Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and 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 |
| 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 |
| 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 |
| 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 |
| Whole exome sequencing analyses identified novel genes for Alzheimer's disease and related dementia. Alzheimer's & dementia : the journal of the Alzheimer's Association 2024 8 . Ya-Ru Zhang, Bang-Sheng Wu, Shi-Dong Chen, Liu Yang, Yue-Ting Deng, Yu Guo, Xin-Rui Wu, Wei-Shi Liu, Ju-Jiao Kang, Jian-Feng Feng, Wei Cheng, Jin-Tai |
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