Nakamura Y - Search Results

1

Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.

Toda T, Miyake M, Kobayashi K, Mizuno K, Saito K, Osawa M, Nakamura Y, Kanazawa I, Nakagome Y, Tokunaga K, Nakahori Y. Toda T, et al. Among authors: nakamura y. Am J Hum Genet. 1996 Dec;59(6):1313-20. Am J Hum Genet. 1996. PMID: 8940277 Free PMC article.

2

Dinucleotide repeat polymorphism on chromosome 9q32.

Toda T, Ikegawa S, Miyake M, Nakahori Y, Nakamura Y. Toda T, et al. Among authors: nakamura y. Jpn J Hum Genet. 1995 Dec;40(4):333-4. doi: 10.1007/BF01900600. Jpn J Hum Genet. 1995. PMID: 8851767

3

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.

Kobayashi K, Nakahori Y, Miyake M, Matsumura K, Kondo-Iida E, Nomura Y, Segawa M, Yoshioka M, Saito K, Osawa M, Hamano K, Sakakihara Y, Nonaka I, Nakagome Y, Kanazawa I, Nakamura Y, Tokunaga K, Toda T. Kobayashi K, et al. Among authors: nakamura y. Nature. 1998 Jul 23;394(6691):388-92. doi: 10.1038/28653. Nature. 1998. PMID: 9690476

4

Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD).

Kobayashi K, Nakahori Y, Mizuno K, Miyake M, Kumagai T, Honma A, Nonaka I, Nakamura Y, Tokunaga K, Toda T. Kobayashi K, et al. Among authors: nakamura y. Hum Genet. 1998 Sep;103(3):323-7. doi: 10.1007/s004390050824. Hum Genet. 1998. PMID: 9799088

5

Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD).

Kondo-Iida E, Kobayashi K, Watanabe M, Sasaki J, Kumagai T, Koide H, Saito K, Osawa M, Nakamura Y, Toda T. Kondo-Iida E, et al. Among authors: nakamura y. Hum Mol Genet. 1999 Nov;8(12):2303-9. doi: 10.1093/hmg/8.12.2303. Hum Mol Genet. 1999. PMID: 10545611

6

The Fukuyama congenital muscular dystrophy story.

Toda T, Kobayashi K, Kondo-Iida E, Sasaki J, Nakamura Y. Toda T, et al. Among authors: nakamura y. Neuromuscul Disord. 2000 Mar;10(3):153-9. doi: 10.1016/s0960-8966(99)00109-1. Neuromuscul Disord. 2000. PMID: 10734260 Review.

7

Isolation and characterization of a novel gene encoding nuclear protein at a locus (D11S636) tightly linked to multiple endocrine neoplasia type 1 (MEN1).

Toda T, Iida A, Miwa T, Nakamura Y, Imai T. Toda T, et al. Among authors: nakamura y. Hum Mol Genet. 1994 Mar;3(3):465-70. doi: 10.1093/hmg/3.3.465. Hum Mol Genet. 1994. PMID: 7912130

8

Neuronal expression of the fukutin gene.

Sasaki J, Ishikawa K, Kobayashi K, Kondo-Iida E, Fukayama M, Mizusawa H, Takashima S, Sakakihara Y, Nakamura Y, Toda T. Sasaki J, et al. Among authors: nakamura y. Hum Mol Genet. 2000 Dec 12;9(20):3083-90. doi: 10.1093/hmg/9.20.3083. Hum Mol Genet. 2000. PMID: 11115853

9

Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin.

Kobayashi K, Sasaki J, Kondo-Iida E, Fukuda Y, Kinoshita M, Sunada Y, Nakamura Y, Toda T. Kobayashi K, et al. Among authors: nakamura y. FEBS Lett. 2001 Feb 2;489(2-3):192-6. doi: 10.1016/s0014-5793(01)02088-9. FEBS Lett. 2001. PMID: 11165248 Free article.

10

Localization of 24 cosmid clones on the human Y chromosome.

Nagafuchi S, Nakahori Y, Nakamura Y, England SB, Tamura T, Numabe H, Nakagome Y. Nagafuchi S, et al. Among authors: nakamura y. Jpn J Hum Genet. 1992 Dec;37(4):307-10. doi: 10.1007/BF01883322. Jpn J Hum Genet. 1992. PMID: 1297451

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