Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis.

Ähnliche Einträge

• A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis.
  von: Hassoun, H, et al.
  Veröffentlicht: (1994)
• Ankyrin and beta-spectrin accumulate independently of alpha-spectrin in Drosophila.
  von: Dubreuil, R R, et al.
  Veröffentlicht: (1994)
• Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.
  von: Becker, P S, et al.
  Veröffentlicht: (1987)
• Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.
  von: Becker, P S, et al.
  Veröffentlicht: (1993)
• Defective spectrin dimer-dimer association with hereditary elliptocytosis.
  von: Liu, S C, et al.
  Veröffentlicht: (1982)