Cargando…
JAK/STAT Signalling in Huntington’s Disease Immune Cells
Huntington’s disease (HD) is an inherited neurodegenerative disorder caused by a CAG repeat expansion in the huntingtin (HTT) gene. Both central and peripheral innate immune activation have been described as features of the disease. Isolated human HD monocytes have been shown to produce more cytokin...
Autores principales: | Träger, Ulrike, Magnusson, Anna, Lahiri Swales, Nayana, Wild, Edward, North, Janet, Lowdell, Mark, Björkqvist, Maria |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871417/ https://www.ncbi.nlm.nih.gov/pubmed/24459609 http://dx.doi.org/10.1371/currents.hd.5791c897b5c3bebeed93b1d1da0c0648 |
Ejemplares similares
-
The PDE1/5 Inhibitor SCH-51866 Does Not Modify Disease Progression in the R6/2 Mouse Model of Huntington’s Disease
por: Beaumont, Vahri, et al.
Publicado: (2014) -
Abnormal peripheral chemokine profile in Huntington’s disease
por: Wild, Edward, et al.
Publicado: (2011) -
Expression of the Helicobacter pylori adhesin SabA is controlled via phase variation and the ArsRS signal transduction system
por: Goodwin, Andrew C., et al.
Publicado: (2008) -
Identification of a signalling molecule involved in bacterial intergeneric communication
por: Xie, Hua, et al.
Publicado: (2007) -
Functional studies of intimin in vivo and ex vivo: implications for host specificity and tissue tropism
por: Mundy, Rosanna, et al.
Publicado: (2007)