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Sawan Hurst

Researcher at Oregon Health & Science University

Publications -  13
Citations -  1277

Sawan Hurst is an academic researcher from Oregon Health & Science University. The author has contributed to research in topics: Hemostasis & Factor XII. The author has an hindex of 9, co-authored 13 publications receiving 1183 citations.

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Three dimensional optical angiography.

TL;DR: The technique effectively separates the moving and static scattering elements within tissue to achieve high resolution images of blood flow, mapped into the 3-D optically sectioned tissue beds, at speeds that allow for perfusion assessment in vivo.
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Prevention of vascular graft occlusion and thrombus-associated thrombin generation by inhibition of factor XI

TL;DR: Data suggest that endogenous FXI contributes to arterial thrombus propagation through a striking amplification of thrombin generation at the throm Bus luminal surface, supporting the concept that FXI blockade may offer therapeutic advantages over other antithrombotic agents in terms of bleeding complications.
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Mapping of cerebro-vascular blood perfusion in mice with skin and skull intact by Optical Micro-AngioGraphy at 1.3 mum wavelength.

TL;DR: It is shown that high quality imaging of cerebrovascular blood perfusion down to capillary level resolution with the intact skin and cranium are obtained in vivo with OMAG, without the interference from the blood perfusions in the overlaying skin.
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Inhibition of factor XI activation attenuates inflammation and coagulopathy while improving the survival of mouse polymicrobial sepsis

TL;DR: Systemic anticoagulation by inhibitingFXI activation or FXIIa procoagulant activity during sepsis may limit the development of disseminated intravascular coagulation without increasing bleeding risks, and suggest that severe polymicrobial abdominal infection induces prothrombotic FXI activation, to the detriment of the host.
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Survival advantage of coagulation factor XI-deficient mice during peritoneal sepsis

TL;DR: It is found thatFXI-deficient mice have reduced coagulopathy and increased survival relative to FXI-expressing wild-type mice during cecal ligation and puncture-induced acute peritonitis/sepsis and that pharmacologic inhibition of FXI activity may alter the course and outcome of some infections.