Inherited Disorders of the Red Cell Membrane Skeleton
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Abstract
References (125)
THE ORGANIZATION OF PROTEINS IN THE HUMAN RED BLOOD CELL MEMBRANE
1974 • 1,554 citations
Membrane Asymmetry
1977 • 965 citations
Selective solubilization of proteins and phospholipids from red blood cell membranes by nonionic detergents
1973 • 687 citations
The molecular structure of human erythrocyte spectrin
1979 • 539 citations
The membrane attachment protein for spectrin is associated with band 3 in human erythrocyte membranes
1979 • 423 citations
Post splenectomy sepsis
1973 • 393 citations
Hazard of Overwhelming Infection after Splenectomy in Childhood
1967 • 377 citations
Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin
1979 • 355 citations
Spectrin as a stabilizer of the phospholipid asymmetry in the human erythrocyte membrane
1978 • 346 citations
ANIONIC SITES OF HUMAN ERYTHROCYTE MEMBRANES
1973 • 307 citations
Purification of two spectrin-binding proteins: biochemical and electron microscopic evidence for site-specific reassociation between spectrin and bands 2.1 and 4.1.
1979 • 286 citations
In vitro formation of a complex between cytoskeletal proteins of the human erythrocyte
1979 • 254 citations
On the mechanism of ATP-induced shape changes in human erythrocyte membranes. I. The role of the spectrin complex.
1977 • 248 citations
Spectrin-actin membrane skeleton of normal and abnormal red blood cells.
1979 • 244 citations
Irreversible deformation of the spectrin-actin lattice in irreversibly sickled cells.
1976 • 214 citations
Dissecting the red cell membrane skeleton
1979 • 212 citations
Pneumococcal Polysaccharide Immunization in Infants and Children
1978 • 208 citations
Hematology of Infancy and Childhood
1981 • 206 citations
REPAIR OF SKIN DEFECTS
1947 • 195 citations
Selective alteration of erythrocyte deformability by SH-reagents. Evidence for an involvement of spectrin in membrane shear elasticity
1978 • 175 citations
CONGENITAL HEMOLYTIC JAUNDICE. THE PATHOGENESIS OF THE "HEMOLYTIC CRISIS"
1948 • 172 citations
Increased Cell Membrane Permeability in the Pathogenesis of Hereditary Spherocytosis *
1964 • 169 citations
Relation Between Splenectomy and Subsequent Infection: A Clinical Study
1962 • 167 citations
Integral membrane protein interaction with triton cytoskeletons of erythrocytes
1979 • 165 citations
Red-Cell Antibodies in Acquired Hemolytic Anemia with Negative Antiglobulin Serum Tests
1971 • 149 citations
Lateral mobility of human erythrocyte integral membrane proteins
1977 • 145 citations
Intra- and intermolecular cross-linking of membrane proteins in intact erythrocytes and ghosts by SH-oxidizing agents
1977 • 133 citations
A Congenital Haemolytic Anaemia with Thermal Sensitivity of the Erythrocyte Membrane
1975 • 121 citations
Hereditary Spherocytosis
1951 • 115 citations
Spectrin/actin complex isolated from sheep erythrocytes accelerates actin polymerization by simple nucleation. Evidence for oligomeric actin in the erythrocyte cytoskeleton.
1980 • 110 citations
Selective Depression of Blood Group Antigens Associated with Hereditary Ovalocytosis among Melanesians
1977 • 103 citations
Studies on the Destruction of Red Blood Cells
1956 • 102 citations
The role of membrane lipids in the survival of red cells in hereditary spherocytosis
1969 • 100 citations
A Scanning Electron Microscopic Study of the Spleen
1974 • 100 citations
Appearance and distribution of surface proteins of the human erythrocyte membrane. An electron microscope and immunochemical labeling study.
1978 • 97 citations
Control of interaction of spectrin and actin by phosphorylation
1977 • 96 citations
Studies on Spontaneous In Vitro Autohemolysis in Hemolytic Disorders
1956 • 96 citations
Clustering and endocytosis of membrane receptors can be induced in mature erythrocytes of neonatal but not adult humans.
1976 • 95 citations
Genetics of spherocytosis.
1962 • 91 citations
Dependence of spectrin organization in red blood cell membranes on cell metabolism: implications for control of red cell shape, deformability, and surface area.
1979 • 86 citations
Malaria and hereditary ovalocytosis
1977 • 83 citations
Membrane protein phosphorylation of intact normal and hereditary spherocytic erythrocytes.
