Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability
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Red cell membrane: past, present, and futureSpectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissuesHomozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 geneAn isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cellsMolecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangementsMolecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeletonMultiple protein 4.1 isoforms produced by alternative splicing in human erythroid cellsHematopoietic protein-1 regulates the actin membrane skeleton and membrane stability in murine erythrocytesA member of the Plasmodium falciparum PHIST family binds to the erythrocyte cytoskeleton component band 4.1Cysteine shotgun-mass spectrometry (CS-MS) reveals dynamic sequence of protein structure changes within mutant and stressed cellsMetabolic remodeling of the human red blood cell membrane.Membrane remodeling during reticulocyte maturationProtein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities.Loss of the putative tumor suppressor band 4.1B/Dal1 gene is dispensable for normal development and does not predispose to cancerMolecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations.Identification of the protein 4.1 binding interface on glycophorin C and p55, a homologue of the Drosophila discs-large tumor suppressor protein.Heterogeneity of mRNA and protein products arising from the protein 4.1 gene in erythroid and nonerythroid tissues.Modulation of erythrocyte membrane material properties by Ca2+ and calmodulin. Implications for their role in regulation of skeletal protein interactions.Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia.Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosisDisorders of red cell membrane.Lack of protein 4.1G causes altered expression and localization of the cell adhesion molecule nectin-like 4 in testis and can cause male infertility.A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.Protein 4.1R links E-cadherin/beta-catenin complex to the cytoskeleton through its direct interaction with beta-catenin and modulates adherens junction integrity.Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane.Tropomyosin modulates erythrocyte membrane stabilityRBFOX2 promotes protein 4.1R exon 16 selection via U1 snRNP recruitment.Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1.Protein 4.1B suppresses prostate cancer progression and metastasis.Partial purification and characterization of an actin-bundling protein, band 4.9, from human erythrocytesThe 4.1-like proteins of the bovine lens: spectrin-binding proteins closely related in structure to red blood cell protein 4.1.Erythrocyte membrane deformability and stability: two distinct membrane properties that are independently regulated by skeletal protein associations.Defective spectrin dimer-dimer association with hereditary elliptocytosisMechanochemistry of protein 4.1's spectrin-actin-binding domain: ternary complex interactions, membrane binding, network integration, structural strengtheningThe human Kell blood group binds the erythroid 4.1R protein: new insights into the 4.1R-dependent red cell membrane complex.Protein 4.1R-dependent multiprotein complex: new insights into the structural organization of the red blood cell membraneImpaired intestinal calcium absorption in protein 4.1R-deficient mice due to altered expression of plasma membrane calcium ATPase 1b (PMCA1b).Spectrin beta-chain variant associated with hereditary elliptocytosis.Missing band 7 membrane protein in two patients with high Na, low K erythrocytes.
P2860
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P2860
Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability
description
1981 nî lūn-bûn
@nan
1981 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1981 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
name
Deficiency of skeletal membran ...... erythrocyte membrane stability
@ast
Deficiency of skeletal membran ...... erythrocyte membrane stability
@en
Deficiency of skeletal membran ...... erythrocyte membrane stability
@en-gb
Deficiency of skeletal membran ...... erythrocyte membrane stability
@nl
type
label
Deficiency of skeletal membran ...... erythrocyte membrane stability
@ast
Deficiency of skeletal membran ...... erythrocyte membrane stability
@en
Deficiency of skeletal membran ...... erythrocyte membrane stability
@en-gb
Deficiency of skeletal membran ...... erythrocyte membrane stability
@nl
prefLabel
Deficiency of skeletal membran ...... erythrocyte membrane stability
@ast
Deficiency of skeletal membran ...... erythrocyte membrane stability
@en
Deficiency of skeletal membran ...... erythrocyte membrane stability
@en-gb
Deficiency of skeletal membran ...... erythrocyte membrane stability
@nl
P2093
P2860
P3181
P356
P1476
Deficiency of skeletal membran ...... erythrocyte membrane stability
@en
P2093
G Tchernia
N Mohandas
S B Shohet
P2860
P304
P3181
P356
10.1172/JCI110275
P407
P577
1981-08-01T00:00:00Z