Oshima J - Search Results

1

An encouraging progress report on the treatment of progeria and its implications for atherogenesis.

Oshima J, Hisama FM, Martin GM. Oshima J, et al. Circulation. 2014 Jul 1;130(1):4-6. doi: 10.1161/CIRCULATIONAHA.114.010648. Epub 2014 May 2. Circulation. 2014. PMID: 24795391 Free PMC article. No abstract available.

2

Regulation of c-fos expression in senescing Werner syndrome fibroblasts differs from that observed in senescing fibroblasts from normal donors.

Oshima J, Campisi J, Tannock TC, Martin GM. Oshima J, et al. J Cell Physiol. 1995 Feb;162(2):277-83. doi: 10.1002/jcp.1041620213. J Cell Physiol. 1995. PMID: 7822435

3

Integrated mapping analysis of the Werner syndrome region of chromosome 8.

Oshima J, Yu CE, Boehnke M, Weber JL, Edelhoff S, Wagner MJ, Wells DE, Wood S, Disteche CM, Martin GM, et al. Oshima J, et al. Genomics. 1994 Sep 1;23(1):100-13. doi: 10.1006/geno.1994.1464. Genomics. 1994. PMID: 7829057 Free article.

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

6

A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.

Yu CE, Oshima J, Hisama FM, Matthews S, Trask BJ, Schellenberg GD. Yu CE, et al. Among authors: oshima j. Genomics. 1996 Aug 1;35(3):431-40. doi: 10.1006/geno.1996.0382. Genomics. 1996. PMID: 8812476 Free article.

7

No detectable mutations at Werner helicase locus in progeria.

Oshima J, Brown WT, Martin GM. Oshima J, et al. Lancet. 1996 Oct 19;348(9034):1106. doi: 10.1016/S0140-6736(05)64456-X. Lancet. 1996. PMID: 8874483 No abstract available.

8

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

9

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

10

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: oshima j. Nat Genet. 1997 Sep;17(1):100-3. doi: 10.1038/ng0997-100. Nat Genet. 1997. PMID: 9288107

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