Xue-Jun Li
Affiliations: | University of Connecticut, Storrs, CT, United States |
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| Chai E, Chen Z, Mou Y, et al. (2023) Liver-X-receptor agonists rescue axonal degeneration in SPG11-deficient neurons via regulating cholesterol trafficking. Neurobiology of Disease. 106293 |
| Mou Y, Dein J, Chen Z, et al. (2021) MFN2 Deficiency Impairs Mitochondrial Transport and Downregulates Motor Protein Expression in Human Spinal Motor Neurons. Frontiers in Molecular Neuroscience. 14: 727552 |
| Karpe Y, Chen Z, Li XJ. (2021) Stem Cell Models and Gene Targeting for Human Motor Neuron Diseases. Pharmaceuticals (Basel, Switzerland). 14 |
| Mou Y, Dong Y, Chen Z, et al. (2020) Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia. Acta Neuropathologica Communications. 8: 214 |
| Mou Y, Mukte S, Chai E, et al. (2020) Analyzing Mitochondrial Transport and Morphology in Human Induced Pluripotent Stem Cell-Derived Neurons in Hereditary Spastic Paraplegia. Journal of Visualized Experiments : Jove |
| Qin J, Wang M, Zhao T, et al. (2019) Early Forebrain Neurons and Scaffold Fibers in Human Embryos. Cerebral Cortex (New York, N.Y. : 1991) |
| Rani Bijukumar D, Segu A, Mou Y, et al. (2018) Differential toxicity of processed and non-processed states of CoCrMo degradation products generated from a hip simulator on neural cells. Nanotoxicology. 1-16 |
| Denton K, Mou Y, Xu CC, et al. (2018) Impaired Mitochondrial Dynamics Underlie Axonal Defects in Hereditary Spastic Paraplegias. Human Molecular Genetics |
| Denton KR, Xu C, Shah H, et al. (2016) Modeling Axonal Defects in Hereditary Spastic Paraplegia with Human Pluripotent Stem Cells. Frontiers in Biology. 11: 339-354 |
| Xu CC, Denton KR, Wang ZB, et al. (2015) Abnormal mitochondrial transport and morphology as early pathological changes in human models of spinal muscular atrophy. Disease Models & Mechanisms |