CREPT/RPRD1B, a recently identified novel protein highly expressed in tumors, enhances the β-catenin·TCF4 transcriptional activity in response to Wnt signaling

Journal of Biological Chemistry

Volumn 289, Issue 33, 2014, Pages 22589-22599

  Zhang, Yanquan ^a,b   Liu, Chunxiao ^a,b   Duan, Xiaolin ^c   Ren, Fangli ^a,b   Li, Shan ^a   Jin, Zhe ^a,b   Wang, Yinyin ^a,b   Feng, Yarui ^a,b   Liu, Zewen ^a   Chang, Zhijie ^a,b  

^a Tsinghua University   (China)

^b SICHUAN UNIVERSITY   (China)

^c Second People Hospital of Zhuhai   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROLIFERATION; GENES; NUCLEIC ACIDS; PROTEINS; TUMORS;

CATENIN SIGNALING; DOMAIN-CONTAINING PROTEINS; GENE TRANSCRIPTIONS; NOVEL PROTEINS; OVER-EXPRESSION; RNA POLYMERASE II; SIGNALING PATHWAYS; TRANSCRIPTIONAL ACTIVITY;

TRANSCRIPTION;

BETA CATENIN; CELL CYCLE RELATED AND EXPRESSION ELEVATED PROTEIN IN TUMOR PROTEIN; CELL PROTEIN; TCF4 PROTEIN; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; WNT PROTEIN; BASIC HELIX LOOP HELIX LEUCINE ZIPPER TRANSCRIPTION FACTOR; CELL CYCLE PROTEIN; CREPT PROTEIN, HUMAN; CREPT PROTEIN, MOUSE; MULTIPROTEIN COMPLEX; TCF4 PROTEIN, HUMAN; TCF4 PROTEIN, MOUSE; TUMOR PROTEIN;

ARTICLE; BINDING AFFINITY; BINDING SITE; CARCINOGENESIS; CELL INVASION; CELL PROLIFERATION; COMPLEX FORMATION; CONTROLLED STUDY; EMBRYO; GENE ACTIVATION; GENE TARGETING; HUMAN; HUMAN CELL; MOLECULAR DYNAMICS; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; UPREGULATION; 3T3 CELL LINE; ANIMAL; GENETIC TRANSCRIPTION; GENETICS; HEK293 CELL LINE; HELA CELL LINE; METABOLISM; MOUSE; PHYSIOLOGY; WNT SIGNALING PATHWAY;

ANIMALS; BASIC HELIX-LOOP-HELIX LEUCINE ZIPPER TRANSCRIPTION FACTORS; BETA CATENIN; CELL CYCLE PROTEINS; CELL PROLIFERATION; HEK293 CELLS; HELA CELLS; HUMANS; MICE; MULTIPROTEIN COMPLEXES; NEOPLASM PROTEINS; NIH 3T3 CELLS; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC; UP-REGULATION; WNT SIGNALING PATHWAY;

EID: 84905979953     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M114.560979     Document Type: Article

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