Gene, Cell and Tissue

Published by: Kowsar

Novel Poly (ADP-Ribose) Polymerase Inhibitor AZD2461 Combined with Valproic Acid Exerts Mild Antagonistic Effects in Hela Cells

Saman Sargazi 1 , 2 , Ramin Saravani 3 , 4 , * , Javad Zavar Reza 2 , 5 , ** , Hossein Zarei Jaliani 6 , Shekoufeh Mirinejad 4 , Mahdiyeh Moudi 7 and Hamidreza Galavi 3 , 4
Authors Information
1 International Campus, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
2 Biotechnology Research Center, International Campus, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
3 Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran
4 Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan, Iran
5 Department of Clinical Biochemistry, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
6 Protein Engineering Laboratory, Department of Medical Genetics, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
7 Genetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran
Corresponding Authors:
Article information
  • Gene, Cell and Tissue: July 2018, 5 (3); e81645
  • Published Online: October 1, 2018
  • Article Type: Research Article
  • Received: July 2, 2018
  • Revised: August 19, 2018
  • Accepted: September 15, 2018
  • DOI: 10.5812/gct.81645

To Cite: Sargazi S, Saravani R, Zavar Reza J , Zarei Jaliani H , Mirinejad S , et al. Novel Poly (ADP-Ribose) Polymerase Inhibitor AZD2461 Combined with Valproic Acid Exerts Mild Antagonistic Effects in Hela Cells, Gene Cell Tissue. 2018 ; 5(3):e81645. doi: 10.5812/gct.81645.

Copyright © 2018, Gene, Cell and Tissue. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License ( which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
1. Background
2. Methods
3. Results
4. Discussion
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