Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton
about
Merozoite surface protein 1 recognition of host glycophorin A mediates malaria parasite invasion of red blood cellsPerinatal synthetic lethality and hematopoietic defects in compound mafG::mafK mutant micePhysiological roles and regulation of mammalian sulfate transportersErythrocyte scaffolding protein p55/MPP1 functions as an essential regulator of neutrophil polarity.Red Blood Cell Function and Dysfunction: Redox Regulation, Nitric Oxide Metabolism, Anemia.Characterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice.Analysis of the mobilities of band 3 populations associated with ankyrin protein and junctional complexes in intact murine erythrocytes.Comparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in β-adducin null red cells.Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.Oligomeric state of human erythrocyte band 3 measured by fluorescence resonance energy homotransfer.Actin protofilament orientation at the erythrocyte membrane.Flexibility of the cytoplasmic domain of the anion exchange protein, band 3, in human erythrocytesThe SLC4 family of bicarbonate (HCO₃⁻) transporters.Band 3 is a host receptor binding merozoite surface protein 1 during the Plasmodium falciparum invasion of erythrocytes.Effect of radiographic contrast media on the spectrin/band3-network of the membrane skeleton of erythrocytesCharacterization of ENU-induced Mutations in Red Blood Cell Structural Proteins.Band 3 missense mutations and stomatocytosis: insight into the molecular mechanism responsible for monovalent cation leak.Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins.An 11-amino acid beta-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes.Spectrin functions upstream of ankyrin in a spectrin cytoskeleton assembly pathway.SLC4 base (HCO3 -, CO3 2-) transporters: classification, function, structure, genetic diseases, and knockout models.Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A.Gene disruption of dematin causes precipitous loss of erythrocyte membrane stability and severe hemolytic anemiaNovel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutant.Adducin forms a bridge between the erythrocyte membrane and its cytoskeleton and regulates membrane cohesion.Loss of the AE3 Cl(-)/HCO(-) 3 exchanger in mice affects rate-dependent inotropy and stress-related AKT signaling in heart.Mis-trafficking of bicarbonate transporters: implications to human diseases.Bicarbonate transport in health and disease.Enhanced suicidal death of erythrocytes from gene-targeted mice lacking the Cl-/HCO(3)(-) exchanger AE1.The Role of pH Regulation in Cancer Progression.The chromatin-remodeling enzyme BRG1 plays an essential role in primitive erythropoiesis and vascular development.Insights into the structure and function of membrane polypeptides carrying blood group antigens.Reduced DIDS-sensitive chloride conductance in Ae1-/- mouse erythrocytes.The structure and function of band 3 (AE1): recent developments (review).Mapping of an ankyrin-sensitive, phosphatidylethanolamine/phosphatidylcholine mono- and bi-layer binding site in erythroid beta-spectrin.Augmented erythrocyte band-3 phosphorylation in septic miceAnalysis of integral membrane protein contributions to the deformability and stability of the human erythrocyte membrane.Molecular mechanism for the red blood cell senescence clock.Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied.Hereditary stomatocytosis: An underdiagnosed condition.
P2860
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P2860
Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton
description
1996 nî lūn-bûn
@nan
1996 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Targeted disruption of the mur ...... ite a normal membrane skeleton
@ast
Targeted disruption of the mur ...... ite a normal membrane skeleton
@en
Targeted disruption of the mur ...... ite a normal membrane skeleton
@en-gb
Targeted disruption of the mur ...... ite a normal membrane skeleton
@nl
type
label
Targeted disruption of the mur ...... ite a normal membrane skeleton
@ast
Targeted disruption of the mur ...... ite a normal membrane skeleton
@en
Targeted disruption of the mur ...... ite a normal membrane skeleton
@en-gb
Targeted disruption of the mur ...... ite a normal membrane skeleton
@nl
prefLabel
Targeted disruption of the mur ...... ite a normal membrane skeleton
@ast
Targeted disruption of the mur ...... ite a normal membrane skeleton
@en
Targeted disruption of the mur ...... ite a normal membrane skeleton
@en-gb
Targeted disruption of the mur ...... ite a normal membrane skeleton
@nl
P2093
P356
P1433
P1476
Targeted disruption of the mur ...... ite a normal membrane skeleton
@en
P2093
P2888
P304
P356
10.1038/NG1096-227
P407
P577
1996-10-01T00:00:00Z
P5875
P6179
1022794405