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Suppression of c-Cbl Tyrosine Phosphorylation Inhibits Neointimal Formation in Balloon-Injured Rat Arteries
Author(s) -
Zhihui Tang,
Ying Wang,
Yanbo Fan,
Yi Zhu,
Shu Chien,
Nanping Wang
Publication year - 2008
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.107.761932
Subject(s) - phosphorylation , platelet derived growth factor receptor , tyrosine phosphorylation , protein kinase b , vascular smooth muscle , pi3k/akt/mtor pathway , platelet derived growth factor , microbiology and biotechnology , tyrosine , growth factor , medicine , signal transduction , cancer research , endocrinology , biology , biochemistry , receptor , smooth muscle
c-Cbl, a ubiquitously expressed protooncogene, is tyrosine phosphorylated in response to a variety of stimuli, including growth factors such as platelet-derived growth factor (PDGF), and consequently activates signaling proteins such as phosphatidylinositol-3 kinase (PI3K) and Akt. In the present study, we examined the role of c-Cbl tyrosine phosphorylation in vascular injury.

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