Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 68 Records) |
Query Trace: ERCC6[original query] |
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Polymorphism of DNA repair genes OGG1, XRCC1, XPD and ERCC6 in bladder cancer in Belarus. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2014 Sep 19 (6): 509-16. Ramaniuk Volha P, Nikitchenko Nataliya V, Savina Nataliya V, Kuzhir Tatyana D, Rolevich Alexander I, Krasny Sergei A, Sushinsky Vadim E, Goncharova Roza |
Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes. Human genetics 2014 Oct 133 (10): 1311-8. Martins Sandra, Pearson Christopher E, Coutinho Paula, Provost Sylvie, Amorim António, Dubé Marie-Pierre, Sequeiros Jorge, Rouleau Guy |
[Study on gene-gene, gene-environmental interactions of DNA repair genes related with age-related cataract]. Zhonghua yi xue za zhi 2014 Apr 94 (15): 1147-51. Yang Mei, Su Shu, Zhou Jing, Zhu Rongrong, Qin Bai, Yang Ling, Zhang Junfang, Shi Jian, Liang Congkai, Liu Bihong, Qi Yingxiang, Guan Huaij |
Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors. Cancer causes & control : CCC 2014 Jun 25 (6): 759-69. Huhn Stefanie, Bevier Melanie, Pardini Barbara, Naccarati Alessio, Vodickova Ludmila, Novotny Jan, Vodicka Pavel, Hemminki Kari, Försti As |
Genetic Variants That Predispose to DNA Double-Strand Breaks in Lymphocytes From a Subset of Patients With Familial Colorectal Carcinomas. Gastroenterology 2015 Sep . Arora Sanjeevani, Yan Hong, Cho Iltaeg, Fan Hua-Ying, Luo Biao, Gai Xiaowu, Bodian Dale L, Vockley Joseph G, Zhou Yan, Handorf Elizabeth, Egleston Brian L, Andrake Mark, Nicolas Emmanuelle, Serebriiskii Ilya, Yen Timothy J, Hall Michael J, Golemis Erica A, Enders Greg |
[The polymorphism of DNA repair genes XPD, XRCC1, OGG1, and ERCC6, life expectancy, and the inclination to smoke]. Genetika 2014 Aug 50 (8): 975-85. Romaniuk O P, Nikitchenko N V, Savina N V, Kuzhir T D, Goncharova R |
The Cellular Response to Oxidatively Induced DNA Damage and Polymorphism of Some DNA Repair Genes Associated with Clinicopathological Features of Bladder Cancer. Oxidative medicine and cellular longevity 2016 2016 5710403. Savina Nataliya V, Nikitchenko Nataliya V, Kuzhir Tatyana D, Rolevich Alexander I, Krasny Sergei A, Goncharova Roza |
Polymorphisms of multiple genes involved in NER pathway predict prognosis of gastric cancer. Oncotarget 2016 Jun . Liu Jingwei, Deng Na, Xu Qian, Sun Liping, Tu Huakang, Wang Zhenning, Xing Chengzhong, Yuan Yu |
Meta-analysis reveals no significant association between ERCC6 polymorphisms and bladder cancer risk. The International journal of biological markers 2016 Oct 0. Hong Zhengdong, Wu Jinxian, Li Qiang, Zhang Shouhua, Shi Zim |
Single nucleotide polymorphisms of nucleotide excision repair pathway are significantly associated with outcomes of platinum-based chemotherapy in lung cancer. Scientific reports 2017 Sep 7 (1): 11785. Song Xiao, Wang Shiming, Hong Xuan, Li Xiaoying, Zhao Xueying, Huai Cong, Chen Hongyan, Gao Zhiqiang, Qian Ji, Wang Jiucun, Han Baohui, Bai Chunxue, Li Qiang, Wu Junjie, Lu Da |
