Taosheng Huang
Affiliations: | Biomedical Sciences - Ph.D. | University of California, Irvine, Irvine, CA |
Area:
Human Development, Cell Biology, OncologyGoogle:
"Taosheng Huang"
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Publications
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| Yang L, Slone J, Zou W, et al. (2020) Systemic Delivery of AAV- Mitigates the Phenotypes of Mitochondrial Disorders in Mutant Mice. Molecular Therapy. Methods & Clinical Development. 18: 84-97 |
| Yu J, Liang X, Ji Y, et al. (2020) PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy. The Journal of Clinical Investigation |
| Slone JD, Yang L, Peng Y, et al. (2020) Integrated analysis of the molecular pathogenesis of FDXR-associated disease. Cell Death & Disease. 11: 423 |
| Li H, Slone J, Huang T. (2020) The Role of Mitochondrial-related Nuclear Genes in Age-related Common Disease. Mitochondrion |
| Slone J, Huang T. (2020) The special considerations of gene therapy for mitochondrial diseases. Npj Genomic Medicine. 5: 7 |
| Yang L, Slone J, Li Z, et al. (2020) Systemic administration of AAV-Slc25a46 mitigates mitochondrial neuropathy in Slc25a46-/- mice. Human Molecular Genetics |
| Zou W, Slone J, Cao Y, et al. (2019) Mitochondria and Their Role in Human Reproduction. Dna and Cell Biology |
| Li H, Slone J, Fei L, et al. (2019) Mitochondrial DNA Variants and Common Diseases: A Mathematical Model for the Diversity of Age-Related mtDNA Mutations. Cells. 8 |
| Kang E, Wu J, Gutierrez NM, et al. (2019) Author Correction: Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations. Nature |
| Ji Y, Zhang J, Yu J, et al. (2018) Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy. Human Molecular Genetics |