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September 1, 1982BloodOpen Access

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

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Authors

SGSteven R. GoodmanUniversity of Tennessee Health Science CenterKSKA ShifferGenesys (United States)LCLA CasoriaPennsylvania State University

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Cite This Study

Goodman et al. (1982) studied this question.

synapsesocial.com/papers/6a6f5fe1ac440176ef280eadhttps://doi.org/10.1182/blood.v60.3.772.772
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Erythrocyte membrane skeletal protein bands 4.1 a and b are sequence-related phosphoproteins.1982 · 76 citations
  2. 2Binding of spectrin alpha 2-beta 2 tetramers to human erythrocyte membranes.1980 · 49 citations
  3. 3Reassociation of ankyrin with band 3 in erythrocyte membranes and in lipid vesicles.1980 · 198 citations
  4. 4Purification of two spectrin-binding proteins: biochemical and electron microscopic evidence for site-specific reassociation between spectrin and bands 2.1 and 4.1.1979 · 284 citations
  5. 5The role of membrane lipids in the survival of red cells in hereditary spherocytosis1969 · 101 citations