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Iron activates microglia and directly stimulates indoleamine-2,3-dioxygenase activity in the N171-82Q mouse model of Huntington’s disease

Huntington’s disease (HD) is a neurodegenerative disorder caused by a dominant CAG-repeat expansion in the huntingtin gene. Microglial activation is a key feature of HD pathology, and is present before clinical disease onset. The kynurenine pathway (KP) of tryptophan degradation is activated in HD,...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Donley, David W., Realing, Marley, Gigley, Jason P., Fox, Jonathan H.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8121302/
https://ncbi.nlm.nih.gov/pubmed/33989290
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0250606
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