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Volumn 22, Issue 7-8, 2003, Pages 625-629
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Oncogenic and Activated Wild-Type ras-p21 Proteins Induce Different Isoforms of Protein Kinase C in Mitogenic Signal Transduction
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Author keywords
Insulin; Isoforms; Oocyte maturation; Peptide inhibitors; Protein kinase C (PKC); Ras p21 protein
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Indexed keywords
GLUTAMINYLGLUTAMYLVALYLISOLEUCYLARGINYLASPARAGINE;
GLUTAMYLALANYLVALYLSERYLLEUCYLLYSYLPROLYLTHREONINE;
ISOENZYME;
LYSYLLEUCYLPHENYLALANYLISOLEUCYLMETHIONYLASPARAGINE;
PROTEIN KINASE C;
PROTEIN KINASE C BETA;
PROTEIN KINASE C BETA 1;
PROTEIN KINASE C BETA 2;
PROTEIN KINASE C EPSILON;
PROTEIN KINASE C INHIBITOR;
PROTEIN P21;
RAS PROTEIN;
UNCLASSIFIED DRUG;
ANIMAL CELL;
ANIMAL TISSUE;
ARTICLE;
CARCINOGENICITY;
CONTROLLED STUDY;
DRUG MECHANISM;
ENZYME ANALYSIS;
ENZYME INDUCTION;
ENZYME INHIBITION;
IN VITRO STUDY;
IN VIVO STUDY;
MITOGENICITY;
NONHUMAN;
OOCYTE MATURATION;
PROTEIN ANALYSIS;
PROTEIN FUNCTION;
PROTEIN TRANSPORT;
SIGNAL TRANSDUCTION;
WILD TYPE;
ANIMALS;
CELLS, CULTURED;
DOSE-RESPONSE RELATIONSHIP, DRUG;
INSULIN;
ISOENZYMES;
MITOSIS;
ONCOGENE PROTEIN P21(RAS);
OOCYTES;
PEPTIDES;
PROTEIN KINASE C;
RAS PROTEINS;
SIGNAL TRANSDUCTION;
TRANSFECTION;
XENOPUS LAEVIS;
ANIMALIA;
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EID: 0347992860
PISSN: 02778033
EISSN: None
Source Type: Journal
DOI: 10.1023/B:JOPC.0000008727.46554.9e Document Type: Article |
Times cited : (2)
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References (12)
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