Characterization of Gene Expression Phenotype in Amyotrophic Lateral Sclerosis Monocytes

IMPORTANCE: Amyotrophic lateral sclerosis (ALS) is a common adult-onset neurodegenerative disease characterized by selective loss of upper and lower motor neurons. Patients with ALS have persistent peripheral and central inflammatory responses including abnormally functioning T cells and activated m...

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Detalhes bibliográficos
Publicado no:JAMA Neurol
Main Authors: Zhao, Weihua, Beers, David R., Hooten, Kristopher G., Sieglaff, Douglas H., Zhang, Aijun, Kalyana-Sundaram, Shanker, Traini, Christopher M., Halsey, Wendy S., Hughes, Ashley M., Sathe, Ganesh M., Livi, George P., Fan, Guo-Huang, Appel, Stanley H.
Formato: Artigo
Idioma:Inglês
Publicado em: American Medical Association 2017
Assuntos:
Original Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5822209/
https://ncbi.nlm.nih.gov/pubmed/28437540
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamaneurol.2017.0357
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