HuGE Literature Finder
Records 1-16
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Brief Report: Novel Germline Mutations in DNA Damage Repair in Patients with Malignant Pleural Mesotheliomas.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2019 Dec . Guo Robin, DuBoff Mariel, Jayakumaran Gowtham, Kris Mark G, Ladanyi Marc, Robson Mark E, Mandelker Diana, Zauderer Marjorie |
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Breast cancer risk associated with genes encoding DNA repair MRN complex: a study from Punjab, Pakistan.
Breast cancer (Tokyo, Japan) 2018 May 25 (3): 350-355. Khan Rabbia Tariq, Siddique Ayesha, Shahid Naeem, Khokher Samina, Fatima War |
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Contribution of Double-strand Break Repair Gene Nijmegen Breakage Syndrome 1 Genotypes, Gender Difference and Smoking Status to Taiwanese Lung Cancer.
Anticancer research 2017 05 37 (5): 2417-2423. Chuang Chin-Liang, Wang Chung-Hsing, Hsu Chang-Hsien, Hsiao Chieh-Lun, Chen Guan-Liang, Yen Shiou-Ting, Li Hsin-Ting, Chang Wen-Shin, Tsai Chia-Wen, Wang Shou-Cheng, Bau DA-Ti |
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Increased age-adjusted hazard of death associated with a common single nucleotide polymorphism of the human RAD52 gene in a cardiovascular cohort.
Mechanisms of ageing and development 2017 10 167 56-63. Lenart Peter, Zlámal Filip, Machal Jan, Hlinomaz Ota, Groch Ladislav, Bienertová-Vašku Jul |
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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? |
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Genetic factors in individual radiation sensitivity.
DNA repair 2014 Apr 16 54-65. Hornhardt Sabine, Rößler Ute, Sauter Wiebke, Rosenberger Albert, Illig Thomas, Bickeböller Heike, Wichmann Hans-Erich, Gomolka Mar |
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Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study.
Breast cancer research : BCR 2014 16 (3): R58. Damiola Francesca, Pertesi Maroulio, Oliver Javier, Le Calvez-Kelm Florence, Voegele Catherine, Young Erin L, Robinot Nivonirina, Forey Nathalie, Durand Geoffroy, Vallée Maxime P, Tao Kayoko, Roane Terrell C, Williams Gareth J, Hopper John L, Southey Melissa C, Andrulis Irene L, John Esther M, Goldgar David E, Lesueur Fabienne, Tavtigian Sean |
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Comprehensive SNP scan of DNA repair and DNA damage response genes reveal multiple susceptibility loci conferring risk to tobacco associated leukoplakia and oral cancer.
PloS one 2013 8 (2): e56952. Mondal Pinaki, Datta Sayantan, Maiti Guru Prasad, Baral Aradhita, Jha Ganga Nath, Panda Chinmay Kumar, Chowdhury Shantanu, Ghosh Saurabh, Roy Bidyut, Roychoudhury Susan |
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Non-homologous end-joining pathway associated with occurrence of myocardial infarction: gene set analysis of genome-wide association study data.
PloS one 2013 8 (2): e56262. Verschuren Jeffrey J W, Trompet Stella, Deelen Joris, Stott David J, Sattar Naveed, Buckley Brendan M, Ford Ian, Heijmans Bastiaan T, Guchelaar Henk-Jan, Houwing-Duistermaat Jeanine J, Slagboom P Eline, Jukema J Wout |
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Variants in activators and downstream targets of ATM, radiation exposure, and contralateral breast cancer risk in the WECARE study.
Human mutation 2012 Jan 33 (1): 158-64. Brooks Jennifer D, Teraoka Sharon N, Reiner Anne S, Satagopan Jaya M, Bernstein Leslie, Thomas Duncan C, Capanu Marinela, Stovall Marilyn, Smith Susan A, Wei Shan, Shore Roy E, Boice John D, Lynch Charles F, Mellemkjaer Lene, Malone Kathleen E, Liang Xiaolin, , Haile Robert W, Concannon Patrick, Bernstein Jonine |
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Involvement of MRE11A and XPA gene polymorphisms in the modulation of DNA double-strand break repair activity: a genotype-phenotype correlation study.
DNA repair 2011 Oct 10 (10): 1044-50. Ricceri Fulvio, Porcedda Paola, Allione Alessandra, Turinetto Valentina, Polidoro Silvia, Guarrera Simonetta, Rosa Fabio, Voglino Floriana, Pezzotti Annamaria, Minieri Valentina, Accomasso Lisa, Cibrario Rocchietti Elisa, Orlando Luca, Giachino Claudia, Matullo Giusep |
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Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk.
Carcinogenesis 2010 Oct 31 (10): 1762-9. Liu Yanhong, Shete Sanjay, Wang Li-E, El-Zein Randa, Etzel Carol J, Liang Fu-Wen, Armstrong Georgina, Tsavachidis Spyros, Gilbert Mark R, Aldape Kenneth D, Xing Jinliang, Wu Xifeng, Wei Qingyi, Bondy Melissa |
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Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population.
Breast cancer research and treatment 2010 May 121 (1): 147-56. Loizidou Maria A, Cariolou Marios A, Neuhausen Susan L, Newbold Robert F, Bashiardes Evy, Marcou Yiola, Michael Thalia, Daniel Maria, Kakouri Eleni, Papadopoulos Panayiotis, Malas Simon, Hadjisavvas Andreas, Kyriacou Kyriac |
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Sequence variant discovery in DNA repair genes from radiosensitive and radiotolerant prostate brachytherapy patients.
Clinical cancer research : an official journal of the American Association for Cancer Research 2009 Aug 15 (15): 5008-16. Pugh Trevor J, Keyes Mira, Barclay Lorena, Delaney Allen, Krzywinski Martin, Thomas Dallas, Novik Karen, Yang Cindy, Agranovich Alexander, McKenzie Michael, Morris W Jim, Olive Peggy L, Marra Marco A, Moore Richard |
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Analysis of variants in DNA damage signalling genes in bladder cancer.
BMC medical genetics 2008 9 69. Choudhury Ananya, Elliott Faye, Iles Mark M, Churchman Michael, Bristow Robert G, Bishop D Timothy, Kiltie Anne |
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Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 Oct 16 (10): 2024-32. Hsu Huan-Ming, Wang Hui-Chun, Chen Sou-Tong, Hsu Giu-Cheng, Shen Chen-Yang, Yu Jyh-Cher |
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- Page last updated:Feb 20, 2020
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