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Valery Combes

Researcher at University of Technology, Sydney

Publications -  85
Citations -  6217

Valery Combes is an academic researcher from University of Technology, Sydney. The author has contributed to research in topics: Cerebral Malaria & Endothelium. The author has an hindex of 40, co-authored 84 publications receiving 5665 citations. Previous affiliations of Valery Combes include University of Sydney & Centre national de la recherche scientifique.

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In vitro generation of endothelial microparticles and possible prothrombotic activity in patients with lupus anticoagulant

TL;DR: Examination of morphological, immunological, and functional characteristics of MPs derived from human umbilical vein endothelial cells stimulated by TNF provides evidence that endothelial-derived MPs are detectable in normal human blood and are increased in patients with a coagulation abnormality characterized by the presence of lupus anticoagulant.
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Type 1 and type 2 diabetic patients display different patterns of cellular microparticles.

TL;DR: Results showed that a wide vesiculation process, resulting from activation or apoptosis of several cell types, occurs in diabetes, however, diabetic patients differ by the procoagulant activity and the cellular origin of microparticles.
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A unified hypothesis for the genesis of cerebral malaria: sequestration, inflammation and hemostasis leading to microcirculatory dysfunction

TL;DR: The events resulting in the development of cerebral malaria complications are multi-factorial, encompassing a dynamic interaction between three processes, thereby explaining the complexity of this deadly syndrome.
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Membrane microparticles mediate transfer of P-glycoprotein to drug sensitive cancer cells.

TL;DR: It is established that MPs shed in vitro from drug-resistant cancer cells incorporate cell surface P- gp from their donor cells, effectively bind to drug-sensitive recipient cells and transfer functional P-gp to the latter.
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Endothelial microparticles: a potential contribution to the thrombotic complications of the antiphospholipid syndrome.

TL;DR: Ex vivo and in vitro observations indicate that generation of EMP in APS and SLE patients results from an autoimmune process involving aPL, which may represent a new pathogenic mechanism for the thrombotic complications of this disease.