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Divaker Choubey

Researcher at University of Cincinnati

Publications -  96
Citations -  15448

Divaker Choubey is an academic researcher from University of Cincinnati. The author has contributed to research in topics: Gene & AIM2. The author has an hindex of 45, co-authored 93 publications receiving 13664 citations. Previous affiliations of Divaker Choubey include University of Texas MD Anderson Cancer Center & Veterans Health Administration.

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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

Type-I interferon receptor deficiency reduces lupus-like disease in NZB mice.

TL;DR: The data indicate that type-I IFNs are important mediators in the pathogenesis of murine lupus, and that reducing their activity in the human counterpart may be beneficial.
Journal ArticleDOI

Evidence for an Interferon-Inducible Gene, Ifi202, in the Susceptibility to Systemic Lupus

TL;DR: These results, together with analyses of promoter region polymorphisms, strain distribution of expression, and effects on cell proliferation and apoptosis, implicate Ifi202 as a candidate gene for lupus.
Journal ArticleDOI

DU-145 and PC-3 human prostate cancer cell lines express androgen receptor: implications for the androgen receptor functions and regulation.

TL;DR: Using antipeptide antibodies directed against three distinct regions of the human AR protein and an improved method to detect AR protein in immunoblotting, it is reported that DU‐145 and PC‐3 cell lines express AR protein.