Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 30 Records) |
| Query Trace: Disease and DNMT1[original query] |
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| Association analyses of DNA methyltransferase-1 (DNMT1) polymorphisms with systemic lupus erythematosus. Journal of human genetics 2004 49 (11): 642-6. Park Byung Lae, Kim Lyoung Hyo, Shin Hyoung Doo, Park Yong Wook, Uhm Wan Sik, Bae Sang-Che |
| Investigating the potential role of genetic and epigenetic variation of DNA methyltransferase genes in hyperplastic polyposis syndrome. PloS one 2011 6 (2): e16831. Drini Musa, Wong Nicholas C, Scott Hamish S, Craig Jeffrey M, Dobrovic Alexander, Hewitt Chelsee A, Dow Christofer, Young Joanne P, Jenkins Mark A, Saffery Richard, Macrae Finlay |
| A population-specific uncommon variant in GRIN3A associated with schizophrenia. Biological psychiatry 2012 Dec . Takata A, Iwayama Y, Fukuo Y, Ikeda M, Okochi T, Maekawa M, Toyota T, Yamada K, Hattori E, Ohnishi T, Toyoshima M, Ujike H, Inada T, Kunugi H, Ozaki N, Nanko S, Nakamura K, Mori N, Kanba S, Iwata N, Kato T, Yoshikawa T |
| Association of polymorphisms in DNMT1, DNMT3A, DNMT3B, MTHFR and MTRR genes with global DNA methylation levels and prognosis of autoimmune thyroid disease. Clinical and experimental immunology 2012 Nov 170 (2): 2. Arakawa Y, Watanabe M, Inoue N, Sarumaru M, Hidaka Y, Iwatani Y |
| DNMT3B (C46359T) polymorphisms and immunoexpression of DNMT3b and DNMT1 proteins in oral lichen planus. Pathobiology : journal of immunopathology, molecular and cellular biology 2012 79 (1): 18-23. Fonseca-Silva Thiago, Oliveira Marcos Vinícius Macedo de, Fraga Carlos Alberto de Carvalho, Farias Lucyana Conceição, Gomes Erika Patrícia Pereira, Barros Lucas Oliveira, Roy Ashbeel, Santiago Gomez Ricardo, Paula Alfredo Maurício Batista De, Guimarães André Luiz Se |
| DNA methyltransferase haplotype is associated with Alzheimer's disease. Neuroscience letters 2014 Sep 579 70-4. Pezzi Julio Carlos, Ens Cintia Monique Boschmann, Borba Ericksen Mielle, Schumacher-Schuh Artur F, de Andrade Fabiana Michelsen, Chaves Marcia Lorena Fagundes, Fiegenbaum Marilu, Camozzato Ana Lui |
| Global changes in DNA methylation in Alzheimer's disease peripheral blood mononuclear cells. Brain, behavior, and immunity 2015 Mar 45 139-44. Di Francesco Andrea, Arosio Beatrice, Falconi Anastasia, Micioni Di Bonaventura Maria Vittoria, Karimi Mohsen, Mari Daniela, Casati Martina, Maccarrone Mauro, D'Addario Claud |
| Risk-Association of DNMT1 Gene Polymorphisms with Coronary Artery Disease in Chinese Han Population. International journal of molecular sciences 2014 15 (12): 22694-22705. Peng Chunyan, Deng Qianyun, Li Zuhua, Xiong Chenling, Li Cong, Zheng Fa |
| Methylation analysis of multiple genes in blood DNA of Alzheimer's disease and healthy individuals. Neuroscience letters 2015 Jul 600 143-7. Tannorella Pierpaola, Stoccoro Andrea, Tognoni Gloria, Petrozzi Lucia, Salluzzo Maria Grazia, Ragalmuto Alda, Siciliano Gabriele, Haslberger Alexander, Bosco Paolo, Bonuccelli Ubaldo, Migliore Lucia, Coppedè Fab |
| EIF3G is associated with narcolepsy across ethnicities. European journal of human genetics : EJHG 2015 Feb . Holm Anja, Lin Ling, Faraco Juliette, Mostafavi Sara, Battle Alexis, Zhu Xiaowei, Levinson Douglas F, Han Fang, Gammeltoft Steen, Jennum Poul, Mignot Emmanuel, Kornum Birgitte |
