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Gilbert R. Upchurch

Researcher at University of Florida

Publications -  525
Citations -  19791

Gilbert R. Upchurch is an academic researcher from University of Florida. The author has contributed to research in topics: Aortic aneurysm & Medicine. The author has an hindex of 68, co-authored 460 publications receiving 17175 citations. Previous affiliations of Gilbert R. Upchurch include Wayne State University & Brigham and Women's Hospital.

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Journal ArticleDOI

Phosphorylation of AKT and Abdominal Aortic Aneurysm Formation

TL;DR: The data suggest that AKT phosphorylation is important in the upstream regulation of MMP activity, and that differential phosphorylated levels may be important in sex differences in AAA.
Journal ArticleDOI

Acute limb ischemia associated with type B aortic dissection: clinical relevance and therapy.

TL;DR: ALI secondary to AoD is predictive of death and visceral ischemia, and endovascular therapy confers excellent limb salvage and allows diagnosis of unsuspected visceral isChemia.
Journal ArticleDOI

Acute aortic dissection presenting with primarily abdominal pain: A rare manifestation of a deadly disease

TL;DR: Increased mortality in patients with acute thoracic aortic dissections who present primarily with abdominal pain is documented, underscoring the importance of maintaining a high index of suspicion for an aorta dissection in patients who have appropriate risk factors.
Journal ArticleDOI

Aortic branch artery pseudoaneurysms accompanying aortic dissection. Part I. Pseudoaneurysm anatomy.

TL;DR: Angiographic and necropsy evidence shows that some of these lesions represent branch artery pseudoaneurysms and, as such, are secondary to an intramural hematoma, not the primary cause of it.
Book ChapterDOI

S-Nitrosothiols: Chemistry, Biochemistry, and Biological Actions

TL;DR: The physiological relevance of RSNOs has been confirmed the observation that the predominant form of NO in mammalian plasma is that of an adduct between NO and serum albumin, S -nitrosoalbumin, which possesses EDRF-like properties in vivo, including vasorelaxation and platelet inhibition.