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In turn, enhancing KCC2 activity not only potentiated L838,417-induced analgesia, it rescued its analgesic potential at high doses, revealing a novel strategy for analgesia in pathological pain, by combined targeting of the appropriate GABA A R-subtypes and restoring Cl - homeostasis

Presupplementary motor area hyperactivity during response inhibition: a candidate endophenotype of obsessive-compulsive disorder

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Impaired mitochondrial fatty acid oxidation and insulin resistance in aging: novel protective role of glutathione