Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ruxu Sun"'
Autor:
Ruxu Sun1, Hongjing Zhu1, Ying Wang1, Jianan Wang1, Chao Jiang1, Qiuchen Cao1, Yeran Zhang1, Yichen Zhang1, Songtao Yuan1 yuansongtao@vip.sina.com, Qinghuai Liu1 liuqh@njmu.edu.cn
Publikováno v:
Journal of Biomedical Research. Sep2023, Vol. 37 Issue 5, p367-381. 15p.
Publikováno v:
Mol Ther
Age-related macular degeneration (AMD) is a universal leading cause for irreversible blindness in the elderly population. Dedifferentiation of retinal pigment epithelium (RPE) cells initiates early pathological events in atrophic AMD. Herein, we aim
Publikováno v:
Molecular Therapy. Nucleic Acids
Increasing evidence has indicated that long non-coding RNAs (lncRNAs) play significant roles in various diseases; however, their roles in age-related macular degeneration (AMD) remain unclear. Dedifferentiation and dysfunction of retinal pigment epit
Autor:
Xue Chen, Ping Xie, Chao Jiang, Qinghuai Liu, Biao Yan, Chen Zhao, Xiantao Sun, Guohua Liu, Meidong Zhu, Sijia Ding, Ruxu Sun
Publikováno v:
Cell Death and Disease, Vol 9, Iss 5, Pp 1-14 (2018)
Cell Death & Disease
Cell Death & Disease
Dedifferentiation of retinal pigment epithelium (RPE) cells and choroidal neovascularization (CNV) contributes to the pathogenesis of age-related macular degeneration (AMD). MicroRNAs (miRNAs) have crucial roles in AMD onset and progression. We thus
Autor:
Qinghuai Liu, Luyin Zhou, Xue Chen, Min Wang, Biao Yan, Ruxu Sun, Mingkang Chen, Hong Sun, Chen Zhao, Chao Jiang, Min Xu, Ping Xie, Daidi Yang
Publikováno v:
Experimental eye research. 180
Retinitis pigmentosa (RP), the most common form of inherited retinal dystrophies, exhibits significant genetic heterogeneity. The crumbs homolog 2 (CRB2) protein, together with CRB1 and CRB3, belongs to the Crumbs family. Given that CRB1 mutations ac