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Albert Haas

Researcher at University of Bonn

Publications -  75
Citations -  10913

Albert Haas is an academic researcher from University of Bonn. The author has contributed to research in topics: Phagosome & Endosome. The author has an hindex of 35, co-authored 69 publications receiving 9931 citations. Previous affiliations of Albert Haas include University of Würzburg & University of California, Los Angeles.

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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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Insights into the Mode of Action of Chitosan as an Antibacterial Compound

TL;DR: The antimicrobial mode of action of chitosan is investigated using a combination of approaches, including in vitro assays, killing kinetics, cellular leakage measurements, membrane potential estimations, and electron microscopy, in addition to transcriptional response analysis, and a possible mechanism for chitOSan's activity is postulated.
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Sec18p (NSF)-Driven Release of Sec17p (α-SNAP) Can Precede Docking and Fusion of Yeast Vacuoles

TL;DR: It is reported thatSec17p, Sec18p, and ATP are only needed for an early stage of the reaction that results in Sec17p release, and may function in a predocking stage ofThe reaction, rather than in bilayer fusion per se.
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Homotypic vacuolar fusion mediated by t- and v-SNAREs

TL;DR: Typical v- and t-SNAREs are identified on the yeast vacuolar membrane, demonstrating that docking is mediated by cognate SNAREs on the two organelle membranes.
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The Phagosome: Compartment with a License to Kill

TL;DR: Research into phagosome biogenesis has flourished in recent years – the purpose of this review is to give a glimpse of where this research stands, with emphasis on the cell biology of macrophage phagosomes.