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Neuroprotective effects of PPAR-γ agonist rosiglitazone in N171-82Q mouse model of Huntington’s disease

Huntington’s disease (HD) is a devastating genetic neurodegenerative disease caused by CAG trinucleotide expansion in the exon-1 region of the huntingtin gene. Currently, no cure is available. It is becoming increasingly apparent that mutant HTT impairs metabolic homeostasis and causes transcription...

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Detalhes bibliográficos
Main Authors: Jin, Jing, Albertz, Jennifer, Guo, Zhihong, Peng, Qi, Rudow, Gay, Troncoso, Juan C., Ross, Christopher A., Duan, Wenzhen
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3642978/
https://ncbi.nlm.nih.gov/pubmed/23373812
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jnc.12190
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