1978 • 83 citations
Incidence of Gallbladder Disease in Chronic Hemolytic Anemia (Spherocytosis)
1952 • 78 citations
Hereditary Spherocytosis
1951 • 77 citations
Abnormal membrane protein of red blood cells in hereditary spherocytosis
1971 • 74 citations
The selective and conjoint loss of red cell lipids
1969 • 73 citations
Domains of receptor mobility and endocytosis in the membranes of neonatal human erythrocytes in the membranes of neonatal human erythrocytes and reticulocytes are deficient in spectrin
1979 • 67 citations
Diminished spectrin extraction from ATP-depleted human erythrocytes. Evidence relating spectrin to changes in erythrocyte shape and deformability.
1978 • 66 citations
HEREDITARY SPHEROCYTOSIS WITH SECONDARY HÆMOCHROMATOSIS
1968 • 64 citations
Elliptocytosis with hemolytic anemia: the effects of splenectomy.
1955 • 57 citations
Abnormality in a specific protein of the erythrocyte membrane in hereditary spherocytosis
1974 • 57 citations
Reconstitution of spectrin-deficient, spherocytic mouse erythrocyte membranes.
1979 • 56 citations
Extramedullary Hematopoiesis in Anemias
1928 • 55 citations
ALTERATIONS IN OSMOTIC AND MECHANICAL FRAGILITY RELATED TO IN VIVO ERYTHROCYTE AGING AND SPLENIC SEQUESTRATION IN HEREDITARY SPHEROCYTOSIS*†
1960 • 53 citations
ELLIPTIC ERYTHROCYTES IN MAN
1941 • 51 citations
Red cell life span after splenectomy in hereditary spherocytosis
1968 • 50 citations
Phosphorylation in erythrocyte membranes from abnormally shaped cells
1976 • 49 citations
The Life Span of the Elliptocyte
1954 • 46 citations
Massive Thoracic Extramedullary Hemopoiesis
1960 • 46 citations
Participation of spectrin in Sendai virus-induced fusion of human erythrocyte ghosts.
1978 • 46 citations
The hereditary elliptocytoses: clinical and linkage data
1962 • 42 citations
Membrane polypeptide aggregates in glucose 6-phosphate dehydrogenase-deficient and in vitro aged red blood cells.
1978 • 41 citations
Red cell survival studies in hereditary spherocytosis
1970 • 40 citations
Fine Structure of the Red Pulp of the Spleen in Hereditary Spherocytosis
1972 • 40 citations
Congenital Spherocytosis in Infancy
1958 • 39 citations
Heat‐Induced Erythrocyte Fragmentation in Neonatal Elliptocytosis
1979 • 39 citations
Hereditary Spherocytosis: Observations on Hemolytic Mechanisms and Iron Metabolism
1960 • 38 citations
Fatty Acid Composition of Erythrocytes in Hereditary Spherocytosis
1979 • 37 citations
ASCERTAINING GENETIC CARRIERS OF HEREDITARY SPHEROCYTOSIS BY STATISTICAL ANALYSIS OF MULTIPLE LABORATORY TESTS*
1962 • 36 citations
Congenital Hemolytic Anemia in the Newborn
1957 • 36 citations
HEREDITARY ELLIPTOCYTOSIS: AN UNUSUAL PRESENTATION OF HEMOLYSIS IN THE NEWBORN ASSOCIATED WITH TRANSIENT MORPHOLOGIC ABNORMALITIES
1969 • 35 citations
Association of decreased membrane protein phosphorylation with red blood cell spherocytosis
1977 • 34 citations
Red cell calcium leak in congenital hemolytic anemia with extreme microcytosis
1976 • 33 citations
Fragmentation and myelin formation in hereditary xerocytosis and other hemolytic anemias
1978 • 33 citations
A New Familial Disorder with Abnormal Erythrocyte Morphology and Increased Permeability of the Erythrocytes to Sodium and Potassium
1971 • 31 citations
Hereditary spherocytosis in 100 children.
1966 • 31 citations
Autosomal dominant hemolytic anemia characterized by ovalocytosis
1965 • 30 citations
Differences in fatty acid composition between normal human erythrocytes and hereditary spherocytosis affected cells
1972 • 30 citations
Neonatal Manifestations of Hereditary Spherocytosis
1967 • 28 citations
Relative deficiency of Ca2+-dependent adenosine triphosphatase activity of red cell membranes in hereditary spherocytosis
1974 • 28 citations
Spinal cord disease in hereditary spherocytosis: report of two cases with a hypothesized common mechanism for neurologic and red cell abnormalities
1976 • 26 citations
Spectrin rearrangement early in erythrocyte ghost endocytosis.
1979 • 26 citations
Atypical Autohemolysis in Hereditary Spherocytosis as a Reflection of Two Cell Populations: Relationship of Cell Lipids to Conditioning by the Spleen
1968 • 26 citations
Increased Erythrocyte Ca2+ Content in Hereditary Spherocytosis
1975 • 25 citations
CONGENITAL AND FAMILIAL HEMOLYTIC DISEASE IN CHILDREN
1938 • 25 citations
Absence of one component of spectrin adenosine triphosphatase in hereditary spherocytosis
1975 • 25 citations
Involvement of spectrin in membrane fusion: induction of fusion in human erythrocyte ghosts by proteolytic enzymes and its inhibition by antispectrin antibody.
