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An Optimization of AAV-82Q-Delivered Rat Model of Huntington’s Disease
Kyoung-Ha So, Jai Ho Choi, Jaisan Islam, Elina KC, Hyeong Cheol Moon, So Yoon Won, Hyong Kyu Kim, Soochong Kim, Sang-Hwan Hyun, Young Seok Park
Journal of Korean Neurosurgical Society. 2020;63(5):579-589.   Published online 2020 March 5    DOI: https://doi.org/10.3340/jkns.2019.0182

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An Optimization of AAV-82Q-Delivered Rat Model of Huntington’s Disease
Journal of Korean Neurosurgical Society. 2020;63(5):579-589   Crossref logo
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52. AAV-Delivered RNAi Improves Cellular and Motor Phenotypes in a Mouse Model for Huntington's Disease
Molecular Therapy. 2005;11:S22   Crossref logo
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AAV-BDNF augments neurogenesis in both the normal adult rat brain and the quinolinic acid lesion model of Huntington's disease
Experimental Neurology. 2006;198(2):565   Crossref logo
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545. Attenuation of Functional Deficits in the QA Model of Huntington's Disease Following AAV Therapeutic Delivery
Molecular Therapy. 2007;15:S209   Crossref logo
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77. Dose-Dependent Neuroprotective Effect of CNTF Delivered Via Tetracycline-Regulated Lentiviral Vectors in the Quinolonic Acid Rat Model of Huntington's Disease
Molecular Therapy. 2002;5(5):S28   Crossref logo
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282. Silencing Mutant Htt by AAV-Mediated Expression of RNAi Ameliorates Disease Manifestations in the YAC128 Mouse Model of Huntington's Disease
Molecular Therapy. 2013;21:S108   Crossref logo
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Sertraline slows disease progression and increases neurogenesis in N171-82Q mouse model of Huntington's disease
Neurobiology of Disease. 2008;30(3):312-322   Crossref logo
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Altered selenium status in Huntington's disease: Neuroprotection by selenite in the N171-82Q mouse model
Neurobiology of Disease. 2014;71:34-42   Crossref logo
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NMDA-receptor binding in QUIN-induced huntington's disease rat model
Neurochemistry International. 1990;16:29   Crossref logo
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507. Allele-Specific Silencing of Mutant Huntingtin in a Lentiviral-Based Rat Model of Huntington's Disease
Molecular Therapy. 2009;17:S194-S195   Crossref logo
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