Mice lacking Zfhx1b, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of hirschsprung disease-mental retardation syndrome

American Journal of Human Genetics

Volumn 72, Issue 2, 2003, Pages 465-470

  De Putte, Tom Van ^a   Maruhashi, Mitsuji ^b   Francis, Annick ^a   Nelles, Luc ^a   Kondoh, Hisato ^b   Huylebroeck, Danny ^a   Higashi, Yujiro ^b  

^a DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^b OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; SMAD INTERACTING PROTEIN 1; SMAD PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; EMBRYO; GENE; GENE FUNCTION; GENE MUTATION; GENETIC CODE; HIRSCHSPRUNG DISEASE; HIRSCHSPRUNG DISEASE MENTAL RETARDATION SYNDROME; INTESTINE INNERVATION; KNOCKOUT MOUSE; MENTAL RETARDATION MALFORMATION SYNDROME; MOLECULAR MECHANICS; NEURAL CREST CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; STEM CELL; VERTEBRATE;

ANIMALIA; VERTEBRATA;

EID: 0037322308     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/346092     Document Type: Article

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