Altered Erythrocyte Membrane Protein Phosphorylation in an Unusual Case of Hereditary Spherocytosis

Author:

Boivin Pierre,Delaunay Jean,Galand Colette

Publisher

Wiley

Subject

Hematology

Reference14 articles.

1. Isoelectric focusing of spectrin components in hereditary spherocytosis;Boivin;Clin Chim Acta,1976

2. Erythrocyte membrane phosphorylation in hereditary ***spherocytosis;Boivin;Biomed Express,1977

3. Properties of a nonspecific nucleotidase in the membrane of rabbit red cells;Delaunay;Biochim Biophys Acta,1978

4. Properties of a membrane-bound phosphatase activity in normal and abnormal red blood cells;Delaunay;Clin Chim Acta,1979

5. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes;Dodge;Arch Biochem Biophys,1963

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1. Evidence for Imbalanced Furosemide-Sensitive Na+, K+ Cotransport in Hereditary Stomatocytosis;Scandinavian Journal of Haematology;2009-04-24

2. Diagnose und Differentialdiagnose hämolytischer Anämien;Diagnostische Hämatologie;1992

3. Genetic Variants Affecting the Structure and Function of the Human Red Cell Membrane;Clinical Disorders of Membrane Transport Processes;1987

4. Hereditary Spherocytosis and Related Disorders;Clinics in Haematology;1985-02

5. Inherited Disorders of the Red Cell Membrane Skeleton;Pediatric Clinics of North America;1980-05

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