Protein kinase C isoforms α, δ and θ require insulin receptor substrate-1 to inhibit the tyrosine kinase activity of the insulin receptor in human kidney embryonic cells (HEK 293 cells)

Diabetologia

Volumn 41, Issue 7, 1998, Pages 833-838

  Kellerer, M ^a   Mushack, J ^a   Seffer, E ^a   Mischak, H ^b   Ullrich, A ^c   Haring H U ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b Hämatologisches Institut   (Germany)

^c MAX PLANCK INSTITUTE OF BIOCHEMISTRY   (Germany)

Author keywords

Insulin receptor; Insulin receptor substrate; Insulin resistance; Protein kinase C; Serine phosphorylation

Indexed keywords

INSULIN RECEPTOR SUBSTRATE 1; PROTEIN KINASE C; PROTEIN TYROSINE KINASE;

ARTICLE; CONTROLLED STUDY; CYTOKINE RELEASE; ENZYME INHIBITION; HORMONE RECEPTOR INTERACTION; HUMAN; HUMAN CELL; HYPERGLYCEMIA; INSULIN RESISTANCE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; SIGNAL TRANSDUCTION;

ALKALINE PHOSPHATASE; CELL LINE; ENZYME ACTIVATION; HUMANS; INSULIN; ISOENZYMES; KIDNEY; PHOSPHOPROTEINS; PHOSPHORYLATION; PROTEIN KINASE C; PROTEIN KINASE C-ALPHA; PROTEIN KINASE C-DELTA; PROTEIN-TYROSINE KINASES; RECEPTOR, INSULIN; RECOMBINANT PROTEINS; TETRADECANOYLPHORBOL ACETATE; TRANSFECTION;

EID: 0031809427     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001250050995     Document Type: Article

References (10)

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