Essential function of Chk1 can be uncoupled from DNA damage checkpoint and replication control

Proceedings of the National Academy of Sciences of the United States of America

Volumn 105, Issue 52, 2008, Pages 20752-20757

  Wilsker, Deborah ^a   Petermann, Eva ^b   Helleday, Thomas ^b,c   Bunz, Fred ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c STOCKHOLM UNIVERSITY   (Sweden)

Author keywords

ATR; Centrosome; Gene targeting; Mitosis; Phosphorylation

Indexed keywords

CHECKPOINT KINASE 1; DNA;

ARTICLE; CELL VIABILITY; CENTROSOME; CODON; CONTROLLED STUDY; DNA DAMAGE; DNA REPLICATION; GENE CONTROL; GENE MUTATION; GENE TARGETING; GENETIC LINKAGE; HUMAN; HUMAN CELL; MITOSIS RATE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; SIGNAL TRANSDUCTION;

CELL LINE, TUMOR; CELL SURVIVAL; CENTROSOME; DNA DAMAGE; DNA REPLICATION; G2 PHASE; GENE TARGETING; HUMANS; METAPHASE; MUTATION, MISSENSE; PHOSPHORYLATION; PROTEIN KINASES; QUANTITATIVE TRAIT LOCI;

EID: 58549089689     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0806917106     Document Type: Article

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