Nakamura Y - Search Results

1

Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease.

Yamada R, Tanaka T, Unoki M, Nagai T, Sawada T, Ohnishi Y, Tsunoda T, Yukioka M, Maeda A, Suzuki K, Tateishi H, Ochi T, Nakamura Y, Yamamoto K. Yamada R, et al. Among authors: nakamura y. Am J Hum Genet. 2001 Mar;68(3):674-85. doi: 10.1086/318789. Epub 2001 Feb 14. Am J Hum Genet. 2001. PMID: 11179015 Free PMC article.

2

Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population.

Ohnishi Y, Tanaka T, Yamada R, Suematsu K, Minami M, Fujii K, Hoki N, Kodama K, Nagata S, Hayashi T, Kinoshita N, Sato H, Sato H, Kuzuya T, Takeda H, Hori M, Nakamura Y. Ohnishi Y, et al. Among authors: nakamura y. Hum Genet. 2000 Mar;106(3):288-92. doi: 10.1007/s004390051039. Hum Genet. 2000. PMID: 10798356

3

Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population.

Yamada R, Tanaka T, Ohnishi Y, Suematsu K, Minami M, Seki T, Yukioka M, Maeda A, Murata N, Saiki O, Teshima R, Kudo O, Ishikawa K, Ueyosi A, Tateishi H, Inaba M, Goto H, Nishizawa Y, Tohma S, Ochi T, Yamamoto K, Nakamura Y. Yamada R, et al. Among authors: nakamura y. Hum Genet. 2000 Mar;106(3):293-7. doi: 10.1007/s004390051040. Hum Genet. 2000. PMID: 10798357

4

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

5

Association studies of 33 single nucleotide polymorphisms (SNPs) in 29 candidate genes for bronchial asthma: positive association a T924C polymorphism in the thromboxane A2 receptor gene.

Unoki M, Furuta S, Onouchi Y, Watanabe O, Doi S, Fujiwara H, Miyatake A, Fujita K, Tamari M, Nakamura Y. Unoki M, et al. Among authors: nakamura y. Hum Genet. 2000 Apr;106(4):440-6. doi: 10.1007/s004390000267. Hum Genet. 2000. PMID: 10830912

6

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

7

Identification and allelic frequencies of novel single-nucleotide polymorphisms in the DUSP1 and BTG1 genes.

Suzuki C, Unoki M, Nakamura Y. Suzuki C, et al. Among authors: nakamura y. J Hum Genet. 2001;46(3):155-7. doi: 10.1007/s100380170105. J Hum Genet. 2001. PMID: 11310585

8

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

9

A high-throughput SNP typing system for genome-wide association studies.

Ohnishi Y, Tanaka T, Ozaki K, Yamada R, Suzuki H, Nakamura Y. Ohnishi Y, et al. Among authors: nakamura y. J Hum Genet. 2001;46(8):471-7. doi: 10.1007/s100380170047. J Hum Genet. 2001. PMID: 11501945

10

High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2.

Iida A, Ohnishi Y, Ozaki K, Ariji Y, Nakamura Y, Tanaka T. Iida A, et al. Among authors: nakamura y. J Hum Genet. 2001;46(10):604-8. doi: 10.1007/s100380170029. J Hum Genet. 2001. PMID: 11589220

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