Human FEM1B is required for Rad9 recruitment and CHK1 activation in response to replication stress

Oncogene

Volumn 28, Issue 18, 2009, Pages 1971-1981

  Sun, T P ^a,b   Shieh, S Y ^b  

^a NATIONAL DEFENSE MEDICAL CENTER   (Taiwan)

^b INSTITUTE OF BIOMEDICAL SCIENCES   (Taiwan)

Author keywords

CHK1; FEM1B; Replication stress

Indexed keywords

CHECKPOINT KINASE 1; COMPLEMENTARY DNA; FEM1 PROTEIN; FEM1B PROTEIN; GLUTATHIONE TRANSFERASE; PROTEIN RAD9; RECOMBINANT PROTEIN; SMALL INTERFERING RNA; UNCLASSIFIED DRUG; ATR PROTEIN, HUMAN; CARRIER PROTEIN; CELL CYCLE PROTEIN; FEM1B PROTEIN, HUMAN; PROTEIN KINASE; PROTEIN SERINE THREONINE KINASE;

ARTICLE; CAENORHABDITIS ELEGANS; CELL CYCLE; CELL FRACTIONATION; CELL STRAIN HCT116; CELL STRESS; CHROMATIN; CONTROLLED STUDY; DNA REPLICATION; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME PHOSPHORYLATION; FLOW CYTOMETRY; HELA CELL; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; TWO HYBRID SYSTEM; YEAST; CELL LINE; CYTOLOGY; GENETIC TRANSFECTION; GENETICS; ISOLATION AND PURIFICATION; KIDNEY; METABOLISM; PHYSIOLOGY;

ATAXIA TELANGIECTASIA; CAENORHABDITIS ELEGANS;

CARRIER PROTEINS; CELL CYCLE PROTEINS; CELL LINE, TRANSFORMED; DNA REPLICATION; ENZYME ACTIVATION; HCT116 CELLS; HELA CELLS; HUMANS; KIDNEY; PROTEIN KINASES; PROTEIN-SERINE-THREONINE KINASES; RECOMBINANT PROTEINS; RNA, SMALL INTERFERING; TRANSFECTION; TWO-HYBRID SYSTEM TECHNIQUES;

EID: 66149104550     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/onc.2009.58     Document Type: Article

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