Disease: Overhydrated hereditary stomatocytosis
- <em>PIEZO1</em> Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells
- A case of hereditary over-hydrated stomatocytosis with stomatospherocytes and spherocytes in the blood
- A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis
- Acquired stomatocytosis in alcoholic liver disease
- Advances in understanding the pathogenesis of red cell membrane disorders
- Alterations of red blood cell metabolome in overhydrated hereditary stomatocytosis
- ATP-dependent vesiculation in red cell membranes from different hereditary stomatocytosis variants
- Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context
- Cocaine induces a reversible stomatocytosis of red blood cells and increases blood viscosity
- Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis
- Genetic diseases of erythrocyte membrane permeability
- Hereditary dehydrated and overhydrated stomatocytosis: recent advances
- Hereditary red cell membrane disorders and laboratory diagnostic testing
- Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied
- Hereditary stomatocytosis and cation-leaky red cells--recent developments
- Hereditary stomatocytosis: an unusual cause of severe neonatal jaundice
- Hereditary stomatocytosis: association of low 2,3-diphosphoglycerate with increased cation pumping by the red cell
- Hereditary stomatocytosis: phenotypical expression of sodium transport and band 7 peptides in 44 cases
- Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells
- Inherited hemolytic anemia: a possessive beginner's guide
- Mechanosensitive Pannexin 1 Activity Is Modulated by Stomatin in Human Red Blood Cells
- Membrane raft actin deficiency and altered Ca2+-induced vesiculation in stomatin-deficient overhydrated hereditary stomatocytosis
- Mice deficient in the putative phospholipid flippase ATP11C exhibit altered erythrocyte shape, anemia, and reduced erythrocyte life span
- Mild erythrocytosis as a presenting manifestation of <em>PIEZO1</em> associated erythrocyte volume disorders
- Model organisms: new insights into ion channel and transporter function. Stomatin homologues interact in Caenorhabditis elegans
- Molecular basis of red cell membrane disorders
- Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants
- Overhydrated stomatocytosis associated with a complex <em>RHAG</em> genotype including a novel <em>de novo</em> mutation
- Previously misdiagnosed red cell membrane disorder and familial consequences
- Primary red cell hydration disorders: Pathogenesis and diagnosis
- Purification of band 7.2b, a 31-kDa integral phosphoprotein absent in hereditary stomatocytosis
- Red blood cell membrane defects
- Red cell membrane disorders
- Reticulocyte Maturation and Variant Red Blood Cells
- Rh-null phenotype and stomatocytosis
- Sitosterolemia's stomatocytosis and macrothrombocytopenia
- SNPs altering ammonium transport activity of human Rhesus factors characterized by a yeast-based functional assay
- Stomatin is mis-trafficked in the erythrocytes of overhydrated hereditary stomatocytosis, and is absent from normal primitive yolk sac-derived erythrocytes
- Stomatocytosis of Standard Schnauzers is not associated with stomatin deficiency
- The "stomatin" gene and protein in overhydrated hereditary stomatocytosis
- The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations
- The membrane defect in hereditary stomatocytosis
- The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells
- The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein
- The structure of a conserved piezo channel domain reveals a topologically distinct β sandwich fold
- Transient presence of stomatocytes: A clue to the diagnosis of overhydrated hereditary stomatocytosis in a child with beta-thalassemia