Chondroitin sulfate A is a cell surface receptor for Plasmodium falciparum-infected erythrocytes
about
Antigenic variation in malaria: in situ switching, relaxed and mutually exclusive transcription of var genes during intra-erythrocytic development in Plasmodium falciparumMolecular aspects of severe malariaThe var genes of Plasmodium falciparum are located in the subtelomeric region of most chromosomesAnalysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolatesAntibodies from malaria-exposed pregnant women recognize trypsin resistant epitopes on the surface of Plasmodium falciparum-infected erythrocytes selected for adhesion to chondroitin sulphate ALiver accumulation of Plasmodium chabaudi-infected red blood cells and modulation of regulatory T cell and dendritic cell responsesRelease of sequestered malaria parasites upon injection of a glycosaminoglycanDifferential induction of functional IgG using the Plasmodium falciparum placental malaria vaccine candidate VAR2CSAStructural modifications to a high-activity binding peptide located within the PfEMP1 NTS domain induce protection against P. falciparum malaria in Aotus monkeysStructure of the DBL3x domain of pregnancy-associated malaria protein VAR2CSA complexed with chondroitin sulfate AA recombinant peptide based on PfEMP-1 blocks and reverses adhesion of malaria-infected red blood cells to CD36 under flowclag9: A cytoadherence gene in Plasmodium falciparum essential for binding of parasitized erythrocytes to CD36Inhibition of Plasmepsin V activity demonstrates its essential role in protein export, PfEMP1 display, and survival of malaria parasitesSevere falciparum malaria. World Health Organization, Communicable Diseases ClusterSkeleton-binding protein 1 functions at the parasitophorous vacuole membrane to traffic PfEMP1 to the Plasmodium falciparum-infected erythrocyte surfaceFunctional analysis of the exported type IV HSP40 protein PfGECO in Plasmodium falciparum gametocytesPTEX is an essential nexus for protein export in malaria parasitesNew var reconstruction algorithm exposes high var sequence diversity in a single geographic location in MaliClag9 is not essential for PfEMP1 surface expression in non-cytoadherent Plasmodium falciparum parasites with a chromosome 9 deletion.Characterization of proteoglycans of human placenta and identification of unique chondroitin sulfate proteoglycans of the intervillous spaces that mediate the adherence of Plasmodium falciparum-infected erythrocytes to the placenta.Plasmodium strain determines dendritic cell function essential for survival from malariaPlasmodium falciparum uses gC1qR/HABP1/p32 as a receptor to bind to vascular endothelium and for platelet-mediated clumping.Identification of glycosaminoglycan binding regions in the Plasmodium falciparum encoded placental sequestration ligand, VAR2CSABlood coagulation, inflammation, and malaria.High throughput functional assays of the variant antigen PfEMP1 reveal a single domain in the 3D7 Plasmodium falciparum genome that binds ICAM1 with high affinity and is targeted by naturally acquired neutralizing antibodiesDifferential recognition of P. falciparum VAR2CSA domains by naturally acquired antibodies in pregnant women from a malaria endemic area.Using an improved phagocytosis assay to evaluate the effect of HIV on specific antibodies to pregnancy-associated malaria.Identification of glycosaminoglycan binding domains in Plasmodium falciparum erythrocyte membrane protein 1 of a chondroitin sulfate A-adherent parasitePlasmodium chabaudi-infected erythrocytes adhere to CD36 and bind to microvascular endothelial cells in an organ-specific wayFucosylated chondroitin sulfate inhibits Plasmodium falciparum cytoadhesion and merozoite invasion.Inhibition of binding of malaria-infected erythrocytes by a tetradecasaccharide fraction from chondroitin sulfate ABiological and biochemical characteristics of cytoadhesion of Plasmodium falciparum-infected erythrocytes to chondroitin-4-sulfate.Rapid acquisition of isolate-specific antibodies to chondroitin sulfate A-adherent plasmodium falciparum isolates in Ghanaian primigravidae.Evaluation of the antigenic diversity of placenta-binding Plasmodium falciparum variants and the antibody repertoire among pregnant women.Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching patternMolecular mechanistic insights into the endothelial receptor mediated cytoadherence of Plasmodium falciparum-infected erythrocytes.Effects of pregnancy and intensity of Plasmodium falciparum transmission on immunoglobulin G subclass responses to variant surface antigens.Inhibition of chondroitin-4-sulfate-specific adhesion of Plasmodium falciparum-infected erythrocytes by sulfated polysaccharidesEvidence of promiscuous endothelial binding by Plasmodium falciparum-infected erythrocytes.Differential binding of clonal variants of Plasmodium falciparum to allelic forms of intracellular adhesion molecule 1 determined by flow adhesion assay.
P2860
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P2860
Chondroitin sulfate A is a cell surface receptor for Plasmodium falciparum-infected erythrocytes
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh
1995年學術文章
@zh-hant
name
Chondroitin sulfate A is a cel ...... lciparum-infected erythrocytes
@ast
Chondroitin sulfate A is a cel ...... lciparum-infected erythrocytes
@en
type
label
Chondroitin sulfate A is a cel ...... lciparum-infected erythrocytes
@ast
Chondroitin sulfate A is a cel ...... lciparum-infected erythrocytes
@en
prefLabel
Chondroitin sulfate A is a cel ...... lciparum-infected erythrocytes
@ast
Chondroitin sulfate A is a cel ...... lciparum-infected erythrocytes
@en
P2093
P2860
P356
P1476
Chondroitin sulfate A is a cel ...... lciparum-infected erythrocytes
@en
P2093
P2860
P356
10.1084/JEM.182.1.15
P407
P577
1995-07-01T00:00:00Z