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

Year Number of Results
1998 3
1999 3
2000 2
2002 1
2003 1
2005 1
2006 2
2007 3
2008 3
2011 1
2020 0
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18 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.
Phenomics and lamins: from disease to therapy.
Hegele RA, Oshima J. Hegele RA, et al. Exp Cell Res. 2007 Jun 10;313(10):2134-43. doi: 10.1016/j.yexcr.2007.03.023. Epub 2007 Mar 30. Exp Cell Res. 2007. PMID: 17466974 Review.
The spectrum of WRN mutations in Werner syndrome patients.
Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, Poot M, Rubin CD, Chen DF, Yang CC, Juch H, Dorn T, Spiegel R, Oral EA, Abid M, Battisti C, Lucci-Cordisco E, Neri G, Steed EH, Kidd A, Isley W, Showalter D, Vittone JL, Konstantinow A, Ring J, Meyer P, Wenger SL, von Herbay A, Wollina U, Schuelke M, Huizenga CR, Leistritz DF, Martin GM, Mian IS, Oshima J. Huang S, et al. Hum Mutat. 2006 Jun;27(6):558-67. doi: 10.1002/humu.20337. Hum Mutat. 2006. PMID: 16673358 Free PMC article.
Accumulation of Werner protein at DNA double-strand breaks in human cells.
Lan L, Nakajima S, Komatsu K, Nussenzweig A, Shimamoto A, Oshima J, Yasui A. Lan L, et al. J Cell Sci. 2005 Sep 15;118(Pt 18):4153-62. doi: 10.1242/jcs.02544. Epub 2005 Sep 1. J Cell Sci. 2005. PMID: 16141234 Free article.
Werner helicase expression in human fetal and adult aortas.
Wang L, Evans AE, Ogburn CE, Youssoufian H, Martin GM, Oshima J. Wang L, et al. Exp Gerontol. 1999 Dec;34(8):935-41. doi: 10.1016/s0531-5565(99)00066-2. Exp Gerontol. 1999. PMID: 10673147
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. 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.
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