Nkx2-5 pathways and congenital heart disease: Loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block

Cell

Volumn 117, Issue 3, 2004, Pages 373-386

  Pashmforoush, Mohammad ^a   Lu, Jonathan T ^a   Chen, Hanying ^f   St Amand, Tara ^a   Kondo, Richard ^a   Pradervand, Sylvain ^a   Evans, Sylvia M ^a   Clark, Bob ^b   Feramisco, James R ^a   Giles, Wayne ^a   Ho, Siew Yen ^c   Benson, D Woodrow ^d   Silberbach, Michael ^e   Shou, Weinian ^f   Chien, Kenneth R ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALGARY   (Canada)

^c ROYAL BROMPTON HOSPITAL   (United Kingdom)

^d UNIVERSITY OF CINCINNATI   (United States)

^e OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^f INDIANA UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN 10; PROTEIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CARDIOMYOPATHY; CELL LINEAGE; COMPLETE HEART BLOCK; CONGENITAL HEART DISEASE; CONTROLLED STUDY; DISEASE COURSE; GENE; GENE MUTATION; HEART ATRIOVENTRICULAR NODE; HEART ATRIUM CONDUCTION; HEART VENTRICLE; KNOCKOUT GENE; MOUSE; MUSCLE CELL; NKX2 5 GENE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ANIMALIA;

EID: 11144357335     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(04)00405-2     Document Type: Article

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