Role of the stress-activated/c-Jun NH2-terminal protein kinase pathway in the cellular response to adriamycin and other chemotherapeutic drugs

Journal of Biological Chemistry

Volumn 271, Issue 48, 1996, Pages 30950-30955

  Osborn, Maudie T ^a   Chambers, Timothy C ^a  

^a UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIINFECTIVE AGENT; DOXORUBICIN; ETOPOSIDE; MITOGEN ACTIVATED PROTEIN KINASE; VINBLASTINE;

ARTICLE; CANCER CHEMOTHERAPY; CARCINOMA CELL; CONTROLLED STUDY; DOSE TIME EFFECT RELATION; DRUG RESISTANCE; DRUG RESPONSE; ENZYME ACTIVATION; HEAT SHOCK; HUMAN; HUMAN CELL; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION;

ANTIBIOTICS, ANTINEOPLASTIC; CA(2+)-CALMODULIN DEPENDENT PROTEIN KINASE; DOXORUBICIN; DRUG RESISTANCE, MULTIPLE; ENZYME ACTIVATION; ENZYME INHIBITORS; ETOPOSIDE; GENE EXPRESSION; HUMANS; JNK MITOGEN-ACTIVATED PROTEIN KINASES; MITOGEN-ACTIVATED PROTEIN KINASES; P-GLYCOPROTEIN; PHOSPHORYLATION; PROTO-ONCOGENE PROTEINS C-JUN; RNA, MESSENGER; TUMOR CELLS, CULTURED; VINBLASTINE;

EID: 0029851730     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.271.48.30950     Document Type: Article

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