ATM is required for the cellular response to thymidine induced replication fork stress

Human Molecular Genetics

Volumn 13, Issue 23, 2004, Pages 2937-2945

  Bolderson, Emma ^a   Scorah, Jennifer ^a,b   Helleday, Thomas ^a   Smythe, Carl ^a   Meuth, Mark ^a  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATM PROTEIN; CELL PROTEIN; CHECKPOINT KINASE 2; COHESIN; DEOXYCYTIDINE TRIPHOSPHATE; DNA; NIJMEGEN BREAKAGE SYNDROME PROTEIN; PROTEIN SMC1; THYMIDINE; UNCLASSIFIED DRUG;

ARTICLE; CELL CYCLE; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; DNA REPLICATION; ENZYME PHOSPHORYLATION; EXPOSURE; GENETIC TRANSFECTION; HOMOLOGOUS RECOMBINATION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION;

BLOTTING, WESTERN; CELL CYCLE PROTEINS; CELL LINE, TRANSFORMED; DNA REPLICATION; DNA-BINDING PROTEINS; ELECTROPHORESIS, GEL, PULSED-FIELD; HUMANS; PROTEIN-SERINE-THREONINE KINASES; RECOMBINATION, GENETIC; RNA, SMALL INTERFERING; THYMIDINE; TUMOR SUPPRESSOR PROTEINS;

ATAXIA; ATAXIA TELANGIECTASIA;

EID: 9744284973     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddh316     Document Type: Article

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