554 related articles for article (PubMed ID: 12927431)
1. 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]
2. Novel LMNA gene mutation in a patient with Atypical Werner's Syndrome.
Doh YJ; Kim HK; Jung ED; Choi SH; Kim JG; Kim BW; Lee IK
Korean J Intern Med; 2009 Mar; 24(1):68-72. PubMed ID: 19270485
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. First Japanese case of atypical progeroid syndrome/atypical Werner syndrome with heterozygous LMNA mutation.
Motegi S; Yokoyama Y; Uchiyama A; Ogino S; Takeuchi Y; Yamada K; Hattori T; Hashizume H; Ishikawa Y; Goto M; Ishikawa O
J Dermatol; 2014 Dec; 41(12):1047-52. PubMed ID: 25327215
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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; 179(4):279-87. PubMed ID: 19011155
[TBL] [Abstract][Full Text] [Related]
8. Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA.
Rodríguez-López AM; Jackson DA; Nehlin JO; Iborra F; Warren AV; Cox LS
Mech Ageing Dev; 2003 Feb; 124(2):167-74. PubMed ID: 12633936
[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. Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population.
Matsumoto T; Imamura O; Yamabe Y; Kuromitsu J; Tokutake Y; Shimamoto A; Suzuki N; Satoh M; Kitao S; Ichikawa K; Kataoka H; Sugawara K; Thomas W; Mason B; Tsuchihashi Z; Drayna D; Sugawara M; Sugimoto M; Furuichi Y; Goto M
Hum Genet; 1997 Jul; 100(1):123-30. PubMed ID: 9225981
[TBL] [Abstract][Full Text] [Related]
11. Down-regulation of the defective transcripts of the Werner's syndrome gene in the cells of patients.
Yamabe Y; Sugimoto M; Satoh M; Suzuki N; Sugawara M; Goto M; Furuichi Y
Biochem Biophys Res Commun; 1997 Jul; 236(1):151-4. PubMed ID: 9223443
[TBL] [Abstract][Full Text] [Related]
12. Localization of the Bloom syndrome helicase to punctate nuclear structures and the nuclear matrix and regulation during the cell cycle: comparison with the Werner's syndrome helicase.
Gharibyan V; Youssoufian H
Mol Carcinog; 1999 Dec; 26(4):261-73. PubMed ID: 10569803
[TBL] [Abstract][Full Text] [Related]
13. Phenotypic heterogeneity in body fat distribution in patients with atypical Werner's syndrome due to heterozygous Arg133Leu lamin A/C mutation.
Jacob KN; Baptista F; dos Santos HG; Oshima J; Agarwal AK; Garg A
J Clin Endocrinol Metab; 2005 Dec; 90(12):6699-706. PubMed ID: 16174718
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. LMNA mutations in atypical Werner's syndrome.
Bonne G; Levy N
Lancet; 2003 Nov; 362(9395):1585-6; author reply 1586. PubMed ID: 14615129
[No Abstract] [Full Text] [Related]
16. 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]
17. Analysis of Werner's expression within the brain and primary neuronal culture.
Gee J; Ding Q; Keller JN
Brain Res; 2002 Jun; 940(1-2):44-8. PubMed ID: 12020873
[TBL] [Abstract][Full Text] [Related]
18. LMNA mutations in atypical Werner's syndrome.
Vigouroux C; Caux F; Capeau J; Christin-Maitre S; Cohen A
Lancet; 2003 Nov; 362(9395):1585; author reply 1586. PubMed ID: 14615128
[No Abstract] [Full Text] [Related]
19. 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]
20. Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1.
Kawabe Y; Seki M; Seki T; Wang WS; Imamura O; Furuichi Y; Saitoh H; Enomoto T
J Biol Chem; 2000 Jul; 275(28):20963-6. PubMed ID: 10806190
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
