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Thomas Wollert

Researcher at Pasteur Institute

Publications -  28
Citations -  8713

Thomas Wollert is an academic researcher from Pasteur Institute. The author has contributed to research in topics: Autophagy & Vesicle. The author has an hindex of 14, co-authored 26 publications receiving 7125 citations. Previous affiliations of Thomas Wollert include Max Planck Society & National Institutes of Health.

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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.
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky, +2983 more
- 08 Feb 2021 - 
TL;DR: In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
Journal ArticleDOI

Molecular mechanism of multivesicular body biogenesis by ESCRT complexes

TL;DR: It is shown that ESCRT-0 forms domains of clustered cargo but does not deform membranes, which explains how the ESCRTs direct membrane budding and scission from the cytoplasmic side of the bud without being consumed in the reaction.
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Membrane scission by the ESCRT-III complex

TL;DR: Three subunits of ESCRT-III, Vps20, Snf7 and Vps24, are sufficient to detach intralumenal vesicles and are reconstituted and visualized by fluorescence microscopy.
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Extending the Host Range of Listeria monocytogenes by Rational Protein Design

TL;DR: Analyzing the recognition complex of the listerial invasion protein InlA and its human receptor E-cadherin, two single substitutions are postulated and verified to increase binding affinity by four orders of magnitude and extend binding specificity to include formerly incompatible murine E- cadher in a versatile murine model of human listeriosis.