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Utility of the Hebb–Williams maze paradigm for translational research in Fragile X syndrome: A direct comparison of mice and humans

Authors :
Boutet, I. (Isabelle)
Collin, C.A. (Charles A.)
Macleod, L.S. (Lindsey S.)
Messier, C. (Claude)
Holahan, M.R. (Matthew R.)
Berry-Kravis, E. (Elizabeth)
Gandhi, R.M. (Reno M.)
Kogan, C.S. (Cary S.)
Boutet, I. (Isabelle)
Collin, C.A. (Charles A.)
Macleod, L.S. (Lindsey S.)
Messier, C. (Claude)
Holahan, M.R. (Matthew R.)
Berry-Kravis, E. (Elizabeth)
Gandhi, R.M. (Reno M.)
Kogan, C.S. (Cary S.)
Source :
Frontiers in Molecular Neuroscience vol. 11
Publication Year :
2018

Abstract

To generate meaningful information, translational research must employ paradigms that allow extrapolation from animal models to humans. However, few studies have evaluated translational paradigms on the basis of defined validation criteria. We outline three criteria for validating translational paradigms. We then evaluate the Hebb–Williams maze paradigm (Hebb and Williams, 1946; Rabinovitch and Rosvold, 1951) on the basis of these criteria using Fragile X syndrome (FXS) as model disease. We focused

Details

Database :
OAIster
Journal :
Frontiers in Molecular Neuroscience vol. 11
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1051044323
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.3389.fnmol.2018.00099