Oshima J - Search Results

1

Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and ex vivo studies.

Horvath S, Oshima J, Martin GM, Lu AT, Quach A, Cohen H, Felton S, Matsuyama M, Lowe D, Kabacik S, Wilson JG, Reiner AP, Maierhofer A, Flunkert J, Aviv A, Hou L, Baccarelli AA, Li Y, Stewart JD, Whitsel EA, Ferrucci L, Matsuyama S, Raj K. Horvath S, et al. Among authors: oshima j. Aging (Albany NY). 2018 Jul 26;10(7):1758-1775. doi: 10.18632/aging.101508. Aging (Albany NY). 2018. PMID: 30048243 Free PMC article.

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

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.

5

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.

6

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

7

Structure and function of the human Werner syndrome gene promoter: evidence for transcriptional modulation.

Wang L, Hunt KE, Martin GM, Oshima J. Wang L, et al. Among authors: oshima j. Nucleic Acids Res. 1998 Aug 1;26(15):3480-5. doi: 10.1093/nar/26.15.3480. Nucleic Acids Res. 1998. PMID: 9671808 Free PMC article.

8

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: oshima j. Exp Cell Res. 1998 Aug 1;242(2):487-94. doi: 10.1006/excr.1998.4124. Exp Cell Res. 1998. PMID: 9683536

9

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: oshima j. Am J Med Genet. 1999 Feb 19;82(5):399-403. Am J Med Genet. 1999. PMID: 10069711

10

The Werner syndrome protein is involved in RNA polymerase II transcription.

Balajee AS, Machwe A, May A, Gray MD, Oshima J, Martin GM, Nehlin JO, Brosh R, Orren DK, Bohr VA. Balajee AS, et al. Among authors: oshima j. Mol Biol Cell. 1999 Aug;10(8):2655-68. doi: 10.1091/mbc.10.8.2655. Mol Biol Cell. 1999. PMID: 10436020 Free PMC article.

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