Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome

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

Volumn 97, Issue 26, 2000, Pages 14536-14541

  Yu, Kai ^a   Herr, Andrew B ^a   Waksman, Gabriel ^a   Ornitz, David M ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Craniosynostosis; FGF; FGF receptor; Mutation; Syndactyly

Indexed keywords

FIBROBLAST GROWTH FACTOR 10; FIBROBLAST GROWTH FACTOR 2; FIBROBLAST GROWTH FACTOR 9; FIBROBLAST GROWTH FACTOR RECEPTOR; KERATINOCYTE GROWTH FACTOR;

ACROCEPHALOSYNDACTYLY; ALTERNATIVE RNA SPLICING; ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CENTRAL NERVOUS SYSTEM MALFORMATION; CONTROLLED STUDY; CRANIOFACIAL SYNOSTOSIS; GENE MUTATION; MESENCHYME; MISSENSE MUTATION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RECEPTOR BINDING; SYNDACTYLY;

3T3 CELLS; ACROCEPHALOSYNDACTYLIA; ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; FIBROBLAST GROWTH FACTORS; HUMANS; LIGANDS; MICE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR;

EID: 0034687699     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.97.26.14536     Document Type: Article

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