Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: NEIL2[original query] |
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Functional variants of the NEIL1 and NEIL2 genes and risk and progression of squamous cell carcinoma of the oral cavity and oropharynx. Clinical cancer research : an official journal of the American Association for Cancer Research 2008 Jul 14 (13): 4345-52. Zhai Xiadong, Zhao Hui, Liu Zhensheng, Wang Li-E, El-Naggar Adel K, Sturgis Erich M, Wei Qing |
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3. Gut 2008 Sep 57 (9): 1252-5. Dallosso A R, Dolwani S, Jones N, Jones S, Colley J, Maynard J, Idziaszczyk S, Humphreys V, Arnold J, Donaldson A, Eccles D, Ellis A, Evans D G, Frayling I M, Hes F J, Houlston R S, Maher E R, Nielsen M, Parry S, Tyler E, Moskvina V, Cheadle J P, Sampson J |
DNA base excision repair gene polymorphisms modulate human cognitive performance and decline during normal life span. Mechanisms of ageing and development 2011 Aug 132 (8-9): 449-58. Lillenes Meryl S, Espeseth Thomas, Støen Mari, Lundervold Astri J, Frye Stephan A, Rootwelt Helge, Reinvang Ivar, Tønjum To |
Analysis of DNA repair gene polymorphisms and survival in low-grade and anaplastic gliomas. Journal of neuro-oncology 2011 Dec 105 (3): 531-8. Berntsson Shala Ghaderi, Wibom Carl, Sjöström Sara, Henriksson Roger, Brännström Thomas, Broholm Helle, Johansson Christoffer, Fleming Sarah J, McKinney Patricia A, Bethke Lara, Houlston Richard, Smits Anja, Andersson Ulrika, Melin Beatrice |
Association of polymorphisms in oxidative stress genes with clinical outcomes for bladder cancer treated with Bacillus Calmette-Guérin. PloS one 2012 7 (6): e38533. Wei Hua, Kamat Ashish, Chen Meng, Ke Hung-Lung, Chang David W, Yin Jikai, Grossman H Barton, Dinney Colin P, Wu Xife |
Increased risk of lung cancer associated with a functionally impaired polymorphic variant of the human DNA glycosylase NEIL2. DNA repair 2012 Jun 11 (6): 570-8. Dey Sanjib, Maiti Amit K, Hegde Muralidhar L, Hegde Pavana M, Boldogh Istvan, Sarkar Partha S, Abdel-Rahman Sherif Z, Sarker Altaf H, Hang Bo, Xie Jingwu, Tomkinson Alan E, Zhou Mian, Shen Binghui, Wang Guanghai, Wu Chen, Yu Dianke, Lin Dongxin, Cardenas Victor, Hazra Tapas |
Variation within 3'-UTRs of base excision repair genes and response to therapy in colorectal cancer patients: A potential modulation of microRNAs binding. Clinical cancer research : an official journal of the American Association for Cancer Research 2013 Nov 19 (21): 6044-56. Pardini Barbara, Rosa Fabio, Barone Elisa, Di Gaetano Cornelia, Slyskova Jana, Novotny Jan, Levy Miroslav, Garritano Sonia, Vodickova Ludmila, Buchler Tomas, Gemignani Federica, Landi Stefano, Vodicka Pavel, Naccarati Aless |
Genetic variation in the base excision repair pathway, environmental risk factors, and colorectal adenoma risk. PloS one 2013 8 (8): e71211. Corral Roman, Lewinger Juan Pablo, Joshi Amit D, Levine A Joan, Vandenberg David J, Haile Robert W, Stern Mariana |
