Silencing Of The Drosophila Ortholog Of SOX5 Leads To Abnormal Neuronal Development And Behavioral Impairment.

Li, A., Hooli, B., Mullin, K. et al. (7 more authors) (2017) Silencing Of The Drosophila Ortholog Of SOX5 Leads To Abnormal Neuronal Development And Behavioral Impairment. Human Molecular Genetics, 26 (8). pp. 1472-1482. ISSN 0964-6906

Abstract

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Authors/Creators:
Copyright, Publisher and Additional Information: © 2017 Oxford University Press.
Keywords: Presynaptic terminals; Alzheimer's disease; signal transduction; mutation; dendrites; drosophila; genes; intellectual disability; nerve degeneration; neurons; repression; smell perception; brain; genetics; developmental delay; rna interference; neuroblastoma cell; candidate disease gene
Dates:
  • Accepted: 7 February 2017
  • Published (online): 10 February 2017
  • Published: 15 April 2017
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Neuroscience (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 14 Mar 2017 15:47
Last Modified: 13 Jul 2023 14:19
Published Version: https://doi.org/10.1093/hmg/ddx051
Status: Published
Publisher: Oxford University Press
Refereed: Yes
Identification Number: https://doi.org/10.1093/hmg/ddx051
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