330 related articles for article (PubMed ID: 16673358)
1. The spectrum of WRN mutations in Werner syndrome patients.
Huang S; Lee L; Hanson NB; Lenaerts C; Hoehn H; Poot M; Rubin CD; Chen DF; Yang CC; Juch H; Dorn T; Spiegel R; Oral EA; Abid M; Battisti C; Lucci-Cordisco E; Neri G; Steed EH; Kidd A; Isley W; Showalter D; Vittone JL; Konstantinow A; Ring J; Meyer P; Wenger SL; von Herbay A; Wollina U; Schuelke M; Huizenga CR; Leistritz DF; Martin GM; Mian IS; Oshima J
Hum Mutat; 2006 Jun; 27(6):558-67. PubMed ID: 16673358
[TBL] [Abstract][Full Text] [Related]
2. 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]
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 clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.
Muftuoglu M; Oshima J; von Kobbe C; Cheng WH; Leistritz DF; Bohr VA
Hum Genet; 2008 Nov; 124(4):369-77. PubMed ID: 18810497
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Cellular Werner phenotypes in mice expressing a putative dominant-negative human WRN gene.
Wang L; Ogburn CE; Ware CB; Ladiges WC; Youssoufian H; Martin GM; Oshima J
Genetics; 2000 Jan; 154(1):357-62. PubMed ID: 10628995
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Comparative aspects of the Werner syndrome gene.
Oshima J
In Vivo; 2000; 14(1):165-72. PubMed ID: 10757074
[TBL] [Abstract][Full Text] [Related]
11. WRN protein as a novel erythroblast immunohistochemical marker with applications for the diagnosis of Werner syndrome.
Sadahira Y; Sugihara T; Fujiwara H; Nishimura H; Suetsugu Y; Takeshita M; Okamura S; Goto M
Virchows Arch; 2015 Mar; 466(3):343-50. PubMed ID: 25503078
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Modulation of Werner syndrome protein function by a single mutation in the conserved RecQ domain.
Lee JW; Kusumoto R; Doherty KM; Lin GX; Zeng W; Cheng WH; von Kobbe C; Brosh RM; Hu JS; Bohr VA
J Biol Chem; 2005 Nov; 280(47):39627-36. PubMed ID: 16150736
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Diverse dealings of the Werner helicase/nuclease.
Cheng WH; Bohr VA
Sci Aging Knowledge Environ; 2003 Aug; 2003(31):PE22. PubMed ID: 12904570
[TBL] [Abstract][Full Text] [Related]
16. The Werner syndrome helicase-nuclease--one protein, many mysteries.
Fry M
Sci Aging Knowledge Environ; 2002 Apr; 2002(13):re2. PubMed ID: 14602980
[TBL] [Abstract][Full Text] [Related]
17. Mismatch repair in extracts of Werner syndrome cell lines.
Bennett SE; Umar A; Oshima J; Monnat RJ; Kunkel TA
Cancer Res; 1997 Jul; 57(14):2956-60. PubMed ID: 9230208
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Functional interaction between the Werner Syndrome protein and DNA polymerase delta.
Kamath-Loeb AS; Johansson E; Burgers PM; Loeb LA
Proc Natl Acad Sci U S A; 2000 Apr; 97(9):4603-8. PubMed ID: 10781066
[TBL] [Abstract][Full Text] [Related]
20. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.
Friedrich K; Lee L; Leistritz DF; Nürnberg G; Saha B; Hisama FM; Eyman DK; Lessel D; Nürnberg P; Li C; Garcia-F-Villalta MJ; Kets CM; Schmidtke J; Cruz VT; Van den Akker PC; Boak J; Peter D; Compoginis G; Cefle K; Ozturk S; López N; Wessel T; Poot M; Ippel PF; Groff-Kellermann B; Hoehn H; Martin GM; Kubisch C; Oshima J
Hum Genet; 2010 Jul; 128(1):103-11. PubMed ID: 20443122
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]