A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
about
sameAs
Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stabilityA 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-associationAbnormalities of the erythrocyte membraneThe ring-infected erythrocyte surface antigen (RESA) of Plasmodium falciparum stabilizes spectrin tetramers and suppresses further invasionA comprehensive model of the spectrin divalent tetramer binding region deduced using homology modeling and chemical cross-linking of a mini-spectrin.Disorders of red cell membrane.Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.Erythrocyte disorders in the perinatal periodAnalysis of factors regulating erythrocyte deformability.Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-association.Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis.Tryptic digestion of spectrin in variants of hereditary elliptocytosis.Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosisA molecular defect in two families with hemolytic poikilocytic anemia: reduction of high affinity membrane binding sites for ankyrinEffect of heat on the circular dichroism of spectrin in hereditary pyropoikilocytosisPseudopyropoikilocytosis: a striking artefact.Pseudopyropoikilocytosis leading to spurious results.Red cell membrane disorders.Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred.Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis.Conformational stabilities of the structural repeats of erythroid spectrin and their functional implications.
P2860
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P2860
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
description
1975 nî lūn-bûn
@nan
1975 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1975 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1975年の論文
@ja
1975年論文
@yue
1975年論文
@zh-hant
1975年論文
@zh-hk
1975年論文
@zh-mo
1975年論文
@zh-tw
1975年论文
@wuu
name
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@ast
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@en
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@nl
type
label
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@ast
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@en
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@nl
prefLabel
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@ast
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@en
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@nl
P2093
P1476
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane
@en
P2093
C B Speaker
H S Zarkowsky
N Mohandas
S B Shohet
P2860
P304
P356
10.1111/J.1365-2141.1975.TB02740.X
P407
P577
1975-04-01T00:00:00Z