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MONOGENIC MOUSE MODELS OF AUTISM SPECTRUM DISORDERS: COMMON MECHANISMS AND MISSING LINKS

Journal

NEUROSCIENCE
Volume 321, Issue -, Pages 3-23

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2015.12.040

Keywords

autism mouse models; Mecp2; Fmr1; Ube3a; Pten; Shank3

Categories

Funding

  1. NIH - United States grants [5R01-MH098114-03, 1R21-HD077197-01, 1R21-MH104316-01]
  2. Duke Institute for Brain Science Incubator award
  3. Autism Speaks
  4. Marcus Foundation
  5. Foundation for Prader-Willi Research
  6. Phelan-McDermid Syndrome Foundation
  7. Ruth. K. Broad Foundation
  8. Roche

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Autism spectrum disorders (ASDs) present unique challenges in the fields of genetics and neurobiology because of the clinical and molecular heterogeneity underlying these disorders. Genetic mutations found in ASD patients provide opportunities to dissect the molecular and circuit mechanisms underlying autistic behaviors using animal models. Ongoing studies of genetically modified models have offered critical insight into possible common mechanisms arising from different mutations, but links between molecular abnormalities and behavioral phenotypes remain elusive. The challenges encountered in modeling autism in mice demand a new analytic paradigm that integrates behavioral assessment with circuit-level analysis in genetically modified models with strong construct validity. This article is part of a Special Issue entitled: Neuropsychiatric Disease. (C) 2016 IBRO. Published by Elsevier Ltd. All rights reserved.

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