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Sangita C. Sinha

Researcher at North Dakota State University

Publications -  47
Citations -  11339

Sangita C. Sinha is an academic researcher from North Dakota State University. The author has contributed to research in topics: Autophagy & BECN1. The author has an hindex of 23, co-authored 42 publications receiving 9591 citations. Previous affiliations of Sangita C. Sinha include University of Texas Southwestern Medical Center & Purdue University.

Papers
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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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JNK1-Mediated Phosphorylation of Bcl-2 Regulates Starvation-Induced Autophagy

Yongjie Wei, +5 more
- 20 Jun 2008 - 
TL;DR: It is demonstrated that JNK1-mediated multisite phosphorylation of Bcl-2 stimulates starvation-induced autophagy by disrupting the B cl-2/Beclin 1 complex, which defines a mechanism that cells use to regulate autophagic activity in response to nutrient status.
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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.
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Bcl-2 family members: dual regulators of apoptosis and autophagy.

Beth Levine, +4 more
- 01 Jul 2008 - 
TL;DR: This hitherto neglected crosstalk between the core machineries regulating autophagy and apoptosis may redefine the role of Bcl-2 family proteins in oncogenesis and tumor progression.
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Regulation of innate antiviral defenses through a shared repressor domain in RIG-I and LGP2

Takeshi Saito, +8 more
- 09 Jan 2007 - 
TL;DR: RIG-I is a cytoplasmic sensor of HCV and is governed by RD interactions that are shared with LGP2 as an on/off switch controlling innate defenses, which may have therapeutic implications for immune regulation.