Partial Ankyrin and Spectrin Deficiency in Severe, Atypical Hereditary Spherocytosis

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1970 • 253,849 citations

Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

1971 • 8,619 citations

The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes

1963 • 4,433 citations

[17] Isolation of microgram quantities of proteins from polyacrylamide gels for amino acid sequence analysis

1983 • 1,115 citations

Visualization of the hexagonal lattice in the erythrocyte membrane skeleton.

1987 • 405 citations

Visualization of the protein associations in the erythrocyte membrane skeleton.

1985 • 398 citations

Association between ankyrin and the cytoplasmic domain of band 3 isolated from the human erythrocyte membrane.

1980 • 377 citations

Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin

1979 • 355 citations

Glycophorin is linked by band 4.1 protein to the human erythrocyte membrane skeleton

1984 • 283 citations

Selective association of spectrin with the cytoplasmic surface of human erythrocyte plasma membranes. Quantitative determination with purified (32P)spectrin.

1977 • 278 citations

Interactions between protein 4.1 and band 3. An alternative binding site for an element of the membrane skeleton.

1985 • 274 citations

The molecular organization of the red cell membrane skeleton.

1983 • 206 citations

Partial deficiency of erythrocyte spectrin in hereditary spherocytosis

1985 • 200 citations

Human erythrocyte ankyrin. Purification and properties.

1980 • 198 citations

Spectrin deficient inherited hemolytic anemias in the mouse: Characterization by spectrin synthesis and mRNA activity in reticulocytes

1984 • 176 citations

The Molecular Basis for Membrane – Cytoskeleton Association in Human Erythrocytes

1982 • 157 citations

Inheritance Pattern and Clinical Response to Splenectomy as a Reflection of Erythrocyte Spectrin Deficiency in Hereditary Spherocytosis

1986 • 153 citations

Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis.

1981 • 148 citations

A Genetic Defect in the Binding of Protein 4.1 to Spectrin in a Kindred with Hereditary Spherocytosis

1982 • 125 citations

Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis

1982 • 94 citations

Acute leukemias associated with the 4;11 chromosome translocation have rearranged immunoglobulin heavy chain genes

1985 • 74 citations

Hereditary Spherocytosis and Related Disorders

1985 • 74 citations

Ultrastructure of unit fragments of the skeleton of the human erythrocyte membrane.

1984 • 64 citations

A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.

1984 • 59 citations

Binding of spectrin alpha 2-beta 2 tetramers to human erythrocyte membranes.

1980 • 49 citations

Partial spectrin deficiency in hereditary pyropoikilocytosis

1986 • 47 citations

Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.

1984 • 36 citations