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Ken Sato

Researcher at Gunma University

Publications -  244
Citations -  17525

Ken Sato is an academic researcher from Gunma University. The author has contributed to research in topics: Endoplasmic reticulum & Golgi apparatus. The author has an hindex of 48, co-authored 228 publications receiving 15459 citations. Previous affiliations of Ken Sato include Dartmouth College & National Presto Industries.

Papers
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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

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy 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

Degradation of Paternal Mitochondria by Fertilization-Triggered Autophagy in C. elegans Embryos

Miyuki Sato, +1 more
- 25 Nov 2011 - 
TL;DR: It is shown that autophagy, which delivers cytosolic components to lysosomes for degradation, is required for the elimination of paternal mitochondria in Caenorhabditis elegans and thereby maternal inheritance of mitochondrial DNA.
Journal ArticleDOI

Defining the functions of trans -SNARE pairs

TL;DR: Data indicate that SNARE pairing may transiently signal to downstream factors, leading to fusion of yeast vacuoles, as the function of this trans-SNARE complex must be transient.
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The Rab8 GTPase regulates apical protein localization in intestinal cells

TL;DR: It is found that apical peptidases and transporters localized to lysosomes in the small intestine of Rab8-deficient mice, and this led to a marked reduction in the absorption rate of nutrients in theSmall intestine, and ultimately to death.