Alternatively spliced FGFR-1 isoforms differentially modulate endothelial cell activation of c-YES

Archives of Biochemistry and Biophysics

Volumn 450, Issue 1, 2006, Pages 50-62

  Zhang, Pei ^a   Greendorfer, Jessica S ^a   Jiao, Jing ^a   Kelpke, Stacey C ^a   Thompson, John A ^a  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

Angiogenesis; c YES; Endothelial cells; FGFR 1 isoforms; Signal transduction

Indexed keywords

CORTACTIN; FIBROBLAST GROWTH FACTOR 1; FIBROBLAST GROWTH FACTOR RECEPTOR 1; ISOPROTEIN; MATRIGEL; PROTEIN SH2; PROTEIN SH3; TYROSINE;

ANIMAL TISSUE; ARTICLE; CELL DENSITY; CELL GROWTH; CELL PROLIFERATION; CONTROLLED STUDY; DNA TRANSFECTION; ENDOTHELIUM CELL; IMMUNOPRECIPITATION; IN VITRO STUDY; NONHUMAN; PRIORITY JOURNAL; RAT; SRC HOMOLOGY DOMAIN;

ALTERNATIVE SPLICING; ANIMALS; BRAIN; CELL PROLIFERATION; CELLS, CULTURED; ENDOTHELIAL CELLS; FIBROBLAST GROWTH FACTOR 1; HUMANS; NEOVASCULARIZATION, PHYSIOLOGIC; PROTEIN ISOFORMS; PROTO-ONCOGENE PROTEINS C-YES; RATS; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 1; SIGNAL TRANSDUCTION; SRC HOMOLOGY DOMAINS; TRANSFECTION;

ANIMALIA;

EID: 33646861363     PISSN: 00039861     EISSN: 10960384     Source Type: Journal    
DOI: 10.1016/j.abb.2006.03.017     Document Type: Article

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