The epigenetic regulation of synaptic genes contributes to the etiology of autism
Author:
Affiliation:
1. Institute of Experimental Endocrinology, Biomedical Research Center , Slovak Academy of Sciences , Dubravska cesta 9, 845 05 Bratislava , Slovakia
2. Institute of Physiology, Faculty of Medicine , Comenius University , Bratislava , Slovakia
Abstract
Publisher
Walter de Gruyter GmbH
Subject
General Neuroscience
Link
https://www.degruyter.com/document/doi/10.1515/revneuro-2021-0014/pdf
Reference109 articles.
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2. Alex, A.M., Saradalekshmi, K.R., Shilen, N., Suresh, P.A., and Banerjee, M. (2019). Genetic association of DNMT variants can play a critical role in defining the methylation patterns in autism. IUBMB Life 71: 901–907, https://doi.org/10.1002/iub.2021.
3. Andari, E., Nishitani, S., Kaundinya, G., Caceres, G.A., Morrier, M.J., Ousley, O., Smith, A.K., Cubells, J.F., and Young, L.J. (2020). Epigenetic modification of the oxytocin receptor gene: implications for autism symptom severity and brain functional connectivity. Neuropsychopharmacology 45: 1150–1158, https://doi.org/10.1038/s41386-020-0610-6.
4. Bakos, J., Bacova, Z., Grant, S.G., Castejon, A.M., and Ostatnikova, D. (2015). Are molecules involved in neuritogenesis and axon guidance related to autism pathogenesis? Neuromol. Med. 17: 297–304, https://doi.org/10.1007/s12017-015-8357-7.
5. Barnett Burns, S., Almeida, D., and Turecki, G. (2018). The epigenetics of early life adversity: current limitations and possible solutions. Prog. Mol. Biol. Transl. Sci. 157: 343–425, https://doi.org/10.1016/bs.pmbts.2018.01.008.
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