Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: DNA Damage and FANCD2[original query] |
---|
Haplotype analysis of eight genes of the monoubiquitinated FANCD2-DNA damage-repair pathway in breast cancer patients. Cancer epidemiology 2013 Jun 37 (3): 311-7. Tang Li-Li, Chen Fei-Yu, Wang Hao, Hu Xue-Li, Dai Xu, Mao Jie, Shen Zheng-Tang, Wu Yu-Hui, Wang Shou-Man, Hai Jian, Yan Guo-Jiao, Li Hui, Huang Ju |
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility. Scientific reports 2017 Apr 7 (1): 681. Mantere Tuomo, Tervasmäki Anna, Nurmi Anna, Rapakko Katrin, Kauppila Saila, Tang Jiangbo, Schleutker Johanna, Kallioniemi Anne, Hartikainen Jaana M, Mannermaa Arto, Nieminen Pentti, Hanhisalo Riitta, Lehto Sini, Suvanto Maija, Grip Mervi, Jukkola-Vuorinen Arja, Tengström Maria, Auvinen Päivi, Kvist Anders, Borg Åke, Blomqvist Carl, Aittomäki Kristiina, Greenberg Roger A, Winqvist Robert, Nevanlinna Heli, Pylkäs Kat |
Analysis of polymorphisms in genes associated with the FA/BRCA pathway in three patients with multiple primary malignant neoplasms. Artificial cells, nanomedicine, and biotechnology 2019 Dec 47 (1): 1101-1112. Wang Le, Wang Hao, Wang Ting, Liu Jinhui, Chen Wei, Wang Yamin, Chen Chao, Zhu Hongli, Dai Pengg |
Association of Single-Nucleotide Polymorphisms in Monoubiquitinated FANCD2-DNA Damage Repair Pathway Genes With Breast Cancer in the Chinese Population. Technology in cancer research & treatment 2018 Jan 17 1533033818819841. Chen Fei-Yu, Wang Hao, Li Hui, Hu Xue-Li, Dai Xu, Wang Shou-Man, Yan Guo-Jiao, Jiang Ping-Lan, Hu Yuan-Ping, Huang Juan, Tang Li- |
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 |
Genomic Landscape of Primary and Recurrent Anal Squamous Cell Carcinomas in Relation to HPV Integration, Copy-Number Variation, and DNA Damage Response Genes. Molecular cancer research : MCR 2021 4 19 (8): 1308-1321. Aldersley Jordan, Lorenz David R, Mouw Kent W, D'Andrea Alan D, Gabuzda Da |
A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene. Genome medicine 2021 12 13 (1): 186. Fierheller Caitlin T, Guitton-Sert Laure, Alenezi Wejdan M, Revil Timothée, Oros Kathleen K, Gao Yuandi, Bedard Karine, Arcand Suzanna L, Serruya Corinne, Behl Supriya, Meunier Liliane, Fleury Hubert, Fewings Eleanor, Subramanian Deepak N, Nadaf Javad, Bruce Jeffrey P, Bell Rachel, Provencher Diane, Foulkes William D, El Haffaf Zaki, Mes-Masson Anne-Marie, Majewski Jacek, Pugh Trevor J, Tischkowitz Marc, James Paul A, Campbell Ian G, Greenwood Celia M T, Ragoussis Jiannis, Masson Jean-Yves, Tonin Patricia |
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 |
Genomic characterization of metastatic castration-resistant prostate cancer patients undergoing PSMA radioligand therapy: A single-center experience. The Prostate 2022 Oct . Satapathy Swayamjeet, Das Chandan K, Aggarwal Piyush, Sood Ashwani, Parihar Ashwin S, Singh Shrawan K, Mittal Bhagwant |
Next generation sequencing reveals a high prevalence of pathogenic mutations in homologous recombination DNA damage repair genes among patients with uterine sarcoma. Gynecologic oncology 2023 8 177 14-19. Dimitrios Nasioudis, Nawar A Latif, Emily M Ko, Lori Cory, Sarah H Kim, Lainie Martin, Fiona Simpkins, Robert Giunto |
- Page last reviewed:Oct 1, 2023
- Page last updated:Nov 28, 2023
- Content source: