Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: DNA Damage and MSH6[original query] |
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Association of DNA repair and steroid metabolism gene polymorphisms with clinical late toxicity in patients treated with conformal radiotherapy for prostate cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2006 Apr 12 (8): 2545-54. Damaraju Sambasivarao, Murray David, Dufour Jennifer, Carandang Diana, Myrehaug Sten, Fallone Gino, Field Colin, Greiner Russell, Hanson John, Cass Carol E, Parliament Matth |
DNA repair and cell cycle control genes and the risk of young-onset lung cancer. Cancer research 2006 Nov 66 (22): 11062-9. Landi Stefano, Gemignani Federica, Canzian Federico, Gaborieau Valérie, Barale Roberto, Landi Debora, Szeszenia-Dabrowska Neonilia, Zaridze David, Lissowska Jolanta, Rudnai Peter, Fabianova Eleonora, Mates Dana, Foretova Lenka, Janout Vladimir, Bencko Vladimir, Gioia-Patricola Lydie, Hall Janet, Boffetta Paolo, Hung Rayjean J, Brennan Pa |
Polygenic model of DNA repair genetic polymorphisms in human breast cancer risk. Carcinogenesis 2008 Nov 29 (11): 2132-8. Smith Tasha R, Levine Edward A, Freimanis Rita I, Akman Steven A, Allen Glenn O, Hoang Kimberly N, Liu-Mares Wen, Hu Jennifer |
DNA mismatch repair gene polymorphisms affect survival in pancreatic cancer. The oncologist 2011 16 (1): 61-70. Dong Xiaoqun, Li Yanan, Hess Kenneth R, Abbruzzese James L, Li Dongh |
Genetic variants in BRIP1 (BACH1) contribute to risk of nonsyndromic cleft lip with or without cleft palate. Birth defects research. Part A, Clinical and molecular teratology 2014 Sep 100 (9): 670-8. Mostowska Adrianna, Hozyasz Kamil K, Wójcicki Piotr, Galas-Filipowicz Daria, Lasota Agnieszka, Dunin-Wilczy?ska Izabella, Lianeri Margarita, Jagodzi?ski Pawe? |
Germline Mutations in Cancer Predisposition Genes are Frequent in Sporadic Sarcomas. Scientific reports 2017 9 7 (1): 10660. Chan Sock Hoai, Lim Weng Khong, Ishak Nur Diana Binte, Li Shao-Tzu, Goh Wei Lin, Tan Gek San, Lim Kiat Hon, Teo Melissa, Young Cedric Ng Chuan, Malik Simeen, Tan Mann Hong, Teh Jonathan Yi Hui, Chin Francis Kuok Choon, Kesavan Sittampalam, Selvarajan Sathiyamoorthy, Tan Patrick, Teh Bin Tean, Soo Khee Chee, Farid Mohamad, Quek Richard, Ngeow Joan |
Germline mutations in pancreatic cancer and potential new therapeutic options. Oncotarget 2017 10 8 (42): 73240-73257. Pihlak Rille, Valle Juan W, McNamara Mairéad |
Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas. Genome medicine 2018 9 10 (1): 69. Buckley Alexandra R, Ideker Trey, Carter Hannah, Harismendy Olivier, Schork Nicholas |
Whole exome sequencing of breast cancer (TNBC) cases from India: association of MSH6 and BRIP1 variants with TNBC risk and oxidative DNA damage. Molecular biology reports 2018 Aug . Aravind Kumar M, Naushad Shaik Mohammad, Narasimgu Narasimhulu, Nagaraju Naik S, Kadali Srilatha, Shanker Uday, Lakshmi Narasu |
Assessment of DNA repair susceptibility genes identified by whole exome sequencing in head and neck cancer. DNA repair 2018 5 66-67 50-63. Das Raima, Kundu Sharbadeb, Laskar Shaheen, Choudhury Yashmin, Ghosh Sankar Kum |
High throughput gene sequencing reveals altered landscape in DNA damage responses and chromatin remodeling in sporadic pancreatic neuroendocrine tumors. Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2018 Apr 18 (3): 318-327. Ji Shunrong, Yang Wenting, Liu Jiang, Zhao Jingjing, Chen Liang, Ni Quanxing, Long Jiang, Yu Xianj |
Overexpression of NEIL3 associated with altered genome and poor survival in selected types of human cancer. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2020 5 42 (5): 1010428320918404. Tran Oanh Tn, Tadesse Serkalem, Chu Christopher, Kidane Daw |
Clinical Impact of Somatic Variants in Homologous Recombination Repair-Related Genes in Ovarian High-Grade Serous Carcinoma. Cancer research and treatment : official journal of Korean Cancer Association 2020 Jan . Choi Min Chul, Hwang Sohyun, Kim Sewha, Jung Sang Geun, Park Hyun, Joo Won Duk, Song Seung Hun, Lee Chan, Kim Tae-Heon, Kang Haeyoun, An Hee Ju |
Polymorphisms and rare variants identified by next-generation sequencing confer risk for lung cancer in han Chinese population. Pathology, research and practice 2020 Feb 152873. Li Xiaoqi, Liu Jinsheng, Wang Ke, Zhou Juan, Zhang Hang, Zhang Mancang, Shi Yongyo |
Using next-generation sequencing to redefine BRCAness in triple-negative breast cancer. Cancer science 2020 1 111 (4): 1375-1384. Lin Po-Han, Chen Ming, Tsai Li-Wei, Lo Chiao, Yen Tzu-Chun, Huang Thomas Yoyan, Chen Chih-Kai, Fan Sheng-Chih, Kuo Sung-Hsin, Huang Chiun-She |
