Keratins modulate hepatic cell adhesion, size and G1/S transition

Experimental Cell Research

Volumn 313, Issue 1, 2007, Pages 179-194

  Galarneau, Luc ^a,b   Loranger, Anne ^a   Gilbert, Stéphane ^a,b   Marceau, Normand ^a,b  

^a Centre de Recherche en Cancerologie   (Canada)

^b UNIVERSITÉ LAVAL   (Canada)

Author keywords

Cell cycle; Cell size; Cell spreading; Cyclins; Integrin; Keratin; Plectin; Protein synthesis; RACK1

Indexed keywords

BETA1 INTEGRIN; COMPLEMENTARY DNA; CYCLIN A; CYCLINE; CYTOKERATIN 18; CYTOKERATIN 8; FAS ANTIGEN; FLICE INHIBITORY PROTEIN; FOCAL ADHESION KINASE; INTERMEDIATE FILAMENT PROTEIN; KERATIN; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; PLECTIN; PROTEIN KINASE B; RECEPTOR FOR ACTIVATED C KINASE 1; RECEPTOR PROTEIN; VINCULIN;

ANIMAL CELL; APOPTOSIS; ARTICLE; AUTOPHOSPHORYLATION; CELL ADHESION; CELL CYCLE G1 PHASE; CELL CYCLE PROGRESSION; CELL CYCLE S PHASE; CELL GROWTH; CELL SIZE; CELL SPREADING; CELL STIMULATION; CELL STRUCTURE; CONTROLLED STUDY; DNA TRANSFER; ENZYME ACTIVATION; ENZYME PHOSPHORYLATION; EPITHELIUM CELL; FOCAL ADHESION; HEPATOMA CELL; INTERMEDIATE FILAMENT; LIVER CELL; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN SYNTHESIS; RAT; SIGNAL TRANSDUCTION;

EID: 33845631306     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.yexcr.2006.10.007     Document Type: Article

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