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Updated: Jul 6, 2025

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阅读器YTHDC2通过调节PPEF2和PDE6B的翻译来维持视觉功能和视网膜光受体的生存

Yeming Yang1, Xiaoyan Jiang1, Junyao Chen1

  • 1The Sichuan Provincial Key Laboratory for Human Disease Gene Study, Center for Medical Genetics, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan 610072, China.

Journal of genetics and genomics = Yi chuan xue bao
|December 29, 2023
PubMed
概括

YTHDC2蛋白对视力至关重要. 它在杆光受体中缺少,会通过影响关键基因翻译导致视网膜退化和视力受损,从而为遗传性视网膜变提供了新的见解.

关键词:
史诗转录组学 史诗转录组学遗传性视网膜变症 遗传性视网膜变症 遗传性视网膜变症N(6) -甲基氨酸 (m(6) A) 是一种摄影受体退化 摄影受体退化视网膜功能 视网膜功能这就是YTHDC2

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