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Monica Hagedorn

Researcher at Jacobs University Bremen

Publications -  39
Citations -  6887

Monica Hagedorn is an academic researcher from Jacobs University Bremen. The author has contributed to research in topics: Phagosome & Dictyostelium discoideum. The author has an hindex of 24, co-authored 38 publications receiving 6272 citations. Previous affiliations of Monica Hagedorn include University of Geneva & Bernhard Nocht Institute for Tropical Medicine.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Infection by Tubercular Mycobacteria Is Spread by Nonlytic Ejection from Their Amoeba Hosts

TL;DR: Using the social amoeba Dictyostelium as a genetically tractable host for pathogenic mycobacteria, it is discovered that M. tuberculosis and M. marinum, but not M. avium, are ejected from the cell through an actin-based structure, the ejectosome, and this conserved nonlytic spreading mechanism requires a cytoskeleton regulator from the host and an intactMycobacterial ESX-1 secretion system.
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Flotillin and RacH modulate the intracellular immunity of Dictyostelium to Mycobacterium marinum infection

TL;DR: It is found that two host proteins – the flotillin homologue vacuolin and p80, a predicted copper transporter – accumulate at the vacuole during pathogen replication until it finally ruptures and the bacteria are released into the host cytosol.
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Dynamic life and death interactions between Mycobacterium smegmatis and J774 macrophages.

TL;DR: A systematic analysis addressing how macrophages kill ‘non‐pathogenic’ Mycobacterium smegmatis found that map kinase p38 is a crucial regulator of all processes investigated, except NO synthesis, that facilitated the host for some functions while being usurped by live bacteria for others.