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MicroRNAs as potential therapeutics for treating spinal cord injury 被引量:3
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作者 hualin yan Peiwei Hong +1 位作者 Mei Jiang Hedong Li 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第17期1352-1359,共8页
MicroRNAs are a class of recently discovered, small non-coding RNAs that have been shown to play essential roles in a vast majority of biological processes. Very little is known about the role of microRNAs during spin... MicroRNAs are a class of recently discovered, small non-coding RNAs that have been shown to play essential roles in a vast majority of biological processes. Very little is known about the role of microRNAs during spinal cord injury. This review summarizes the changes in expression levels of microRNAs after spinal cord injury. These aberrant changes suggest that microRNAs play an important role in inflammation, oxidative stress, apoptosis, glial scar formation and axonal regeneration. Given their small size and specificity of action, microRNAs could be potential therapeutics for treating spinal cord injury in the future. There are rapidly developing techniques for manipulating microRNA levels in animals; we review different chemical modification and delivery strategies. These may provide platforms for designing efficient microRNA delivery protocols for use in the clinic. 展开更多
关键词 MICRORNAS spinal cord injury reactive astrogliosis axonal regeneration antagomir anti-miR neural regeneration REVIEWS
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Non-cell-autonomous manner of AAV administration to attenuate cardiomyocyte hypertrophy by targeting paracrine signaling on ECM to reduce viral dosage
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作者 Lei Liu Peng Yue +7 位作者 Yue Zhang Yimin Hua Wenwei Bi hualin yan Hongyu Liao Jiawen Li Kaiyu Zhou Yifei Li 《Signal Transduction and Targeted Therapy》 SCIE CSCD 2022年第2期352-355,共4页
Dear Editor,Adeno-associated virus(AAV)is one of the most powerful vectors for exogenous gene delivery.1 However,the risks associated with the high dosages of AAV administration that are required to achieve meaningful... Dear Editor,Adeno-associated virus(AAV)is one of the most powerful vectors for exogenous gene delivery.1 However,the risks associated with the high dosages of AAV administration that are required to achieve meaningful effects limit the applicability of this method.Generally,AAV only presents cell autonomous manner in infected cells.Besides,mosaic genetic editing or gene therapy would trigger global biological function restore by above 30–40%infective ratio in heart diseases. 展开更多
关键词 DOSAGE AAV AUTONOMOUS
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