Cargando…
Extracellular Vesicles in Sickle Cell Disease: A Promising Tool
Sickle cell disease (SCD) is the most common hemoglobinopathy worldwide. It is characterized by an impairment of shear stress-mediated vasodilation, a pro-coagulant, and a pro-adhesive state orchestrated among others by the depletion of the vasodilator nitric oxide, by the increased phosphatidylseri...
Autores principales: | Lamarre, Yann, Nader, Elie, Connes, Philippe, Romana, Marc, Garnier, Yohann |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495982/ https://www.ncbi.nlm.nih.gov/pubmed/36134985 http://dx.doi.org/10.3390/bioengineering9090439 |
Ejemplares similares
-
Extracellular Vesicles in Sickle Cell Disease: Plasma Concentration, Blood Cell Types Origin Distribution and Biological Properties
por: Nader, Elie, et al.
Publicado: (2021) -
The Red Blood Cell—Inflammation Vicious Circle in Sickle Cell Disease
por: Nader, Elie, et al.
Publicado: (2020) -
Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study
por: Renoux, Céline, et al.
Publicado: (2016) -
Lipid profiles in French West Indies sickle cell disease cohorts, and their general population
por: Lalanne-Mistrih, Marie-Laure, et al.
Publicado: (2018) -
Differences of microparticle patterns between sickle cell anemia and hemoglobin SC patients
por: Garnier, Yohann, et al.
Publicado: (2017)