Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: NEIL1[original query] |
---|
OGG1 expression and OGG1 Ser326Cys polymorphism and risk of lung cancer in a prospective study. Mutation research 2008 Mar 639 (1-2): 45-54. Hatt Lotte, Loft Steffen, Risom Lotte, Møller Peter, Sørensen Mette, Raaschou-Nielsen Ole, Overvad Kim, Tjønneland Anne, Vogel Ul |
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 |
Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma. Carcinogenesis 2009 Jul 30 (7): 1147-54. Forsbring Monika, Vik Erik S, Dalhus Bjørn, Karlsen Tom H, Bergquist Annika, Schrumpf Erik, Bjørås Magnar, Boberg Kirsten M, Alseth Ingr |
Three novel NEIL1 promoter polymorphisms in gastric cancer patients. World journal of gastrointestinal oncology 2010 Feb 2 (2): 2. Goto M, Shinmura K, Tao H, Tsugane S, Sugimura H |
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 |
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome. Kidney international 2011 Jun . Sanna-Cherchi S, Burgess KE, Nees SN, Caridi G, Weng PL, Dagnino M, Bodria M, Carrea A, Allegretta MA, Kim HR, Perry BJ, Gigante M, Clark LN, Kisselev S, Cusi D, Gesualdo L, Allegri L, Scolari F, D'Agati V, Shapiro LS, Pecoraro C, Palomero T, Ghiggeri GM, Gharavi AG |
Influence of the OGG1 Ser326Cys polymorphism on oxidatively damaged DNA and repair activity. Free radical biology & medicine 2012 Jan 52 (1): 118-25. Jensen Annie, Løhr Mille, Eriksen Louise, Grønbæk Morten, Dorry Elad, Loft Steffen, Møller Pet |
Prevalence of the DNA repair enzyme-NEIL1 gene mutation in patients with type 2 diabetes in the Turkish population. Journal of endocrinological investigation 2012 Apr 35 (4): 401-6. Salmanoglu M, Kucukardali Y, Kucukodaci Z, Fenercioglu A, Solmazgul E, Onem Y, Baloglu H, Ozata |
A NEIL1 single nucleotide polymorphism (rs4462560) predicts the risk of radiation-induced toxicities in esophageal cancer patients treated with definitive radiotherapy. Cancer 2013 Dec 119 (23): 4205-11. Chen Yun, Zhu Meiling, Zhang Zhen, Jiang Guoliang, Fu Xiaolong, Fan Min, Sun Menghong, Wei Qingyi, Zhao Kuai |
Polymorphism of the DNA base excision repair genes in keratoconus. International journal of molecular sciences 2014 15 (11): 19682-99. Wojcik Katarzyna A, Synowiec Ewelina, Sobierajczyk Katarzyna, Izdebska Justyna, Blasiak Janusz, Szaflik Jerzy, Szaflik Jacek |
Variation in DNA Base Excision Repair Genes in Fuchs Endothelial Corneal Dystrophy. Medical science monitor : international medical journal of experimental and clinical research 2015 21 2809-27. Wójcik Katarzyna A, Synowiec Ewelina, Polakowski Piotr, B?asiak Janusz, Szaflik Jerzy, Szaflik Jacek |
Association between single nucleotide polymorphisms of MUTYH, hOGG1 and NEIL1 genes, and depression. Journal of affective disorders 2015 Sep 184 90-6. Czarny Piotr, Kwiatkowski Dominik, Galecki Piotr, Talarowska Monika, Orzechowska Agata, Bobinska Kinga, Bielecka-Kowalska Anna, Szemraj Janusz, Maes Michael, Su Kuan-Pin, Sliwinski Toma |
Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease. Arthritis & rheumatology (Hoboken, N.J.) 2015 Dec . Ognenovski Mikhail, Renauer Paul, Gensterblum Elizabeth, Kötter Ina, Xenitidis Theodoros, Henes Jörg C, Casali Bruno, Salvarani Carlo, Direskeneli Haner, Kaufman Kenneth M, Sawalha Amr |
Genetic variants involved in oxidative stress, base excision repair, DNA methylation, and folate metabolism pathways influence myeloid neoplasias susceptibility and prognosis. Molecular carcinogenesis 2016 Mar . Gonçalves Ana Cristina, Alves Raquel, Baldeiras Inês, Cortesão Emília, Carda José Pedro, Branco Claudia C, Oliveiros Bárbara, Loureiro Luísa, Pereira Amélia, Nascimento Costa José Manuel, Sarmento-Ribeiro Ana Bela, Mota-Vieira Lui |
