Martin GM - Search Results

1

Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference.

Huang S, Chen L, Libina N, Janes J, Martin GM, Campisi J, Oshima J. Huang S, et al. Among authors: martin gm. Hum Genet. 2005 Dec;118(3-4):444-50. doi: 10.1007/s00439-005-0051-7. Epub 2005 Oct 6. Hum Genet. 2005. PMID: 16208517

2

Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A.

Huang S, Risques RA, Martin GM, Rabinovitch PS, Oshima J. Huang S, et al. Among authors: martin gm. Exp Cell Res. 2008 Jan 1;314(1):82-91. doi: 10.1016/j.yexcr.2007.08.004. Epub 2007 Aug 16. Exp Cell Res. 2008. PMID: 17870066 Free PMC article.

3

DNA methylation signatures in Blood DNA of Hutchinson-Gilford Progeria syndrome.

Bejaoui Y, Razzaq A, Yousri NA, Oshima J, Megarbane A, Qannan A, Potabattula R, Alam T, Martin GM, Horn HF, Haaf T, Horvath S, El Hajj N. Bejaoui Y, et al. Among authors: martin gm. Aging Cell. 2022 Feb;21(2):e13555. doi: 10.1111/acel.13555. Epub 2022 Jan 19. Aging Cell. 2022. PMID: 35045206 Free PMC article.

4

Review of How Genetic Research on Segmental Progeroid Syndromes Has Documented Genomic Instability as a Hallmark of Aging But Let Us Now Pursue Antigeroid Syndromes!

Martin GM, Hisama FM, Oshima J. Martin GM, et al. J Gerontol A Biol Sci Med Sci. 2021 Jan 18;76(2):253-259. doi: 10.1093/gerona/glaa273. J Gerontol A Biol Sci Med Sci. 2021. PMID: 33295962 Free PMC article. Review.

5

LMNA mutations in atypical Werner's syndrome.

Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, Shafeghati Y, Botha EG, Garg A, Hanson NB, Martin GM, Mian IS, Kennedy BK, Oshima J. Chen L, et al. Among authors: martin gm. Lancet. 2003 Aug 9;362(9382):440-5. doi: 10.1016/S0140-6736(03)14069-X. Lancet. 2003. PMID: 12927431

6

Collagen expression in fibroblasts with a novel LMNA mutation.

Nguyen D, Leistritz DF, Turner L, MacGregor D, Ohson K, Dancey P, Martin GM, Oshima J. Nguyen D, et al. Among authors: martin gm. Biochem Biophys Res Commun. 2007 Jan 19;352(3):603-8. doi: 10.1016/j.bbrc.2006.11.070. Epub 2006 Nov 27. Biochem Biophys Res Commun. 2007. PMID: 17150192 Free PMC article.

7

SOD2 polymorphisms: unmasking the effect of polymorphism on splicing.

Shao J, Chen L, Marrs B, Lee L, Huang H, Manton KG, Martin GM, Oshima J. Shao J, et al. Among authors: martin gm. BMC Med Genet. 2007 Mar 1;8:7. doi: 10.1186/1471-2350-8-7. BMC Med Genet. 2007. PMID: 17331249 Free PMC article.

8

Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.

Hisama FM, Lessel D, Leistritz D, Friedrich K, McBride KL, Pastore MT, Gottesman GS, Saha B, Martin GM, Kubisch C, Oshima J. Hisama FM, et al. Among authors: martin gm. Am J Med Genet A. 2011 Dec;155A(12):3002-6. doi: 10.1002/ajmg.a.34336. Epub 2011 Nov 7. Am J Med Genet A. 2011. PMID: 22065502 Free PMC article.

9

Clinical utility gene card for: Werner syndrome.

Hisama FM, Kubisch C, Martin GM, Oshima J. Hisama FM, et al. Among authors: martin gm. Eur J Hum Genet. 2012 May;20(5). doi: 10.1038/ejhg.2011.265. Epub 2012 Jan 18. Eur J Hum Genet. 2012. PMID: 22258520 Free PMC article. No abstract available.

10

DNA damage accumulation and TRF2 degradation in atypical Werner syndrome fibroblasts with LMNA mutations.

Saha B, Zitnik G, Johnson S, Nguyen Q, Risques RA, Martin GM, Oshima J. Saha B, et al. Among authors: martin gm. Front Genet. 2013 Jul 5;4:129. doi: 10.3389/fgene.2013.00129. eCollection 2013. Front Genet. 2013. PMID: 23847654 Free PMC article.

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