Gene-gene and gene-environment interactions influence platinum-based chemotherapy response and toxicity in non-small cell lung cancer patients. Scientific reports 2017 Jul 7 (1): 5082. Cui Jia-Jia, Wang Lei-Yun, Zhu Tao, Gong Wei-Jing, Zhou Hong-Hao, Liu Zhao-Qian, Yin Ji- |
Epistatic SNP interaction of ERCC6 with ERCC8 and their joint protein expression contribute to gastric cancer/atrophic gastritis risk. Oncotarget 2017 May . Jing Jing-Jing, Lu You-Zhu, Sun Li-Ping, Liu Jing-Wei, Gong Yue-Hua, Xu Qian, Dong Nan-Nan, Yuan Yu |
Polymorphisms of cancer-related genes and risk of multipleprimary malignancies involving colorectal cancer. Turkish journal of medical sciences 2017 11 47 (5): 1549-1554. Cao Peiguo, Yu Li, Wu Anshan, Li Jingjing, Liu Ling, Liu Chunlan, Zhou Jianda, Cao Ke, Guo Chengxi |
Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A. Scientific reports 2017 Oct 7 (1): 13686. Wang Xiaozhu, Huang Yu, Yan Ming, Li Jiuwei, Ding Changhong, Jin Hong, Fang Fang, Yang Yanling, Wu Baiyan, Chen Dafa |
Somatic mutations in early onset luminal breast cancer. Oncotarget 2018 Apr 9 (32): 22460-22479. Encinas Giselly, Sabelnykova Veronica Y, de Lyra Eduardo Carneiro, Hirata Katayama Maria Lucia, Maistro Simone, de Vasconcellos Valle Pedro Wilson Mompean, de Lima Pereira Gláucia Fernanda, Rodrigues Lívia Munhoz, de Menezes Pacheco Serio Pedro Adolpho, de Gouvêa Ana Carolina Ribeiro Chaves, Geyer Felipe Correa, Basso Ricardo Alves, Pasini Fátima Solange, Del Pilar Esteves Diz Maria, Brentani Maria Mitzi, Guedes Sampaio Góes João Carlos, Chammas Roger, Boutros Paul C, Koike Folgueira Maria Aparecida Azeve |
Genetic variants in the nucleotide excision repair genes are associated with the risk of developing endometriosis. Biology of reproduction 2019 Aug . Shen Te-Chun, Tsai Chia-Wen, Chang Wen-Shin, Wang Yun-Chi, Hsu Huai-Mei, Li Hsin-Ting, Gu Jian, Bau Da-Ti |
Genetic Variant Screening of DNA Repair Genes in Myelodysplastic Syndrome Identifies a Novel Mutation in the XRCC2 Gene. Oncology research and treatment 2019 Mar 1-6. Valka Jan, Vesela Jitka, Votavova Hana, Dostalova-Merkerova Michaela, Urbanova Zuzana, Jonasova Anna, Cermak Jaroslav, Belickova Moni |
Haplotypes of HTRA1 rs1120638, TIMP3 rs9621532, VEGFA rs833068, CFI rs10033900, ERCC6 rs3793784, and KCTD10 rs56209061 Gene Polymorphisms in Age-Related Macular Degeneration. Disease markers 2019 2019 9602949. Liutkeviciene Rasa, Vilkeviciute Alvita, Gedvilaite Greta, Kaikaryte Kriste, Kriauciuniene Lore |
Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia. Scientific reports 2020 9 10 (1): 14297. Kim Borahm, Yun Woobin, Lee Seung-Tae, Choi Jong Rok, Yoo Keon Hee, Koo Hong Hoe, Jung Chul Won, Kim Sun H |
Early-onset nucleotide excision repair disorders with neurological impairment: Clues for early diagnosis and prognostic counseling. Clinical genetics 2020 6 98 (3): 251-260. Baer Sarah, Obringer Cathy, Julia Sophie, Chelly Jameleddine, Capri Yline, Gras Domitille, Baujat Geneviève, Felix Têmis Maria, Doray Berenice, Sanchez Del Pozo Jaime, Ramos Lina M, Burglen Lydie, Laugel Vincent, Calmels Nadè |