| Association of DNMT1 Gene Polymorphisms with Congenital Heart Disease in Child Patients. Pediatric cardiology 2015 Jun 36 (5): 906-11. Wang FengYu, Zhou ShiYuan, Wang YanLi, Wang LiNa, Zhou JiPing, Wang HaiLi, Li CongMin, Chang MingX |
| Associations of ChREBP and Global DNA Methylation with Genetic and Environmental Factors in Chinese Healthy Adults. PloS one 2016 11 (6): e0157128. Gao Jiajia, Qiu Xueping, Wang Xuebin, Peng Chunyan, Zheng Fa |
| Gene-gene and gene-sex epistatic interactions of DNMT1, DNMT3A and DNMT3B in autoimmune thyroid disease. Endocrine journal 2016 May . Cai Tian-Tian, Zhang Jian, Wang Xuan, Song Rong-Hua, Qin Qiu, Muhali Fatuma-Said, Zhou Jiao-Zhen, Xu Jian, Zhang Jin- |
| Prenatal Air Pollution Exposures, DNA Methyl Transferase Genotypes, and Associations with Newborn LINE1 and Alu Methylation and Childhood Blood Pressure and Carotid Intima-Media Thickness in the Children's Health Study. Environmental health perspectives 2016 May . Breton Carrie V, Yao Jin, Millstein Josh, Gao Lu, Siegmund Kimberly D, Mack Wendy, Whitfield-Maxwell Lora, Lurmann Fred, Hodis Howard, Avol Ed, Gilliland Frank |
| Association of DNA methyltransferase polymorphisms with susceptibility to primary gouty arthritis. Biomedical reports 2016 Oct 5 (4): 467-472. Zhong Xiaowu, Peng Yuanhong, Yao Chengjiao, Qing Yufeng, Yang Qibin, Guo Xiaolan, Xie Wenguang, Zhao Mingcai, Cai Xiaoming, Zhou Jing-G |
| Studying the Association between Sudden Hearing Loss and DNA N-Methyltransferase 1 (DNMT1) Genetic Polymorphism. The journal of international advanced otology 2017 Apr . ?eker Y?ld?z Kübra, Durmu? Kas?m, Dönmez Gonca, Arslan Serdal, Altunta? Emine El |
| RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia. Nature communications 2017 12 8 (1): 2126. Lipka Daniel B, Witte Tania, Toth Reka, Yang Jing, Wiesenfarth Manuel, Nöllke Peter, Fischer Alexandra, Brocks David, Gu Zuguang, Park Jeongbin, Strahm Brigitte, Wlodarski Marcin, Yoshimi Ayami, Claus Rainer, Lübbert Michael, Busch Hauke, Boerries Melanie, Hartmann Mark, Schönung Maximilian, Kilik Umut, Langstein Jens, Wierzbinska Justyna A, Pabst Caroline, Garg Swati, Catalá Albert, De Moerloose Barbara, Dworzak Michael, Hasle Henrik, Locatelli Franco, Masetti Riccardo, Schmugge Markus, Smith Owen, Stary Jan, Ussowicz Marek, van den Heuvel-Eibrink Marry M, Assenov Yassen, Schlesner Matthias, Niemeyer Charlotte, Flotho Christian, Plass Christo |
| Association between DNA methyltransferase gene polymorphism and Parkinson's disease. Neuroscience letters 2016 Dec 639 146-150. Pezzi Julio Carlos, de Bem Cintia Monique Boschmann Ens, da Rocha Tatiane Jacobsen, Schumacher-Schuh Artur F, Chaves Marcia Lorena Fagundes, Rieder Carlos Roberto, Hutz Mara H, Fiegenbaum Marilu, Camozzato Ana Lui |
| Loss of Chromatin-Remodeling Proteins and/or CDKN2A Associates With Metastasis of Pancreatic Neuroendocrine Tumors and Reduced Patient Survival Times. Gastroenterology 2018 2 154 (8): 2060-2063.e8. Roy Somak, LaFramboise William A, Liu Ta-Chiang, Cao Dengfeng, Luvison Alyssa, Miller Caitlyn, Lyons Maureen A, O'Sullivan Roderick J, Zureikat Amer H, Hogg Melissa E, Tsung Allan, Lee Kenneth K, Bahary Nathan, Brand Randall E, Chennat Jennifer S, Fasanella Kenneth E, McGrath Kevin, Nikiforova Marina N, Papachristou Georgios I, Slivka Adam, Zeh Herbert J, Singhi Aatur |
