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BACHD rats expressing full-length mutant huntingtin exhibit differences in social behavior compared to wild-type littermates

机译:与野生型同窝仔相比,表达全长突变型亨廷顿蛋白的BACHD大鼠表现出社会行为差异

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摘要

BackgroundHuntington disease (HD) is a devastating inherited neurodegenerative disorder characterized by progressive motor, cognitive, and psychiatric symptoms without any cure to slow down or stop the progress of the disease. The BACHD rat model for HD carrying the human full-length mutant huntingtin protein (mHTT) with 97 polyQ repeats has been recently established as a promising model which reproduces several HD-like features. While motor and cognitive functions have been characterized in BACHD rats, little is known about their social phenotype.
机译:背景亨廷顿舞蹈病(HD)是一种破坏性的遗传性神经退行性疾病,其特征是进行性运动,认知和精神病性症状,无法治愈或延缓疾病进展。最近已经建立了带有人类全长突变亨廷顿蛋白(mHTT)和97个polyQ重复序列的HD的BACHD大鼠模型,该模型可再现多种HD样特征。虽然在BACHD大鼠中已表征了运动和认知功能,但对其社交表型知之甚少。

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