Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes
about
Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissuesAnkyrin-B targets beta2-spectrin to an intracellular compartment in neonatal cardiomyocytescDNA sequence for human erythrocyte ankyrinIsolation and characterization of cDNA clones for human erythrocyte beta-spectrinSmall, membrane-bound, alternatively spliced forms of ankyrin 1 associated with the sarcoplasmic reticulum of mammalian skeletal muscleStructurally Similar but Functionally Diverse ZU5 Domains in Human Erythrocyte AnkyrinAnkyrin 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 anemiaComparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in β-adducin null red cells.Changing patterns in cytoskeletal mRNA expression and protein synthesis during murine erythropoiesis in vivoChromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells.AnkB, a periplasmic ankyrin-like protein in Pseudomonas aeruginosa, is required for optimal catalase B (KatB) activity and resistance to hydrogen peroxide.Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi.Absence of a red blood cell phenotype in mice with hematopoietic deficiency of SEC23B.Genes encoding alpha and beta subunits of Na,K-ATPase are located on three different chromosomes in the mouseStructure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing.Cardiac ankyrins in health and diseaseAbnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.Clinicopathologic features of young and old sphha/sphha mice. Mutants with congenital hemolytic anemiaThe murine mutation jaundiced is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of beta-spectrin.Ankyrin and beta-spectrin accumulate independently of alpha-spectrin in Drosophila.A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.Tissue-specific expression of distinct spectrin and ankyrin transcripts in erythroid and nonerythroid cellsControl of erythroid differentiation: asynchronous expression of the anion transporter and the peripheral components of the membrane skeleton in AEV- and S13-transformed cells.Synthesis and assembly of membrane skeletal proteins in mammalian red cell precursors.Drosophilia spectrin. I. Characterization of the purified proteinHeterogeneity in lymphocyte spectrin distribution: ultrastructural identification of a new spectrin-rich cytoplasmic structureUnequal synthesis and differential degradation of alpha and beta spectrin during murine erythroid differentiationRemarkable homology among the internal repeats of erythroid and nonerythroid spectrin.Distinct ankyrin isoforms at neuron cell bodies and nodes of Ranvier resolved using erythrocyte ankyrin-deficient miceVascular dysfunction in a murine model of severe hemolysis.Diffusion of target cell membrane proteins allows recognition of cryptic binding sites by Mycoplasma pulmonis hemagglutinin.Novel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutant.The alpha-spectrin gene is on chromosome 1 in mouse and man.Membrane Injury and Repair in the Muscular Dystrophies.Trypsin-sensitive, bovine serum albumin-dependent hemolysis activity in Mycoplasma pulmonis.β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations.Of mice and men: the mice were right.Brain spectrin (fodrin) interacts with phospholipids as revealed by intrinsic fluorescence quenching and monolayer experiments.
P2860
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P2860
Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes
description
1984 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1984 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1984
@ast
im Juli 1984 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1984/07/01)
@sk
vědecký článek publikovaný v roce 1984
@cs
wetenschappelijk artikel (gepubliceerd op 1984/07/01)
@nl
наукова стаття, опублікована в липні 1984
@uk
مقالة علمية (نشرت في يوليو 1984)
@ar
name
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@ast
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@en
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@nl
type
label
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@ast
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@en
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@nl
prefLabel
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@ast
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@en
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@nl
P2093
P921
P1433
P1476
Spectrin deficient inherited h ...... mRNA activity in reticulocytes
@en
P2093
C. S. Birkenmeier
D. M. Bodine
J. E. Barker
P304
P356
10.1016/0092-8674(84)90408-2
P407
P577
1984-07-01T00:00:00Z