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Items: 1 to 20 of 32

1.
CSB affected on the sensitivity of lung cancer cells to platinum-based drugs through the global decrease of let-7 and miR-29
Zhenbang Yang, Chunling Liu, Hongjiao Wu, Yuning Xie, Hui Gao, Xuemei Zhang
BMC Cancer. 2019; 19: 948. Published online 2019 Oct 15. doi: 10.1186/s12885-019-6194-z
PMCID:
PMC6792260
AbstractArticlePDF–5.7M
2.
Prognostic Value of Excision Repair Cross-Complementing mRNA Expression in Gastric Cancer
Shan-Shan Luo, Xi-Wen Liao, Xiao-Dong Zhu
Biomed Res Int. 2018; 2018: 6204684. Published online 2018 Oct 17. doi: 10.1155/2018/6204684
PMCID:
PMC6207904
AbstractArticlePDF–3.7M
3.
CSA and CSB play a role in the response to DNA breaks
Barbara Pascucci, Alessandra Fragale, Veronica Marabitti, Giuseppe Leuzzi, Angelo Salvatore Calcagnile, Eleonora Parlanti, Annapaola Franchitto, Eugenia Dogliotti, Mariarosaria D’Errico
Oncotarget. 2018 Feb 20; 9(14): 11581–11591. Published online 2018 Jan 29. doi: 10.18632/oncotarget.24342
PMCID:
PMC5837770
AbstractArticlePDF–2.5M
4.
ATM and CDK2 control chromatin remodeler CSB to inhibit RIF1 in DSB repair pathway choice
Nicole L. Batenburg, John R. Walker, Sylvie M. Noordermeer, Nathalie Moatti, Daniel Durocher, Xu-Dong Zhu
Nat Commun. 2017; 8: 1921. Published online 2017 Dec 4. doi: 10.1038/s41467-017-02114-x
PMCID:
PMC5715124
AbstractArticlePDF–2.0M
5.
Single nucleotide polymorphisms of nucleotide excision repair pathway are significantly associated with outcomes of platinum-based chemotherapy in lung cancer
Xiao Song, Shiming Wang, Xuan Hong, Xiaoying Li, Xueying Zhao, Cong Huai, Hongyan Chen, Zhiqiang Gao, Ji Qian, Jiucun Wang, Baohui Han, Chunxue Bai, Qiang Li, Junjie Wu, Daru Lu
Sci Rep. 2017; 7: 11785. Published online 2017 Sep 18. doi: 10.1038/s41598-017-08257-7
PMCID:
PMC5603542
AbstractArticlePDF–2.7M
6.
Cockayne syndrome B protein regulates recruitment of the Elongin A ubiquitin ligase to sites of DNA damage
Juston C. Weems, Brian D. Slaughter, Jay R. Unruh, Stefan Boeing, Shawn M. Hall, Merry B. McLaird, Takashi Yasukawa, Teijiro Aso, Jesper Q. Svejstrup, Joan W. Conaway, Ronald C. Conaway
J Biol Chem. 2017 Apr 21; 292(16): 6431–6437. Published online 2017 Mar 14. doi: 10.1074/jbc.C117.777946
PMCID:
PMC5399097
AbstractArticlePDF–873K
7.
Polymorphisms of multiple genes involved in NER pathway predict prognosis of gastric cancer
Jingwei Liu, Na Deng, Qian Xu, Liping Sun, Huakang Tu, Zhenning Wang, Chengzhong Xing, Yuan Yuan
Oncotarget. 2016 Jul 26; 7(30): 48130–48142. Published online 2016 Jun 20. doi: 10.18632/oncotarget.10173
PMCID:
PMC5217006
AbstractArticlePDF–2.1M
8.
The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair
Yooksil Sin, Kiyoji Tanaka, Masafumi Saijo
J Biol Chem. 2016 Jan 15; 291(3): 1387–1397. Published online 2015 Nov 30. doi: 10.1074/jbc.M115.683235
PMCID:
PMC4714222
AbstractArticlePDF–1.6M
9.
CSB-PGBD3 Mutations Cause Premature Ovarian Failure
Yingying Qin, Ting Guo, Guangyu Li, Tie-Shan Tang, Shidou Zhao, Xue Jiao, Juanjuan Gong, Fei Gao, Caixia Guo, Joe Leigh Simpson, Zi-Jiang Chen
PLoS Genet. 2015 Jul; 11(7): e1005419. Published online 2015 Jul 28. doi: 10.1371/journal.pgen.1005419
PMCID:
PMC4517778
AbstractArticlePDF–5.2M
10.
Cockayne syndrome group B protein regulates DNA double-strand break repair and checkpoint activation
Nicole L Batenburg, Elizabeth L Thompson, Eric A Hendrickson, Xu-Dong Zhu
EMBO J. 2015 May 12; 34(10): 1399–1416. Published online 2015 Mar 27. doi: 10.15252/embj.201490041
PMCID:
PMC4491999
AbstractArticlePDF–2.4M
11.
