Literature DB >> 7641880

Genetic disorders of the red cell membranes.

J Delaunay1.   

Abstract

The red cell membrane is comprised of a lipid bilayer studded with transmembrane proteins, and laminated by a protein network, the membrane skeleton, at the surface of the inner monolayer. The erythrocyte owes its mechanical properties to the membrane skeleton. Hereditary spherocytosis, hereditary elliptocytosis or poikilocytosis, Southeast Asian ovalocytosis are hereditary hemolytic anemias, due to mutations in the genes encoding ankyrin, the anion exchanger, spectrin, protein 4.1 or protein 4.2, which are main proteins of the membrane. Recent advances in the field have led to fundamental questions.

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Year:  1995        PMID: 7641880     DOI: 10.1016/0014-5793(95)00460-q

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  2 in total

Review 1.  The molecular basis of disorders of the red cell membrane.

Authors:  M F McMullin
Journal:  J Clin Pathol       Date:  1999-04       Impact factor: 3.411

2.  Clinical course of 63 children with hereditary spherocytosis: a retrospective study.

Authors:  Maria Christina Lopes Araujo Oliveira; Rachel Aparecida Ferreira Fernandes; Carolina Lins Rodrigues; Daniela Aguiar Ribeiro; Maria Fernanda Giovanardi; Marcos Borato Viana
Journal:  Rev Bras Hematol Hemoter       Date:  2012
  2 in total

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