色素性视网膜炎
诱导多能干细胞
干细胞
黄斑变性
视网膜变性
遗传增强
移植
视网膜
人类视网膜的基因治疗
干细胞疗法
医学
神经科学
生物
生物信息学
眼科
基因
遗传学
胚胎干细胞
外科
作者
Akiko Maeda,Michiko Mandai,Masayo Takahashi
出处
期刊:Annual Review of Genomics and Human Genetics
[Annual Reviews]
日期:2019-08-31
卷期号:20 (1): 201-216
被引量:32
标识
DOI:10.1146/annurev-genom-083118-015043
摘要
Given the importance of visual information to many daily activities, retinal degenerative diseases—which include both inherited conditions (such as retinitis pigmentosa) and acquired conditions (such as age-related macular degeneration)—can have a dramatic impact on human lives. The therapeutic options for these diseases remain limited. Since the discovery of the first causal gene for retinitis pigmentosa almost three decades ago, more than 250 genes have been identified, and gene therapies have been rapidly developed. Simultaneously, stem cell technologies such as induced pluripotent stem cell–based transplantation have advanced and have been applied to the treatment of retinal degenerative diseases. Here, we review recent progress in these expanding fields and discuss the potential for precision medicine in ophthalmic care.
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