Identification and characterization of mercaptopyrimidine‐based small molecules as inhibitors of nonhomologous <scp>DNA</scp> end joining-Reference-Cited by-同舟云学术

Identification and characterization of mercaptopyrimidine‐based small molecules as inhibitors of nonhomologous DNA end joining

Published:2022-09-11 Issue:3 Volume:290 Page:796-820
ISSN:1742-464X
Container-title:The FEBS Journal
language:en
Short-container-title:The FEBS Journal

Author:

Ray Ujjayinee¹,Gopinatha Vindya K.¹²,Sharma Shivangi¹³,Goyary Laijau¹,Choudhary Bibha³^ORCID,Mantelingu Kempegowda²,Rangappa Kanchugarakoppal S.²⁴,Raghavan Sathees C.¹^ORCID

Affiliation:

1. Department of Biochemistry Indian Institute of Science Bangalore India

2. Department of Studies in Chemistry University of Mysore India

3. Institute of Bioinformatics and Applied Biotechnology Electronics City Bangalore India

4. Institution of Excellence, Vijnana Bhavana University of Mysore India

Funder

Department of Atomic Energy, Government of India

Department of Biotechnology, Ministry of Science and Technology, India

Indo-French Centre for the Promotion of Advanced Research

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/febs.16615

Reference90 articles.

1. Modulation of DNA double-strand break repair as a strategy to improve precise genome editing

2. DNA Double-Strand Break Repair Inhibitors as Cancer Therapeutics

3. Nonhomologous end joining: new accessory factors fine tune the machinery

4. Strategies to improve radiotherapy with targeted drugs

5. DNA repair dysregulation from cancer driver to therapeutic target

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