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Stefaan J. Soenen

Researcher at Katholieke Universiteit Leuven

Publications -  125
Citations -  13395

Stefaan J. Soenen is an academic researcher from Katholieke Universiteit Leuven. The author has contributed to research in topics: Nanoparticle & Cell morphology. The author has an hindex of 40, co-authored 109 publications receiving 10803 citations. Previous affiliations of Stefaan J. Soenen include Ghent University & Catholic University of Leuven.

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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

Cellular toxicity of inorganic nanoparticles: Common aspects and guidelines for improved nanotoxicity evaluation

TL;DR: An overview of the cytotoxic effects of commonly used inorganic NPs: quantum dots, gold and iron oxide nanoparticles is presented and suggestions are made on how to optimize NP design in view of minimal cytotoxicity.
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Polymer-Coated Nanoparticles Interacting with Proteins and Cells: Focusing on the Sign of the Net Charge

TL;DR: This study shows that the number of adsorbed human serum albumin molecules per NP was not influenced by their surface charge, and cytot toxicity assays revealed a higher cytotoxicity for positively charged NPs, associated with their enhanced uptake.