Rac and Cdc42 are potent stimulators of E2F-dependent transcription capable of promoting retinoblastoma susceptibility gene product hyperphosphorylation

Journal of Biological Chemistry

Volumn 273, Issue 30, 1998, Pages 18812-18818

  Gjoerup, Ole ^a   Lukas, Jiri ^b   Bartek, Jiri ^b   Willumsen, Berthe M ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b DANISH CANCER SOCIETY RESEARCH CENTER   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN; CYCLIN D1; GENE PRODUCT; GUANOSINE TRIPHOSPHATASE;

ARTICLE; CELL GROWTH; CYTOSKELETON; DNA SYNTHESIS; ENZYME ACTIVITY; ENZYME INHIBITION; ENZYME PHOSPHORYLATION; PRIORITY JOURNAL; TRANSCRIPTION REGULATION;

3T3 CELLS; ANIMALS; CARRIER PROTEINS; CDC42 GTP-BINDING PROTEIN; CELL CYCLE PROTEINS; CYCLIN-DEPENDENT KINASE INHIBITOR P16; CYCLIN-DEPENDENT KINASE INHIBITOR P21; CYCLINS; DNA REPLICATION; DNA-BINDING PROTEINS; E2F TRANSCRIPTION FACTORS; GENETIC PREDISPOSITION TO DISEASE; GTP-BINDING PROTEINS; MICE; PHOSPHORYLATION; RAC GTP-BINDING PROTEINS; RETINOBLASTOMA PROTEIN; TRANSCRIPTION FACTOR DP1; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC; UP-REGULATION;

EID: 0032563216     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.273.30.18812     Document Type: Article

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