Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color

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

Volumn 93, Issue 2, 1996, Pages 867-872

  Gariepy, Cheryl E ^a   Cass, Daniel T ^b   Yanagisawa, Masashi ^a  

^a UNIVERSITY OF TEXAS AT DALLAS   (United States)

^b CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

Author keywords

enteric neurons; Hirschsprung disease; melanocytes; neural crest; Shah Waardenburg syndrome

Indexed keywords

ENDOTHELIN B RECEPTOR;

ANIMAL MODEL; ARTICLE; CELL MATURATION; GENE DELETION; GENE LOCATION; GROWTH REGULATION; HIRSCHSPRUNG DISEASE; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN CONFORMATION; RAT; RECEPTOR BINDING; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CLONING, MOLECULAR; COLON; DNA, COMPLEMENTARY; ENDOTHELINS; GANGLIA; GENES, LETHAL; HAIR; HETEROZYGOTE; HOMOZYGOTE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RADIOLIGAND ASSAY; RATS; RATS, MUTANT STRAINS; RECEPTOR, ENDOTHELIN B; RECEPTORS, ENDOTHELIN; RNA SPLICING; RNA, MESSENGER; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION;

EID: 0030033185     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.93.2.867     Document Type: Article

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