Constitutive receptor activation by Crouzon syndrome mutations in fibrobast growth factor receptor (FGFR) 2 and FGFR2/Neu chimeras

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

Volumn 93, Issue 15, 1996, Pages 7894-7899

  Galvin, Brendan D ^a   Hart, Kristen C ^b   Meyer, April N ^a   Webster, Melanie K ^a   Donoghue, Daniel J ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR 2; FIBROBLAST GROWTH FACTOR RECEPTOR; PROTEIN TYROSINE KINASE;

ACHONDROPLASIA; ACROCEPHALOSYNDACTYLY; AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CELL STRAIN 3T3; CHIMERA; CONTROLLED STUDY; CROUZON SYNDROME; DISULFIDE BOND; GENE DELETION; MOUSE; NONHUMAN; ONCOGENE NEU; POINT MUTATION; PRIORITY JOURNAL; REPORTER GENE; SIGNAL TRANSDUCTION; THANATOPHORIC DWARFISM;

3T3 CELLS; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CLONING, MOLECULAR; CRANIOSYNOSTOSES; GENES, ERBB-2; HUMANS; MICE; MOLECULAR SEQUENCE DATA; POINT MUTATION; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, ERBB-2; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR; RECOMBINANT FUSION PROTEINS; SEQUENCE DELETION; SYNDROME; TRANSFECTION;

ANIMALIA;

EID: 0029816813     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.93.15.7894     Document Type: Article

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