Utility of the Hebb–Williams Maze Paradigm for Translational Research in Fragile X Syndrome: A Direct Comparison of Mice and Humans-Reference-Cited by-同舟云学术

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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

Published:2018-03-28 Issue: Volume:11 Page:
ISSN:1662-5099
Container-title:Frontiers in Molecular Neuroscience
language:
Short-container-title:Front. Mol. Neurosci.

Author:

Boutet Isabelle,Collin Charles A.,MacLeod Lindsey S.,Messier Claude,Holahan Matthew R.,Berry-Kravis Elizabeth,Gandhi Reno M.,Kogan Cary S.

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience,Molecular Biology

Reference81 articles.

1. Intentional maps in posterior parietal cortex.;Andersen;Annu. Rev. Neurosci.,2002

2. Cognitive and behavioural profile of fragile X boys: correlations to molecular data.;Backes;Am. J. Med. Genet.,2002

3. Male and female Fmr1 knockout mice on C57 albino background exhibit spatial learning and memory impairments.;Baker;Genes Brain Behav.,2010

4. Specification of the neurobehavioral phenotype in males with fragile X syndrome.;Baumgardner;Pediatrics,1995

5. Arbaclofen in fragile X syndrome: results of phase 3 trials.;Berry-Kravis;J. Neurodev. Disord.,2017

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