Additive effects of variants of unknown significance in replication repair-associated DNA polymerase genes on mutational burden and prognosis across diverse cancers. Journal for immunotherapy of cancer 2021 9 9 (9): . Ying Jieer, Yang Lin, Yin Jiani C, Xia Guojie, Xing Minyan, Chen Xiaoxi, Pang Jiaohui, Wu Yong, Bao Hua, Wu Xue, Shao Yang, Zhu Lingjun, Cheng Xiangdo |
Prevalence and spectrum of germline cancer susceptibility gene variants and somatic second hits in colorectal cancer. American journal of cancer research 2021 12 11 (11): 5571-5580. Liao Haiyan, Cai Songhua, Bai Yuezong, Zhang Bei, Sheng Yuling, Tong Shuang, Cai Jinping, Zhao Feilong, Zhao Xiaochen, Chen Shiqing, Zhang Cheng, Gao Ji |
Germline DNA damage repair gene mutations in pancreatic cancer patients with personal/family histories of pancreas/breast/ovarian/prostate cancer in a Japanese population. Annals of gastroenterological surgery 2021 11 5 (6): 853-864. Hata Tatsuo, Mizuma Masamichi, Motoi Fuyuhiko, Ishida Masaharu, Ohtsuka Hideo, Nakagawa Kei, Morikawa Takanori, Furukawa Toru, Unno Michia |
Looking beyond the cytogenetics in haematological malignancies: decoding the role of tandem repeats in DNA repair genes. Molecular biology reports 2022 9 49 (11): 10293-10305. Bhattacharya Priyanjali, Patel Trupti |
Identification of Germline Mutations in Upper Tract Urothelial Carcinoma With Suspected Lynch Syndrome. Frontiers in oncology 2022 4 12 774202. Guan Bao, Wang Jie, Li Xuesong, Lin Lin, Fang Dong, Kong Wenwen, Tian Chuangyu, Li Juan, Yang Kunlin, Han Guanpeng, Wu Yucai, He Yuhui, Peng Yiji, Yu Yanfei, He Qun, He Shiming, Gong Yanqing, Zhou Liqun, Tang |
Prevalence and Spectrum of Predisposition Genes With Germline Mutations Among Chinese Patients With Bowel Cancer. Frontiers in genetics 2022 2 12 755629. Xie Zhengyong, Ke Yongli, Chen Junyong, Li Zehang, Wang Changzheng, Chen Yuhong, Ding Hongliang, Cheng Liya |
Mismatch repair gene germline mutations in patients with prostate cancer. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2023 6 52 (2): 133-138. Bangwei Fang, Yu Wei, Jian Pan, Tingwei Zhang, Dingwei Ye, Yao Z |
Clinicopathological and molecular analysis of microsatellite instability in prostate cancer: a multi-institutional study in China. Frontiers in oncology 2023 10 13 1277233. Huizhi Zhang, Xiaoqun Yang, Jialing Xie, Xiao Cheng, Jiayi Chen, Miaomiao Shen, Wenyi Ding, Suying Wang, Zhe Zhang, Chaofu Wang, Ming Zh |
Long-term response to camrelizumab in a pretreated metastatic mixed testicular germ-cell tumor patient with co-mutations in DNA damage-repair genes. Immunotherapy 2023 1 15 (1): 17-25. Zhang Hui, Jiang Da, Meng Erhong, Zhao Meng, Niu Beifa |
Genomic landscape of Chinese patients with hepatocellular carcinoma using next-generation sequencing and its association with the prognosis. Annals of hepatology 2023 1 28 (2): 100898. Yang Zhao, Liu Jianwei, Xue Feng, Zhang Lei, Xue Hui, Wu Yeye, Bai Shilei, Du Furong, Wang Xiaoxuan, Deng Wanglong, Song Chao, Wang K |
Age- and ethnic-driven molecular and clinical disparity of East Asian breast cancers. BMC medicine 2024 9 22 (1): 422. Ji Yoon Lee, Ji Won Lee, Min Sung Chung, Jong Gwon Choi, Sung Hoon Sim, Hyo Jeong Kim, Jeong Eun Kim, Kyoung Eun Lee, Yeon Hee Park, Myoung Joo Kang, Mi Sun Ahn, Yee Soo Chae, Ji Hyun Park, Jee Hyun Kim, Gun Min Kim, Jae Ho Byun, Keon Uk Park, Ju Won Kim, Seung Pil Jung, Jung Hyun Lee, Jung Seok An, Byunghyun Jang, Dayoung Yoon, Jiwon Kim, Jisoo Hong, Harim Koo, Kyu Ran Cho, Cheol Yong Kim, Jason K Sa, Kyong Hwa Pa |
The Impact of Li Fraumeni and Germline Retinoblastoma Mutations on Leiomyosarcoma Initiation, Outcomes and Genetic Testing Recommendations. Clinical cancer research : an official journal of the American Association for Cancer Research 2024 8 . Josephine K Dermawan, David H Abramson, Sarah Chiang, Martee L Hensley, William D Tap, Sujana Movva, Robert G Maki, Diana Mandelker, Cristina R Antones |
Mutation Analysis of TMB-High Colorectal Cancer: Insights Into Molecular Pathways and Clinical Implications. Cancer science 2025 1 . Yuko Chikaishi, Hiroshi Matsuoka, Eiji Sugihara, Mayu Takeda, Makoto Sumitomo, Seiji Yamada, Gaku Inaguma, Yusuke Omura, Yeongcheol Cheong, Yosuke Kobayashi, Masaya Nakauchi, Junichiro Hiro, Koji Masumori, Koki Otsuka, Hiroshi Nishihara, Koichi Suda, Hideyuki Saya, Tetsuya Takimo |
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