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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
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1986 2
1987 1
1989 8
1991 2
1992 4
1993 5
1994 5
1995 3
1996 7
1997 3
1998 2
1999 5
2000 2
2001 1
2002 4
2003 9
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2005 10
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2007 3
2008 3
2009 6
2010 4
2012 2
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96 results

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Page 1
WRN mutations in Werner syndrome.
Moser MJ, Oshima J, Monnat RJ Jr. Moser MJ, et al. Hum Mutat. 1999;13(4):271-9. doi: 10.1002/(SICI)1098-1004(1999)13:4<271::AID-HUMU2>3.0.CO;2-Q. Hum Mutat. 1999. PMID: 10220139 Review.
Mitochondrial dysfunction measured in vivo.
Marcinek DJ. Marcinek DJ. Acta Physiol Scand. 2004 Dec;182(4):343-52. doi: 10.1111/j.1365-201X.2004.01372.x. Acta Physiol Scand. 2004. PMID: 15569095 Review.
Modulation of paraoxonase (PON1) activity.
Costa LG, Vitalone A, Cole TB, Furlong CE. Costa LG, et al. Biochem Pharmacol. 2005 Feb 15;69(4):541-50. doi: 10.1016/j.bcp.2004.08.027. Biochem Pharmacol. 2005. PMID: 15670573 Review.
Syndromes of accelerated aging.
Martin GM. Martin GM. Natl Cancer Inst Monogr. 1982;60:241-7. Natl Cancer Inst Monogr. 1982. PMID: 6214719 Review.
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. Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258. Science. 1996. PMID: 8602509
96 results