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Volumn 20, Issue 13, 2001, Pages 3459-3472
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Pin1 is overexpressed in breast cancer and cooperates with Ras signaling in increasing the transcriptional activity of c-Jun towards cyclin D1
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Author keywords
c Jun; Cancer; Cyclin D1; Pin1; Ras signaling
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Indexed keywords
ACTIN;
CYCLIN D1;
ESTROGEN RECEPTOR;
ISOMERASE;
MESSENGER RNA;
PEPTIDYLPROLYL ISOMERASE PIN1;
PROLINE;
PROLYL ISOMERASE;
RAS PROTEIN;
SERINE;
THREONINE;
UNCLASSIFIED DRUG;
ADULT;
AGED;
ARTICLE;
BREAST CANCER;
BREAST CARCINOGENESIS;
CONTROLLED STUDY;
GENE OVEREXPRESSION;
GENETIC TRANSCRIPTION;
HUMAN;
HUMAN CELL;
HUMAN TISSUE;
ONCOGENE C JUN;
ONCOGENE H RAS;
ONCOGENE NEU;
PRIORITY JOURNAL;
PROMOTER REGION;
PROTEIN CONFORMATION;
PROTEIN PHOSPHORYLATION;
TUMOR GROWTH;
ADULT;
AGED;
AGED, 80 AND OVER;
BREAST;
BREAST NEOPLASMS;
CARCINOMA IN SITU;
CELLS, CULTURED;
CYCLIN D1;
FEMALE;
GENE EXPRESSION REGULATION;
GENE EXPRESSION REGULATION, NEOPLASTIC;
HUMANS;
JNK MITOGEN-ACTIVATED PROTEIN KINASES;
MIDDLE AGED;
MITOGEN-ACTIVATED PROTEIN KINASES;
PEPTIDYLPROLYL ISOMERASE;
PHOSPHORYLATION;
PROMOTER REGIONS (GENETICS);
PROTO-ONCOGENE PROTEINS C-JUN;
RAS PROTEINS;
RECEPTOR, ERBB-2;
RECEPTORS, ESTROGEN;
SIGNAL TRANSDUCTION;
TRANSCRIPTION, GENETIC;
TUMOR CELLS, CULTURED;
TUMOR MARKERS, BIOLOGICAL;
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EID: 0035796405
PISSN: 02614189
EISSN: None
Source Type: Journal
DOI: 10.1093/emboj/20.13.3459 Document Type: Article |
Times cited : (506)
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References (59)
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