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本文引用的文献

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In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration.通过CRISPR/Cas9介导的同源性非依赖靶向整合进行体内基因组编辑。
Nature. 2016 Dec 1;540(7631):144-149. doi: 10.1038/nature20565. Epub 2016 Nov 16.
2
Retinal regeneration mechanisms linked to multiple cancer molecules: A therapeutic conundrum.与多种癌症分子相关的视网膜再生机制:治疗难题。
Prog Retin Eye Res. 2017 Jan;56:19-31. doi: 10.1016/j.preteyeres.2016.08.003. Epub 2016 Aug 30.
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Neural activity promotes long-distance, target-specific regeneration of adult retinal axons.神经活动促进成年视网膜轴突的长距离、靶向特异性再生。
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EPIRETINAL MEMBRANE FORMATION AFTER INTRAVITREAL AUTOLOGOUS STEM CELL IMPLANTATION IN A RETINITIS PIGMENTOSA PATIENT.视网膜色素变性患者玻璃体内自体干细胞植入术后的视网膜前膜形成
Retin Cases Brief Rep. 2017;11(3):227-231. doi: 10.1097/ICB.0000000000000327.
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Visual Acuity after Retinal Gene Therapy for Choroideremia.视网膜基因治疗脉络膜视网膜萎缩后的视力
N Engl J Med. 2016 May 19;374(20):1996-8. doi: 10.1056/NEJMc1509501. Epub 2016 Apr 27.
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Report on the National Eye Institute Audacious Goals Initiative: Regenerating the Optic Nerve.美国国立眼科研究所大胆目标计划报告:视神经再生
Invest Ophthalmol Vis Sci. 2016 Mar;57(3):1271-5. doi: 10.1167/iovs.15-18500.
7
Efficacy and Safety of rAAV2-ND4 Treatment for Leber's Hereditary Optic Neuropathy.重组腺相关病毒2型- ND4治疗Leber遗传性视神经病变的疗效与安全性
Sci Rep. 2016 Feb 19;6:21587. doi: 10.1038/srep21587.
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Molecular Mechanisms Mediating Retinal Reactive Gliosis Following Bone Marrow Mesenchymal Stem Cell Transplantation.骨髓间充质干细胞移植后介导视网膜反应性胶质增生的分子机制
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N Engl J Med. 2015 May 14;372(20):1887-97. doi: 10.1056/NEJMoa1414221. Epub 2015 May 4.
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From mice to mind: Strategies and progress in translating neuroregeneration.从老鼠到大脑:神经再生转化的策略和进展。
Eur J Pharmacol. 2015 Jul 15;759:90-100. doi: 10.1016/j.ejphar.2015.03.041. Epub 2015 Mar 23.

保护视网膜神经节细胞。

Protecting retinal ganglion cells.

作者信息

Khatib T Z, Martin K R

机构信息

Department of Clinical Neurosciences, John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, UK.

Eye Department, Addenbrooke's Hospital, Cambridge, UK.

出版信息

Eye (Lond). 2017 Feb;31(2):218-224. doi: 10.1038/eye.2016.299. Epub 2017 Jan 13.

DOI:10.1038/eye.2016.299
PMID:28085136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5306473/
Abstract

Retinal ganglion cell degeneration underlies several conditions which give rise to significant visual compromise, including glaucoma, hereditary optic neuropathies, ischaemic optic neuropathies, and demyelinating disease. In this review, we discuss the emerging strategies for neuroprotection specifically in the context of glaucoma, including pharmacological neuroprotection, mesenchymal stem cells, and gene therapy approaches. We highlight potential pitfalls that need to be considered when developing these strategies and outline future directions, including the prospects for clinical trials.

摘要

视网膜神经节细胞变性是导致严重视力损害的多种病症的基础,这些病症包括青光眼、遗传性视神经病变、缺血性视神经病变和脱髓鞘疾病。在本综述中,我们将讨论特别是在青光眼背景下的新兴神经保护策略,包括药理学神经保护、间充质干细胞和基因治疗方法。我们强调在制定这些策略时需要考虑的潜在陷阱,并概述未来的方向,包括临床试验的前景。