G
Geoffrey C. Gurtner
Researcher at Stanford University
Publications - 478
Citations - 32002
Geoffrey C. Gurtner is an academic researcher from Stanford University. The author has contributed to research in topics: Wound healing & Medicine. The author has an hindex of 76, co-authored 423 publications receiving 25985 citations. Previous affiliations of Geoffrey C. Gurtner include Duke University & York University.
Papers
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Journal ArticleDOI
Short Hairpin RNA Silencing of PHD-2 Improves Neovascularization and Functional Outcomes in Diabetic Wounds and Ischemic Limbs.
Kevin J. Paik,Zeshaan N. Maan,Elizabeth R. Zielins,Dominik Duscher,Alexander J. Whittam,Shane D. Morrison,Elizabeth A. Brett,Ryan C. Ransom,Michael S. Hu,Joseph C. Wu,Geoffrey C. Gurtner,Michael T. Longaker,Derrick C. Wan +12 more
TL;DR: In this article, the authors investigated the therapeutic potential of inhibiting HIF-1α degradation through short hairpin RNA silencing of PHD-2 in the setting of diabetic wounds and limb ischemia.
Journal ArticleDOI
Nipple Reconstruction with the Biodesign Nipple Reconstruction Cylinder: A Prospective Clinical Study.
Brendan Collins,Jeremy Z. Williams,Heather Karu,Jason P. Hodde,Victoria A. Martin,Geoffrey C. Gurtner +5 more
TL;DR: The Biodesign NRC offers a safe alternative to nipple reconstruction, resulting in stable projection and a high level of patient satisfaction for 12 months after placement.
Journal ArticleDOI
Using intraoperative laser angiography to safeguard nipple perfusion in nipple-sparing mastectomies.
Monica M. Dua,Danielle M. Bertoni,Dung Nguyen,Shannon Meyer,Geoffrey C. Gurtner,Irene Wapnir +5 more
TL;DR: A classification system of NAC perfusion patterns defined as V1 (from subjacent breast), V2 (surrounding skin), and V3 (combination of V1 + V2) is reviewed, which describes the benefits of a first stage operation to devascularize the NAC as a means of improving blood flow to the Nac in preparation for NSM.
Patent
Profiling of cell populations
TL;DR: In this paper, a single cell analysis method was used to characterize transcriptional programs across hundreds of individual murine long-term hematopoietic stem cells (LT-SCs).
Journal ArticleDOI
Black, White, and Gray: Macrophages in Skin Repair and Disease.
TL;DR: Macrophages may exist as one population where all cells alter their phenotype in response to signals from the microenvironment or as distinct subsets that can control wound outcomes.