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Items: 1 to 20 of 36

1.

Werner syndrome: molecular genetics and mechanistic hypotheses.

Monnat RJ Jr.

Exp Gerontol. 1992 Jul-Aug;27(4):447-53. Review. No abstract available.

PMID:
1459221
2.

Mutation-causing mutations.

Ellis NA.

Nature. 1996 May 9;381(6578):110-1. No abstract available.

PMID:
8610002
3.
4.

Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines.

Fukuchi K, Tanaka K, Nakura J, Kumahara Y, Uchida T, Okada Y.

Somat Cell Mol Genet. 1985 Jul;11(4):303-8.

PMID:
2992100
5.

[Mutagen sensitivity and the repair process of the lymphocytes in the Werner syndrome].

Deknudt G, Verellen-Dumoulin C, Léonard A.

C R Seances Soc Biol Fil. 1985;179(4):518-21. French.

PMID:
2938680
6.

The Werner syndrome protein at the crossroads of DNA repair and apoptosis.

Comai L, Li B.

Mech Ageing Dev. 2004 Aug;125(8):521-8. Review.

PMID:
15336909
7.

Analysis of microsatellite instability and hypermutation of immunoglobulin variable genes in Werner syndrome.

Rosner K, Winter DB, Skovgaard GL, Oshima J, Gearhart PJ, Bohr VA.

Mech Ageing Dev. 2001 Aug;122(11):1121-33.

PMID:
11389928
8.

Disorders of DNA replication and repair.

Auerbach AD, Verlander PC.

Curr Opin Pediatr. 1997 Dec;9(6):600-16. Review.

PMID:
9425594
9.

Dna repair: pathways and defects.

Bartram CR.

Eur J Pediatr. 1980 Dec;135(2):121-8. Review.

PMID:
7004875
10.

Werner syndrome: a molecular genetic hypothesis.

Goldstein S, Murano S, Shmookler Reis RJ.

J Gerontol. 1990 Jan;45(1):B3-8. Review.

PMID:
2404059
11.

DNA damage and repair in telomeres: relation to aging.

Kruk PA, Rampino NJ, Bohr VA.

Proc Natl Acad Sci U S A. 1995 Jan 3;92(1):258-62.

12.

Immortalization of Werner syndrome and progeria fibroblasts.

Saito H, Moses RE.

Exp Cell Res. 1991 Feb;192(2):373-9.

PMID:
1671011
13.

The Werner syndrome protein is a DNA helicase.

Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA.

Nat Genet. 1997 Sep;17(1):100-3.

PMID:
9288107
14.

32nd annual meeting of European Environmental Mutagen Society. DNA damage and repair fundamental aspects and contribution to human disorders.

Tudek B, Ciesla Z, Janion C, Boiteux S, Bebenek K, Shinagawa H, Bartsch H, Laval J, van Zeeland AA, Mullenders LF, Szyfter K, Collins A, Kruszewski M.

DNA Repair (Amst). 2003 Jun 11;2(6):765-81. No abstract available.

PMID:
12767355
15.

Meningioma arising in Werner syndrome confirmed by mutation analysis.

Nakamura Y, Shimizu T, Ohigashi Y, Itou N, Ishikawa Y.

J Clin Neurosci. 2005 May;12(4):503-6.

PMID:
15925797
16.

Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases.

Gangloff S, Soustelle C, Fabre F.

Nat Genet. 2000 Jun;25(2):192-4.

PMID:
10835635
17.

Evidence against DNA polymerase beta as a candidate gene for Werner syndrome.

Chang M, Burmer GC, Sweasy J, Loeb LA, Edelhoff S, Disteche CM, Yu CE, Anderson L, Oshima J, Nakura J, et al.

Hum Genet. 1994 May;93(5):507-12.

PMID:
8168825
18.

Telomere-based proliferative lifespan barriers in Werner-syndrome fibroblasts involve both p53-dependent and p53-independent mechanisms.

Davis T, Singhrao SK, Wyllie FS, Haughton MF, Smith PJ, Wiltshire M, Wynford-Thomas D, Jones CJ, Faragher RG, Kipling D.

J Cell Sci. 2003 Apr 1;116(Pt 7):1349-57.

19.

Altered frequency of initiation sites of DNA replication in Werner's syndrome cells.

Takeuchi F, Hanaoka F, Goto M, Akaoka I, Hori T, Yamada M, Miyamoto T.

Hum Genet. 1982;60(4):365-8. No abstract available.

PMID:
7106772
20.

Werner and Bloom helicases are involved in DNA repair in a complementary fashion.

Imamura O, Fujita K, Itoh C, Takeda S, Furuichi Y, Matsumoto T.

Oncogene. 2002 Jan 31;21(6):954-63.

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