Nakura J - Search Results

1

Homozygous and compound heterozygous mutations at the Werner syndrome locus.

Oshima J, Yu CE, Piussan C, Klein G, Jabkowski J, Balci S, Miki T, Nakura J, Ogihara T, Ells J, Smith M, Melaragno MI, Fraccaro M, Scappaticci S, Matthews J, Ouais S, Jarzebowicz A, Schellenberg GD, Martin GM. Oshima J, et al. Among authors: nakura j. Hum Mol Genet. 1996 Dec;5(12):1909-13. doi: 10.1093/hmg/5.12.1909. Hum Mol Genet. 1996. PMID: 8968742

2

Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.

Yu CE, Oshima J, Goddard KA, Miki T, Nakura J, Ogihara T, Poot M, Hoehn H, Fraccaro M, Piussan C, et al. Yu CE, et al. Among authors: nakura j. Am J Hum Genet. 1994 Aug;55(2):356-64. Am J Hum Genet. 1994. PMID: 8037212 Free PMC article.

3

Evidence against DNA polymerase beta as a candidate gene for Werner syndrome.

Chang M, Burmer GC, Sweasy J, Loeb LA, Edelhoff S, Disteche CM, Yu CE, Anderson L, Oshima J, Nakura J, et al. Chang M, et al. Among authors: nakura j. Hum Genet. 1994 May;93(5):507-12. doi: 10.1007/BF00202813. Hum Genet. 1994. PMID: 8168825

4

Positional cloning of the Werner's syndrome gene.

Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Yu CE, et al. Among authors: nakura j. Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258. Science. 1996. PMID: 8602509

5

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

Goddard KA, Yu CE, Oshima J, Miki T, Nakura J, Piussan C, Martin GM, Schellenberg GD, Wijsman EM. Goddard KA, et al. Among authors: nakura j. Am J Hum Genet. 1996 Jun;58(6):1286-302. Am J Hum Genet. 1996. PMID: 8651307 Free PMC article.

6

Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Yu CE, Oshima J, Wijsman EM, Nakura J, Miki T, Piussan C, Matthews S, Fu YH, Mulligan J, Martin GM, Schellenberg GD. Yu CE, et al. Among authors: nakura j. Am J Hum Genet. 1997 Feb;60(2):330-41. Am J Hum Genet. 1997. PMID: 9012406 Free PMC article.

7

Homozygosity mapping and Werner's syndrome.

Schellenberg GD, Martin GM, Wijsman EM, Nakura J, Miki T, Ogihara T. Schellenberg GD, et al. Among authors: nakura j. Lancet. 1992 Apr 18;339(8799):1002. doi: 10.1016/0140-6736(92)91590-5. Lancet. 1992. PMID: 1348795 No abstract available.

8

Homozygosity mapping of the Werner syndrome locus (WRN).

Nakura J, Wijsman EM, Miki T, Kamino K, Yu CE, Oshima J, Fukuchi K, Weber JL, Piussan C, Melaragno MI, et al. Nakura J, et al. Genomics. 1994 Oct;23(3):600-8. doi: 10.1006/geno.1994.1548. Genomics. 1994. PMID: 7851888

9

Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus.

Kihara K, Nakura J, Ye L, Mitsuda N, Kamino K, Zhao Y, Fujioka Y, Miki T, Ogihara T. Kihara K, et al. Among authors: nakura j. Jpn J Hum Genet. 1994 Dec;39(4):403-9. doi: 10.1007/BF01892385. Jpn J Hum Genet. 1994. PMID: 7873752

10

Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.

Nakura J, Miki T, Ye L, Mitsuda N, Zhao Y, Kihara K, Yu CE, Oshima J, Fukuchi KI, Wijsman EM, Schellenberg GD, Martin GM, Murano Si, Hashimoto K, Fujiwara Y, Ogihara T. Nakura J, et al. Genomics. 1996 Aug 15;36(1):130-41. doi: 10.1006/geno.1996.0433. Genomics. 1996. PMID: 8812424

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