Mingli Hsieh

Affiliations: 
Department of Life Science Tunghai University, Taiwan 
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"Mingli Hsieh"
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Publications

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Wu YL, Chang JC, Chao YC, et al. (2022) In Vitro Efficacy and Molecular Mechanism of Curcumin Analog in Pathological Regulation of Spinocerebellar Ataxia Type 3. Antioxidants (Basel, Switzerland). 11
Chi TH, Hsieh BY, Liang PS, et al. (2020) Expression and Functional Study of Single Mutations of Carbonic Anhydrase 8 in Neuronal Cells. Cellular and Molecular Neurobiology
Hsieh M, Hsieh BY, Ma CY, et al. (2019) Protective roles of carbonic anhydrase 8 in Machado-Joseph Disease. Journal of Neuroscience Research
Lo CM, Ma YS, Wei YH, et al. (2018) Promoter analysis and transcriptional regulation of human carbonic anhydrase VIII gene in a MERRF disease cell model. Archives of Biochemistry and Biophysics. 641: 50-61
Wu YL, Chang JC, Lin WY, et al. (2017) Caffeic Acid and Resveratrol Ameliorate Cellular Damage in Cell and Drosophila Models of Spinocerebellar Ataxia Type 3 through Upregulation of Nrf2 Pathway. Free Radical Biology & Medicine
Chang JC, Wu SL, Hoel F, et al. (2016) Far-infrared radiation protects viability in a cell model of Spinocerebellar Ataxia by preventing polyQ protein accumulation and improving mitochondrial function. Scientific Reports. 6: 30436
Wang TK, Cheng CK, Chi TH, et al. (2014) Effects of carbonic anhydrase-related protein VIII on human cells harbouring an A8344G mitochondrial DNA mutation. The Biochemical Journal. 459: 149-60
Chang JC, Liu KH, Li YC, et al. (2013) Functional recovery of human cells harbouring the mitochondrial DNA mutation MERRF A8344G via peptide-mediated mitochondrial delivery. Neuro-Signals. 21: 160-73
Chen HF, Chen CY, Lin TH, et al. (2012) The protective roles of phosphorylated heat shock protein 27 in human cells harboring myoclonus epilepsy with ragged-red fibers A8344G mtDNA mutation. The Febs Journal. 279: 2987-3001
Chen CY, Chen HF, Gi SJ, et al. (2011) Decreased heat shock protein 27 expression and altered autophagy in human cells harboring A8344G mitochondrial DNA mutation. Mitochondrion. 11: 739-49
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