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Disposition of Proteins and Lipids in Synaptic Membrane Compartments Is Altered in Q175/Q7 Huntington’s Disease Mouse Striatum

Dysfunction at synapses is thought to be an early change contributing to cognitive, psychiatric and motor disturbances in Huntington’s disease (HD). In neurons, mutant Huntingtin collects in aggregates and distributes to the same sites as wild-type Huntingtin including on membranes and in synapses....

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Detalhes bibliográficos
Publicado no:Front Synaptic Neurosci
Main Authors: Iuliano, Maria, Seeley, Connor, Sapp, Ellen, Jones, Erin L., Martin, Callie, Li, Xueyi, DiFiglia, Marian, Kegel-Gleason, Kimberly B.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8013775/
https://ncbi.nlm.nih.gov/pubmed/33815086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnsyn.2021.618391
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