Functional attenuation of Ufd1l, a 22q11.2 deletion syndrome candidate gene, leads to cardiac outflow septation defects in chicken embryos

Pediatric Research

Volumn 53, Issue 4, 2003, Pages 546-553

  Yamagishi, Chihiro ^a   Hierck, Beerend P ^b   Gittenberger De Groot, Adriana C ^b   Yamagishi, Hiroyuki ^a   Srivastava, Deepak ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; PROTEIN;

ANIMAL TISSUE; ARTICLE; CELL MIGRATION; CHICK EMBRYO; CHICKEN; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; EMBRYO; GENE EXPRESSION; GENE FUNCTION; HEAD; INCIDENCE; MESENCHYME; NEURAL CREST CELL; NEURAL TUBE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RETROVIRUS; SEPTATION DEFECT; STRUCTURE ANALYSIS;

AMINO ACID SEQUENCE; ANIMALS; CHICK EMBRYO; CHICKENS; CHROMOSOME DELETION; DNA, COMPLEMENTARY; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENETIC VECTORS; HEART SEPTAL DEFECTS; MOLECULAR SEQUENCE DATA; NEURAL CREST; PROTEINS; RETROVIRIDAE;

EID: 0037383523     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/01.PDR.0000055765.11310.E3     Document Type: Article

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