Depletion of the bloom syndrome helicase stimulates homology-dependent repair at double-strand breaks in human chromosomes

DNA Repair

Volumn 10, Issue 4, 2011, Pages 416-426

  Wang, Yibin ^a   Smith, Krissy ^a   Waldman, Barbara Criscuolo ^a   Waldman, Alan S ^a  

^a UNIVERSITY OF SOUTH CAROLINA   (United States)

Author keywords

Bloom syndrome; Double strand break repair; Homologous recombination; Human cell culture; Nonhomologous end joining

Indexed keywords

BLOOM SYNDROME HELICASE; ENDONUCLEASE; THYMIDINE KINASE; TUBULIN;

ACCURACY; ARTICLE; BLOOM SYNDROME; CANCER SUSCEPTIBILITY; CLONE; CONTROLLED STUDY; DNA REPAIR; DOUBLE STRANDED DNA BREAK; FUSION GENE; GENE CONVERSION; GENE DISRUPTION; GENE EXPRESSION; GENE MUTATION; GENETIC RECOMBINATION; GENETIC TRANSFECTION; GENOMIC INSTABILITY; HOMOLOGOUS RECOMBINATION; HUMAN; HUMAN CELL; HUMAN CHROMOSOME; PRIORITY JOURNAL; PROTEIN EXPRESSION; RNA INTERFERENCE; SISTER CHROMATID EXCHANGE; TK NEO FUSION GENE;

BASE SEQUENCE; BLOOM SYNDROME; CELL LINE; CHROMOSOMES, HUMAN; DNA BREAKS, DOUBLE-STRANDED; DNA HELICASES; DNA REPAIR; GENE KNOCKDOWN TECHNIQUES; GENE ORDER; GENETIC VECTORS; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; RECOMBINATION, GENETIC; RNA, SMALL INTERFERING; SEQUENCE ALIGNMENT;

EID: 79952689584     PISSN: 15687864     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dnarep.2011.01.009     Document Type: Article

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