subject area of
- A molecular defect in two families with hemolytic poikilocytic anemia: reduction of high affinity membrane binding sites for ankyrin. Journal Articles
- Alterations in erythrocyte membrane material properties: a marker of the membrane abnormality in human and chicken muscular dystrophy. Journal Articles
- Alterations of Membrane Phosphorylation in Erythrocyte Membranes from Patients with Duchenne Muscular Dystrophy Journal Articles
- Alterations of erythrocyte ghost protein phosphorylation in the duchenne and myotonic muscular dystrophies Journal Articles
- Identification of Dp71 Isoforms in the Platelet Membrane Cytoskeleton Journal Articles
- Myotonic muscular dystrophy Journal Articles
- Partial Ankyrin and Spectrin Deficiency in Severe, Atypical Hereditary Spherocytosis Journal Articles
- Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome Journal Articles
- Phosphorylation of casein by human erythrocyte membrane-bound protein kinase: competition of casein with endogenous substrates Journal Articles
- Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis Journal Articles
- The bending rigidity of the red blood cell cytoplasmic membrane Journal Articles
- The effect of membrane cholesterol depletion upon erythrocyte membrane-bound enzymes Journal Articles