G
Giuseppe Pintucci
Researcher at New York University
Publications - 33
Citations - 4057
Giuseppe Pintucci is an academic researcher from New York University. The author has contributed to research in topics: Vascular endothelial growth factor A & Angiogenesis. The author has an hindex of 25, co-authored 33 publications receiving 3871 citations.
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Journal ArticleDOI
Biological roles of fibroblast growth factor-2.
TL;DR: Roles of FGF-2 in Development and Differentiation in Various Organ Systems and Mechanisms of Action: Extra- and Intracellular Signaling.
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Fibroblast Growth Factor-2 (FGF-2) Induces Vascular Endothelial Growth Factor (VEGF) Expression in the Endothelial Cells of Forming Capillaries: An Autocrine Mechanism Contributing to Angiogenesis
Graziano Seghezzi,Sundeep Patel,Christine J. Ren,Anna Gualandris,Giuseppe Pintucci,Edith S. Robbins,Richard L. Shapiro,Aubrey C. Galloway,Daniel B. Rifkin,Paolo Mignatti +9 more
TL;DR: Angiogenesis in vivo can be modulated by a novel mechanism that involves the autocrine action of vascular endothelial cell-derived FGF-2 and VEGF and is demonstrated to be an important autocrine mediator of F GF-2-induced angiogenesis.
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TRANSFORMING GROWTH FACTOR-BETA 1 (TGF-β1) INDUCES ANGIOGENESIS THROUGH VASCULAR ENDOTHELIAL GROWTH FACTOR (VEGF)-MEDIATED APOPTOSIS
TL;DR: It is reported that VEGF‐mediated apoptosis is required for TGF‐β1 induction of angiogenesis, and this novel, unexpected role of V EGF and VEGFR2 indicates VEGf‐ mediated apoptosis as a potential target to controlAngiogenesis.
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Novel p27kip1 C-terminal scatter domain mediates rac-dependent cell migration independent of cell cycle arrest functions
Sandra S. McAllister,Michelle Becker-Hapak,Michelle Becker-Hapak,Giuseppe Pintucci,Michele Pagano,Steven F. Dowdy,Steven F. Dowdy +6 more
TL;DR: A novel role for p27 in cell motility that is independent of its function in cell cycle inhibition is defined and predicted in p27-deficient cells.
Journal ArticleDOI
Differential modulation of cell phenotype by different molecular weight forms of basic fibroblast growth factor: possible intracellular signaling by the high molecular weight forms.
TL;DR: Results indicate that increased cell migration and FGF receptor down-regulation are mediated by the extracellular interaction of 18-kD bFGF with its cell surface receptor.