Corticostriatal dysfunction and glutamate transporter 1 (GLT1) in Huntington's disease: interactions between neurons and astrocytes.
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Corticostriatal Dysfunction in Huntington's Disease: The BasicsNew Insights on Astrocyte Ion Channels: Critical for Homeostasis and Neuron-Glia SignalingThe choreography of neuroinflammation in Huntington's diseaseRole of cerebral cortex in the neuropathology of Huntington's diseaseCurrent approaches to enhance glutamate transporter function and expressionSynaptic dysfunction and septin protein family members in neurodegenerative diseasesThe chicken or the egg: mitochondrial dysfunction as a cause or consequence of toxicity in Huntington's diseaseAscorbic acid and the brain: rationale for the use against cognitive decline.Altered Neuronal Dynamics in the Striatum on the Behavior of Huntingtin Interacting Protein 14 (HIP14) Knockout MiceAstrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model miceDysfunctional behavioral modulation of corticostriatal communication in the R6/2 mouse model of Huntington's diseaseNeurological and psychiatric disorders as a neuroglial failure.Cortical efferents lacking mutant huntingtin improve striatal neuronal activity and behavior in a conditional mouse model of Huntington's diseaseBiological sources of inflexibility in brain and behavior with aging and neurodegenerative diseases.Neurovascular and Immuno-Imaging: From Mechanisms to Therapies. Proceedings of the Inaugural Symposium.Early exposure to dynamic environments alters patterns of motor exploration throughout the lifespan.Astroglia in neurological diseasesSLC1 glutamate transportersDiversity of astrocyte functions and phenotypes in neural circuits.Astrocytes: a central element in neurological diseases.The role of glial-specific Kir4.1 in normal and pathological states of the CNS.Dysregulation of Corticostriatal Connectivity in Huntington's Disease: A Role for Dopamine ModulationDysregulation of corticostriatal ascorbate release and glutamate uptake in transgenic models of Huntington's disease.Striatal Network Models of Huntington's Disease Dysfunction Phenotypes.Stratification of astrocytes in healthy and diseased brain.Astrogliopathology: a central element of neuropsychiatric diseases?Circadian Regulation of Glutamate Transporters.
P2860
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P2860
Corticostriatal dysfunction and glutamate transporter 1 (GLT1) in Huntington's disease: interactions between neurons and astrocytes.
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Corticostriatal dysfunction an ...... etween neurons and astrocytes.
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type
label
Corticostriatal dysfunction an ...... etween neurons and astrocytes.
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prefLabel
Corticostriatal dysfunction an ...... etween neurons and astrocytes.
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P2860
P1433
P1476
Corticostriatal dysfunction an ...... etween neurons and astrocytes.
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P2093
Ana María Estrada-Sánchez
George V Rebec
P2860
P356
10.1016/J.BAGA.2012.04.029
P577
2012-07-01T00:00:00Z