Lack of WRN results in extensive deletion at nonhomologous joining ends

Cancer Research

Volumn 62, Issue 2, 2002, Pages 547-551

  Oshima, Junko ^a   Pae, Chong ^a   Huang, Shurong ^b   Campisi, Judith ^b   Schiestl, Robert H ^c  

^a UNIVERSITY OF WASHINGTON   (United States)

^b LAWRENCE BERKELEY NATIONAL LABORATORY   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DOUBLE STRANDED DNA; PROTEIN; UNCLASSIFIED DRUG; WERNER SYNDROME PROTEIN;

ARTICLE; DNA STRAND BREAKAGE; FIBROBLAST CULTURE; GENE DELETION; GENE LOCUS; GENE MUTATION; HUMAN; HUMAN CELL; PLASMID; PRIORITY JOURNAL; PROGERIA; WERNER SYNDROME;

DNA; DNA HELICASES; DNA REPAIR; FEMALE; FIBROBLASTS; GENE DELETION; HUMANS; MALE; PLASMIDS; RECQ HELICASES; TRANSFECTION; WERNER SYNDROME;

EID: 0037081095     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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