Manipulation of cell cycle progression can counteract the apparent loss of correction frequency following oligonucleotide-directed gene repair

BMC Molecular Biology

Volumn 8, Issue , 2007, Pages

  Engstrom, Julia U ^a   Kmiec, Eric B ^a  

^a UNIVERSITY OF DELAWARE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

OLIGONUCLEOTIDE; SINGLE STRANDED DNA; THYMIDINE;

ARTICLE; CELL CYCLE G1 PHASE; CELL CYCLE PROGRESSION; CELL CYCLE S PHASE; CONTROLLED STUDY; DNA REPAIR; DNA REPLICATION; HUMAN; HUMAN CELL; MITOSIS INHIBITION; SENESCENCE;

CELL AGING; CELL CYCLE; CELL DIVISION; CELLS, CULTURED; DNA REPAIR; DNA REPLICATION; GENETIC THERAPY; HUMANS; OLIGONUCLEOTIDES; THYMIDINE; TIME FACTORS;

MAMMALIA;

EID: 33847197563     PISSN: None     EISSN: 14712199     Source Type: Journal    
DOI: 10.1186/1471-2199-8-9     Document Type: Article

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