Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm

Development

Volumn 129, Issue 7, 2002, Pages 1795-1806

  Dunwoodie, Sally L ^a   Clements, Melanie ^a   Sparrow, Duncan B ^a   Sa, Xin ^a   Conlon, Ronald A ^a   Beddington, Rosa S P ^a  

^a VICTOR CHANG CARDIAC RESEARCH INSTITUTE   (Australia)

Author keywords

Dll3; Mouse; Notch signalling; Pudgy; Somite; Spondylocostal dysplasia

Indexed keywords

GENE PRODUCT; PROTEIN DLL3; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; BONE DYSPLASIA; CONTROLLED STUDY; EMBRYO SEGMENTATION; GENE EXPRESSION; GENE MUTATION; HUMAN; JARCHO LEVIN SYNDROME; MESODERM; MOLECULAR CLOCK; MOUSE; NONHUMAN; NULL ALLELE; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SKELETON MALFORMATION; SOMITE;

ALLELES; ANIMALS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE TARGETING; HUMANS; IN SITU HYBRIDIZATION; MEMBRANE PROTEINS; MICE; MICE, KNOCKOUT; MICE, MUTANT STRAINS; MUTATION; NAPHTHOLS; OSTEOCHONDRODYSPLASIAS; RECEPTORS, NOTCH; SIGNAL TRANSDUCTION; SOMITES; TRIAZINES;

ANIMALIA; MAMMALIA;

EID: 0036332950     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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