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Angelika Amon

Researcher at Massachusetts Institute of Technology

Publications -  201
Citations -  29098

Angelika Amon is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Aneuploidy & Mitotic exit. The author has an hindex of 78, co-authored 200 publications receiving 26171 citations. Previous affiliations of Angelika Amon include Cold Spring Harbor Laboratory & University of California, San Francisco.

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Journal ArticleDOI

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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CDC20 and CDH1: a family of substrate-specific activators of APC-dependent proteolysis.

Rosella Visintin, +2 more
- 17 Oct 1997 - 
TL;DR: Overexpression of either CDC20 or CDH1 was sufficient to induce APC-dependent proteolysis of the appropriate target in stages of the cell cycle in which substrates are normally stable.
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Effects of Aneuploidy on Cellular Physiology and Cell Division in Haploid Yeast

Eduardo M. Torres, +12 more
- 17 Aug 2007 - 
TL;DR: It is concluded that aneuploidy causes not only a proliferative disadvantage but also a set of phenotypes that is independent of the identity of the individual extra chromosomes.
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The Phosphatase Cdc14 Triggers Mitotic Exit by Reversal of Cdk-Dependent Phosphorylation

Rosella Visintin, +5 more
- 01 Dec 1998 - 
TL;DR: This work shows that the Cdc14 phosphatase triggers mitotic exit by three parallel mechanisms, each of which inhibits Cdk activity, and induces degradation of mitotic cyclins.
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Cfi1 prevents premature exit from mitosis by anchoring Cdc14 phosphatase in the nucleolus

Rosella Visintin, +2 more
- 29 Apr 1999 - 
TL;DR: It is shown that Cdc14 is sequestered in the nucleolus for most of the cell cycle, allowing it to reach its targets during nuclear division and a highly conserved signalling cascade, critical for the exit from mitosis, is required for this movement of CDC14 during anaphase.