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Results: 1 to 20 of 101

1.

The Werner syndrome gene and global sequence variation.

Passarino G, Shen P, Van Kirk JB, Lin AA, De Benedictis G, Cavalli Sforza LL, Oefner PJ, Underhill PA.

Genomics. 2001 Jan 1;71(1):118-22.

PMID:
11161804
[PubMed - indexed for MEDLINE]
2.

Possible associations between successful aging and polymorphic markers in the Werner gene region.

Sild M, Koca C, Bendixen MH, Frederiksen H, McGue M, Kølvraa S, Christensen K, Nexø B.

Ann N Y Acad Sci. 2006 May;1067:309-10.

PMID:
16804003
[PubMed - indexed for MEDLINE]
3.

Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mapping.

Ye L, Nakura J, Mitsuda N, Fujioka Y, Kamino K, Ohta T, Jinno Y, Niikawa N, Miki T, Ogihara T.

Genomics. 1995 Aug 10;28(3):566-9.

PMID:
7490095
[PubMed - indexed for MEDLINE]
4.

The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C.

Kamath-Loeb AS, Welcsh P, Waite M, Adman ET, Loeb LA.

J Biol Chem. 2004 Dec 31;279(53):55499-505. Epub 2004 Oct 15.

PMID:
15489508
[PubMed - indexed for MEDLINE]
Free Article
5.

Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians.

Castro E, Ogburn CE, Hunt KE, Tilvis R, Louhija J, Penttinen R, Erkkola R, Panduro A, Riestra R, Piussan C, Deeb SS, Wang L, Edland SD, Martin GM, Oshima J.

Am J Med Genet. 1999 Feb 19;82(5):399-403.

PMID:
10069711
[PubMed - indexed for MEDLINE]
6.

Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.

Nakura J, Miki T, Ye L, Mitsuda N, Zhao Y, Kihara K, Yu CE, Oshima J, Fukuchi KI, Wijsman EM, Schellenberg GD, Martin GM, Murano Si, Hashimoto K, Fujiwara Y, Ogihara T.

Genomics. 1996 Aug 15;36(1):130-41.

PMID:
8812424
[PubMed - indexed for MEDLINE]
7.

Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population.

Ye L, Miki T, Nakura J, Oshima J, Kamino K, Rakugi H, Ikegami H, Higaki J, Edland SD, Martin GM, Ogihara T.

Am J Med Genet. 1997 Feb 11;68(4):494-8. Erratum in: Am J Med Genet 1997 May 2;70(1):103.

PMID:
9021029
[PubMed - indexed for MEDLINE]
8.

Werner syndrome and mutations of the WRN and LMNA genes in France.

Uhrhammer NA, Lafarge L, Dos Santos L, Domaszewska A, Lange M, Yang Y, Aractingi S, Bessis D, Bignon YJ.

Hum Mutat. 2006 Jul;27(7):718-9.

PMID:
16786514
[PubMed - indexed for MEDLINE]
9.

[Genetic analysis of Werner syndrome in a family].

Morishima A, Mitsuda N, Nakura J, Kamino K, Sato N, Miki T, Ogihara T.

Nihon Ronen Igakkai Zasshi. 1995 Dec;32(12):817-21. Japanese.

PMID:
8865743
[PubMed - indexed for MEDLINE]
Free Article
10.

A novel mutation of the WRN gene in a Chinese patient with Werner syndrome.

Zhao N, Hao F, Qu T, Zuo YG, Wang BX.

Clin Exp Dermatol. 2008 May;33(3):278-81. doi: 10.1111/j.1365-2230.2007.02641.x. Epub 2008 Jan 16.

PMID:
18205852
[PubMed - indexed for MEDLINE]
11.

Variation in the type I interferon gene cluster on 9p21 influences susceptibility to asthma and atopy.

Chan A, Newman DL, Shon AM, Schneider DH, Kuldanek S, Ober C.

Genes Immun. 2006 Mar;7(2):169-78.

PMID:
16437122
[PubMed - indexed for MEDLINE]
12.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
[PubMed - indexed for MEDLINE]
13.

High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2.

Iida A, Ohnishi Y, Ozaki K, Ariji Y, Nakamura Y, Tanaka T.

J Hum Genet. 2001;46(10):604-8.

PMID:
11589220
[PubMed - indexed for MEDLINE]
14.

Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.

Hutcheson KA, Paluru PC, Bernstein SL, Koh J, Rappaport EF, Leach RA, Young TL.

Mol Vis. 2005 Jul 14;11:501-8.

PMID:
16052165
[PubMed - indexed for MEDLINE]
Free Article
15.

The bovine PPARGC1A gene: molecular characterization and association of an SNP with variation of milk fat synthesis.

Weikard R, Kühn C, Goldammer T, Freyer G, Schwerin M.

Physiol Genomics. 2005 Mar 21;21(1):1-13.

PMID:
15781588
[PubMed - indexed for MEDLINE]
Free Article
16.

The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.

Muftuoglu M, Oshima J, von Kobbe C, Cheng WH, Leistritz DF, Bohr VA.

Hum Genet. 2008 Nov;124(4):369-77. doi: 10.1007/s00439-008-0562-0. Epub 2008 Sep 23. Review.

PMID:
18810497
[PubMed - indexed for MEDLINE]
17.

Genomic organization and sequence variation of the human integrin subunit alpha8 gene (ITGA8).

Ekwa-Ekoka C, Diaz GA, Carlson C, Hasegawa T, Samudrala R, Lim KC, Yabu JM, Levy B, Schnapp LM.

Matrix Biol. 2004 Nov;23(7):487-96.

PMID:
15579315
[PubMed - indexed for MEDLINE]
18.

Denaturing high-performance liquid chromatography for the detection of mutations and polymorphisms in UBE3A.

Bercovich D, Beaudet AL.

Genet Test. 2003 Fall;7(3):189-94.

PMID:
14641994
[PubMed - indexed for MEDLINE]
19.

Genetic variations of regulator of G-protein signaling 2 in hypertensive patients and in the general population.

Yang J, Kamide K, Kokubo Y, Takiuchi S, Tanaka C, Banno M, Miwa Y, Yoshii M, Horio T, Okayama A, Tomoike H, Kawano Y, Miyata T.

J Hypertens. 2005 Aug;23(8):1497-505.

PMID:
16003176
[PubMed - indexed for MEDLINE]
20.

Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene region.

Hisama FM, Oshima J, Yu CE, Fu YH, Mulligan J, Weissman SM, Schellenberg GD.

Genomics. 1998 Sep 15;52(3):352-7.

PMID:
9790753
[PubMed - indexed for MEDLINE]

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