Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins.
about
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple hePoint mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-associationFour different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosisAnkyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrinRapid capping in alpha-spectrin-deficient MEL cells from mice afflicted with hereditary hemolytic anemiaThe lamprey (Lampetra fluviatilis) erythrocyte; morphology, ultrastructure, major plasma membrane proteins and phospholipids, and cytoskeletal organization.Red blood cell-mimicking synthetic biomaterial particles.Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.The membrane skeleton of erythrocytes. A percolation model.Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe).Membrane protein dynamics and functional implications in mammalian cells.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.Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins.Vascular dysfunction in a murine model of severe hemolysis.Current problems in haematology. 2: Hereditary spherocytosis.Evaluation of red cell membrane cytoskeletal disorders using a flow cytometric method in South iran.A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings.Amphiphile-induced vesiculation in aged hereditary spherocytosis erythrocytes indicates normal membrane stability properties under non-starving conditions.Reduction of membrane band 7 and activation of volume stimulated (K+, Cl-)-cotransport in a case of congenital stomatocytosis.
P2860
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P2860
Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh
1987年學術文章
@zh-hant
name
Hereditary elliptocytosis, sph ...... of membrane skeletal proteins.
@en
Hereditary elliptocytosis, sph ...... of membrane skeletal proteins.
@nl
type
label
Hereditary elliptocytosis, sph ...... of membrane skeletal proteins.
@en
Hereditary elliptocytosis, sph ...... of membrane skeletal proteins.
@nl
prefLabel
Hereditary elliptocytosis, sph ...... of membrane skeletal proteins.
@en
Hereditary elliptocytosis, sph ...... of membrane skeletal proteins.
@nl
P1433
P1476
Hereditary elliptocytosis, sph ...... of membrane skeletal proteins.
@en
P2093
P304
P356
10.1016/0268-960X(87)90031-2
P577
1987-09-01T00:00:00Z