Tzu-Kang Sang, Ph.D.
Affiliations: | Purdue University, West Lafayette, IN, United States |
Area:
developmentGoogle:
"Tzu-Kang Sang"Mean distance: 16.03 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentorDonald Ready | grad student | 2001 | Purdue | |
(Eyes closed, a Drosophila p47 homolog, is essential for membrane biogenesis.) |
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Publications
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Hsiao MC, Huang TY, Yu BH, et al. (2022) Whole-mount immunofluorescent labeling of the adult fly retina. Star Protocols. 3: 101430 |
Chi H, Sun L, Shiu RH, et al. (2020) Cleavage of human tau at Asp421 inhibits hyperphosphorylated tau induced pathology in a Drosophila model. Scientific Reports. 10: 13482 |
Chi H, Chang HY, Sang TK. (2018) Neuronal Cell Death Mechanisms in Major Neurodegenerative Diseases. International Journal of Molecular Sciences. 19 |
Chang HY, Sang TK, Chiang AS. (2018) Untangling the Tauopathy for Alzheimer's disease and parkinsonism. Journal of Biomedical Science. 25: 54 |
Liang CJ, Chang YC, Chang HC, et al. (2014) Derlin-1 regulates mutant VCP-linked pathogenesis and endoplasmic reticulum stress-induced apoptosis. Plos Genetics. 10: e1004675 |
Chang YC, Hung WT, Chang YC, et al. (2011) Pathogenic VCP/TER94 alleles are dominant actives and contribute to neurodegeneration by altering cellular ATP level in a Drosophila IBMPFD model. Plos Genetics. 7: e1001288 |
Chatterjee S, Sang TK, Lawless GM, et al. (2009) Dissociation of tau toxicity and phosphorylation: role of GSK-3beta, MARK and Cdk5 in a Drosophila model. Human Molecular Genetics. 18: 164-77 |
Sang TK, Chang HY, Lawless GM, et al. (2007) A Drosophila model of mutant human parkin-induced toxicity demonstrates selective loss of dopaminergic neurons and dependence on cellular dopamine. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 981-92 |
Sang TK, Jackson GR. (2005) Drosophila models of neurodegenerative disease. Neurorx : the Journal of the American Society For Experimental Neurotherapeutics. 2: 438-46 |
Mee L, Honkala H, Kopra O, et al. (2005) Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1. Human Molecular Genetics. 14: 1475-88 |