The transcription factor B-Myb is maintained in an inhibited state in target cells through its interaction with the nuclear corepressors N-CoR and SMRT

Molecular and Cellular Biology

Volumn 22, Issue 11, 2002, Pages 3663-3673

  Li, Xiaolin ^a   McDonnell, Donald P ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN A; NUCLEAR RECEPTOR COREPRESSOR; PROTEIN SMRT; REPRESSOR PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR B MYB; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING SITE; CELL CYCLE; CONTROLLED STUDY; GENE EXPRESSION REGULATION; GENE MUTATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; TRANSCRIPTION REGULATION;

ANIMALS; CDC2-CDC28 KINASES; CELL CYCLE PROTEINS; CELL LINE; CYCLIN A; CYCLIN-DEPENDENT KINASE 2; CYCLIN-DEPENDENT KINASES; DNA-BINDING PROTEINS; MEMBRANE PROTEINS; MICE; MODELS, BIOLOGICAL; MUTATION; NUCLEAR PROTEINS; PHOSPHOPROTEINS; PHOSPHORYLATION; PROTEIN STRUCTURE, TERTIARY; PROTEIN-SERINE-THREONINE KINASES; PROTO-ONCOGENE PROTEINS C-MYB; RECOMBINANT FUSION PROTEINS; REPRESSOR PROTEINS; TRANS-ACTIVATORS; TRANSCRIPTION, GENETIC;

ANIMALIA;

EID: 0036097193     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.22.11.3663-3673.2002     Document Type: Article

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