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 he
about
Probing large conformational rearrangements in wild-type and mutant spectrin using structural mass spectrometryLow expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46.Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi.Genomic anatomy of a premier major histocompatibility complex paralogous region on chromosome 1q21-q22Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosisProbing structures of large protein complexes using zero-length cross-linking.The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation.Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred.Modulation of erythrocyte membrane mechanical function by protein 4.1 phosphorylation.
P2860
Q30571286-9C7E6499-A972-40CE-9E54-7E812D2BB93FQ33899236-D2ED19B9-028F-4F99-9126-5E0ABAB0EE79Q34083706-6DD57BB0-3CB2-4FA8-9C68-5417F722A514Q35033356-63E52486-894A-4A1F-B967-4F6543792788Q35553297-CC28F3C6-C1DE-4638-B88B-13DE0E81FC6FQ35881989-B067D286-AB9E-4EF0-9414-CC186BE12678Q36236942-7F5E361A-DCCB-461E-9F13-F3EB944DF0E5Q37263172-AFAF10C4-4083-49EA-87DF-CDD7454CB059Q37362461-E8E599E4-F803-41D0-8459-9067FD4A6356Q42742478-5C7815F8-55FD-44AA-A2D9-2760E6D7EF4EQ45195797-B3BC8452-2E2E-49CB-B7D5-31F2F060B893
P2860
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 he
description
1992 nî lūn-bûn
@nan
1992 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի մարտին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
A common type of the spectrin ...... al importance of the triple he
@nl
type
label
A common type of the spectrin ...... al importance of the triple he
@nl
prefLabel
A common type of the spectrin ...... al importance of the triple he
@nl
P2093
P2860
P356
P1476
A common type of the spectrin ...... iple helical model of spectrin
@en
P2093
A Baruchel
H S Zarkowsky
M C Lecomte
P G Gallagher
S K Ballas
P2860
P356
10.1172/JCI115669
P407
P577
1992-03-01T00:00:00Z