WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.

Aging cell

Volumn 2, Issue 4, 2003, Pages 191-199

  Chen, Lishan ^a   Huang, Shurong ^a   Lee, Lin ^a   Davalos, Albert ^a   Schiestl, Robert H ^a   Campisi, Judith ^a   Oshima, Junko ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; BLOOM SYNDROME PROTEIN; DNA; EXODEOXYRIBONUCLEASE; HELICASE; RECQ HELICASE; WRN PROTEIN, HUMAN;

ARTICLE; CELL AGING; CELL LINE; DNA DAMAGE; DNA REPAIR; ENZYMOLOGY; FIBROBLAST; GENETIC RECOMBINATION; GENETICS; HUMAN; METABOLISM; MUTATION; PATHOPHYSIOLOGY; WERNER SYNDROME;

ADENOSINE TRIPHOSPHATASES; CELL AGING; CELL LINE, TRANSFORMED; DNA; DNA DAMAGE; DNA HELICASES; DNA REPAIR; EXODEOXYRIBONUCLEASES; FIBROBLASTS; HUMANS; MUTATION; RECOMBINATION, GENETIC; RECQ HELICASES; WERNER SYNDROME;

EID: 0141740425     PISSN: 14749718     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1474-9728.2003.00052.x     Document Type: Article

References (0)