Reduction of membrane band 7 and activation of volume stimulated (K+, Cl−)-cotransport in a case of congenital stomatocytosis
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1989.tb06288.x/fullpdf
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1. The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]
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3. Comparison of instruments for measurement of erythrocyte deformability
4. Congenital Stomatocytosis and Chronic Haemolytic Anaemia
5. Partial Ankyrin and Spectrin Deficiency in Severe, Atypical Hereditary Spherocytosis
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1. The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells;Frontiers in Physiology;2018-04-16
2. Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells;American Journal of Physiology-Cell Physiology;2012-01-15
3. The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein;Blood;2009-02-05
4. Regulation of K-Cl Cotransport: from Function to Genes;Journal of Membrane Biology;2004-11
5. Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction;British Journal of Haematology;2004-04-27
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