Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities.
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Protein 4.1 R-135 interacts with a novel centrosomal protein (CPAP) which is associated with the gamma-tubulin complexSpectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissuesA nonerythroid isoform of protein 4.1R interacts with components of the contractile apparatus in skeletal myofibersZFP36L2 is required for self-renewal of early burst-forming unit erythroid progenitorsMild spherocytosis and altered red cell ion transport in protein 4. 2-null miceHematopoietic protein-1 regulates the actin membrane skeleton and membrane stability in murine erythrocytesCortical dynein and asymmetric membrane elongation coordinately position the spindle in anaphaseCharacterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice.Protein 4.1R regulates cell adhesion, spreading, migration and motility of mouse keratinocytes by modulating surface expression of beta1 integrin.Mitotic regulation of protein 4.1R involves phosphorylation by cdc2 kinaseNeuroacanthocytosis associated with a defect of the 4.1R membrane proteinCirculating primitive erythroblasts establish a functional, protein 4.1R-dependent cytoskeletal network prior to enucleating.Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleationProperties of the C-terminal domain of 4.1 proteins.Loss of the putative tumor suppressor band 4.1B/Dal1 gene is dispensable for normal development and does not predispose to cancerStructural protein 4.1R is integrally involved in nuclear envelope protein localization, centrosome-nucleus association and transcriptional signaling.The cytoskeletal adaptor protein band 4.1B is required for the maintenance of paranodal axoglial septate junctions in myelinated axons.Formation of mammalian erythrocytes: chromatin condensation and enucleation.Characterization of cytoskeletal protein 4.1R interaction with NHE1 (Na(+)/H(+) exchanger isoform 1).ICln: a new regulator of non-erythroid 4.1R localisation and functionProtein 4.1R links E-cadherin/beta-catenin complex to the cytoskeleton through its direct interaction with beta-catenin and modulates adherens junction integrity.Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis.Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell TraitsThe 4.1B cytoskeletal protein regulates the domain organization and sheath thickness of myelinated axons.Quantitative analysis of murine terminal erythroid differentiation in vivo: novel method to study normal and disordered erythropoiesis.Deletion of the intestinal plasma membrane calcium pump, isoform 1, Atp2b1, in mice is associated with decreased bone mineral density and impaired responsiveness to 1, 25-dihydroxyvitamin D3.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).Strain-specific variations in cation content and transport in mouse erythrocytes.Gene disruption of dematin causes precipitous loss of erythrocyte membrane stability and severe hemolytic anemiaCytoskeletal protein 4.1R negatively regulates T-cell activation by inhibiting the phosphorylation of LATAtomic force microscopy demonstration of cytoskeleton instability in mouse erythrocytes with dematin-headpiece and β-adducin deficiency.Proper cytoskeletal architecture beneath the plasma membrane of red blood cells requires Ttll4.Protein 4.1R Influences Myogenin Protein Stability and Skeletal Muscle Differentiation.Genome-wide identification of TAL1's functional targets: insights into its mechanisms of action in primary erythroid cells.Cardiac cytoskeleton and arrhythmia: an unexpected role for protein 4.1R in cardiac excitability.Protein 4.1R, a microtubule-associated protein involved in microtubule aster assembly in mammalian mitotic extract.Innate B-1 B Cells Are Not Enriched in Red Blood Cell Autoimmune Mice: Importance of B Cell Receptor Transgenic Selection.Microfluidic assay of the deformability of primitive erythroblasts.In-depth analysis of cysteine oxidation by the RBC proteome: advantage of peroxiredoxin II knockout mice.
P2860
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P2860
Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities.
description
1999 nî lūn-bûn
@nan
1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Protein 4.1R-deficient mice ar ...... mbrane skeleton abnormalities.
@ast
Protein 4.1R-deficient mice ar ...... mbrane skeleton abnormalities.
@en
type
label
Protein 4.1R-deficient mice ar ...... mbrane skeleton abnormalities.
@ast
Protein 4.1R-deficient mice ar ...... mbrane skeleton abnormalities.
@en
prefLabel
Protein 4.1R-deficient mice ar ...... mbrane skeleton abnormalities.
@ast
Protein 4.1R-deficient mice ar ...... mbrane skeleton abnormalities.
@en
P2093
P2860
P356
P1476
Protein 4.1R-deficient mice ar ...... mbrane skeleton abnormalities.
@en
P2093
J A Chasis
J G Conboy
L L Peters
L Walensky
P2860
P304
P356
10.1172/JCI3858
P407
P577
1999-02-01T00:00:00Z