Cytochrome P4501A1 Promotes G1 Phase Cell Cycle Progression by Controlling Aryl Hydrocarbon Receptor Activity

Molecular Pharmacology

Volumn 65, Issue 2, 2004, Pages 461-469

  Levine Fridman, Aviva ^a,b   Chen, Li ^a   Elferink, Cornelis J ^a  

^a University of Texas Medical Branch School of Medicine   (United States)

^b WAYNE STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1 (1 PROPYNYL)PYRENE; 2,3,7,8 TETRACHLORODIBENZO PARA DIOXIN; ALKYNE; AROMATIC HYDROCARBON RECEPTOR; CYROCHROME P450 1A1 INHIBITOR; CYTOCHROME P450 1A1; CYTOCHROME P450 INHIBITOR; ETHOXYRESORUFIN DEETHYLASE; PROTEIN P27; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ANIMAL; ANIMAL CELL; ARTICLE; CELL CYCLE; CELL CYCLE G1 PHASE; CELL CYCLE S PHASE; CELL FUNCTION; COMPARATIVE STUDY; CONTROLLED STUDY; DOSE RESPONSE; DRUG EFFECT; GENETICS; HEPATOMA CELL; INHIBITION KINETICS; LIGAND BINDING; METABOLIC REGULATION; METABOLISM; MITOSIS INHIBITION; NONHUMAN; PHASE TRANSITION; PHYSIOLOGY; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; RECEPTOR UPREGULATION; REGULATORY MECHANISM; TUMOR CELL LINE;

ANIMALS; CELL LINE, TUMOR; CYTOCHROME P-450 CYP1A1; DOSE-RESPONSE RELATIONSHIP, DRUG; G1 PHASE; RATS; RECEPTORS, ARYL HYDROCARBON; TETRACHLORODIBENZODIOXIN;

EID: 1642579495     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: 10.1124/mol.65.2.461     Document Type: Article

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