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Volumn 4, Issue JULY2015, 2015, Pages

NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets

(18)  Bouveret, Romaric a,b   Waardenberg, Ashley J a,c   Schonrock, Nicole a,b   Ramialison, Mirana a,b,d   Doan, Tram a   de jong, Danielle a   Bondue, Antoine e,f   Kaur, Gurpreet d   Mohamed, Stephanie a   Fonoudi, Hananeh a,b,g   Chen, Chiann Mun h   Wouters, Merridee A i,j   Bhattacharya, Shoumo h   Plachta, Nicolas d   Dunwoodie, Sally L a,b   Chapman, Gavin a,b   Blanpain, Cédric e   Harvey, Richard P a,b  


Author keywords

[No Author keywords available]

Indexed keywords

DNA; DNA ADENINE METHYLTRANSFERASE; ETS PROTEIN; HEAT SHOCK PROTEIN; HEAT SHOCK PROTEIN 68; HOX PROTEIN; NUCLEAR FACTOR I; PONASTERONE A; SERUM RESPONSE FACTOR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR ELK 1; TRANSCRIPTION FACTOR ELK 4; TRANSCRIPTION FACTOR GATA 4; TRANSCRIPTION FACTOR NKX2.5; TRANSCRIPTION FACTOR TBX5; UNCLASSIFIED DRUG; HOMEOBOX PROTEIN NKX-2.5; HOMEODOMAIN PROTEIN; MUTANT PROTEIN; NKX2-5 PROTEIN, MOUSE; PROTEIN BINDING;

EID: 84940567692     PISSN: None     EISSN: 2050084X     Source Type: Journal    
DOI: 10.7554/eLife.06942     Document Type: Article
Times cited : (64)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.