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Rajesh Agarwal

Researcher at University of Montana

Publications -  483
Citations -  32284

Rajesh Agarwal is an academic researcher from University of Montana. The author has contributed to research in topics: Silibinin & Apoptosis. The author has an hindex of 92, co-authored 416 publications receiving 29843 citations. Previous affiliations of Rajesh Agarwal include University of Lucknow & Anschutz Medical Campus.

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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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Green Tea Constituent Epigallocatechin-3-Gallate and Induction of Apoptosis and Cell Cycle Arrest in Human Carcinoma Cells

TL;DR: Green tea may protect against cancer by causing cell cycle arrest and inducing apoptosis, and needs to be evaluated in human trials.
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Multitargeted therapy of cancer by silymarin.

TL;DR: The protective effects of silymarin and its major active constituent, silibinin, studied in various tissues, suggest a clinical application in cancer patients as an adjunct to established therapies, to prevent or reduce chemotherapy as well as radiotherapy-induced toxicity.
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Protective Effects of Silymarin Against Photocarcinogenesis in a Mouse Skin Model

TL;DR: Silymarin can provide substantial protection against different stages of UVB-induced carcinogenesis, possibly via its strong antioxidant properties.
Journal Article

Silibinin Strongly Synergizes Human Prostate Carcinoma DU145 Cells to Doxorubicin-induced Growth Inhibition, G2-M Arrest, and Apoptosis

TL;DR: Findings suggest a need for in vivo studies with this combination of silibinin and doxorubicin against prostate cancer, which is limited because of high systemic toxicity, and might be relevant for a clinical application in prostate cancer patients.