| Genetic variants in DNMT1 and the risk of cardiac autonomic neuropathy in women with type 1 diabetes. Journal of diabetes investigation 2019 Jul 10 (4): 985-989. Santos-Bezerra Daniele Pereira, Admoni Sharon Nina, Mori Rosana Cristina, Pelaes Tatiana Souza, Perez Ricardo Vesoni, Machado Cleide Guimarães, Monteiro Maria Beatriz, Parisi Maria Candida, Pavin Elizabeth Joao, Queiroz Marcia Silva, Passarelli Marisa, Machado Ubiratan Fabres, Correa-Giannella Maria Luc |
| DNMT1 and DNMT3B genetic polymorphisms affect the clinical course and outcome of melanoma patients. Melanoma research 2019 Apr . Maric Helena, Supic Gordana, Kandolf-Sekulovic Lidija, Maric Veljko, Mijuskovic Zeljko, Radevic Tatjana, Rajovic Milica, Magic Zvon |
| Genetic association of DNMT variants can play a critical role in defining the methylation patterns in autism. IUBMB life 2019 Feb . Alex Ann Mary, Saradalekshmi Korammannil R, Shilen Neena, Suresh Poovathinal A, Banerjee Moin |
| Polymorphisms of genes required for methionine synthesis and DNA methylation influence mitochondrial DNA methylation. Epigenomics 2020 5 12 (12): 1003-1012. Stoccoro Andrea, Tannorella Pierpaola, Migliore Lucia, Coppedè Fab |
| Inflammatory Pathways Are Impaired in Alzheimer Disease and Differentially Associated With Apolipoprotein E Status. Journal of neuropathology and experimental neurology 2021 9 80 (10): 922-932. Kloske Courtney M, Dugan Adam J, Weekman Erica M, Winder Zachary, Patel Ela, Nelson Peter T, Fardo David W, Wilcock Donna |
| Analysis of Relationships between Immune Checkpoint and Methylase Gene Polymorphisms and Outcomes after Unrelated Bone Marrow Transplantation. Cancers 2021 Jun 13 (11): . Takahashi Hidekazu, Okayama Naoko, Yamaguchi Natsu, Nomura Moe, Miyahara Yuta, Mahbub M H, Hase Ryosuke, Morishima Yasuo, Suehiro Yutaka, Yamasaki Takahiro, Tamada Koji, Takahashi Satoshi, Tojo Arinobu, Tanabe Tsuyos |
| DNMT1 and DNMT3B gene variants and their association with endometriosis in South Indian women. Molecular biology reports 2021 Oct . Veena K V, Siddamalla Swapna, Deenadayal Mamata, Shivaji Sisinthy, Bhanoori Manju |
| Association of the DNA Methyltransferase and Folate Cycle Enzymes' Gene Polymorphisms with Coronary Restenosis. Life (Basel, Switzerland) 2022 Feb 12 (2): . Timizheva Kalima B, Ahmed Abdulbary A M, Ait Aissa Amira, Aghajanyan Anna V, Tskhovrebova Leyla V, Azova Madina |
| Role of clusterin gene 3'-UTR polymorphisms and promoter hypomethylation in the pathogenesis of pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Biochimica et biophysica acta. Gene regulatory mechanisms 2023 8 1866 (4): 194980. Ramani Shyam Kapuganti, Lipsa Sahoo, Pranjya Paramita Mohanty, Bushra Hayat, Sucheta Parija, Debasmita Pankaj Alo |
| Gene-wide significant association analyses of DNMT1 genetic variants with Parkinson's disease. Frontiers in genetics 2023 3 14 1112388. Wang Jian-Yong, Cui Lei, Shi Hong-Yi, Chen Ling-Hao, Jin Ren-Wei, Jiang Xiao-Xia, Chen Zhu-Ling, Zhu Jian-Hong, Zhang Xio |
Ultra-low-coverage genome-wide association study-insights into gestational age using 17,844 embryo samples with preimplantation genetic testing.
Genome medicine 2023 2 15 (1): 10. Li Shumin, Yan Bin, Li Thomas K T, Lu Jianliang, Gu Yifan, Tan Yueqiu, Gong Fei, Lam Tak-Wah, Xie Pingyuan, Wang Yuexuan, Lin Ge, Luo Ruiba |
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