Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: DNMT3L[original query] |
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No evidence for mutations of CTCFL/BORIS in Silver-Russell syndrome patients with IGF2/H19 imprinting control region 1 hypomethylation. PloS one 2009 4 (8): e6631. Bernier-Latmani Jeremiah, Baumer Alessandra, Shaw Phill |
A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation. Human molecular genetics 2009 May 18 (10): 1755-68. El-Maarri Osman, Kareta Michael S, Mikeska Thomas, Becker Tim, Diaz-Lacava Amalia, Junen Judith, Nüsgen Nicole, Behne Frank, Wienker Thomas, Waha Andreas, Oldenburg Johannes, Chédin Frédér |
Human intelligence and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking. PloS one 2010 5 (6): e11329. Haggarty Paul, Hoad Gwen, Harris Sarah E, Starr John M, Fox Helen C, Deary Ian J, Whalley Lawrence |
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 |
Risk-association of DNA methyltransferases polymorphisms with gastric cancer in the Southern Chinese population. International journal of molecular sciences 2012 13 (7): 7. Yang XX, He XQ, Li FX, Wu YS, Gao Y, Li M |
Genetic polymorphisms of DNMT3L involved in hypermethylation of chromosomal ends are associated with greater risk of developing ovarian endometriosis. The American journal of pathology 2012 May 180 (5): 1781-6. Borghese Bruno, Santulli Pietro, Héquet Delphine, Pierre Guillaume, de Ziegler Dominique, Vaiman Daniel, Chapron Charl |
Association of DNMT1 and DNMT3B polymorphisms with breast cancer risk in Han Chinese women from South China. Genetics and molecular research : GMR 2012 Sep 11 (AOP): AOP. Sun MY, Yang XX, Xu WW, Yao GY, Pan HZ, Li M |
DNA methyltransferase candidate polymorphisms, imprinting methylation, and birth outcome. PloS one 2013 8 (7): e68896. Haggarty Paul, Hoad Gwen, Horgan Graham W, Campbell Doris |
A genetic association study detects haplotypes associated with obstructive heart defects. Human genetics 2014 Sep 133 (9): 1127-38. Li Ming, Cleves Mario A, Mallick Himel, Erickson Stephen W, Tang Xinyu, Nick Todd G, Macleod Stewart L, Hobbs Charlotte A, |
DNA methyl transferase (DNMT) gene polymorphisms could be a primary event in epigenetic susceptibility to schizophrenia. PloS one 2014 9 (5): e98182. Saradalekshmi Koramannil Radha, Neetha Nanoth Vellichiramal, Sathyan Sanish, Nair Indu V, Nair Chandrasekharan M, Banerjee Moin |
Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia. Genetics and molecular research : GMR 2015 14 (4): 16041-9. Dong Y, Pan Y, Wang R, Zhang Z, Xi Q, Liu R |
Idiopathic male infertility and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking. Scientific reports 2017 Sep 7 (1): 11219. Tang Qiuqin, Chen Yiqiu, Wu Wei, Ding Hongjuan, Xia Yankai, Chen Daozhen, Wang Xin |
Polymorphisms in DNA methylation-related genes are linked to the phenotype of Machado-Joseph disease. Neurobiology of aging 2018 12 75 225.e1-225.e8. Ding Dongxue, Wang Chunrong, Chen Zhao, Peng Huirong, Li Kai, Zhou Xin, Peng Yun, Wang Puzhi, Hou Xiaocan, Li Tianjiao, Qiu Rong, Xia Kun, Sequeiros Jorge, Ashizawa Tetsuo, Tang Beisha, Jiang Ho |
Interaction of nutrition and genetics via DNMT3L-mediated DNA methylation determines cognitive decline. Neurobiology of aging 2019 Feb 78 64-73. Flitton Miles, Rielly Nicholas, Warman Rhian, Warden Donald, Smith A David, Macdonald Ian A, Knight Helen Miran |
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 |
DNMT3B rs1569686 and rs2424913 gene polymorphisms are associated with positive family history of preterm birth and smoking status. Croatian medical journal 2020 Feb 61 (1): 8-17. Bariši? Anita, Kolak Maja, Peterlin Ana, Tul Nataša, Gašparovi? Krpina Milena, Ostoji? Saša, Peterlin Borut, Pereza Ni |
A genome-wide association study on frequent exacerbation of asthma depending on smoking status. Respiratory medicine 2022 5 199 106877. Son Ji-Hye, Park Jong-Sook, Lee Jong-Uk, Kim Min Kyung, Min Sun-Ah, Park Choon-Sik, Chang Hun S |
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- Page last updated:Apr 22, 2024
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