DCAF7 is required for maintaining the cellular levels of ERCC1-XPF and nucleotide excision repair-Reference-Cited by-同舟云学术

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DCAF7 is required for maintaining the cellular levels of ERCC1-XPF and nucleotide excision repair

Published:2019-10 Issue:1 Volume:519 Page:204-210
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Kawara Hiroaki,Akahori Ryo,Wakasugi Mitsuo,Sancar Aziz,Matsunaga Tsukasa

Funder

NIH-NCI

Lineberger Comprehensive Cancer Center

JSPS KAKENHI

NIH

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference36 articles.

1. DNA repair endonuclease ERCC1-XPF as a novel therapeutic target to overcome chemoresistance in cancer therapy;McNeil;Nucleic Acids Res.,2012

2. The ERCC1 and ERCC4 (XPF) genes and gene products;Manandhar;Gene,2015

3. Replication protein A confers structure-specific endonuclease activities to the XPF-ERCC1 and XPG subunits of human DNA repair excision nuclease;Matsunaga;J. Biol. Chem.,1996

4. Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease;Sijbers;Cell,1996

5. Mapping of interaction domains between human repair proteins ERCC1 and XPF;de Laat;Nucleic Acids Res.,1998

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4. Advances in molecular characterization of myeloid proliferations associated with Down syndrome;Frontiers in Genetics;2022-08-10

5. Biomarker potentials of miRNA-associated circRNAs in breast cancer (MCF-7) cells: an in vitro and in silico study;Molecular Biology Reports;2021-03

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