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Updated: Jun 5, 2025

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对基因编辑和肌痛性侧面硬化症 (从2004年到2024年) 的文献分析分析

Hejia Wan^1,2, Wenli Qian^1,3, Bingqi Wei^1,4

¹School of Medicine, Henan University of Chinese Medicine, Zhengzhou, China.

Frontiers in neuroscience

|December 11, 2024

概括

对肌缩侧面硬化症 (ALS) 的基因编辑研究显示出稳定的趋势,重点关注免疫和炎症机制. 像RNA编辑这样的新兴领域提供了新的治疗途径.

科学领域:

基因编辑用于肌缩侧面硬化症 (ALS) 的图书统计分析.

背景情况:

基因编辑技术正在探索潜在的ALS治疗方法.
了解研究环境对于推进治疗策略至关重要.

研究的目的:

全面审查ALS的基因编辑研究.
确定ALS基因编辑的当前趋势和未来方向.

主要方法:

在Web of Science,PubMed和Scopus上进行系统的文献搜索.
使用R,CiteSpace和VOSviewer进行文献计量分析.
空间时间分布,作者,主题和关键词的分析.

主要成果:

对于ALS的基因编辑领域在过去十年中稳定了下来.
目前的研究重点是炎症和免疫机制,相关疾病和细胞因子.
确定了潜在的研究合作者和关键主题领域.

结论:

RNA编辑,反意义寡核酸和甘氨酸受体是最先进的主题.
该领域正在迅速发展,为ALS的科学研究和临床应用提供了新的想法.

关键词:

在CiteSpace中使用CiteSpace.在VOSviewer中使用VOSviewer.骨髓缩侧面硬化症 (ALS) 是一种圣经计量学研究研究基因编辑技术基因编辑技术

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