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Alecia Cutler

Researcher at Cleveland Clinic

Publications -  15
Citations -  363

Alecia Cutler is an academic researcher from Cleveland Clinic. The author has contributed to research in topics: Diabetic retinopathy & Neovascularization. The author has an hindex of 8, co-authored 15 publications receiving 305 citations. Previous affiliations of Alecia Cutler include Cleveland Clinic Lerner College of Medicine.

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Cross-talk between vascular endothelial growth factor and matrix metalloproteinases in the induction of neovascularization in vivo.

TL;DR: The results suggest that MMPs act both upstream and downstream of V EGF and imply that potential combination therapies of VEGF and MMP inhibitors may be a useful therapeutic approach in diseases of pathological neovascularization.
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Impaired function of circulating CD34(+) CD45(-) cells in patients with proliferative diabetic retinopathy.

TL;DR: The results from these pilot studies suggest that ECFCs from patients with PDR are mobilized into the circulation but may be unable to migrate and repair damaged capillary endothelium, suggesting that EC FCs may be a potential therapeutic target in the prevention and treatment of diabetic vascular complications.
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Inhibition of EGF Signaling Protects the Diabetic Retina from Insulin-Induced Vascular Leakage

TL;DR: In this study with diabetic mice, insulin treatment resulted in increased vascular leakage apparently mediated by betacellulin and signaling via the epidermal growth factor (EGF) receptor, and treatment with EGF receptor inhibitors reduced retinal vascular leakage in diabetic mice on insulin.
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Increased Neovascularization in Mice Lacking Tissue Inhibitor of Metalloproteinases-3

TL;DR: The results of these studies determine an accentuation of pathologic VEGF-mediated angiogenesis in the cornea and laser-induced CNV in mice lacking TIMP-3, implying that TIMp-3 may regulate the development of the choroidal vasculature and is a likely contributor to increased susceptibility to choroid neovascularization.
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Tissue Inhibitor of Metalloproteinases-3 Peptides Inhibit Angiogenesis and Choroidal Neovascularization in Mice

TL;DR: Tissue inhibitor of metalloproteinases-3 peptides are identified to be efficient inhibitors of angiogenesis and have a potential to be used therapeutically in diseases with increased neovascularization.