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The role of Arl13b in the maintenance of neural tube patterning and
oligodendrocyte development
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Phosphorylation of N-terminal Mutant Huntingtin is Related to its
Preferential Nuclear Accumulation in Striatal Neurons
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Developing a Nonhuman Primate Model of Huntington's Disease
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The role of glia in Huntington's disease pathology
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Toxicity and solubility of mutant superoxide dismutase 1 in
amyotrophic lateral sclerosis
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Mutant Huntingtin Impairs Astrocytic Secretion
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Transcriptional dysregulation of TrkA associates withneurodegeneration in Spinocerebellar Ataxia 17
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Cell Type-Dependent Activities of the Ubiquitin-Proteasome Systemand Selective Neurodegeneration
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The role of Huntingtin-associated protein 1 (Hap1) in postnatal development
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Age-dependent, region-specific mechanisms contribute to Spinocerebellar Ataxia 17 pathogenesis.
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The Role of Oligodendrocyte Dysfunction in Huntington's Disease
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Ubiquitin Targeting and Differential Accumulation of Mutant Huntingtin
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Differential Proteolysis of Mutant Huntingtin in Astrocytes and
Neurons
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Therapeutic effect of Berberine on Huntington's Disease Transgenic Mouse Model
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