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Tzu-Kang Sang, Ph.D.

Affiliations: 
Purdue University, West Lafayette, IN, United States 
Area:
development
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"Tzu-Kang Sang"
Mean distance: 16.03 (cluster 11)
 		SNBCP
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Donald 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
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