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

Volumn 98, Issue 13, 2001, Pages 7182-7187

Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome

(6) Ibrahimi, Omar A a Eliseenkova, Anna V a Plotnikov, Alexander N a Yu, Kai b Ornitz, David M b Mohammadi, Moosa a

a NEW YORK UNIVERSITY SCHOOL OF MEDICINE (United States)

b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR; GROWTH FACTOR RECEPTOR;

ACROCEPHALOSYNDACTYLY; AMINO ACID SUBSTITUTION; ARTICLE; AUTOCRINE EFFECT; BINDING AFFINITY; CRANIOFACIAL SYNOSTOSIS; CRYSTAL STRUCTURE; GENE ACTIVATION; GENE MUTATION; PARACRINE SIGNALING; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SYNDACTYLY;

ACROCEPHALOSYNDACTYLIA; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; BINDING SITES; CRYSTALLOGRAPHY, X-RAY; FIBROBLAST GROWTH FACTORS; HUMANS; HYDROGEN BONDING; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; POINT MUTATION; PROTEIN CONFORMATION; PROTEIN STRUCTURE, SECONDARY; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR; RECOMBINANT PROTEINS; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0035912715 PISSN: 00278424 EISSN: None Source Type: Journal
DOI: 10.1073/pnas.121183798 Document Type: Article

Times cited : (166)

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