Alrahbeni, TahaniSartor, FrancescaAnderson, JihanMiedzybrodzka, ZosiaMcCaig, ColinMuller, Berndt2015-05-272015-05-272015-05-27Alrahbeni, T, Sartor, F, Anderson, J, Miedzybrodzka, Z, McCaig, C & Muller, B 2015, 'Full UPF3B function is critical for neuronal differentiation of neural stem cells', Molecular brain, vol. 8, 33. https://doi.org/10.1186/s13041-015-0122-1, https://doi.org/10.1186/s13041-015-0122-11756-6606ORCID: /0000-0003-1279-5421/work/60546372ORCID: /0000-0001-5151-8254/work/76975431ORCID: /0000-0003-2890-8136/work/175113375ORCID: /0000-0003-1279-5421/work/60546372http://hdl.handle.net/2164/4555Acknowledgments We thank Fred H Gage (Salk Institute, La Jolla, CA, USA) for HCN-A94 cells and Niels Gehring (University of Cologne, Germany) for constructs. We gratefully acknowledge Tenovus Scotland (Project Grant G11-06), Moonlight Prowl (FS) and the Saudi Arabian Ministry of Higher Education via King Abdullah Program for Scholarships for support (TA). JA is supported by a PhD studentship from Medical Research Scotland (PhD-654-2012) and Dundee Cell Products.151880216engautismschizophreniaX-linked intellectual disabilitynonsense-mediated mRNA decayUPF3B mutationUPF1tethered function assayqPCRArhgap24Atf4protein localisationR MedicineMedical Research Council (MRC)PhD-654-2012OtherTenovus ScotlandG11-06Supplementary DataRJournal article10.1186/s13041-015-0122-18