Nakamura Y - Search Results

1

Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.

Tachikawa M, Nagai Y, Nakamura K, Kobayashi K, Fujiwara T, Han HJ, Nakabayashi Y, Ichikawa Y, Goto J, Kanazawa I, Nakamura Y, Toda T. Tachikawa M, et al. Among authors: nakamura y, nakamura k. J Hum Genet. 2002;47(6):275-8. doi: 10.1007/s100380200039. J Hum Genet. 2002. PMID: 12111376

2

Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.

Takeda S, Kondo M, Sasaki J, Kurahashi H, Kano H, Arai K, Misaki K, Fukui T, Kobayashi K, Tachikawa M, Imamura M, Nakamura Y, Shimizu T, Murakami T, Sunada Y, Fujikado T, Matsumura K, Terashima T, Toda T. Takeda S, et al. Among authors: nakamura y. Hum Mol Genet. 2003 Jun 15;12(12):1449-59. doi: 10.1093/hmg/ddg153. Hum Mol Genet. 2003. PMID: 12783852

3

Isolation and characterization of the mouse ortholog of the Fukuyama-type congenital muscular dystrophy gene.

Horie M, Kobayashi K, Takeda S, Nakamura Y, Lyons GE, Toda T. Horie M, et al. Among authors: nakamura y. Genomics. 2002 Nov;80(5):482-6. Genomics. 2002. PMID: 12408965

4

Thirteen single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase 4 (ADH4) gene locus.

Iida A, Saito S, Sekine A, Kondo K, Mishima C, Kitamura Y, Harigae S, Osawa S, Nakamura Y. Iida A, et al. Among authors: nakamura y. J Hum Genet. 2002;47(2):74-6. doi: 10.1007/s100380200003. J Hum Genet. 2002. PMID: 11916005

5

Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR.

Saito S, Iida A, Sekine A, Miura Y, Ogawa C, Kawauchi S, Higuchi S, Nakamura Y. Saito S, et al. Among authors: nakamura y. J Hum Genet. 2002;47(4):147-71. doi: 10.1007/s100380200018. J Hum Genet. 2002. PMID: 12166651

6

Catalog of 77 single-nucleotide polymorphisms (SNPs) in the carbohydrate sulfotransferase 1 (CHST1) and carbohydrate sulfotransferase 3 (CHST3) genes.

Iida A, Saito S, Sekine A, Mishima C, Kitamura Y, Kondo K, Harigae S, Osawa S, Nakamura Y. Iida A, et al. Among authors: nakamura y. J Hum Genet. 2002;47(1):14-9. doi: 10.1007/s10038-002-8650-9. J Hum Genet. 2002. PMID: 11829137

7

Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8.

Iida A, Saito S, Sekine A, Mishima C, Kitamura Y, Kondo K, Harigae S, Osawa S, Nakamura Y. Iida A, et al. Among authors: nakamura y. J Hum Genet. 2002;47(6):285-310. doi: 10.1007/s100380200041. J Hum Genet. 2002. PMID: 12111378

8

Three hundred twenty-six genetic variations in genes encoding nine members of ATP-binding cassette, subfamily B (ABCB/MDR/TAP), in the Japanese population.

Saito S, Iida A, Sekine A, Miura Y, Ogawa C, Kawauchi S, Higuchi S, Nakamura Y. Saito S, et al. Among authors: nakamura y. J Hum Genet. 2002;47(1):38-50. doi: 10.1007/s10038-002-8653-6. J Hum Genet. 2002. PMID: 11829140

9

Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy.

Takei T, Iida A, Nitta K, Tanaka T, Ohnishi Y, Yamada R, Maeda S, Tsunoda T, Takeoka S, Ito K, Honda K, Uchida K, Tsuchiya K, Suzuki Y, Fujioka T, Ujiie T, Nagane Y, Miyano S, Narita I, Gejyo F, Nihei H, Nakamura Y. Takei T, et al. Among authors: nakamura y. Am J Hum Genet. 2002 Mar;70(3):781-6. doi: 10.1086/339077. Epub 2002 Feb 1. Am J Hum Genet. 2002. PMID: 11828340 Free PMC article.

10

Characterization of a VNTR polymorphism in the coding region of the CEL gene.

Higuchi S, Nakamura Y, Saito S. Higuchi S, et al. Among authors: nakamura y. J Hum Genet. 2002;47(4):213-5. doi: 10.1007/s100380200027. J Hum Genet. 2002. PMID: 12166660

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