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers. PLoS genetics 2014 Apr 10 (4): e1004256. Osorio Ana, Milne Roger L, Kuchenbaecker Karoline, Vaclová Tereza, Pita Guillermo, Alonso Rosario, Peterlongo Paolo, Blanco Ignacio, de la Hoya Miguel, Duran Mercedes, Díez Orland, Ramón Y Cajal Teresa, Konstantopoulou Irene, Martínez-Bouzas Cristina, Andrés Conejero Raquel, Soucy Penny, McGuffog Lesley, Barrowdale Daniel, Lee Andrew, Swe-Brca , Arver Brita, Rantala Johanna, Loman Niklas, Ehrencrona Hans, Olopade Olufunmilayo I, Beattie Mary S, Domchek Susan M, Nathanson Katherine, Rebbeck Timothy R, Arun Banu K, Karlan Beth Y, Walsh Christine, Lester Jenny, John Esther M, Whittemore Alice S, Daly Mary B, Southey Melissa, Hopper John, Terry Mary B, Buys Saundra S, Janavicius Ramunas, Dorfling Cecilia M, van Rensburg Elizabeth J, Steele Linda, Neuhausen Susan L, Ding Yuan Chun, Hansen Thomas V O, Jønson Lars, Ejlertsen Bent, Gerdes Anne-Marie, Infante Mar, Herráez Belén, Moreno Leticia Thais, Weitzel Jeffrey N, Herzog Josef, Weeman Kisa, Manoukian Siranoush, Peissel Bernard, Zaffaroni Daniela, Scuvera Giulietta, Bonanni Bernardo, Mariette Frederique, Volorio Sara, Viel Alessandra, Varesco Liliana, Papi Laura, Ottini Laura, Tibiletti Maria Grazia, Radice Paolo, Yannoukakos Drakoulis, Garber Judy, Ellis Steve, Frost Debra, Platte Radka, Fineberg Elena, Evans Gareth, Lalloo Fiona, Izatt Louise, Eeles Ros, Adlard Julian, Davidson Rosemarie, Cole Trevor, Eccles Diana, Cook Jackie, Hodgson Shirley, Brewer Carole, Tischkowitz Marc, Douglas Fiona, Porteous Mary, Side Lucy, Walker Lisa, Morrison Patrick, Donaldson Alan, Kennedy John, Foo Claire, Godwin Andrew K, Schmutzler Rita Katharina, Wappenschmidt Barbara, Rhiem Kerstin, Engel Christoph, Meindl Alfons, Ditsch Nina, Arnold Norbert, Plendl Hans Jörg, Niederacher Dieter, Sutter Christian, Wang-Gohrke Shan, Steinemann Doris, Preisler-Adams Sabine, Kast Karin, Varon-Mateeva Raymonda, Gehrig Andrea, Stoppa-Lyonnet Dominique, Sinilnikova Olga M, Mazoyer Sylvie, Damiola Francesca, Poppe Bruce, Claes Kathleen, Piedmonte Marion, Tucker Kathy, Backes Floor, Rodríguez Gustavo, Brewster Wendy, Wakeley Katie, Rutherford Thomas, Caldés Trinidad, Nevanlinna Heli, Aittomäki Kristiina, Rookus Matti A, van Os Theo A M, van der Kolk Lizet, de Lange J L, Meijers-Heijboer Hanne E J, van der Hout A H, van Asperen Christi J, Gómez Garcia Encarna B, Hoogerbrugge Nicoline, Collée J Margriet, van Deurzen Carolien H M, van der Luijt Rob B, Devilee Peter, Hebon , Olah Edith, Lázaro Conxi, Teulé Alex, Menéndez Mireia, Jakubowska Anna, Cybulski Cezary, Gronwald Jacek, Lubinski Jan, Durda Katarzyna, Jaworska-Bieniek Katarzyna, Johannsson Oskar Th, Maugard Christine, Montagna Marco, Tognazzo Silvia, Teixeira Manuel R, Healey Sue, Investigators Kconfab, Olswold Curtis, Guidugli Lucia, Lindor Noralane, Slager Susan, Szabo Csilla I, Vijai Joseph, Robson Mark, Kauff Noah, Zhang Liying, Rau-Murthy Rohini, Fink-Retter Anneliese, Singer Christian F, Rappaport Christine, Geschwantler Kaulich Daphne, Pfeiler Georg, Tea Muy-Kheng, Berger Andreas, Phelan Catherine M, Greene Mark H, Mai Phuong L, Lejbkowicz Flavio, Andrulis Irene, Mulligan Anna Marie, Glendon Gord, Toland Amanda Ewart, Bojesen Anders, Pedersen Inge Sokilde, Sunde Lone, Thomassen Mads, Kruse Torben A, Jensen Uffe Birk, Friedman Eitan, Laitman Yael, Shimon Shani Paluch, Simard Jacques, Easton Douglas F, Offit Kenneth, Couch Fergus J, Chenevix-Trench Georgia, Antoniou Antonis C, Benitez Javi |
Polymorphisms in NEIL-2, APE-1, CYP2E1 and MDM2 Genes are Independent Predictors of Gastric Cancer Risk in a Northern Jiangsu Population (China). Journal of nanoscience and nanotechnology 2015 Jul 15 (7): 4815-28. Elingarami Sauli, Liu Hongna, Kalinjuma Aneth Vedastus, Hu Weiyue, Li Song, He Nongy |
[Characteristic of the Genetic Variability of Four Polymorphic Variants (rs2069705, rs17880053, rs11126176, and rs804271) in Representative Samples of Indigenous and Alien Populations of Siberia]. Genetika 2015 Aug 51 (8): 946-52. Kucher A N, Babushkina N P, Kulish E V, Makeeva O A, Bragina E Yu, Goncharova I A, Eremina E R, Puzyrev V |
