Associated Papers
Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1.
Allegrini B et al.
Blood Cells, Molecules & Diseases, 2023
An erythrocyte-centric view on the MFSD2B sphingosine-1-phosphate transporter.
Ghaderi S et al.
Pharmacology & Therapeutics, 2023
Borate Transporters and SLC4 Bicarbonate Transporters Share Key Functional Properties.
Beltran JL et al.
Membranes, 2023
Cell physiology and molecular mechanism of anion transport by erythrocyte band 3/AE1.
Jennings ML
American Journal of Physiology. Cell Physiology, 2021
Hereditary stomatocytosis: An underdiagnosed condition.
Andolfo I et al.
American Journal of Hematology, 2018
The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.
Flatt JF et al.
Frontiers in Physiology, 2018
Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context.
Reithmeier RA et al.
Biochimica Et Biophysica Acta, 2016
Crystal structure of the anion exchanger domain of human erythrocyte band 3.
Arakawa T et al.
Science (new York, N.y.), 2015
Rapid Cl⁻/HCO⁻₃exchange kinetics of AE1 in HEK293 cells and hereditary stomatocytosis red blood cells.
Frumence E et al.
American Journal of Physiology. Cell Physiology, 2013
South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.
Guizouarn H et al.
British Journal of Haematology, 2011
Band 3 missense mutations and stomatocytosis: insight into the molecular mechanism responsible for monovalent cation leak.
Barneaud-Rocca D et al.
International Journal of Cell Biology, 2011
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