Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice

Proceedings of the National Academy of Sciences of the United States of America

Volumn 100, Issue 4, 2003, Pages 1763-1768

  Vermot, Julien ^a   Niederreither, Karen ^a,b   Garnier, Jean Marie ^a   Chambon, Pierre ^a   Dollé, Pascal ^a  

^a INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RETINOIC ACID;

ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; AORTA ARCH ANOMALY; ARTICLE; BRANCHIAL ARCH; CARTILAGE HYPOPLASIA; CHONDRODYSPLASIA; CLINICAL FEATURE; CONGENITAL BLOOD VESSEL MALFORMATION; CONTROLLED STUDY; DIGEORGE SYNDROME; DOWN REGULATION; EMBRYO; EMBRYO DEVELOPMENT; GENE DELETION; GENETIC ANALYSIS; HEART SEPTUM DEFECT; LARYNX CARTILAGE; MOUSE; NEWBORN; NONHUMAN; PARATHYROID DISEASE; PHENOTYPE; PRIORITY JOURNAL; THYMUS APLASIA; TRACHEA DISEASE; VELOCARDIOFACIAL SYNDROME; VITAMIN METABOLISM;

ALDEHYDE OXIDOREDUCTASES; ANIMALS; ANIMALS, NEWBORN; DIGEORGE SYNDROME; EMBRYO; FEMALE; GENE TARGETING; IMMUNOHISTOCHEMISTRY; MALE; MICE; MICE, INBRED C57BL; PHENOTYPE; RETINAL DEHYDROGENASE; TRETINOIN;

ANIMALIA; MAMMALIA;

EID: 0037452691     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0437920100     Document Type: Article

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