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Small-molecule TrkB receptor agonists improve motor function and extend survival in a mouse model of Huntington's disease

Huntington's disease (HD) is a fatal neurodegenerative disease characterized by abnormal motor coordination, cognitive decline and psychiatric disorders. This disease is caused by an expanded CAG trinucleotide repeat in the gene encoding the protein huntingtin. Reduced levels of brain-derived n...

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Dettagli Bibliografici
Autori principali: Jiang, Mali, Peng, Qi, Liu, Xia, Jin, Jing, Hou, Zhipeng, Zhang, Jiangyang, Mori, Susumu, Ross, Christopher A., Ye, Keqiang, Duan, Wenzhen
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3658168/
https://ncbi.nlm.nih.gov/pubmed/23446639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt098
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