163 related articles for article (PubMed ID: 12722926)
1. Lack of amyloid plaque formation in the central nervous system of a patient with Werner syndrome.
Mori H; Tomiyama T; Maeda N; Ozawa K; Wakasa K
Neuropathology; 2003 Mar; 23(1):51-6. PubMed ID: 12722926
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 9012406
[TBL] [Abstract][Full Text] [Related]
3. Werner syndrome: a changing pattern of clinical manifestations in Japan (1917~2008).
Goto M; Ishikawa Y; Sugimoto M; Furuichi Y
Biosci Trends; 2013 Feb; 7(1):13-22. PubMed ID: 23524889
[TBL] [Abstract][Full Text] [Related]
4. A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay.
Müller FB; Tsianakas A; Kuwert C; Korge BP; Hunzelmann N
Br J Dermatol; 2005 May; 152(5):1030-2. PubMed ID: 15888165
[TBL] [Abstract][Full Text] [Related]
5. Werner syndrome: clinical evaluation of two cases and a novel mutation.
Mansur AT; Elçioglu NH; Demirci GT
Genet Couns; 2014; 25(2):119-27. PubMed ID: 25059010
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 16804003
[TBL] [Abstract][Full Text] [Related]
7. Genetic analyses of two cases of Werner's syndrome.
Sogabe Y; Yasuda M; Yokoyama Y; Tamura A; Negishi I; Ohnishi K; Shinozaki T; Ishikawa O
Eur J Dermatol; 2004; 14(6):379-82. PubMed ID: 15564200
[TBL] [Abstract][Full Text] [Related]
8. Comparative aspects of the Werner syndrome gene.
Oshima J
In Vivo; 2000; 14(1):165-72. PubMed ID: 10757074
[TBL] [Abstract][Full Text] [Related]
9. Human premature aging syndromes and genomic instability.
Bohr VA
Mech Ageing Dev; 2002 Apr; 123(8):987-93. PubMed ID: 12044947
[No Abstract] [Full Text] [Related]
10. Homozygous and compound heterozygous mutations at the Werner syndrome locus.
Oshima J; Yu CE; Piussan C; Klein G; Jabkowski J; Balci S; Miki T; Nakura J; Ogihara T; Ells J; Smith M; Melaragno MI; Fraccaro M; Scappaticci S; Matthews J; Ouais S; Jarzebowicz A; Schellenberg GD; Martin GM
Hum Mol Genet; 1996 Dec; 5(12):1909-13. PubMed ID: 8968742
[TBL] [Abstract][Full Text] [Related]
11. Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer.
Agrelo R; Cheng WH; Setien F; Ropero S; Espada J; Fraga MF; Herranz M; Paz MF; Sanchez-Cespedes M; Artiga MJ; Guerrero D; Castells A; von Kobbe C; Bohr VA; Esteller M
Proc Natl Acad Sci U S A; 2006 Jun; 103(23):8822-7. PubMed ID: 16723399
[TBL] [Abstract][Full Text] [Related]
12. [Utilization of Werner syndrome mouse model in studying premature aging and tumor].
Jia ST; Yang SH; Luo Y
Yi Chuan; 2009 Aug; 31(8):785-90. PubMed ID: 19689938
[TBL] [Abstract][Full Text] [Related]
13. Failure to complement abnormal phenotypes of simian virus 40-transformed Werner syndrome cells by introduction of a normal human chromosome 8.
Kodama S; Kashino G; Suzuki K; Takatsuji T; Okumura Y; Oshimura M; Watanabe M; Barrett JC
Cancer Res; 1998 Nov; 58(22):5188-95. PubMed ID: 9823331
[TBL] [Abstract][Full Text] [Related]
14. WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.
Chen L; Huang S; Lee L; Davalos A; Schiestl RH; Campisi J; Oshima J
Aging Cell; 2003 Aug; 2(4):191-9. PubMed ID: 12934712
[TBL] [Abstract][Full Text] [Related]
15. [Human genes in premature aging].
Miki T; Morishima A; Nakura J
Nihon Naika Gakkai Zasshi; 1999 Sep; 88(9):1701-5. PubMed ID: 10581749
[No Abstract] [Full Text] [Related]
16. Deficient DNA repair in the human progeroid disorder, Werner syndrome.
Bohr VA
Mutat Res; 2005 Sep; 577(1-2):252-9. PubMed ID: 15916783
[TBL] [Abstract][Full Text] [Related]
17. Increased frequency of DNA deletions in pink-eyed unstable mice carrying a mutation in the Werner syndrome gene homologue.
Lebel M
Carcinogenesis; 2002 Jan; 23(1):213-6. PubMed ID: 11756244
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 16786514
[TBL] [Abstract][Full Text] [Related]
19. The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases.
Shen JC; Loeb LA
Trends Genet; 2000 May; 16(5):213-20. PubMed ID: 10782115
[TBL] [Abstract][Full Text] [Related]
20. Werner syndrome: genetic and molecular basis of a premature aging disorder.
Lebel M
Cell Mol Life Sci; 2001 Jun; 58(7):857-67. PubMed ID: 11497235
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]