P21 is required for dextrose-mediated inhibition of mouse liver regeneration

Hepatology

Volumn 50, Issue 1, 2009, Pages 207-215

  Weymann, Alexander ^a   Hartman, Eric ^a   Gazit, Vered ^a   Wang, Connie ^a   Glauber, Martin ^a   Turmelle, Yumirle ^a   Rudnick, David A ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BROXURIDINE; CCAAT ENHANCER BINDING PROTEIN ALPHA; CYCLIN DEPENDENT KINASE INHIBITOR 1; CYCLIN DEPENDENT KINASE INHIBITOR 1B; GAG PROTEIN; GLUCOSE; IMMEDIATE EARLY PROTEIN; INTERLEUKIN 6; MITOGEN ACTIVATED PROTEIN KINASE; PROTEIN P21; PROTEIN P44; SCATTER FACTOR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR FOXM1; TRANSFORMING GROWTH FACTOR ALPHA; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG; CYCLIN DEPENDENT KINASE INHIBITOR 1A;

ANIMAL TISSUE; ARTICLE; BODY MASS; CELL PROLIFERATION; CONTROLLED STUDY; ENZYME ACTIVATION; LIVER CELL; LIVER REGENERATION; MALE; MOLECULAR MECHANICS; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN INDUCTION; SIGNAL TRANSDUCTION; ANIMAL; C57BL MOUSE; DRUG EFFECT; PHYSIOLOGY;

ANIMALS; CYCLIN-DEPENDENT KINASE INHIBITOR P21; GLUCOSE; LIVER REGENERATION; MALE; MICE; MICE, INBRED C57BL;

EID: 67651184180     PISSN: 02709139     EISSN: None     Source Type: Journal    
DOI: 10.1002/hep.22979     Document Type: Article

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