RH blood group system and molecular basis of Rh-deficiency
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Functional reconstitution into liposomes of purified human RhCG ammonia channelCD47: A Cell Surface Glycoprotein Which Regulates Multiple Functions of Hematopoietic Cells in Health and DiseaseHuman Rhesus B and Rhesus C glycoproteins: properties of facilitated ammonium transport in recombinant kidney cellsPhosphorylation and ankyrin-G binding of the C-terminal domain regulate targeting and function of the ammonium transporter RhBGThe ammonium transporter RhBG: requirement of a tyrosine-based signal and ankyrin-G for basolateral targeting and membrane anchorage in polarized kidney epithelial cellsEvolutionary conservation and diversification of Rh family genes and proteinsMice expressing RHAG and RHD human blood group genesHuman RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cellsCD47 is expressed at normal levels in patients with autoimmune haemolytic anaemia and/or immune thrombocytopenia.Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4.2 (-) cells (mutations Chartres 1 and 2).Resolving the biological role of the Rhesus (Rh) proteins of red blood cells with the aid of a green algaLack of the Rhesus protein Rh1 impairs growth of the green alga Chlamydomonas reinhardtii at high CO2.Spontaneous mutations in the ammonium transport gene AMT4 of Chlamydomonas reinhardtiiDisorders of red cell membrane.Molecular mechanisms of renal ammonia transport.Expression of the non-erythroid Rh glycoproteins in mammalian tissues.The sorting of blood group active proteins during enucleationSevere Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts.Human Rhesus-associated glycoprotein mediates facilitated transport of NH(3) into red blood cells.Refined views of multi-protein complexes in the erythrocyte membrane.Characteristics of mammalian Rh glycoproteins (SLC42 transporters) and their role in acid-base transport.Advances in understanding the pathogenesis of the red cell volume disorders.Blood type biochemistry and human disease.Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.Functional analysis of human RhCG: comparison with E. coli ammonium transporter reveals similarities in the pore and differences in the vestibule.Integrin receptor specificity for human red cell ICAM-4 ligand. Critical residues for alphaIIbeta3 binding.Critical band 3 multiprotein complex interactions establish early during human erythropoiesis.Role of CD47 and Signal Regulatory Protein Alpha (SIRPα) in Regulating the Clearance of Viable or Aged Blood Cells.Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.Eosin-5-maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis.Study of the D-- phenotype reveals erythrocyte membrane alterations in the absence of RHCE.Association between alloantibody specificity and autoantibodies to red blood cells.Modelling the human rhesus proteins: implications for structure and function.Enhancement of red blood cell transfusion compatibility using CRISPR-mediated erythroblast gene editing.A novel nucleotide deletion in RHAG allele identified in a Chinese Rhnull individual.A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene.The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.
P2860
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P2860
RH blood group system and molecular basis of Rh-deficiency
description
1999 nî lūn-bûn
@nan
1999 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի դեկտեմբերին 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
RH blood group system and molecular basis of Rh-deficiency
@ast
RH blood group system and molecular basis of Rh-deficiency
@en
RH blood group system and molecular basis of Rh-deficiency
@nl
type
label
RH blood group system and molecular basis of Rh-deficiency
@ast
RH blood group system and molecular basis of Rh-deficiency
@en
RH blood group system and molecular basis of Rh-deficiency
@nl
prefLabel
RH blood group system and molecular basis of Rh-deficiency
@ast
RH blood group system and molecular basis of Rh-deficiency
@en
RH blood group system and molecular basis of Rh-deficiency
@nl
P356
P1476
RH blood group system and molecular basis of Rh-deficiency
@en
P2093
J P Cartron
P304
P356
10.1053/BEHA.1999.0047
P407
P577
1999-12-01T00:00:00Z