206 related articles for article (PubMed ID: 9352493)
1. Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing.
Goto M
Mech Ageing Dev; 1997 Dec; 98(3):239-54. PubMed ID: 9352493
[TBL] [Abstract][Full Text] [Related]
2. Werner's syndrome: from clinics to genetics.
Goto M
Clin Exp Rheumatol; 2000; 18(6):760-6. PubMed ID: 11138345
[TBL] [Abstract][Full Text] [Related]
3. LMNA mutations in atypical Werner's syndrome.
Chen L; Lee L; Kudlow BA; Dos Santos HG; Sletvold O; Shafeghati Y; Botha EG; Garg A; Hanson NB; Martin GM; Mian IS; Kennedy BK; Oshima J
Lancet; 2003 Aug; 362(9382):440-5. PubMed ID: 12927431
[TBL] [Abstract][Full Text] [Related]
4. Absence of premature senescence in Werner's syndrome keratinocytes.
Ibrahim B; Sheerin AN; Jennert-Burston K; Bird JL; Massala MV; Illsley M; James SE; Faragher RG
Exp Gerontol; 2016 Oct; 83():139-47. PubMed ID: 27492502
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Positional cloning of the Werner's syndrome gene.
Yu CE; Oshima J; Fu YH; Wijsman EM; Hisama F; Alisch R; Matthews S; Nakura J; Miki T; Ouais S; Martin GM; Mulligan J; Schellenberg GD
Science; 1996 Apr; 272(5259):258-62. PubMed ID: 8602509
[TBL] [Abstract][Full Text] [Related]
7. Cellular aging in Werner's syndrome: a unique phenotype?
Norwood TH; Hoehn H; Salk D; Martin GM
J Invest Dermatol; 1979 Jul; 73(1):92-6. PubMed ID: 448183
[TBL] [Abstract][Full Text] [Related]
8. Effect of age and apoptosis on the mouse homologue of the huWRN gene.
Wu J; He J; Mountz JD
Mech Ageing Dev; 1998 Jun; 103(1):27-44. PubMed ID: 9681877
[TBL] [Abstract][Full Text] [Related]
9. Severe toxicity following induction chemotherapy for acute myelogenous leukemia in a patient with Werner's syndrome.
Seiter K; Qureshi A; Liu D; Galvin-Parton P; Arshad M; Agoliati G; Ahmed T
Leuk Lymphoma; 2005 Jul; 46(7):1091-5. PubMed ID: 16019564
[TBL] [Abstract][Full Text] [Related]
10. Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus.
Kihara K; Nakura J; Ye L; Mitsuda N; Kamino K; Zhao Y; Fujioka Y; Miki T; Ogihara T
Jpn J Hum Genet; 1994 Dec; 39(4):403-9. PubMed ID: 7873752
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Werner's syndrome: a review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations.
Salk D
Hum Genet; 1982; 62(1):1-5. PubMed ID: 6759366
[TBL] [Abstract][Full Text] [Related]
13. Werner Syndrome as an example of inflamm-aging: possible therapeutic opportunities for a progeroid syndrome?
Davis T; Kipling D
Rejuvenation Res; 2006; 9(3):402-7. PubMed ID: 16859481
[TBL] [Abstract][Full Text] [Related]
14. Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster.
Masala MV; Scapaticci S; Olivieri C; Pirodda C; Montesu MA; Cuccuru MA; Pruneddu S; Danesino C; Cerimele D
Eur J Dermatol; 2007; 17(3):213-6. PubMed ID: 17478382
[TBL] [Abstract][Full Text] [Related]
15. Werner's syndrome.
Duvic M; Lemak NA
Dermatol Clin; 1995 Jan; 13(1):163-8. PubMed ID: 7712642
[TBL] [Abstract][Full Text] [Related]
16. Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases.
Yamagata K; Kato J; Shimamoto A; Goto M; Furuichi Y; Ikeda H
Proc Natl Acad Sci U S A; 1998 Jul; 95(15):8733-8. PubMed ID: 9671747
[TBL] [Abstract][Full Text] [Related]
17. Asymmetry of DNA replication fork progression in Werner's syndrome.
Rodríguez-López AM; Jackson DA; Iborra F; Cox LS
Aging Cell; 2002 Oct; 1(1):30-9. PubMed ID: 12882351
[TBL] [Abstract][Full Text] [Related]
18. Werner's syndrome lymphoblastoid cells are hypersensitive to topoisomerase II inhibitors in the G2 phase of the cell cycle.
Pichierri P; Franchitto A; Mosesso P; Proietti de Santis L; Balajee AS; Palitti F
Mutat Res; 2000 Mar; 459(2):123-33. PubMed ID: 10725663
[TBL] [Abstract][Full Text] [Related]
19. The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer. Mutations in brief no. 136. Online.
Vidal V; Bay JO; Champomier F; Grancho M; Beauville L; Glowaczower C; Lemery D; Ferrara M; Bignon YJ
Hum Mutat; 1998; 11(5):413-4. PubMed ID: 10206685
[TBL] [Abstract][Full Text] [Related]
20. Premature aging and predisposition to cancers caused by mutations in RecQ family helicases.
Furuichi Y
Ann N Y Acad Sci; 2001 Apr; 928():121-31. PubMed ID: 11795503
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]