Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability.

Eitemau Tebyg

• An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.
  gan: Conboy, J G, et al.
  Cyhoeddwyd: (1993)
• Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1.
  gan: Takakuwa, Y, et al.
  Cyhoeddwyd: (1986)
• Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.
  gan: Tomaselli, M B, et al.
  Cyhoeddwyd: (1981)
• Stabilization of erythrocyte membranes by polyamines.
  gan: Ballas, S K, et al.
  Cyhoeddwyd: (1983)
• Modulation of erythrocyte membrane mechanical stability by 2,3-diphosphoglycerate in the neonatal poikilocytosis/elliptocytosis syndrome.
  gan: Mentzer, W C, et al.
  Cyhoeddwyd: (1987)