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David R. Knighton

Researcher at University of California, Berkeley

Publications -  14
Citations -  2589

David R. Knighton is an academic researcher from University of California, Berkeley. The author has contributed to research in topics: Wound healing & Angiogenesis. The author has an hindex of 11, co-authored 14 publications receiving 2531 citations. Previous affiliations of David R. Knighton include University of California, San Francisco.

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Oxygen tension regulates the expression of angiogenesis factor by macrophages

TL;DR: The control of angiogenesis in wound healing may be the result of macrophages responding to tissue oxygen tension without the necessity of interacting with other cell types or biochemical signals.
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Classification and treatment of chronic nonhealing wounds. Successful treatment with autologous platelet-derived wound healing factors (PDWHF).

TL;DR: This is the first clinical demonstration that locally acting growth factors promote healing of chronic cutaneous ulcers by showing a direct correlation to 100% healing with initial wound size and the initiation of PDWHF therapy.
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Preoperative optimization of cardiovascular hemodynamics improves outcome in peripheral vascular surgery. A prospective, randomized clinical trial.

TL;DR: In this group of patients, preoperative cardiac assessment and optimization is associated with improved outcome, and patients with a PA catheter had significantly fewer adverse intraoperative events than the control group.
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Oxygen as an antibiotic. The effect of inspired oxygen on infection.

TL;DR: Modelling the effect of breathing 12, 21, and 45% oxygen on the size and number of lesions produced by intradermal injections of Escherichia coli revealed that suppression of infection by moderate hyperoxia is comparable with that reported by Burke after timely, adequate doses of type-specific antibiotics.
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Role of platelets and fibrin in the healing sequence: an in vivo study of angiogenesis and collagen synthesis.

TL;DR: The capacity of platelets and fibrin to initiate angiogenesis, fibroplasia, collagen synthesis and monocyte migration in the rabbit cornea assay is investigated and a mononuclear infiltrate with neovascularization and fiboplasia is shown.