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Richard A. Lockshin

Researcher at City University of New York

Publications -  17
Citations -  5056

Richard A. Lockshin is an academic researcher from City University of New York. The author has contributed to research in topics: Programmed cell death & Autophagy. The author has an hindex of 9, co-authored 17 publications receiving 4098 citations. Previous affiliations of Richard A. Lockshin include Stellenbosch University.

Papers
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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.
Journal ArticleDOI

Caspase-independent cell death?

TL;DR: Experimental and therapeutic procedures must account for the possibility that cells that are in trouble can activate numerous physiological pathways toward self-destruction, leading to variant forms of cell death that may display one or more characteristics of apoptosis.
Journal ArticleDOI

The variability of autophagy and cell death susceptibility Unanswered questions

TL;DR: This article attempts to provide answers by explaining how and when a change in autophagic pathway activity such as primary stress response is able to affect cell viability and when not and provides new concepts that set autophagy into an energetic feedback loop, that may assist in the understanding of Autophagy in maintaining healthy cells or when it controls the threshold between cell death and cell survival.
Journal ArticleDOI

Dengue-induced autophagy, virus replication and protection from cell death require ER stress (PERK) pathway activation

TL;DR: It is demonstrated that among the multiple autophagy-inducing pathways during infection, ER stress signaling is more important to viral replication and protection of cells than either ATM or ROS-mediated signaling.
Book ChapterDOI

Cell Death: History and Future

TL;DR: The rapid development of the field has given substantial understanding of how cell death is achieved, and this knowledge has made it possible to understand that there are multiple pathways to death and that the commitment to die is not the same as execution.