In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
about
Proteomic analysis reveals novel proteins associated with the Plasmodium protein exporter PTEX and a loss of complex stability upon truncation of the core PTEX component, PTEX150Host cell remodeling by pathogens: the exomembrane system in Plasmodium-infected erythrocytesThe Plasmodium berghei translocon of exported proteins reveals spatiotemporal dynamics of tubular extensions.Shedding of host autophagic proteins from the parasitophorous vacuolar membrane of Plasmodium berghei.Interaction between Plasmodium Glycosylphosphatidylinositol and the Host Protein Moesin Has No Implication in Malaria Pathology.Contrasting Inducible Knockdown of the Auxiliary PTEX Component PTEX88 in P. falciparum and P. berghei Unmasks a Role in Parasite Virulence.Targeted Deletion of a Plasmodium Site-2 Protease Impairs Life Cycle Progression in the Mammalian Host.An in silico down-scaling approach uncovers novel constituents of the Plasmodium-containing vacuole
P2860
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P2860
In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
@ast
In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
@en
type
label
In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
@ast
In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
@en
prefLabel
In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
@ast
In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
@en
P2093
P2860
P50
P921
P356
P1433
P1476
In Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence.
@en
P2093
Alyssa Ingmundson
Jean Costa Nunes
Werner Stenzel
P2860
P304
P356
10.1128/EC.00276-14
P577
2015-03-27T00:00:00Z