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ELAVL3 Cryptic Exon Inclusion and Pathological TDP-43 in ALS/FTD
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Altered CRABP1 Expression in Fragile-X syndrome
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The role of the histone demethylase LSD1 in hippocampal neuron survival and tau-mediated neurodegeneration.
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Direct reprogramming of astrocytes to enhance recovery after stroke
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Novel role of Cdh1-APC as a regulator of neuronal protein synthesis and stress granule dynamics
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Neurobehavioral effects, and therapeutic-like potential, of MDMA and cortico-striatal trkB
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RNA-binding proteins with mixed charge domains self-assemble, aggregate, and interact with core pathologies in Alzheimer's Disease
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Deciphering how N-terminal phosphorylation alters fused in sarcoma (FUS) function: Implications for FTD/ALS pathogenesis
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Pathogenesis of novel FMR1 mutations in fragile X syndrome
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Ubiquitin Targeting and Differential Accumulation of Mutant Huntingtin
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Age-dependent, region-specific mechanisms contribute to Spinocerebellar Ataxia 17 pathogenesis.
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Stem cell derived monkey neural progenitor cells as a platform for translational research in Huntington's disease
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Functional Analysis of a De Novo Missense GRIN1 Mutation Associated with Intractable Seizures
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Adhesion G Protein-coupled Receptor G1 (GPR56) Regulation by Sorting Nexin 27
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The Role of Oligodendrocyte Dysfunction in Huntington's Disease
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Genetic Diversity in Oxytocin Receptor Sequence, Neural Expression, and Social Behavior
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Investigation of the disruption of miRNA-137 and its effects on the Nrg/ErbB4 pathway in schizophrenia
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Impairments in protein synthesis and signaling in Fragile X human cells
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Shedding light on the spatiotemporal regulation of RGS14
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An In Vivo Model to Study the Regulation of FMRP
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