Association between Single-Nucleotide Polymorphisms of the hOGG1,NEIL1,APEX1, FEN1,LIG1, and LIG3 Genes and Alzheimer's Disease Risk. Neuropsychobiology 2016 73 (2): 98-107. Kwiatkowski Dominik, Czarny Piotr, Toma Monika, Korycinska Anna, Sowinska Katarzyna, Galecki Piotr, Bachurska Agnieszka, Bielecka-Kowalska Anna, Szemraj Janusz, Maes Michael, Sliwinski Toma |
Polymorphism of the XRCC1 Gene Is Associated with Susceptibility and Short-Term Recovery of Ischemic Stroke. International journal of environmental research and public health 2016 Oct 13 (10): . He Wei, Huang Peng, Liu Dinghua, Zhong Lingling, Yu Rongbin, Li Jian |
Defective repair capacity of variant proteins of the DNA glycosylase NTHL1 for 5-hydroxyuracil, an oxidation product of cytosine. Free radical biology & medicine 2018 12 131 264-273. Shinmura Kazuya, Kato Hisami, Kawanishi Yuichi, Goto Masanori, Tao Hong, Yoshimura Katsuhiro, Nakamura Satoki, Misawa Kiyoshi, Sugimura Haruhi |
Investigation of base excision repair gene variants in late-onset Alzheimer's disease. PloS one 2019 14 (8): e0221362. Ertuzun Tugce, Semerci Asli, Cakir Mehmet Emin, Ekmekcioglu Aysegul, Gok Mehmet Oguz, Soltys Daniela T, de Souza-Pinto Nadja C, Sezerman Ugur, Muftuoglu Melt |
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 |
Evaluation of the influence of chronic low-dose radiation on DNA repair gene polymorphisms [XRCC1, XRCC3, PRKDC (XRCC7), LIG1, NEIL1] in individuals from normal and high level natural radiation areas of Kerala Coast. International journal of radiation biology 2020 Mar 1-15. Saini Divyalakshmi, K R Sudheer, P R Vivek Kumar, Soren D C, Jain Vinay, Koya P K M, G Jaikrishan, Das Birajalax |
Genetic variations in DNA repair gene NEIL1 associated with radiation pneumonitis risk in lung cancer patients. Molecular genetics & genomic medicine 2021 Jun e1698. Zheng Yuming, Zheng Leizhen, Yu Jiahua, Jiang Mawei, Zhang Songfang, Cai Xuwei, Zhu Meili |
Deregulated DNA damage response network in Behcet's disease. Clinical immunology (Orlando, Fla.) 2022 11 246 109189. Vlachogiannis Nikolaos I, Ntouros Panagiotis A, Pappa Maria, Verrou Kleio-Maria, Arida Aikaterini, Souliotis Vassilis L, Sfikakis Petros |
Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents. Frontiers in oncology 2022 11 12 870863. Olkinuora Alisa Petriina, Mayordomo Andrea Constanza, Kauppinen Anni Katariina, Cerliani María Belén, Coraglio Mariana, Collia Ávila Karina, Gutiérrez Alejandro, Alvarez Karin, Cassana Alessandra, Lopéz-Köstner Francisco, Jauk Federico, García-Rivello Hernán, Ristimäki Ari, Koskenvuo Laura, Lepistö Anna, Nieminen Taina Tuulikki, Vaccaro Carlos Alberto, Pavicic Walter Hernán, Peltomäki Päi |
Single-Nucleotide Polymorphisms in Base-Excision Repair-Related Genes Involved in the Risk of an Occurrence of Non-Alcoholic Fatty Liver Disease. International journal of molecular sciences 2023 7 24 (14): . Sylwia Zió?kowska, Marcin Kosmalski, ?ukasz Ko?odziej, Aleksandra Jab?kowska, Janusz Zbigniew Szemraj, Tadeusz Pietras, Maciej Jab?kowski, Piotr Lech Czar |
Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases. Frontiers in oncology 2023 3 13 1111191. Alenezi Wejdan M, Fierheller Caitlin T, Serruya Corinne, Revil Timothée, Oros Kathleen K, Subramanian Deepak N, Bruce Jeffrey, Spiegelman Dan, Pugh Trevor, Campbell Ian G, Mes-Masson Anne-Marie, Provencher Diane, Foulkes William D, Haffaf Zaki El, Rouleau Guy, Bouchard Luigi, Greenwood Celia M T, Ragoussis Jiannis, Tonin Patricia |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: