Stem Cell-Derived Human Striatal Progenitors Innervate Striatal Targets and Alleviate Sensorimotor Deficit in a Rat Model of Huntington Disease

Huntington disease (HD) is an inherited late-onset neurological disorder characterized by progressive neuronal loss and disruption of cortical and basal ganglia circuits. Cell replacement using human embryonic stem cells may offer the opportunity to repair the damaged circuits and significantly amel...

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מידע ביבליוגרפי
הוצא לאור ב:Stem Cell Reports
Main Authors: Besusso, Dario, Schellino, Roberta, Boido, Marina, Belloli, Sara, Parolisi, Roberta, Conforti, Paola, Faedo, Andrea, Cernigoj, Manuel, Campus, Ilaria, Laporta, Angela, Bocchi, Vittoria Dickinson, Murtaj, Valentina, Parmar, Malin, Spaiardi, Paolo, Talpo, Francesca, Maniezzi, Claudia, Toselli, Mauro Giuseppe, Biella, Gerardo, Moresco, Rosa Maria, Vercelli, Alessandro, Buffo, Annalisa, Cattaneo, Elena
פורמט: Artigo
שפה:Inglês
יצא לאור: Elsevier 2020
נושאים:
Article
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC7220987/
https://ncbi.nlm.nih.gov/pubmed/32302555
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.stemcr.2020.03.018
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