AG17242/AG/NIA NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2001	1
2002	2
2003	4
2004	1
2005	7
2006	4
2007	4
2008	7
2009	6
2010	4
2011	8
2012	4
2013	7
2014	5
2015	7
2016	2
2021	1
2025	0

1

Vijg J, Suh Y. Vijg J, et al. Annu Rev Physiol. 2013;75:645-68. doi: 10.1146/annurev-physiol-030212-183715. Annu Rev Physiol. 2013. PMID: 23398157 Review.

2

Age to survive: DNA damage and aging.

Schumacher B, Garinis GA, Hoeijmakers JH. Schumacher B, et al. Trends Genet. 2008 Feb;24(2):77-85. doi: 10.1016/j.tig.2007.11.004. Epub 2008 Jan 14. Trends Genet. 2008. PMID: 18192065 Review.

3

Circulating miRNAs in ageing and ageing-related diseases.

Jung HJ, Suh Y. Jung HJ, et al. J Genet Genomics. 2014 Sep 20;41(9):465-72. doi: 10.1016/j.jgg.2014.07.003. Epub 2014 Aug 6. J Genet Genomics. 2014. PMID: 25269672 Free PMC article. Review.

4

Genome instability, cancer and aging.

Maslov AY, Vijg J. Maslov AY, et al. Biochim Biophys Acta. 2009 Oct;1790(10):963-9. doi: 10.1016/j.bbagen.2009.03.020. Epub 2009 Mar 31. Biochim Biophys Acta. 2009. PMID: 19344750 Free PMC article. Review.

5

Chromosomal aneuploidy in the aging brain.

Faggioli F, Vijg J, Montagna C. Faggioli F, et al. Mech Ageing Dev. 2011 Aug;132(8-9):429-36. doi: 10.1016/j.mad.2011.04.008. Epub 2011 Apr 28. Mech Ageing Dev. 2011. PMID: 21549743 Free PMC article. Review.

6

Aging and genome maintenance: lessons from the mouse?

Hasty P, Campisi J, Hoeijmakers J, van Steeg H, Vijg J. Hasty P, et al. Science. 2003 Feb 28;299(5611):1355-9. doi: 10.1126/science.1079161. Science. 2003. PMID: 12610296 Review.

7

SNP discovery in associating genetic variation with human disease phenotypes.

Suh Y, Vijg J. Suh Y, et al. Mutat Res. 2005 Jun 3;573(1-2):41-53. doi: 10.1016/j.mrfmmm.2005.01.005. Mutat Res. 2005. PMID: 15829236 Review.

8

Genetics of longevity and aging.

Vijg J, Suh Y. Vijg J, et al. Annu Rev Med. 2005;56:193-212. doi: 10.1146/annurev.med.56.082103.104617. Annu Rev Med. 2005. PMID: 15660509 Review.

9

Direct mutation analysis by high-throughput sequencing: from germline to low-abundant, somatic variants.

Gundry M, Vijg J. Gundry M, et al. Mutat Res. 2012 Jan 3;729(1-2):1-15. doi: 10.1016/j.mrfmmm.2011.10.001. Epub 2011 Oct 12. Mutat Res. 2012. PMID: 22016070 Free PMC article. Review.

10

The progeroid phenotype of Ku80 deficiency is dominant over DNA-PKCS deficiency.

Reiling E, Dollé ME, Youssef SA, Lee M, Nagarajah B, Roodbergen M, de With P, de Bruin A, Hoeijmakers JH, Vijg J, van Steeg H, Hasty P. Reiling E, et al. PLoS One. 2014 Apr 16;9(4):e93568. doi: 10.1371/journal.pone.0093568. eCollection 2014. PLoS One. 2014. PMID: 24740260 Free PMC article.

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