1. Sui, Xue, Tang, Xiaolong, Wu, Xi, Liu, Yongshuo. 2022. Identification of ERCC8 as a novel cisplatin-resistant gene in esophageal cancer based on genome-scale CRISPR/Cas9 screening. In Biochemical and biophysical research communications, 593, 84-92. doi:10.1016/j.bbrc.2022.01.033. https://pubmed.ncbi.nlm.nih.gov/35063774/
2. Yousefipour, Farideh, Mahjoobi, Forouzandeh. 2021. Identification of two novel homozygous mutations in ERCC8 gene in two unrelated consanguineous families with Cockayne syndrome from Iran. In Clinica chimica acta; international journal of clinical chemistry, 523, 65-71. doi:10.1016/j.cca.2021.08.015. https://pubmed.ncbi.nlm.nih.gov/34461059/
3. Chebly, Alain, Corbani, Sandra, Abou Ghoch, Joelle, Megarbane, André, Chouery, Eliane. 2018. First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene. In BMC medical genetics, 19, 161. doi:10.1186/s12881-018-0677-7. https://pubmed.ncbi.nlm.nih.gov/30200888/
4. van Sluis, Marjolein, Yu, Qing, van der Woude, Melanie, Lans, Hannes, Marteijn, Jurgen A. 2024. Transcription-coupled DNA-protein crosslink repair by CSB and CRL4CSA-mediated degradation. In Nature cell biology, 26, 770-783. doi:10.1038/s41556-024-01394-y. https://pubmed.ncbi.nlm.nih.gov/38600236/
5. Li, Yue, Zheng, Luyao, Chen, Fuying, Yao, Zhirong, Li, Ming. . Two Novel Mutations in the ERCC8 Gene in a Patient with Ultraviolet-sensitive Syndrome. In Acta dermato-venereologica, 99, 117-118. doi:10.2340/00015555-3032. https://pubmed.ncbi.nlm.nih.gov/30182135/
6. Tian, Ye, Ma, Guochen, Li, Haoqi, Xiong, Jingyuan, Cheng, Guo. 2023. Shared Genetics and Comorbid Genes of Amyotrophic Lateral Sclerosis and Parkinson's Disease. In Movement disorders : official journal of the Movement Disorder Society, 38, 1813-1821. doi:10.1002/mds.29572. https://pubmed.ncbi.nlm.nih.gov/37534731/
7. Carnie, Christopher J, Acampora, Aleida C, Bader, Aldo S, Jackson, Stephen P, Stingele, Julian. 2024. Transcription-coupled repair of DNA-protein cross-links depends on CSA and CSB. In Nature cell biology, 26, 797-810. doi:10.1038/s41556-024-01391-1. https://pubmed.ncbi.nlm.nih.gov/38600235/
8. Taghdiri, Maryam, Dastsooz, Hassan, Fardaei, Majid, Farazi Fard, Mohammad Ali, Faghihi, Mohammad Ali. 2017. A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome. In Frontiers in pediatrics, 5, 169. doi:10.3389/fped.2017.00169. https://pubmed.ncbi.nlm.nih.gov/28848724/
9. Hao, Xiao-Dan, Yao, Yi-Zhi, Xu, Kai-Ge, Xu, Wen-Hua, Zhang, Jing-Jing. . Insufficient Dose of ERCC8 Protein Caused by a Frameshift Mutation Is Associated With Keratoconus With Congenital Cataracts. In Investigative ophthalmology & visual science, 63, 1. doi:10.1167/iovs.63.13.1. https://pubmed.ncbi.nlm.nih.gov/36454558/
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