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Neural Regeneration Research|January 12, 2019
Rescue axonal defects by targeting mitochondrial dynamics in hereditary spastic paraplegiasYongchao Mou, Xue-Jun LiGene Therapy|June 28, 2019
AAV9 Vector: a Novel modality in gene therapy for spinal muscular atrophyRithu Pattali, Yongchao Mou, Xue-Jun LiMethods in Molecular Biology (Clifton, N.J.)|March 27, 2021
Monitoring Axonal Degeneration in Human Pluripotent Stem Cell Models of Hereditary Spastic ParaplegiasXue-Jun Li, Yongchao Mou, Conrad Milton, et al.Journal of Visualized Experiments : Jove|February 25, 2020
Analyzing Mitochondrial Transport and Morphology in Human Induced Pluripotent Stem Cell-Derived Neurons in Hereditary Spastic ParaplegiaYongchao Mou, Sukhada Mukte, Eric Chai, et al.Frontiers in Molecular Neuroscience|October 4, 2021
MFN2 Deficiency Impairs Mitochondrial Transport and Downregulates Motor Protein Expression in Human Spinal Motor NeuronsYongchao Mou, Joshua Dein, Zhenyu Chen, et al.Neurobiology of Disease|September 14, 2023
Liver-X-receptor agonists rescue axonal degeneration in SPG11-deficient neurons via regulating cholesterol traffickingEric Chai, Zhenyu Chen, Yongchao Mou, et al.Brain : a Journal of Neurology|January 13, 2022
Inhibiting mitochondrial fission rescues degeneration in hereditary spastic paraplegia neuronsZhenyu Chen, Eric Chai, Yongchao Mou, et al.Human Molecular Genetics|May 5, 2018
Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegiasKyle Denton, Yongchao Mou, Chong-Chong Xu, et al.Journal of Biomedical Materials Research. Part B, Applied Biomaterials|November 28, 2016
Effects of different doses of 2,3-dimercaptosuccinic acid-modified Fe2 O3 nanoparticles on intercalated discs in engineered cardiac tissuesYongchao Mou, Shuanghong Lv, Fei Xiong, et al.Physiology (Bethesda, Md.)|June 16, 2017
Modeling Physiological Events in 2D vs. 3D Cell CultureKayla Duval, Hannah Grover, Li-Hsin Han, et al.Pageof 3