Homologous recombination resolution defect in Werner syndrome

Molecular and Cellular Biology

Volumn 22, Issue 20, 2002, Pages 6971-6978

  Saintigny, Yannick ^a   Makienko, Kate ^a   Swanson, Cristina ^a   Emond, Mary J ^a   Monnat Jr , Raymond J ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL PROTEIN; GENE PRODUCT; HELICASE; PROTEIN RUSA; RAD51 PROTEIN; RECQ HELICASE; RESOLVASE; UNCLASSIFIED DRUG;

AGING; ANIMAL CELL; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CANCER RISK; CELL DIVISION; CELL SURVIVAL; CONTROLLED STUDY; DNA DAMAGE; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; HYPERSENSITIVITY; MICROSATELLITE INSTABILITY; MITOSIS; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROGENY; WERNER SYNDROME;

CELL DIVISION; CELL LINE, TRANSFORMED; DNA DAMAGE; DNA HELICASES; DNA-BINDING PROTEINS; HUMANS; RAD51 RECOMBINASE; RECOMBINATION, GENETIC; RECQ HELICASES; WERNER SYNDROME;

ANIMALIA; BACTERIA (MICROORGANISMS);

EID: 0036787870     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.22.20.6971-6978.2002     Document Type: Article

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