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Ella Borgenheimer et al.
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Shane A. Liddelow et al.
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Lilach Soreq et al.
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Ruotian Jiang et al.
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Pratap Meera et al.
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Mahmoud A. Pouladi et al.
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Lack of huntingtin promotes neural stem cells differentiation into glial cells while neurons expressing huntingtin with expanded polyglutamine tracts undergo cell death
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India Bohanna et al.
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Sarah J. Tabrizi et al.
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Local Ca2+ detection and modulation of synaptic release by astrocytes
Maria Amalia Di Castro et al.
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Ali Khoshnan et al.
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Bahareh Ajami et al.
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