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Items: 14

1.

Human RECQ Helicase Pathogenic Variants, Population Variation and "Missing" Diseases.

Fu W, Ligabue A, Rogers KJ, Akey JM, Monnat RJ Jr.

Hum Mutat. 2017 Feb;38(2):193-203. doi: 10.1002/humu.23148. Epub 2016 Dec 9.

2.

Use of p38 MAPK Inhibitors for the Treatment of Werner Syndrome.

Bagley MC, Davis T, Murziani PG, Widdowson CS, Kipling D.

Pharmaceuticals (Basel). 2010 Jun 4;3(6):1842-1872. Review.

3.

Cigarette smoke induces cellular senescence via Werner's syndrome protein down-regulation.

Nyunoya T, Monick MM, Klingelhutz AL, Glaser H, Cagley JR, Brown CO, Matsumoto E, Aykin-Burns N, Spitz DR, Oshima J, Hunninghake GW.

Am J Respir Crit Care Med. 2009 Feb 15;179(4):279-87. doi: 10.1164/rccm.200802-320OC. Epub 2008 Nov 14.

5.

Complex SNP-based haplotypes in three human helicases: implications for cancer association studies.

Trikka D, Fang Z, Renwick A, Jones SH, Chakraborty R, Kimmel M, Nelson DL.

Genome Res. 2002 Apr;12(4):627-39.

6.
7.

Loss of Werner syndrome protein function promotes aberrant mitotic recombination.

Prince PR, Emond MJ, Monnat RJ Jr.

Genes Dev. 2001 Apr 15;15(8):933-8.

8.

Sp1-mediated transcription of the Werner helicase gene is modulated by Rb and p53.

Yamabe Y, Shimamoto A, Goto M, Yokota J, Sugawara M, Furuichi Y.

Mol Cell Biol. 1998 Nov;18(11):6191-200.

9.
10.

Genetics and the pathobiology of ageing.

Martin GM.

Philos Trans R Soc Lond B Biol Sci. 1997 Dec 29;352(1363):1773-80. Review.

11.

DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system.

Suzuki N, Shimamoto A, Imamura O, Kuromitsu J, Kitao S, Goto M, Furuichi Y.

Nucleic Acids Res. 1997 Aug 1;25(15):2973-8.

12.

Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Yu CE, Oshima J, Wijsman EM, Nakura J, Miki T, Piussan C, Matthews S, Fu YH, Mulligan J, Martin GM, Schellenberg GD.

Am J Hum Genet. 1997 Feb;60(2):330-41.

13.

A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifs.

Shimamoto A, Kitao S, Ichikawa K, Suzuki N, Yamabe Y, Imamura O, Tokutake Y, Satoh M, Matsumoto T, Kuromitsu J, Kataoka H, Sugawara K, Sugawara M, Sugimoto M, Goto M, Furuichi Y.

Proc Natl Acad Sci U S A. 1996 Oct 1;93(20):10913-7.

14.

Deletion mapping of chromosome 8p in colorectal carcinoma and dysplasia arising in ulcerative colitis, prostatic carcinoma, and malignant fibrous histiocytomas.

Chang M, Tsuchiya K, Batchelor RH, Rabinovitch PS, Kulander BG, Haggitt RC, Burmer GC.

Am J Pathol. 1994 Jan;144(1):1-6.

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