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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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Muscle-specific roles for p38K MAP kinase in the regulation of
locomotor activity in Drosophila
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Exploring the neurogenetics of sociality: creation of models toassess the functional role of V1a receptor diversity
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Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of Alzheimer's disease
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Developing a Nonhuman Primate Model of Huntington's Disease
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