Compartment-selective sensitivity of cardiovascular morphogenesis to combinations of retinoic acid receptor gene mutations

Circulation Research

Volumn 80, Issue 6, 1997, Pages 757-764

  Lee, Robin Y ^a   Luo, Jiangming ^b   Evans, Ronald M ^c   Giguere, Vincent ^b   Sucov, Henry M ^a,c  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b ROYAL VICTORIA HOSPITAL   (Canada)

^c HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

gene disruption; genetic deficiency; retinoid teratology; retinoid X receptor

Indexed keywords

RETINOIC ACID RECEPTOR; RETINOID X RECEPTOR; RETINOL;

ANIMAL TISSUE; ARTICLE; CARDIOVASCULAR MALFORMATION; EMBRYO; GENE EXPRESSION; GENE MUTATION; HEART DEVELOPMENT; MOUSE; NONHUMAN; PRIORITY JOURNAL; RETINOL DEFICIENCY;

EID: 0030906262     PISSN: 00097330     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.RES.80.6.757     Document Type: Article

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