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The FEBS Journal|April 26, 2023
Deletion of Emc1 in photoreceptor cells causes retinal degeneration in miceXiao Li, Zhilin Jiang, Yujing Su, et al.
Genetic Testing and Molecular Biomarkers|October 15, 2020
Identification of Novel EYS Mutations by Targeted Sequencing AnalysisWanli Tian, Xiao Li, Ya Li, et al.
Science China. Life Sciences|March 9, 2026
WTAP mediated m6A methylation modulates retinal photoreceptor function via facilitating of REEP6, PDE6B and RDH12 translationKuanxiang Sun, Lin Zhang, Wenjing Liu, et al.
Cell Proliferation|October 8, 2024
Deletion of Transmembrane protein 184b leads to retina degeneration in miceGuo Liu, Tiannan Liu, Junkai Tan, et al.
Frontiers in Cell and Developmental Biology|February 4, 2022
Deletion of Asrgl1 Leads to Photoreceptor Degeneration in MiceYu Zhou, Wanli Tian, Xiaoyan Jiang, et al.
Cell Death & Disease|September 7, 2018
Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cellsYeming Yang, Kuanxiang Sun, Wenjing Liu, et al.
Human Molecular Genetics|May 5, 2018
A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosaYu Zhou, Shujin Li, Lulin Huang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 22, 2022
Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinomaYeming Yang, Jingshu Cai, Xue Yang, et al.
Cell Death & Disease|October 30, 2021
A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axisYeming Yang, Xiao Li, Jieping Wang, et al.
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