Sequestrin, a CD36 recognition protein on Plasmodium falciparum malaria-infected erythrocytes identified by anti-idiotype antibodies
about
Structural modifications to a high-activity binding peptide located within the PfEMP1 NTS domain induce protection against P. falciparum malaria in Aotus monkeysclag9: A cytoadherence gene in Plasmodium falciparum essential for binding of parasitized erythrocytes to CD36Evidence-based annotation of the malaria parasite's genome using comparative expression profilingPlasmodium chabaudi-infected erythrocytes adhere to CD36 and bind to microvascular endothelial cells in an organ-specific wayPlasmodium P36 determines host cell receptor usage during sporozoite invasionComparison of apoptosis in human primary pulmonary endothelial cells and a brain microvascular endothelial cell line co-cultured with Plasmodium falciparum field isolates.Investigating the host binding signature on the Plasmodium falciparum PfEMP1 protein family.Cerebral malaria and immunogenetics.Host-parasite interaction and morbidity in malaria endemic areas.Clinical and molecular aspects of severe malaria.Synthetic peptides based on motifs present in human band 3 protein inhibit cytoadherence/sequestration of the malaria parasite Plasmodium falciparum.Malaria vaccine development.Antibody reactivity to linear epitopes of Plasmodium falciparum cytoadherence-linked asexual gene 9 in asymptomatic children and adults from papua new GuineaAntigenic variation in Plasmodium falciparum.Plasmodium falciparum erythrocyte membrane protein 1 is a parasitized erythrocyte receptor for adherence to CD36, thrombospondin, and intercellular adhesion molecule 1.The s48/45 six-cysteine proteins: mediators of interaction throughout the Plasmodium life cycle.Cytoadherence of Babesia bovis-infected erythrocytes to bovine brain capillary endothelial cells provides an in vitro model for sequestration.In vivo binding of immunoglobulin M to the surfaces of Babesia bigemina-infected erythrocytes.Antigenic and functional differences in adhesion of Plasmodium falciparum-infected erythrocytes to human and bovine CD36.Molecular mechanisms of sequestration in malaria.Evaluation of immunotherapy to reverse sequestration in the treatment of severe Plasmodium falciparum malaria.The effect of proteases and iodination on the adherent behaviour of Plasmodium falciparum-infected erythrocytes.Malaria parasite-specific Th1-like T cells simultaneously reduce parasitemia and promote disease.Protection against malaria by anti-erythropoietin antibody due to suppression of erythropoiesis in the liver and at other sites.CD36 Shunts Eicosanoid Metabolism to Repress CD14 Licensed Interleukin-1β Release and Inflammation.
P2860
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P2860
Sequestrin, a CD36 recognition protein on Plasmodium falciparum malaria-infected erythrocytes identified by anti-idiotype antibodies
description
1991 nî lūn-bûn
@nan
1991 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@ast
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@en
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@nl
type
label
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@ast
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@en
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@nl
prefLabel
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@ast
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@en
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@nl
P2093
P2860
P921
P356
P1476
Sequestrin, a CD36 recognition ...... ed by anti-idiotype antibodies
@en
P2093
C F Ockenhouse
G A Jamieson
N N Tandon
P2860
P304
P356
10.1073/PNAS.88.8.3175
P407
P577
1991-04-15T00:00:00Z