Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

1971 • 8,619 citations

The Metabolic Basis of Inherited Disease.

1988 • 7,933 citations

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1984 • 4,899 citations

The Metabolic Basis of Inherited Disease

1990 • 4,327 citations

High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones

1990 • 1,357 citations

The isolation and characterization of linked δ- and β-globin genes from a cloned library of human DNA

1978 • 1,055 citations

Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins

1990 • 528 citations

Evolution of the Functional Human β-Actin Gene and Its Multi-Pseudogene Family: Conservation of Noncoding Regions and Chromosomal Dispersion of Pseudogenes

1985 • 378 citations

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

1979 • 355 citations

Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1).

1989 • 308 citations

Evolution of the functional human beta-actin gene and its multi-pseudogene family: conservation of noncoding regions and chromosomal dispersion of pseudogenes.

1985 • 211 citations

Partial deficiency of erythrocyte spectrin in hereditary spherocytosis

1985 • 200 citations

cDNA sequence for human erythrocyte ankyrin.

1990 • 166 citations

Chromosome maps of man and mouse, III

1987 • 162 citations

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

1986 • 153 citations

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

1982 • 125 citations

Associations of human erythrocyte band 4.2. Binding to ankyrin and to the cytoplasmic domain of band 3.

1988 • 109 citations

The role of membrane lipids in the survival of red cells in hereditary spherocytosis

1969 • 100 citations

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

1982 • 94 citations

Molecular Basis of Hereditary Elliptocytosis Due to Protein 4.1 Deficiency

1986 • 83 citations

Structure and organization of the murine band 3 gene.

1987 • 82 citations

The alpha-spectrin gene is on chromosome 1 in mouse and man.

1985 • 81 citations

Partial Ankyrin and Spectrin Deficiency in Severe, Atypical Hereditary Spherocytosis

1988 • 80 citations

Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin.

1990 • 74 citations

Association of red cell spherocytosis with deletion of the short arm of chromosome 8

1987 • 63 citations

Localization of the gene for the erythroid anion exchange protein, band 3 (EMPB3), to human chromosome 17

1987 • 54 citations

Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.

1987 • 47 citations

Molecular cloning of the cDNA for human erythrocyte beta-spectrin

1988 • 47 citations

Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21

1986 • 45 citations

Isolation and characterization of cDNA clones for human erythrocyte beta-spectrin.

1987 • 41 citations

Localization of spherocytosis to chromosome 8 or 12 and report of a family with spherocytosis and a reciprocal translocation.

1975 • 37 citations

Linkage and gene localization of hereditary spherocytosis (HS)

1978 • 35 citations

Further Evidence for Location of the Spherocytosis Gene on Chromosome 8

1983 • 34 citations

Localization of the spherocytosis gene to chromosome segment 8p11.22?8p21.1

1988 • 33 citations

Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p

1987 • 29 citations

Association of red cell spherocytosis with deletion of the short arm of chromosome 8

1987 • 24 citations

Exclusion of glutathione reductase from 8pter→8p22 and localization to 8p21

1978 • 7 citations

Deleted Work

1955 • 0 citations