Martin GM - Search Results

1

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: martin gm. Am J Hum Genet. 1997 Feb;60(2):330-41. Am J Hum Genet. 1997. PMID: 9012406 Free PMC article.

2

Clinical utility gene card for: Werner Syndrome--Update 2014.

Hisama FM, Kubisch C, Martin GM, Oshima J. Hisama FM, et al. Among authors: martin gm. Eur J Hum Genet. 2015 Jun;23(6):891-. doi: 10.1038/ejhg.2014.171. Epub 2014 Sep 3. Eur J Hum Genet. 2015. PMID: 25182132 Free PMC article. No abstract available.

3

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: martin gm. Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258. Science. 1996. PMID: 8602509

4

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: martin gm. Am J Hum Genet. 1996 Jun;58(6):1286-302. Am J Hum Genet. 1996. PMID: 8651307 Free PMC article.

5

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. Among authors: martin gm. Genomics. 1996 Aug 15;36(1):130-41. doi: 10.1006/geno.1996.0433. Genomics. 1996. PMID: 8812424

6

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: martin gm. Hum Mol Genet. 1996 Dec;5(12):1909-13. doi: 10.1093/hmg/5.12.1909. Hum Mol Genet. 1996. PMID: 8968742

7

Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population.

Ye L, Miki T, Nakura J, Oshima J, Kamino K, Rakugi H, Ikegami H, Higaki J, Edland SD, Martin GM, Ogihara T. Ye L, et al. Among authors: martin gm. Am J Med Genet. 1997 Feb 11;68(4):494-8. doi: 10.1002/(sici)1096-8628(19970211)68:4<494::aid-ajmg30>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9021029

8

The Werner syndrome protein is a DNA helicase.

Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA. Gray MD, et al. Among authors: martin gm. Nat Genet. 1997 Sep;17(1):100-3. doi: 10.1038/ng0997-100. Nat Genet. 1997. PMID: 9288107

9

Werner helicase is localized to transcriptionally active nucleoli of cycling cells.

Gray MD, Wang L, Youssoufian H, Martin GM, Oshima J. Gray MD, et al. Among authors: martin gm. Exp Cell Res. 1998 Aug 1;242(2):487-94. doi: 10.1006/excr.1998.4124. Exp Cell Res. 1998. PMID: 9683536

10

Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians.

Castro E, Ogburn CE, Hunt KE, Tilvis R, Louhija J, Penttinen R, Erkkola R, Panduro A, Riestra R, Piussan C, Deeb SS, Wang L, Edland SD, Martin GM, Oshima J. Castro E, et al. Among authors: martin gm. Am J Med Genet. 1999 Feb 19;82(5):399-403. Am J Med Genet. 1999. PMID: 10069711

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