1979 • 24 citations
Erythrocyte Membrane Elasticity, Fragmentation and Lysis
1978 • 23 citations
Muscle G-actin is an inhibitor of ATP-induced erythrocyte ghost shape changes and endocytosis
1977 • 22 citations
Comparison of structure and function of human erythrocyte and human muscle actin.
1979 • 22 citations
Hereditary elliptocytosis with hemolytic anemia
1963 • 22 citations
Monoclonal Gammopathy in Hereditary Spherocytosis: A Possible Pathogenetic Relation
1978 • 20 citations
HEREDITARY SPHEROCYTOSIS: A DISEASE OF THE RED CELL MEMBRANE.
1965 • 20 citations
Hereditary Spherocytosis: The Metabolism of Erythrocytes in the Peripheral Blood and in the Splenic Pulp
1974 • 19 citations
Pyknocytosis in a Neonate: An Unusual Presentation of Hereditary Elliptocytosis
1977 • 18 citations
Hereditary Haemolytic Anaemia associated with Elliptocytosis: a Study of Three Families
1961 • 16 citations
Abnormal binding of spectrin to the membrane of erythrocytes in some cases of hereditary spherocytosis
1978 • 16 citations
Homozygous Hereditary Elliptocytosis as the Cause of Haemolytic Anemia in Infancy
1968 • 16 citations
Serum Haptoglobin in Infancy
1961 • 16 citations
CHRONIC ULCER OF THE LEG ASSOCIATED WITH CONGENITAL HEMOLYTIC JAUNDICE
1939 • 15 citations
Hereditary Spherocytosis
1965 • 15 citations
Hereditary Elliptocytosis in Iceland
1967 • 15 citations
Sporadic Congenital Spherocytosis Associated with Congenital Hypoplastic Thrombocytopenia and Malformations
1958 • 15 citations
Haemolytic Anaemia in Infectious Mononucleosis Due to Inapparent Congenital Spherocytosis
1970 • 14 citations
Haemolysis in Athletes due to Hereditary Spherocytosis
1979 • 14 citations
Effect of adrenal steroids in hereditary spherocytic anemia.
1956 • 14 citations
Studies on Calcium Transport and Calcium‐dependent Adenosine Triphosphatase Activity of Erythrocyte Membranes in Hereditary Spherocytosis
1976 • 13 citations
Hereditary elliptocytosis and hyperhaemolysis. A comparative study of 6 families with 145 patients.
1966 • 13 citations
HEREDITARY ELLIPTOCYTOSIS ASSOCIATED WITH INCREASED HEMOLYSIS
1955 • 12 citations
Hereditary Elliptocytosis and Hyperhaemolysis
1966 • 12 citations
Recurrent Hemolytic Anemia Secondary to Accessory Spleens
1978 • 12 citations
Variations of the Mean Diameter in the Ripening of the Erythrocyte.
1950 • 11 citations
Hereditary elliptocytic anaemia
1961 • 10 citations
The surgical treatment of hereditary spherocytosis.
1974 • 9 citations
Altered Erythrocyte Membrane Protein Phosphorylation in an Unusual Case of Hereditary Spherocytosis
1979 • 9 citations
Hereditary elliptical stomatocytosis: A case report
1976 • 8 citations
The Genetic Basis of Hereditary Elliptocytosis With Hemolysis
1968 • 7 citations
Hereditary Haemolytic Ovalocytosis with Defective Erythropoiesis
1979 • 7 citations
THE ROLE OF SPECTRIN AND ACTIN IN IRREVERSIBLY SICKLED CELLS: UNSICKLING OF “IRREVERSIBLY” SICKLED GHOSTS BY CONDITIONS WHICH INTERFERE WITH SPECTRIN-ACTIN POLYMERIZATION11These studies were supported by research grants HL-15963 and HL-15157 and contract no. HB-4–2973 from the National Institutes of Health. The work was done during the tenure of an Established Investigatorship of the American Heart Association (Dr. Lux).
1978 • 7 citations
An unusual variant of hereditary spherocytosis
1970 • 7 citations
Splenectomy in congenital microspherocytosis
1969 • 7 citations
Atypical Hereditary Spherocytosis: Biochemical Studies and Sites of Erythrocyte Destruction
1967 • 6 citations
Hereditary elliptocytosis with hemolytic anemia--a family study of five affected members.
1969 • 6 citations
Erythrocyte membrane proteins in hereditary glucosephosphate isomerase deficiency.
1979 • 5 citations
Red pulp of the spleen in hereditary elliptocytosis
1977 • 4 citations