(Q28307642)

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J C Menninger

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K M John

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P Harris

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O Shalev

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R R Chilcote

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S L Marchesi

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P C Watkins

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V Bennett

Partial deficiency of erythrocyte spectrin in hereditary spherocytosis

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language of work or name

English

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publication date

21 June 1990

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published in

Nature

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volume

345

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issue

6277

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page(s)

736-9

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cites work

1 reference

7 January 2021

Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Further evidence for location of the spherocytosis gene on chromosome 8

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7 January 2021

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

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7 January 2021

Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency

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7 January 2021

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

1 reference

7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

cDNA sequence for human erythrocyte ankyrin

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Chromosome maps of man and mouse, III.

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7 January 2021

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

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7 January 2021

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

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7 January 2021

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

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7 January 2021

Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis

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7 January 2021

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

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7 January 2021

Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

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7 January 2021