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Bioinformatics analysis of the gene expression profile of retinal pigmental epithelial cells based in single-cell RNA sequencing in myopic mice

机译:基于单细胞RNA测序的近视小鼠单细胞RNA测序的视网膜色素上皮细胞基因表达谱的生物信息学

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摘要

Myopia is a very common eye condition that is rapidly increasing in occurrence. It is the most common eye disease in teenagers [1], and uncorrected ametropia is the main cause of moderate or severe visual impairment in people aged 50 years and above [2]. It is estimated that the number of patients with myopia will reach 4.758 billion by 2050, accounting for 49.8% of the global population [3]. The severity of a patient’s myopia is also associated with increased risk of visual impairment due to macular degeneration, cataracts, retinal detachment, and glaucoma caused by high myopia [4]. A decreased visual function in the early stage of myopia [5–7] has also been noted, but the molecular mechanism remains unclear. Due to the existence of a large number of genes that affect biological function, retinal pigmental epithelium (RPE) single-cell captured ribonucleic acid (RNA) sequencing technology was adopted to explore the molecular mechanism of RPE cell apoptosis in myopia and provide a theoretical basis for clinical guidance aimed at protecting early visual function in myopic patients.
机译:近视是一种非常常见的眼部条件,在发生的情况下迅速增加。它是青少年中最常见的眼病[1],未经校正的氛围是50岁及以上的人们中度或严重视力障碍的主要原因[2]。据估计,近视患者的数量将在2050年达到47.58亿,占全球人口的49.8%[3]。患者的近视的严重程度也与由于黄斑变性,白内障,视网膜脱离和由高近视引起的青光眼增加的视力障碍风险增加有关[4]。还注意到了近视早期的视力下降[5-7],但分子机制仍不清楚。由于存在大量影响生物学功能的基因,通过视网膜色素上皮(RPE)单细胞捕获的核糖核酸(RNA)测序技术探讨了近视中RPE细胞凋亡的分子机制,提供了理论基础旨在保护近视患者早期视觉功能的临床指导。

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