 10.1007/s10038-003-0089-0. Epub 2003 Nov 15. J Hum Genet. 2003. PMID: 14618417

10

Linkage and association of childhood asthma with the chromosome 12 genes.

Shao C, Suzuki Y, Kamada F, Kanno K, Tamari M, Hasegawa K, Aoki Y, Kure S, Yang X, Endo H, Takayanagi R, Nakazawa C, Morikawa T, Morikawa M, Miyabayashi S, Chiba Y, Karahashi M, Saito S, Tamura G, Shirakawa T, Matsubara Y. Shao C, et al. Among authors: matsubara y. J Hum Genet. 2004;49(3):115-122. doi: 10.1007/s10038-003-0118-z. Epub 2004 Feb 7. J Hum Genet. 2004. PMID: 14767694

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