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Genetic Diversity in Oxytocin Receptor Sequence, Neural Expression, and Social Behavior
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Focus on the Locus: Elucidating the roles of tau pathology and
the locus coeruleus in Alzheimer's Disease
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The Role of Stress in Two Genetic Models of Epilepsy
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The RNA-binding protein, ZC3H14, is critical for control of
polyadenylation and translation, neuronal development, brain
morphology, and working memory in mice
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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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Assessment of the clinical impact of sequence variants in the
FMR1 gene
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Transcriptional dysregulation of TrkA associates withneurodegeneration in Spinocerebellar Ataxia 17
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Pathogenesis of novel FMR1 mutations in fragile X syndrome
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The polyadenosine RNA-binding protein dNab2 interacts with the fragile X protein homolog and regulates gene expression in Drosophila neurons
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The role of glia in Huntington's disease pathology
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Exploring the neurogenetics of sociality: creation of models toassess the functional role of V1a receptor diversity
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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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An In Vivo Model to Study the Regulation of FMRP
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The role of Arl13b in the maintenance of neural tube patterning and
oligodendrocyte development
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