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    1
    Molecular Genetic studies of spinocerebellar ataxia type 8
    • / Department of Life Science /98/ Doctor
    • Author: I-Cheng Chen   Advisor: Lee, Guey-Jen
    • The autosomal dominant spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerat...
    • Clicks: 141  Downloads: 2 

    2
    Screening of Novel Molecules for SCA 17 Treatment by Using a Microbial Model: Monitoring Protein Solubility by β-Galactosidase Structural Complementation

    3
    Therapeutic evaluation of granulocyte colony-stimulating factor on SCA17 transgenic mice
    • / Department of Life Science /99/ Doctor
    • Author: Ya-Chin Chang   Advisor: Hsieh, Hsiu-Mei
    • SCA17 is an autosomal dominant cerebellar ataxia (ADCA) caused by the polyglutamine (polyQ) expan...
    • Clicks: 305  Downloads: 4 

    4
    Respiratory variability and glottal dysfunction in spinocerebellar ataxia type 17 transgenic mice
    • / Department of Life Science /96/ Master
    • Author: Meng-Wei, Lin   Advisor: Hwang, Ji-Chuu
    • Autosomal dominant spinocerebellar ataxias（SCA）are a clinically and genetically heterogeneous gro...
    • Clicks: 271  Downloads: 27 

    5
    Evaluation of the efficacy of trehalose through the mouse cerebellar organotypic slice culture and SCA17 transgenic mice
    • / Department of Life Science /101/ Master
    • Author: Zhi-Zhong Chen   Advisor: Hsieh, Hsiu-Mei
    • Spinocerebellar ataxia (SCA) is an autosomal dominant and progressive neurodegenerative disease c...
    • Clicks: 288  Downloads: 5 

    6
    Investigation of the neurodegenerative impact of CAG expansion in TBP gene through Taiwan neurodegenerative patients and transgenic mouse model

    7
    Spinocerebellar ataxia type 17: genetic testing and oxidative stress and cytotoxicity studies using SCA17 lymphoblastoid and HEK-293 cell models
    • / Department of Life Science /96/ Master
    • Author: Pei-Ying Lin   Advisor: Lee, Guey-Jen
    • Spinocerebellar ataxia 17 (SCA17) is an inherited progressive neurodegenerative disease. It is ca...
    • Clicks: 210  Downloads: 1 

    8
    Study the association between ERK activation and Purkinje cell degeneration using a mouse model of Spinocerebellar ataxia type 17

    Public on Internet date:
    2025/09/17

    • / Department of Life Science /108/ Doctor
    • Author: Lin, Chia-Wei   Advisor: Hsieh, Hsiu-Mei
    • Spinocerebellar ataxia type 17 (SCA17) is one subtype of autosomal dominant cerebellar ataxia gro...
    • Clicks: 183  Downloads: 0 

    9
    Screening Novel Potential Therapeutic Drugs for Spinocerebellar Ataxia Type 3 through Inducible Cell system
    • / Department of Life Science /99/ Master
    • Author: Hsing-Jung Chen   Advisor: Hsieh, Hsiu-Mei
    • Spinocerebellar ataxia type 3 (SCA3), also called Machado–Joseph disease (MJD), is an autosomal d...
    • Clicks: 222  Downloads: 12 

    10
    Therapeutic Strategies Targeting Chaperone and Proteasome for PolyQ-mediated SCA
    • / Department of Life Science /101/ Master
    • Author: Pin-Jui Kung   Advisor: Lee, Guey-Jen
    • In polyQ-mediated disorders, the expansions of translated CAG repeats in the disease genes result...
    • Clicks: 179  Downloads: 1 
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