Genetic Variation of BCL2 (rs2279115), NEIL2 (rs804270), LTA (rs909253), PSCA (rs2294008) and PLCE1 (rs3765524, rs10509670) Genes and Their Correlation to Gastric Cancer Risk Based on Universal Tagged Arrays and Fe3O4 Magnetic Nanoparticles. Journal of biomedical nanotechnology 2015 Nov 11 (11): 2057-66. Mou Xianbo, Li Taotao, Wang Jiuhai, Ali Zeeshan, Zhang Yuanying, Chen Zhu, Deng Yan, Li Song, Su Enben, Jia Qiongying, He Nongyue, Ni Jian, Cui Daxia |
Variants in FSHB Are Associated With Polycystic Ovary Syndrome and Luteinizing Hormone Level in Han Chinese Women. The Journal of clinical endocrinology and metabolism 2016 Mar jc20153776. Tian Ye, Zhao Han, Chen Haitao, Peng Yingqian, Cui Linlin, Du Yanzhi, Wang Zhao, Xu Jianfeng, Chen Zi-Jia |
Genomic landscape of DNA repair genes in cancer. Oncotarget 2016 Mar . Chae Young Kwang, Anker Jonathan F, Carneiro Benedito A, Chandra Sunandana, Kaplan Jason, Kalyan Aparna, Santa-Maria Cesar A, Platanias Leonidas C, Giles Francis |
Phenotype and Tissue Expression as a Function of Genetic Risk in Polycystic Ovary Syndrome. PloS one 2017 12 (1): e0168870. Pau Cindy T, Mosbruger Tim, Saxena Richa, Welt Corrine |
Polymorphisms of base-excision repair genes and the hepatocarcinogenesis. Gene 2018 Jun . Mattar Manar-Aleslam M, Zekri Abdel-Rahman N, Hussein Nehal, Morsy Heba, Esmat Gamal, Amin Magdy |
Comprehensive Profiling of DNA Repair Defects in Breast Cancer Identifies a Novel Class of Endocrine Therapy Resistance Drivers. Clinical cancer research : an official journal of the American Association for Cancer Research 2018 May . Anurag Meenakshi, Punturi Nindo, Hoog Jeremy, Bainbridge Matthew N, Ellis Matthew J, Haricharan Svas |
Genetic variation in the NEIL2 DNA glycosylase gene is associated with oxidative DNA damage in BRCA2 mutation carriers. Oncotarget 2017 Dec 8 (70): 114626-114636. Benítez-Buelga Carlos, Baquero Juan Miguel, Vaclova Tereza, Fernández Victoria, Martín Paloma, Inglada-Perez Lucia, Urioste Miguel, Osorio Ana, Benítez Javi |
A variant in a microRNA binding site in NEIL2 3'UTR confers susceptibility to age-related cataracts. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2019 Jun fj201802291R. Kang Lihua, Zou Xi, Zhang Guowei, Xiang Jing, Wang Yong, Yang Mei, Chen Xiang, Wu Jian, Guan Huaij |
Cervical carcinoma risk associate with genetic polymorphisms of NEIL2 gene in Chinese population and its significance as predictive biomarker. Scientific reports 2020 Mar 10 (1): 5136. Ye Feng, Liu Jia, Wang Hanzhi, Chen Xiaojing, Cheng Qi, Chen Huaize |
Genetic variations in 3'UTRs of SMUG1 and NEIL2 genes modulate breast cancer risk, survival and therapy response. Mutagenesis 2021 6 36 (4): 269-279. Cumova Andrea, Vymetalkova Veronika, Opattova Alena, Bouskova Veronika, Pardini Barbara, Kopeckova Katerina, Kozevnikovova Renata, Lickova Katerina, Ambrus Miloslav, Vodickova Ludmila, Naccarati Alessio, Soucek Pavel, Vodicka Pav |
aCGH Analysis Reveals Novel Mutations Associated with Congenital Diaphragmatic Hernia Plus (CDH+). Journal of clinical medicine 2023 10 12 (19): . Yannick Schreiner, Teresa Stoll, Oliver Nowak, Meike Weis, Svetlana Hetjens, Eric Steck, Alba Perez Ortiz, Neysan Raf |
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- Page last updated:Mar 25, 2024
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