Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese von Tan, E.K, Lu, C.S, Peng, R, Teo, Y.Y, Wu-Chou, Y.H, Chen, R.S, Weng, Y.H, Chen, C.M, Fung, H.C, Tan, L.C, Zhang, Z.J, An, X.K, Lee-Chen, G.J, Lee, M.C, Fook-Chong, S, Burgunder, J.M, Wu, R.M, Wu, Y.R

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Chinese herbal medicine extracts targeting ubiquitin proteasome pathway to reduce polyq aggregation in cell models of spinocerebellar ataxia 3 von Lee-Chen, G.J., Chang, C.N., Chen, W.L., Lin, T.H., Chen, C.M.

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Variant A320V in vacuolar protein sorting 35 (VPS35) in Taiwanese Parkinson’s disease is associated with endosomal alterations and trafficking defects von Wu, Y.R., Lin, C.H., Chao, C.Y., Chang, C.W., Lee, C.M., Lee-Chen, G.J., Chen, C.M.

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[P88]: Establishment of the SCA17 pathogenic model in C. elegans for gene therapy and pharmaceuticals screening von Pai, C.K., Lee‐Chen, G.J., Su, M.T., Li, M.L.

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DNA Haplotype Analysis of CAG Repeat in Taiwanese Huntington’s Disease Patients von Wang, C.K., Wu, Y.R., Hwu, W.L., Chen, C.M., Ro, L.S., Chen, S.T., Gwinn-Hardy, K., Yang, C.C., Wu, R.M., Chen, T.F., Wang, H.C., Chao, M.C., Chiu, M.J., Lu, C.J., Lee-Chen, G.J.

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[P99]: Molecular genetic and epigenetic studies of SCA8 CTG repeat expansion von Lee‐Chen, G.J., Huang, S.Y., Li, M.L., Wu, Y.R., Chen, C.M.

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[P101]: Apolipoprotein E, angiotensin‐converting enzyme and kallikrein gene polymorphisms and the risk of Alzheimer's disease and vascular dementia von Wang, H.K., Chen, C.M., Fung, H.C., Hsu, W.C., Lee‐Chen, G.J.

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[P100]: Plausible pathogenesis of SCA8 CTG trinucleotide repeats expansion von Chen, I.C., Shiau, H.C, Lin, H.Y., Kao, S.H., Chen, C.M., Lee‐Chen, G.J.

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[P103]: Establishment of spinocerebellar ataxia type 8 transgenic mouse model von Lin, H.Y., Hsu, C.S., Hsieh‐Li, H.M., Chen, C.M., Lu, K.T., Lee‐Chen, G.J.

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[P98]: Biomarker discovery for polyglutamine‐mediated SCA17 using transiently transfected 293 and lymphoblastoid cells with TBP expansion von Lee, L.C., Chen, F.L., Chen, C.M., Chang, K.H., Lee‐Chen, G.J.

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[P102]: The functional role of the PPP2R2B gene, CAG repeat polymorphism and its implication in the genetic susceptibility to Taiwanese Alzheimer's disease von Lin, C.H., Hou, Y.T., Chen, C.M., Hsu, W.C., Fung, H.C., Lee‐Chen, G.J.

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[P209]: Investigation of the neurodegenerative impact of CAG expansion in TBP gene through transgenic mouse model von Hsieh‐Li, H.M., Lin, C.Y., RO, L.S., Chen, C.M., Lee‐Chen, G.J.

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