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Shunbin Ning

Researcher at East Tennessee State University

Publications -  80
Citations -  3288

Shunbin Ning is an academic researcher from East Tennessee State University. The author has contributed to research in topics: DNA damage & T cell. The author has an hindex of 21, co-authored 69 publications receiving 1927 citations. Previous affiliations of Shunbin Ning include University of Miami & University of North Carolina at Chapel Hill.

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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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IRF7: activation, regulation, modification and function

TL;DR: Interferon regulatory factor 7 was originally identified in the context of Epstein–Barr virus infection, and has since emerged as the crucial regulator of type I interferons (IFNs) against pathogenic infections, which activate IRF7 by triggering signaling cascades from pathogen recognition receptors (PRRs) that recognize pathogenic nucleic acids.
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Salt stress induces programmed cell death in prokaryotic organism Anabaena.

TL;DR: This work aims to check if programmed cell death can occur in prokaryotic algae and if the morphological and biochemical features of PCD are conserved.
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TRAF6 and the Three C-Terminal Lysine Sites on IRF7 Are Required for Its Ubiquitination-Mediated Activation by the Tumor Necrosis Factor Receptor Family Member Latent Membrane Protein 1

TL;DR: The last three C-terminal lysine sites of human IRF7 variant A are determined to be essential for activation of IRF9 and support the hypothesis that regulatory ubiquitination of IRf7 is a prerequisite for its phosphorylation.
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Interferon Regulatory Factor 7 Regulates Expression of Epstein-Barr Virus Latent Membrane Protein 1: a Regulatory Circuit

TL;DR: The results of this study indicate that LMP1 is regulated by this host cell gene in addition to the viral factor, EBNA2, and may help to explain how LMP 1 is expressed in type II latency in the absence ofEBNA2.