The emerging role of 5-hydroxymethylcytosine in neurodegenerative diseases
作者： Sahar Al-Mahdawi , Sara Anjomani Virmouni , Mark A. Pook
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摘要: Copyright © 2014 Al-Mahdawi, Anjomani Virmouni and Pook. This is an open-access article distributed under the terms of Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums permitted, provided original author(s) licensor are credited that publication this journal cited, accordance with accepted academic practice. No permitted which does not comply these terms.
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Mark A., DNA Methylation and Trinucleotide Repeat Expansion Diseases DNA Methylation - From Genomics to Technology. ,(2012) , 10.5772/34169
Yan Xiang Yang, Nicholas W. Wood, David S. Latchman, Molecular basis of Parkinson's disease. Neuroreport. ,vol. 20, pp. 150- 156 ,(2009) , 10.1097/WNR.0B013E32831C50DF
Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan, Charles Q. Tran, Uta Francke, Huda Y. Zoghbi, Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. ,vol. 23, pp. 185- 188 ,(1999) , 10.1038/13810
Marian Mellen, Pinar Ayata, Scott Dewell, Skirmantas Kriaucionis, Nathaniel Heintz, MeCP2 binds to 5hmc enriched within active genes and accessible chromatin in the nervous system Epigenetics & Chromatin. ,vol. 6, pp. 52- ,(2013) , 10.1186/1756-8935-6-S1-P52
Marta Kulis, Manel Esteller, DNA methylation and cancer. Advances in Genetics. ,vol. 70, pp. 27- 56 ,(2010) , 10.1016/B978-0-12-380866-0.60002-2
E.I. Rogaev, W.J. Lukiw, O. Lavrushina, E.A. Rogaeva, P.H. St. George-Hyslop, The upstream promoter of the beta-amyloid precursor protein gene (APP) shows differential patterns of methylation in human brain. Genomics. ,vol. 22, pp. 340- 347 ,(1994) , 10.1006/GENO.1994.1393
Ying Cheng, Alison Bernstein, Dahua Chen, Peng Jin, 5-Hydroxymethylcytosine: A new player in brain disorders? Experimental Neurology. ,vol. 268, pp. 3- 9 ,(2015) , 10.1016/J.EXPNEUROL.2014.05.008
Marguerite V. Evans-Galea, Anthony J. Hannan, Nissa Carrodus, Martin B. Delatycki, Richard Saffery, Epigenetic modifications in trinucleotide repeat diseases Trends in Molecular Medicine. ,vol. 19, pp. 655- 663 ,(2013) , 10.1016/J.MOLMED.2013.07.007
Shinpei Yamaguchi, Li Shen, Yuting Liu, Damian Sendler, Yi Zhang, Role of Tet1 in erasure of genomic imprinting Nature. ,vol. 504, pp. 460- 464 ,(2013) , 10.1038/NATURE12805
J S Rao, V L Keleshian, S Klein, S I Rapoport, Epigenetic modifications in frontal cortex from Alzheimer's disease and bipolar disorder patients Translational Psychiatry. ,vol. 2, ,(2012) , 10.1038/TP.2012.55