686 related articles for article (PubMed ID: 8602509)
1. 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]
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. 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]
4. Preferential expression of an intact WRN gene in Werner syndrome cell lines in which a normal chromosome 8 has been introduced.
Kashino G; Kodama S; Suzuki K; Oshimura M; Watanabe M
Biochem Biophys Res Commun; 2001 Nov; 289(1):111-5. PubMed ID: 11708785
[TBL] [Abstract][Full Text] [Related]
5. Premature aging gene discovered.
Pennisi E
Science; 1996 Apr; 272(5259):193-4. PubMed ID: 8602501
[No 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. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. WRN mutations in Werner syndrome.
Moser MJ; Oshima J; Monnat RJ
Hum Mutat; 1999; 13(4):271-9. PubMed ID: 10220139
[TBL] [Abstract][Full Text] [Related]
13. Physical map of the human chromosome 8p12-p21 encompassing tumor suppressor and Werner's syndrome gene loci.
Ichikawa K; Shimamoto A; Imamura O; Tokutake Y; Yamabe Y; Kitao S; Suzuki N; Sugawara K; Matsumoto T; Thomas W; Drayna D; Goto M; Sugimoto M; Sugawara M; Furuichi Y
DNA Res; 1998 Apr; 5(2):103-13. PubMed ID: 9679198
[TBL] [Abstract][Full Text] [Related]
14. The Werner's Syndrome RecQ helicase/exonuclease at the nexus of cancer and aging.
Chun SG; Shaeffer DS; Bryant-Greenwood PK
Hawaii Med J; 2011 Mar; 70(3):52-5. PubMed ID: 21365542
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. [Werner syndrome].
Goto M; Ishikawa Y
Nihon Rinsho; 2000 Jul; 58(7):1490-5. PubMed ID: 10921329
[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. Characterization of the human and mouse WRN 3'-->5' exonuclease.
Huang S; Beresten S; Li B; Oshima J; Ellis NA; Campisi J
Nucleic Acids Res; 2000 Jun; 28(12):2396-405. PubMed ID: 10871373
[TBL] [Abstract][Full Text] [Related]
20. The Werner syndrome protein is involved in RNA polymerase II transcription.
Balajee AS; Machwe A; May A; Gray MD; Oshima J; Martin GM; Nehlin JO; Brosh R; Orren DK; Bohr VA
Mol Biol Cell; 1999 Aug; 10(8):2655-68. PubMed ID: 10436020
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
