A murine model of Holt-Oram syndrome defines roles of the T-Box transcription factor Tbx5 in cardiogenesis and disease

Cell

Volumn 106, Issue 6, 2001, Pages 709-721

  Bruneau, Benoit G ^a   Nemer, Georges ^b   Schmitt, Joachim P ^a   Charron, Frédéric ^b   Robitaille, Lynda ^b   Caron, Sophie ^b   Conner, David A ^a   Gessler, Manfred ^c   Nemer, Mona ^b   Seidman, Christine E ^a,d   Seidman, J G ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

^b CLIN RESEARCH INSTITUTE OF MONTREAL   (Canada)

^c UNIVERSITY OF WÜRZBURG   (Germany)

^d BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATRIAL NATRIURETIC FACTOR; CONNEXIN 40; HOMEODOMAIN PROTEIN; T BOX TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR NKX2.5; TRANSCRIPTION FACTOR TBX5; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; GENE DELETION; GENE EXPRESSION; GENE MUTATION; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HEART DISEASE; HEART MUSCLE CONDUCTION SYSTEM; HETEROZYGOTE; HOLT ORAM SYNDROME; HOMOZYGOTE; HYPOPLASIA; LIMB MALFORMATION; MOUSE; NONHUMAN; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN PROTEIN INTERACTION; TRANSACTIVATION;

EID: 17944378083     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(01)00493-7     Document Type: Article

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