Cockayne Syndrome Group B (Csb) and Group A (Csa) Deficiencies Predispose to Hearing Loss and Cochlear Hair Cell Degeneration in Mice
A. Paul Nagtegaal, Robert N. Rainey, Ingrid van der Pluijm, Renata M.C. Brandt, Gijsbertus T.J. van der Horst, J. Gerard G. Borst, Neil Segil
J Neurosci. 2015 Mar 11; 35(10): 4280–4286. doi: 10.1523/JNEUROSCI.5063-14.2015
PMCID:
PMC4355199
AbstractArticlePDF–4.7M
12.
Identification of Two Missense Mutations of ERCC6 in Three Chinese Sisters with Cockayne Syndrome by Whole Exome Sequencing
Shanshan Yu, Liyuan Chen, Lili Ye, Lingna Fei, Wei Tang, Yujiao Tian, Qian Geng, Xin Yi, Jiansheng Xie
PLoS One. 2014; 9(12): e113914. Published online 2014 Dec 2. doi: 10.1371/journal.pone.0113914
PMCID:
PMC4252064
AbstractArticlePDF–1.6M
13.
Gender and cell-type specific effects of the transcription coupled repair protein, ERCC6/CSB, on repeat expansion in a mouse model of the Fragile X-related disorders
Xiao-Nan Zhao, Karen Usdin
Hum Mutat. Author manuscript; available in PMC 2015 Mar 1.
Published in final edited form as: Hum Mutat. 2014 Mar; 35(3): 341–349. doi: 10.1002/humu.22495
PMCID:
PMC4067466
AbstractArticlePDF–1.1M
14.
The cockayne syndrome B protein is essential for neuronal differentiation and neuritogenesis
F Ciaffardini, S Nicolai, M Caputo, G Canu, E Paccosi, M Costantino, M Frontini, A S Balajee, L Proietti-De-Santis
Cell Death Dis. 2014 May; 5(5): e1268. Published online 2014 May 29. doi: 10.1038/cddis.2014.228
PMCID:
PMC4047889
AbstractArticlePDF–4.0M
15.
Identification of Two Novel ERCC6 Mutations in Old Order Amish with Cockayne Syndrome
B. Xin, H. Wang
Mol Syndromol. 2013 Jan; 3(6): 288–290. Published online 2012 Dec 21. doi: 10.1159/000345924
PMCID:
PMC3569105
AbstractArticlePDF–194K
16.
The conserved Cockayne syndrome B-piggyBac fusion protein (CSB-PGBD3) affects DNA repair and induces both interferon-like and innate antiviral responses in CSB-null cells
Arnold D. Bailey, Lucas T. Gray, Thomas Pavelitz, John C. Newman, Katsuyoshi Horibata, Kiyoji Tanaka, Alan M. Weiner
DNA Repair (Amst) Author manuscript; available in PMC 2013 May 1.
Published in final edited form as: DNA Repair (Amst). 2012 May 1; 11(5): 488–501. Published online 2012 Apr 6. doi: 10.1016/j.dnarep.2012.02.004
PMCID:
PMC3340519
AbstractArticlePDF–2.1M
17.
Defective transcription initiation causes postnatal growth failure in a mouse model of nucleotide excision repair (NER) progeria
Irene Kamileri, Ismene Karakasilioti, Aria Sideri, Theodoros Kosteas, Antonis Tatarakis, Iannis Talianidis, George A. Garinis
Proc Natl Acad Sci U S A. 2012 Feb 21; 109(8): 2995–3000. Published online 2012 Feb 8. doi: 10.1073/pnas.1114941109
PMCID:
PMC3286994
AbstractArticlePDF–725K
18.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
19.
The ERCC6 Gene and Age-Related Macular Degeneration
Dominique C. Baas, Dominiek D. Despriet, Theo G. M. F. Gorgels, Julie Bergeron-Sawitzke, André G. Uitterlinden, Albert Hofman, Cornelia M. van Duijn, Joanna E. Merriam, R. Theodore Smith, Gaetano R. Barile, Jacoline B. ten Brink, Johannes R. Vingerling, Caroline C. W. Klaver, Rando Allikmets, Michael Dean, Arthur A. B. Bergen
PLoS One. 2010; 5(11): e13786. Published online 2010 Nov 1. doi: 10.1371/journal.pone.0013786
PMCID:
PMC2967476
AbstractArticlePDF–726K
20.
A Variant of the Cockayne Syndrome B Gene ERCC6 Confers Risk of Lung Cancer
Zhongning Lin, Xuemei Zhang, Jingsheng Tuo, Yongli Guo, Bridgett Green, Chi-Chao Chan, Wen Tan, Ying Huang, Wenhua Ling, Fred F. Kadlubar, Dongxin Lin, Baitang Ning
Hum Mutat. Author manuscript; available in PMC 2008 Jun 27.
Published in final edited form as: Hum Mutat. 2008 Jan; 29(1): 113–122. doi: 10.1002/humu.20610
PMCID:
PMC2441604
AbstractArticlePDF–475K

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