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Ubiquitin Targeting and Differential Accumulation of Mutant Huntingtin
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The Role of Oligodendrocyte Dysfunction in Huntington's Disease
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The role of Huntingtin-associated protein 1 (Hap1) in postnatal development
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Transcriptional dysregulation of TrkA associates withneurodegeneration in Spinocerebellar Ataxia 17
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The role of glia in Huntington's disease pathology
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The role of cilia transport in oligodendrocyte development and
regulation of PP2A activity
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Developing a Nonhuman Primate Model of Huntington's Disease
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Phosphorylation of N-terminal Mutant Huntingtin is Related to its
Preferential Nuclear Accumulation in Striatal Neurons
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The role of Arl13b in the maintenance of neural tube patterning and
oligodendrocyte development
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Huntingtin-Associated Protein 1 (Hap1) is Involved in Insulin
Secretion From Pancreatic Beta Cells
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