R24 CA078088/CA/NCI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1999	1
2006	3
2007	4
2008	2
2010	4
2011	3
2012	1
2013	3
2014	2
2024	0

1

Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features.

Lessel D, Vaz B, Halder S, Lockhart PJ, Marinovic-Terzic I, Lopez-Mosqueda J, Philipp M, Sim JC, Smith KR, Oehler J, Cabrera E, Freire R, Pope K, Nahid A, Norris F, Leventer RJ, Delatycki MB, Barbi G, von Ameln S, Högel J, Degoricija M, Fertig R, Burkhalter MD, Hofmann K, Thiele H, Altmüller J, Nürnberg G, Nürnberg P, Bahlo M, Martin GM, Aalfs CM, Oshima J, Terzic J, Amor DJ, Dikic I, Ramadan K, Kubisch C. Lessel D, et al. Nat Genet. 2014 Nov;46(11):1239-44. doi: 10.1038/ng.3103. Epub 2014 Sep 28. Nat Genet. 2014. PMID: 25261934 Free PMC article.

2

Rapamycin decreases DNA damage accumulation and enhances cell growth of WRN-deficient human fibroblasts.

Saha B, Cypro A, Martin GM, Oshima J. Saha B, et al. Aging Cell. 2014 Jun;13(3):573-5. doi: 10.1111/acel.12190. Epub 2014 Feb 5. Aging Cell. 2014. PMID: 24308646 Free PMC article.

3

Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry.

Saha B, Lessel D, Nampoothiri S, Rao AS, Hisama FM, Peter D, Bennett C, Nürnberg G, Nürnberg P, Martin GM, Kubisch C, Oshima J. Saha B, et al. Mol Genet Genomic Med. 2013 May 1;1(1):7-14. doi: 10.1002/mgg3.1. Mol Genet Genomic Med. 2013. PMID: 23936869 Free PMC article.

4

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. Front Genet. 2013 Jul 5;4:129. doi: 10.3389/fgene.2013.00129. eCollection 2013. Front Genet. 2013. PMID: 23847654 Free PMC article.

5

Functional deficit associated with a missense Werner syndrome mutation.

Tadokoro T, Rybanska-Spaeder I, Kulikowicz T, Dawut L, Oshima J, Croteau DL, Bohr VA. Tadokoro T, et al. DNA Repair (Amst). 2013 Jun 1;12(6):414-21. doi: 10.1016/j.dnarep.2013.03.004. Epub 2013 Apr 11. DNA Repair (Amst). 2013. PMID: 23583337 Free PMC article.

6

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. 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.

7

The biology of aging: 1985-2010 and beyond.

Martin GM. Martin GM. FASEB J. 2011 Nov;25(11):3756-62. doi: 10.1096/fj.11-1102.ufm. FASEB J. 2011. PMID: 22046003 Free PMC article. Review.

8

Stochastic modulations of the pace and patterns of ageing: impacts on quasi-stochastic distributions of multiple geriatric pathologies.

Martin GM. Martin GM. Mech Ageing Dev. 2012 Apr;133(4):107-11. doi: 10.1016/j.mad.2011.09.001. Epub 2011 Sep 22. Mech Ageing Dev. 2012. PMID: 21963385 Free PMC article. Review.

9

A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features.

Saha B, Lessel D, Hisama FM, Leistritz DF, Friedrich K, Martin GM, Kubisch C, Oshima J. Saha B, et al. Mol Syndromol. 2010 Sep;1(3):127-132. doi: 10.1159/000320166. Epub 2010 Sep 14. Mol Syndromol. 2010. PMID: 21031082 Free PMC article.

10

The demographic and biomedical case for late-life interventions in aging.

Rae MJ, Butler RN, Campisi J, de Grey AD, Finch CE, Gough M, Martin GM, Vijg J, Perrott KM, Logan BJ. Rae MJ, et al. Sci Transl Med. 2010 Jul 14;2(40):40cm21. doi: 10.1126/scitranslmed.3000822. Sci Transl Med. 2010. PMID: 20630854 Free PMC article.

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