Cargando…
Hereditary Xerocytosis: Differential Behavior of PIEZO1 Mutations in the N-Terminal Extracellular Domain Between Red Blood Cells and HEK Cells
Hereditary Xerocytosis, a rare hemolytic anemia, is due to gain of function mutations in PIEZO1, a non-selective cation channel activated by mechanical stress. How these PIEZO1 mutations impair channel function and alter red blood cell (RBC) physiology, is not completely understood. Here, we report...
Autores principales: | Yamaguchi, Yohei, Allegrini, Benoit, Rapetti-Mauss, Raphaël, Picard, Véronique, Garçon, Loïc, Kohl, Peter, Soriani, Olivier, Peyronnet, Rémi, Guizouarn, Hélène |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8562563/ https://www.ncbi.nlm.nih.gov/pubmed/34737711 http://dx.doi.org/10.3389/fphys.2021.736585 |
Ejemplares similares
-
Red blood cell proteomics reveal remnant protein biosynthesis and folding pathways in PIEZO1-related hereditary xerocytosis
por: Caulier, Alexis, et al.
Publicado: (2022) -
PIEZO1 activation delays erythroid differentiation of normal and hereditary xerocytosis-derived human progenitor cells
por: Caulier, Alexis, et al.
Publicado: (2020) -
Rapid Gardos Hereditary Xerocytosis Diagnosis in 8 Families Using Reticulocyte Indices
por: Picard, Véronique, et al.
Publicado: (2021) -
Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients
por: Picard, Véronique, et al.
Publicado: (2019) -
Interplay Between Ion Channels and the Wnt/β-Catenin Signaling Pathway in Cancers
por: Rapetti-Mauss, Raphael, et al.
Publicado: (2020)