Somatic mutations in the DNA repairome in prostate cancers in African Americans and Caucasians. Oncogene 2020 4 39 (21): 4299-4311. Yadav Santosh, Anbalagan Muralidharan, Baddoo Melody, Chellamuthu Vinodh K, Mukhopadhyay Sudurika, Woods Carol, Jiang Wei, Moroz Krzysztof, Flemington Erik K, Makridakis Ni |
Integrative genomic analysis implicates ERCC6 and its interaction with ERCC8 in susceptibility to breast cancer. Scientific reports 2020 12 10 (1): 21276. Moslehi Roxana, Tsao Hui-Shien, Zeinomar Nur, Stagnar Cristy, Fitzpatrick Sean, Dzutsev Amir |
Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries. Human mutation 2021 5 42 (8): 969-977. Forrest Iain S, Chaudhary Kumardeep, Vy Ha My T, Bafna Shantanu, Kim Soyeon, Won Hong-Hee, Loos Ruth J F, Cho Judy, Pasquale Louis R, Nadkarni Girish N, Rocheleau Ghislain, Do R |
Excision Repair Cross-Complementation Group 6 Gene Polymorphism Is Associated with the Response to FOLFIRINOX Chemotherapy in Asian Patients with Pancreatic Cancer. Cancers 2021 Mar 13 (6): . Choi Young Hoon, Lim Younggyun, Ryu Ji Kon, Paik Woo Hyun, Lee Sang Hyub, Kim Yong-Tae, Kim Ju H |
Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing. Journal of assisted reproduction and genetics 2021 Feb . Shen Jiandong, Qu Dianyun, Gao Yan, Sun Fangxi, Xie Jiazi, Sun Xueping, Wang Daowu, Ma Xiang, Cui Yugui, Liu Jiayin, Diao Feiya |
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits. Genome medicine 2022 9 14 (1): 113. Yuan Bo, Schulze Katharina V, Assia Batzir Nurit, Sinson Jefferson, Dai Hongzheng, Zhu Wenmiao, Bocanegra Francia, Fong Chin-To, Holder Jimmy, Nguyen Joanne, Schaaf Christian P, Yang Yaping, Bi Weimin, Eng Christine, Shaw Chad, Lupski James R, Liu Pengf |
Genetic Association of ERCC6 rs2228526 Polymorphism with the Risk of Cancer: Evidence from a Meta-Analysis. BioMed research international 2022 4 2022 2662666. Lin Xiaochun, Wu Yongfu, Li Qingde, Yu Hongying, Li Xugui, Li Xiaohua, Zheng Jink |
Germline Variants in Cancer Genes from Young Breast Cancer Mexican Patients. Cancers 2022 4 14 (7): . Gómez-Flores-Ramos Liliana, Barraza-Arellano Angélica Leticia, Mohar Alejandro, Trujillo-Martínez Miguel, Grimaldo Lizbeth, Ortiz-Lopez Rocío, Treviño Víct |
Role for Nucleotide Excision Repair Gene Variants in Oxaliplatin-Induced Peripheral Neuropathy. JCO precision oncology 2022 2 2 1-18. West Hannah, Coffey Michelle, Wagner Michael J, McLeod Howard L, Colley James P, Adams Richard A, Fleck Oliver, Maughan Timothy S, Fisher David, Kaplan Richard S, Harris Rebecca, Cheadle Jeremy |
The relationship of maternal polymorphisms of genes related to meiosis and DNA damage repair with fetal chromosomal stability. Journal of perinatal medicine 2023 7 . Ying Chan, Xinhua Tang, Dongling Cai, Yize Liu, Dongmei Li, Jie Su, Guowei Neng, Yifei Yin, Zibiao Geng, Shu Zhu, Jinman Zhang, Lihong Jiang, Baosheng Z |
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- Page last updated:Apr 22, 2024
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