Nakamura Y - Search Results

1

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome.

Itoh T, Tanaka T, Nagai R, Kamiya T, Sawayama T, Nakayama T, Tomoike H, Sakurada H, Yazaki Y, Nakamura Y. Itoh T, et al. Among authors: nakamura y. Hum Genet. 1998 Apr;102(4):435-9. doi: 10.1007/s004390050717. Hum Genet. 1998. PMID: 9600240

2

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome.

Tanaka T, Nagai R, Tomoike H, Takata S, Yano K, Yabuta K, Haneda N, Nakano O, Shibata A, Sawayama T, Kasai H, Yazaki Y, Nakamura Y. Tanaka T, et al. Among authors: nakamura y. Circulation. 1997 Feb 4;95(3):565-7. doi: 10.1161/01.cir.95.3.565. Circulation. 1997. PMID: 9024139

3

Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation.

Nakajima T, Furukawa T, Tanaka T, Katayama Y, Nagai R, Nakamura Y, Hiraoka M. Nakajima T, et al. Among authors: nakamura y. Circ Res. 1998 Aug 24;83(4):415-22. doi: 10.1161/01.res.83.4.415. Circ Res. 1998. PMID: 9721698

4

Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome.

Itoh T, Tanaka T, Nagai R, Kikuchi K, Ogawa S, Okada S, Yamagata S, Yano K, Yazaki Y, Nakamura Y. Itoh T, et al. Among authors: nakamura y. Hum Genet. 1998 Sep;103(3):290-4. doi: 10.1007/s004390050819. Hum Genet. 1998. PMID: 9799083

5

Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2.

Nakajima T, Furukawa T, Hirano Y, Tanaka T, Sakurada H, Takahashi T, Nagai R, Itoh T, Katayama Y, Nakamura Y, Hiraoka M. Nakajima T, et al. Among authors: nakamura y. Cardiovasc Res. 1999 Nov;44(2):283-93. doi: 10.1016/s0008-6363(99)00195-9. Cardiovasc Res. 1999. PMID: 10690305

6

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population.

Iwasa H, Itoh T, Nagai R, Nakamura Y, Tanaka T. Iwasa H, et al. Among authors: nakamura y. J Hum Genet. 2000;45(3):182-3. doi: 10.1007/s100380050207. J Hum Genet. 2000. PMID: 10807545

7

Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene.

Seki T, Tanaka T, Nakamura Y. Seki T, et al. Among authors: nakamura y. J Hum Genet. 2000;45(5):299-302. doi: 10.1007/s100380070020. J Hum Genet. 2000. PMID: 11043513

8

Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome.

Itoh T, Kikuchi K, Odagawa Y, Takata S, Yano K, Okada S, Haneda N, Ogawa S, Nakano O, Kawahara Y, Kasai H, Nakayama T, Fukutomi T, Sakurada H, Shimizu A, Yazaki Y, Nagai R, Nakamura Y, Tanaka T. Itoh T, et al. Among authors: nakamura y. J Hum Genet. 2001;46(1):38-40. doi: 10.1007/s100380170123. J Hum Genet. 2001. PMID: 11289718

9

Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome.

Iwasa H, Kurabayashi M, Nagai R, Nakamura Y, Tanaka T. Iwasa H, et al. Among authors: nakamura y. J Hum Genet. 2001;46(3):158-62. doi: 10.1007/s100380170106. J Hum Genet. 2001. PMID: 11310586

10

Genetic variations in five genes involved in the excitement of cardiomyocytes.

Iwasa H, Kurabayashi M, Nagai R, Nakamura Y, Tanaka T. Iwasa H, et al. Among authors: nakamura y. J Hum Genet. 2001;46(9):549-52. doi: 10.1007/s100380170039. J Hum Genet. 2001. PMID: 11558906

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