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Regulation of Dendrite Development and Synapse Formation by Tropomodulin
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Molecular Pathogenesis of Charcot-Marie-Tooth disease caused by
mutations in SIMPLE
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Actin capping protein in dendritic spine development
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Comprehensive Proteome and Transcriptome Studies Reveal RNA
Processing Dysfunction in Alzheimer's disease
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Regulation of translation in neuronal function and development
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SMN functions as a molecular chaperone for mRNP assembly
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Dopamine and dopamine D4 receptor activation: Signaling components,
gene regulation, endogenous circadian systems, and visual function
in mouse retina
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Role of 3' untranslated regions in translation regulation of
GluR2 mRNAs
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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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Regulation and function of the Cdk5/QKI pathway in oligodendroglial
development
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NPAS2 and CLOCK in the mammalian retina: their localization and roles in clock-controlled gene regulation and visual function
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Neuronal Function of hnRNP-Q1: Identification of a Novel Mechanism for Gap-43 mRNA Translation Regulation
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Bidirectional control of dendritic mRNA translation, glutamate
receptor expression, and synapse structure by the CPEB-associated
polyadenylation machinery
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The Role of FMRP in the Regulation of PI3-Kinase Signaling in the
Fragile X Mouse Model
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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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The quaking I Pathway and Regulation of Alternative Splicing in Myelinating Glia
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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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The Role of RGS14 in Learning, Memory, and Synaptic Plasticity
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Inhibition of the schizophrenia-associated microRNA miR-137
disrupts Nrg1α neurodevelopmental signal transduction
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The effect of the Val66Met BDNF polymorphism on axon regeneration after peripheral nerve injury
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Characterizing Motor Neuron-specific mRNA Processing Defects in an Intermediate Mouse Model of Spinal Muscular Atrophy
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