Compartment-Dependent Degradation of Mutant Huntingtin Accounts for Its Preferential Accumulation in Neuronal Processes
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Microglial Activation in the Pathogenesis of Huntington's Disease.The Ubiquitination, Disaggregation and Proteasomal Degradation Machineries in Polyglutamine DiseasemiR-196a Enhances Neuronal Morphology through Suppressing RANBP10 to Provide Neuroprotection in Huntington's Disease.Differential HspBP1 expression accounts for the greater vulnerability of neurons than astrocytes to misfolded proteins.Mutant Huntingtin Inhibits αB-Crystallin Expression and Impairs Exosome Secretion from Astrocytes.
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Compartment-Dependent Degradation of Mutant Huntingtin Accounts for Its Preferential Accumulation in Neuronal Processes
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on August 2016
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vedecký článok
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vetenskaplig artikel
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Compartment-Dependent Degradat ...... mulation in Neuronal Processes
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Compartment-Dependent Degradat ...... ulation in Neuronal Processes.
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type
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Compartment-Dependent Degradat ...... mulation in Neuronal Processes
@en
Compartment-Dependent Degradat ...... ulation in Neuronal Processes.
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Compartment-Dependent Degradat ...... mulation in Neuronal Processes
@en
Compartment-Dependent Degradat ...... ulation in Neuronal Processes.
@nl
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P1476
Compartment-Dependent Degradat ...... mulation in Neuronal Processes
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P2860
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10.1523/JNEUROSCI.0806-16.2016
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P577
2016-08-01T00:00:00Z