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Ting Fen Tsai

Researcher at National Yang-Ming University

Publications -  112
Citations -  9333

Ting Fen Tsai is an academic researcher from National Yang-Ming University. The author has contributed to research in topics: Gene & Transgene. The author has an hindex of 36, co-authored 101 publications receiving 7809 citations. Previous affiliations of Ting Fen Tsai include Taipei Veterans General Hospital & Howard Hughes Medical Institute.

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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.
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MicroRNA-122 plays a critical role in liver homeostasis and hepatocarcinogenesis

TL;DR: It is demonstrated that mice with a targeted deletion of the Mir122a gene possess several key phenotypes of human liver diseases, which provides a rationale for the development of a unique therapy for the treatment of chronic liver disease and HCC.
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Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice.

TL;DR: This study reveals that CISD2 is primarily localized in the mitochondria and that mitochondrial degeneration appears to have a direct phenotypic consequence that triggers the accelerated aging process in Cisd2 knockout mice, and provides strong evidence supporting an earlier clinical hypothesis that WFS is in part a mitochondria-mediated disorder.
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Genetics of Angelman syndrome.

TL;DR: This work is supported by NIH grant HD 37283 and the authors thank Grace Watson for great assistance in preparation of the manuscript.
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Cul3-KLHL20 Ubiquitin Ligase Governs the Turnover of ULK1 and VPS34 Complexes to Control Autophagy Termination

TL;DR: It is shown that ULK1, a serine/threonine kinase critical for autophagy initiation, is a substrate of the Cul3-KLHL20 ubiquitin ligase, and KLHL20 governs the degradation of ATG13, VPS34, Beclin-1, and ATG14 in prolonged starvation through a direct or indirect mechanism.