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pro vyhledávání: '"Van Ngo"'
Autor:
Dowd GC; Department of Microbiology and Immunology, University of Otago, 9054 Dunedin, New Zealand., Mortuza R; Department of Microbiology and Immunology, University of Otago, 9054 Dunedin, New Zealand., Bhalla M; Department of Microbiology and Immunology, University of Otago, 9054 Dunedin, New Zealand., Van Ngo H; Department of Microbiology and Immunology, University of Otago, 9054 Dunedin, New Zealand., Li Y; Department of Microbiology and Immunology, University of Otago, 9054 Dunedin, New Zealand., Rigano LA; Department of Microbiology and Immunology, University of Otago, 9054 Dunedin, New Zealand., Ireton K; Department of Microbiology and Immunology, University of Otago, 9054 Dunedin, New Zealand keith.ireton@otago.ac.nz.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2020 Feb 18; Vol. 117 (7), pp. 3789-3796. Date of Electronic Publication: 2020 Feb 03.
Autor:
Bhalla M; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand., Van Ngo H; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand., Gyanwali GC; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand., Ireton K; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand keith.ireton@otago.ac.nz.
Publikováno v:
Infection and immunity [Infect Immun] 2018 Dec 19; Vol. 87 (1). Date of Electronic Publication: 2018 Dec 19 (Print Publication: 2019).
Autor:
Ireton K; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand., Van Ngo H; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand., Bhalla M; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Publikováno v:
Cellular microbiology [Cell Microbiol] 2018 Aug; Vol. 20 (8), pp. e12861. Date of Electronic Publication: 2018 Jun 20.
Autor:
Van Ngo H; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand., Bhalla M; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand., Chen DY; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand., Ireton K; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Publikováno v:
Cellular microbiology [Cell Microbiol] 2017 Nov; Vol. 19 (11). Date of Electronic Publication: 2017 Aug 25.
Autor:
Hoan Van Ngo, Manmeet Bhalla, Yang Li, Roman Mortuza, Luciano A. Rigano, Keith Ireton, Georgina C. Dowd
Publikováno v:
Proc Natl Acad Sci U S A
The facultative intracellular pathogen Listeria monocytogenes uses an actin-based motility process to spread within human tissues. Filamentous actin from the human cell forms a tail behind bacteria, propelling microbes through the cytoplasm. Motile b
Listeria monocytogenes is a foodborne bacterium that causes gastroenteritis, meningitis, or abortion. Listeria induces its internalization (entry) into some human cells through interaction of the bacterial surface protein InlB with its host receptor,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d28535b29f5fb2332a78e0570842f3b
https://researchonline.lshtm.ac.uk/id/eprint/4651595/1/The-host-scaffolding-protein-Filamin-A.pdf
https://researchonline.lshtm.ac.uk/id/eprint/4651595/1/The-host-scaffolding-protein-Filamin-A.pdf
Publikováno v:
Cellular microbiology. 20(8)
Many microbial pathogens co-opt or perturb host membrane trafficking pathways. This review covers recent examples in which microbes interact with host exocytosis, the fusion of intracellular vesicles with the plasma membrane. The bacterial pathogens
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Publikováno v:
Cellular Microbiology. 19:e12768
The bacterial surface protein InlB mediates internalisation of Listeria monocytogenes into human cells through interaction with the host receptor tyrosine kinase, Met. InlB-mediated entry requires localised polymerisation of the host actin cytoskelet