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本文引用的文献

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Repression of Astrocytic Connexins in Cortical and Subcortical Brain Regions and Prefrontal Enrichment of H3K9me3 in Depression and Suicide.抑郁和自杀中皮质及皮质下脑区星形胶质细胞连接蛋白的抑制及前额叶H3K9me3的富集
Int J Neuropsychopharmacol. 2017 Jan 1;20(1):50-57. doi: 10.1093/ijnp/pyw071.
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Targets of polyamine dysregulation in major depression and suicide: Activity-dependent feedback, excitability, and neurotransmission.重度抑郁症和自杀中多胺失调的靶点:活动依赖性反馈、兴奋性和神经传递。
Neurosci Biobehav Rev. 2016 Jul;66:80-91. doi: 10.1016/j.neubiorev.2016.04.010. Epub 2016 Apr 22.
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KETAMINE: A POTENTIAL RAPID-ACTING ANTISUICIDAL AGENT?氯胺酮:一种潜在的速效抗自杀药物?
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EPIGENETIC VARIATION AT SKA2 PREDICTS SUICIDE PHENOTYPES AND INTERNALIZING PSYCHOPATHOLOGY.SKA2基因的表观遗传变异可预测自杀表型和内化性精神病理学。
Depress Anxiety. 2016 Apr;33(4):308-15. doi: 10.1002/da.22480.
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Long noncoding RNAs in psychiatric disorders.精神疾病中的长链非编码RNA
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Long Non-coding RNA in Neurons: New Players in Early Response to BDNF Stimulation.神经元中的长链非编码RNA:BDNF刺激早期反应中的新角色
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microRNAs as Biomarker in Depression Pathogenesis.微小RNA作为抑郁症发病机制中的生物标志物
Ann Psychiatry Ment Health. 2013;1(1):1003. Epub 2013 Dec 2.
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Depression as a Glial-Based Synaptic Dysfunction.抑郁症作为一种基于胶质细胞的突触功能障碍。
Front Cell Neurosci. 2016 Jan 22;9:521. doi: 10.3389/fncel.2015.00521. eCollection 2015.
9
Interaction between Methylation and CpG Single-Nucleotide Polymorphisms in the HTR2A Gene: Association Analysis with Suicide Attempt in Schizophrenia.5-羟色胺2A受体基因甲基化与CpG单核苷酸多态性的相互作用:与精神分裂症自杀未遂的关联分析
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10
Role of Glia in Stress-Induced Enhancement and Impairment of Memory.神经胶质细胞在应激诱导的记忆增强和损害中的作用。
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理解自杀神经生物学的表观遗传结构:批判性视角。

Understanding epigenetic architecture of suicide neurobiology: A critical perspective.

作者信息

Roy Bhaskar, Dwivedi Yogesh

机构信息

Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Neurosci Biobehav Rev. 2017 Jan;72:10-27. doi: 10.1016/j.neubiorev.2016.10.031. Epub 2016 Nov 9.

DOI:10.1016/j.neubiorev.2016.10.031
PMID:27836463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5183548/
Abstract

Current understanding of environmental cross-talk with genetic makeup is found to be mediated through an epigenetic interface which is associated with prominent reversible and heritable changes at gene expression level. Recent emergence of epigenetic modulation in shaping the genetic information has become a key regulatory factor in answering the underlying complexities associated with several mental disorders. A comprehensive understanding of the pertinent changes in the epigenetic makeup of suicide phenotype exhibits a characteristic signature with the possibility of using it as a biomarker to help predict the risk factors associated with suicide. Within the scope of this current review, the most sought after epigenetic changes of DNA methylation and histone modification are thoroughly scrutinized to understand their close functional association with the broad spectrum of suicide phenotype.

摘要

目前发现,对环境与基因组成相互作用的理解是通过一个表观遗传界面介导的,该界面与基因表达水平上显著的可逆和可遗传变化相关。表观遗传调控在塑造遗传信息方面的最新出现,已成为回答与几种精神障碍相关的潜在复杂性问题的关键调节因素。对自杀表型表观遗传组成相关变化的全面理解展现出一种特征性标志,有可能将其用作生物标志物来帮助预测与自杀相关的风险因素。在本综述范围内,对最受关注的DNA甲基化和组蛋白修饰的表观遗传变化进行了深入研究,以了解它们与广泛的自杀表型的密切功能关联。