Loss of LIN9, a member of the DREAM complex, cooperates with SV40 large T antigen to induce genomic instability and anchorage-independent growth

Oncogene

Volumn 31, Issue 14, 2012, Pages 1859-1868

  Hauser, S ^a   Ulrich, T ^a   Wurster, S ^a   Schmitt, K ^a   Reichert, N ^a,b   Gaubatz, S ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH   (Switzerland)

Author keywords

DREAM complex; genomic instability; mitosis; senescence

Indexed keywords

LIN54 PROTEIN; LIN9 PROTEIN; PRB PROTEIN; PROTEIN; PROTEIN P53; UNCLASSIFIED DRUG; VIRUS LARGE T ANTIGEN;

ANIMAL CELL; ARTICLE; CANCER INHIBITION; CARCINOGENESIS; CELL AGING; FIBROBLAST; GENE CONTROL; GENE EXPRESSION; GENOMIC INSTABILITY; HUMAN; HUMAN CELL; IN VITRO STUDY; MITOSIS; MOUSE; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; ANTIGENS, POLYOMAVIRUS TRANSFORMING; CELL AGING; CELL LINE; CELL PROLIFERATION; CYCLIN-DEPENDENT KINASE INHIBITOR P16; CYCLIN-DEPENDENT KINASE INHIBITOR P21; FIBROBLASTS; GENE EXPRESSION REGULATION, NEOPLASTIC; GENOMIC INSTABILITY; HUMANS; MICE; MITOSIS; NUCLEAR PROTEINS; RETINOBLASTOMA PROTEIN; TUMOR SUPPRESSOR PROTEINS;

EID: 84860422537     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/onc.2011.364     Document Type: Article

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