Apicomplexan parasites co-opt host calpains to facilitate their escape from infected cells. - Wikidata - awgldk - TriplyDB

Apicomplexan parasites co-opt host calpains to facilitate their escape from infected cells.

Apicomplexan parasites co-opt host calpains to facilitate their escape from infected cells.

http://www.wikidata.org/entity/Q36081539

about

Expanding the antimalarial toolkit: Targeting host-parasite interactions Clinically Available Medicines Demonstrating Anti-Toxoplasma Activity The influence of host genetics on erythrocytes and malaria infection: is there therapeutic potential?Recent insights into apicomplexan parasite egress provide new views to a kill Chemical biology approaches for the study of apicomplexan parasites Processing of Plasmodium falciparum Merozoite Surface Protein MSP1 Activates a Spectrin-Binding Function Enabling Parasite Egress from RBCs Calcium-dependent permeabilization of erythrocytes by a perforin-like protein during egress of malaria parasites Biophysics of malarial parasite exit from infected erythrocytes The malarial serine protease SUB1 plays an essential role in parasite liver stage development Inhibition of an Erythrocyte Tyrosine Kinase with Imatinib Prevents Plasmodium falciparum Egress and Terminates Parasitemia Perforin-like protein PPLP2 permeabilizes the red blood cell membrane during egress of Plasmodium falciparum gametocytes A plant-like kinase in Plasmodium falciparum regulates parasite egress from erythrocytes The Apicomplexan CDC/MACPF-like pore-forming proteins.Parasitophorous vacuole poration precedes its rupture and rapid host erythrocyte cytoskeleton collapse in Plasmodium falciparum egress.Using small molecules to dissect mechanisms of microbial pathogenesis.Manipulation of the Host Cell Membrane during Plasmodium Liver Stage Egress An adaptable two-color flow cytometric assay to quantitate the invasion of erythrocytes by Plasmodium falciparum parasites.The Plasmodium falciparum pseudoprotease SERA5 regulates the kinetics and efficiency of malaria parasite egress from host erythrocytes.Apicomplexan perforin-like proteins.The malaria parasite progressively dismantles the host erythrocyte cytoskeleton for efficient egress Inhibition of calpain blocks the phagosomal escape of Listeria monocytogenes.Life cycle-dependent cytoskeletal modifications in Plasmodium falciparum infected erythrocytes Methodology and application of flow cytometry for investigation of human malaria parasites.Global profiling of proteolysis during rupture of Plasmodium falciparum from the host erythrocyte.In vitro genetic analysis of an erythrocyte determinant of malaria infection.Small molecule targeting malaria merozoite surface protein-1 (MSP-1) prevents host invasion of divergent plasmodial species.Quantitative time-course profiling of parasite and host cell proteins in the human malaria parasite Plasmodium falciparum.Calcium signals and calpain-dependent necrosis are essential for release of coxsackievirus B from polarized intestinal epithelial cells The neurotropic parasite Toxoplasma gondii increases dopamine metabolism.Antiparasitic chemotherapy: from genomes to mechanisms.Multiple stiffening effects of nanoscale knobs on human red blood cells infected with Plasmodium falciparum malaria parasite A transient resistance to blood-stage malaria in interferon-γ-deficient mice through impaired production of the host cells preferred by malaria parasites.Toxoplasma on the brain: understanding host-pathogen interactions in chronic CNS infection.A genetic screen to isolate Toxoplasma gondii host-cell egress mutants Functional analysis of erythrocyte determinants of Plasmodium infection Lytic Cycle of Toxoplasma gondii: 15 Years Later.The role of cGMP signalling in regulating life cycle progression of Plasmodium.Proteolytic activation of the essential parasitophorous vacuole cysteine protease SERA6 accompanies malaria parasite egress from its host erythrocyte.Prison break: pathogens' strategies to egress from host cells.New approaches for dissecting protease functions to improve probe development and drug discovery

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P2860

Apicomplexan parasites co-opt host calpains to facilitate their escape from infected cells.

http://www.wikidata.org/entity/Q36081539

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2009 nî lūn-bûn

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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2009年论文

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Apicomplexan parasites co-opt ...... ir escape from infected cells.

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Apicomplexan parasites co-opt ...... ir escape from infected cells.

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Apicomplexan parasites co-opt ...... ir escape from infected cells.

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Apicomplexan parasites co-opt ...... ir escape from infected cells.

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Apicomplexan parasites co-opt ...... ir escape from infected cells.

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Apicomplexan parasites co-opt ...... ir escape from infected cells.

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Claire Darling

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Daniel P Beiting

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Doron C Greenbaum

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Geetha Velmourougane

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Michael B Harbut

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Ming Yeh Lee

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Paul H Davis

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Peter A Greer

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P2860

Erythrocyte G protein as a novel target for malarial chemotherapy

m-Calpain is required for preimplantation embryonic development in mice.

A role for the protease falcipain 1 in host cell invasion by the human malaria parasite

Concerted multi-pronged attack by calpastatin to occlude the catalytic cleft of heterodimeric calpains

Calcium-bound structure of calpain and its mechanism of inhibition by calpastatin

The calpain system

Disruption of the murine calpain small subunit gene, Capn4: calpain is essential for embryonic development but not for cell growth and division

Regulation of cell migration by the calcium-dependent protease calpain.

Subcellular discharge of a serine protease mediates release of invasive malaria parasites from host erythrocytes

Rapid membrane disruption by a perforin-like protein facilitates parasite exit from host cells.

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794-797

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scholarly article

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10.1126/SCIENCE.1171085

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5928

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324

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Rajesh Chandramohanadas

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2009-04-02T00:00:00Z

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24254117

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19342550

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3391539

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