Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Syndrome and DNMT3B[original query] |
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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 |
DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome. Human reproduction (Oxford, England) 2012 Oct . Coppedè F, Bosco P, Tannorella P, Romano C, Antonucci I, Stuppia L, Romano C, Migliore L |
Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects. European journal of human genetics : EJHG 2013 Mar . Weemaes CM, van Tol MJ, Wang J, van Ostaijen-Ten Dam MM, van Eggermond MC, Thijssen PE, Aytekin C, Brunetti-Pierri N, van der Burg M, Graham Davies E, Ferster A, Furthner D, Gimelli G, Gennery A, Kloeckener-Gruissem B, Meyn S, Powell C, Reisli I, Schuetz C, Schulz A, Shugar A, van den Elsen PJ, van der Maarel SM |
Maternal risk for down syndrome and polymorphisms in the promoter region of the DNMT3B gene: a case-control study. Birth defects research. Part A, Clinical and molecular teratology 2015 Apr 103 (4): 299-305. Jaiswal Sushil Kumar, Sukla Krishna Kishore, Kumari Neha, Lakhotia Anjali Rani, Kumar Ashok, Rai Amit Kum |
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 |
DNA (cytosine-5)-methyltransferase 3B (DNMT 3B) polymorphism and risk of Down syndrome offspring. Saudi journal of biological sciences 2018 Jan 25 (1): 101-104. Moura Cláudia Melo de, Bastos Pedro Ribeiro, Ribeiro Julyana S V, Ribeiro Márcia Gonçalves, Amorim Márcia Rodrigues, Costa-Lima Marcelo Agui |
Germline Profiling and Molecular Characterization of Early Onset Metastatic Colorectal Cancer. Frontiers in oncology 2020 10 568911. Xu Ting, Zhang Yinjie, Zhang Jing, Qi Changsong, Liu Dan, Wang Zhenghang, Li Yanyan, Ji Congcong, Li Jian, Lin Xuan, Hou Ting, Liu Hao, Zhang Lu, Han-Zhang Han, Shen Lin, Wang Xiche |
Genetic aetiology of Down syndrome birth: novel variants of maternal DNMT3B and RFC1 genes increase risk of meiosis II nondisjunction in the oocyte. Molecular genetics and genomics : MGG 2022 11 298 (1): 293-313. Halder Pinku, Pal Upamanyu, Ganguly Agnish, Ghosh Papiya, Ray Anirban, Sarkar Sumantra, Ghosh Suj |
DNMT1 SNPs (rs2114724 and rs2228611) associated with positive symptoms in Chinese patients with schizophrenia. Annals of general psychiatry 2023 10 22 (1): 40. Junjiao Ping, Jing Wan, Caiying Huang, Jinming Yu, Jiali Luo, Zhiqiang Xing, Xingguang Luo, Baoguo Du, Tingyun Jiang, Jie Zha |
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