Full-length sequence of the cDNA for human erythroid beta-spectrin
about
A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesiclesbetaIV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the central and peripheral nervous systemSmoothelin, a novel cytoskeletal protein specific for smooth muscle cellsPrimary structure and domain organization of human alpha and beta adducinSpectrin-based skeleton as an actor in cell signalingPoint mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-associationSpectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutationFour different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosisCaenorhabditis elegans beta-G spectrin is dispensable for establishment of epithelial polarity, but essential for muscular and neuronal functionAnkyrin binds to the 15th repetitive unit of erythroid and nonerythroid beta-spectrinProbing conformational stability and dynamics of erythroid and nonerythroid spectrin: effects of urea and guanidine hydrochlorideNa,K-ATPase transport from endoplasmic reticulum to Golgi requires the Golgi spectrin-ankyrin G119 skeleton in Madin Darby canine kidney cellsKaryoplasmic interaction selection strategy: a general strategy to detect protein-protein interactions in mammalian cellsStructural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site.The complete sequence of Drosophila beta-spectrin reveals supra-motifs comprising eight 106-residue segments.Protein 4.2 binds to the carboxyl-terminal EF-hands of erythroid alpha-spectrin in a calcium- and calmodulin-dependent manner.Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.Flexibility of the alpha-spectrin N-terminus by EPR and fluorescence polarization.ATP-dependent mechanism protects spectrin against glycation in human erythrocytes.Invariant tryptophan at a shielded site promotes folding of the conformational unit of spectrin.Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding.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.The murine mutation jaundiced is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of beta-spectrin.Stabilities of folding of clustered, two-repeat fragments of spectrin reveal a potential hinge in the human erythroid spectrin tetramer.A posttranslational modification of beta-actin contributes to the slow dissociation of the spectrin-protein 4.1-actin complex of irreversibly sickled cells.Neural cell adhesion molecule (NCAM) association with PKCbeta2 via betaI spectrin is implicated in NCAM-mediated neurite outgrowth.Localization of dystrophin relative to acetylcholine receptor domains in electric tissue and adult and cultured skeletal muscle.Dystrophin colocalizes with beta-spectrin in distinct subsarcolemmal domains in mammalian skeletal muscle.Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.Spectrin's chimeric E2/E3 enzymatic activity.Molecular epitopes of the ankyrin-spectrin interaction.Spectrin self-association site: characterization and study of beta-spectrin mutations associated with hereditary elliptocytosis.Intertwined αβ spectrin meeting helical actin protofilament in the erythrocyte membrane skeleton: wrap-around vs. point-attachment.Heterogeneous phosphorylation of erythrocyte spectrin beta chain in intact cells.A hybrid model for erythrocyte membrane: a single unit of protein network coupled with lipid bilayer.Organization and dynamics of tryptophan residues in erythroid spectrin: novel structural features of denatured spectrin revealed by the wavelength-selective fluorescence approachMapping of an ankyrin-sensitive, phosphatidylethanolamine/phosphatidylcholine mono- and bi-layer binding site in erythroid beta-spectrin.
P2860
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P2860
Full-length sequence of the cDNA for human erythroid beta-spectrin
description
1990 nî lūn-bûn
@nan
1990 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Full-length sequence of the cDNA for human erythroid beta-spectrin
@ast
Full-length sequence of the cDNA for human erythroid beta-spectrin
@en
Full-length sequence of the cDNA for human erythroid beta-spectrin
@en-gb
Full-length sequence of the cDNA for human erythroid beta-spectrin
@nl
type
label
Full-length sequence of the cDNA for human erythroid beta-spectrin
@ast
Full-length sequence of the cDNA for human erythroid beta-spectrin
@en
Full-length sequence of the cDNA for human erythroid beta-spectrin
@en-gb
Full-length sequence of the cDNA for human erythroid beta-spectrin
@nl
prefLabel
Full-length sequence of the cDNA for human erythroid beta-spectrin
@ast
Full-length sequence of the cDNA for human erythroid beta-spectrin
@en
Full-length sequence of the cDNA for human erythroid beta-spectrin
@en-gb
Full-length sequence of the cDNA for human erythroid beta-spectrin
@nl
P2093
P1476
Full-length sequence of the cDNA for human erythroid beta-spectrin
@en
P2093
A L Scarpa
B G Forget
J C Winkelmann
V T Marchesi
P304
P407
P577
1990-07-15T00:00:00Z