Progranulin functions as a cathepsin D chaperone to stimulate axonal outgrowth in vivo

Loss of function mutations in progranulin (GRN) cause frontotemporal dementia, but how GRN haploinsufficiency causes neuronal dysfunction remains unclear. We previously showed that GRN is neurotrophic in vitro. Here, we used an in vivo axonal outgrowth system and observed a delayed recovery in GRN(−...

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Bibliografiset tiedot
Julkaisussa:Hum Mol Genet
Päätekijät: Beel, Sander, Moisse, Matthieu, Damme, Markus, De Muynck, Louis, Robberecht, Wim, Van Den Bosch, Ludo, Saftig, Paul, Van Damme, Philip
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2017
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Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5886064/
https://ncbi.nlm.nih.gov/pubmed/28453791
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx162
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