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Redefining drug discovery for neuroscience R&D

Redefining drug discovery for neuroscience R&D

Key Papers

Drug connectivity mapping and functional analysis reveal therapeutic small molecules that

differentially modulate myelination

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In this study, we describe how we can determine the optimal concentrations of pharmacogenomically-derived small molecules and show differential mechanistic changes in myelinating glial cells in vivo and ex vivo.

Functional genomic analyses highlight a shift in Gpr17-regulated cellular processes in oligodendrocyte progenitor cells and underlying myelin dysregulation in the aged mouse cerebrum

We unravelled the age-related changes in myelinating glial cells using high-throughput transcriptomic profiling. This information was combined with systems biology and drug discovery for identifying therapeutics which were validated in mouse models of aging and injury.

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Disruption of oligodendrocyte progenitor cells is an early sign of pathology in the triple transgenic mouse model of Alzheimer's disease

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Using transgenic mouse models of aging, we could describe the rapid deterioration of NG2 glia, which impact their ability as a reservoir for myelin turnover and repair.

Astrocytes are direct cellular targets of lithium treatment

Novel roles for lysyl oxidase and peroxisome-proliferator activated receptor-γ as astroglial targets of lithium: This study identified the mechanisms by which lithium regulates astrocye physiology and their relationship to major depressive disorders. The study further revealed and validated novel therapies for the treatment of bipolar disorder.

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Pharmacogenomic identification of small molecules for lineage specific manipulation of

subventricular zone germinal activity

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We established an entirely novel computational-based drug-discovery strategy to identify  of small molecules that can be used to manipulate neural stem cells in different context. We provide proof that, by administration of small molecules in vivo, it is possible to promote the specific generation of neural cells in aging and regenerative contexts.

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