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Inherited Disorders of the Red Cell Membrane Skeleton

Data up to Jan 2025

Published1980
Citations26
References125

Total Citations Per Year

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

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Inherited Disorders of the Red Cell Membrane Skeleton (1980) – Pediatric Clinics of North America | Metascience Observatory Explorer