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There are 8351 results for: content related to: Role for metabotropic glutamate receptor 5 (mGluR5) in the pathogenesis of fragile X syndrome

  1. You have free access to this content
    Genetic manipulation of STEP reverses behavioral abnormalities in a fragile X syndrome mouse model

    Genes, Brain and Behavior

    Volume 11, Issue 5, July 2012, Pages: 586–600, S. M. Goebel-Goody, E. D. Wilson-Wallis, S. Royston, S. M. Tagliatela, J. R. Naegele and P. J. Lombroso

    Version of Record online : 6 APR 2012, DOI: 10.1111/j.1601-183X.2012.00781.x

  2. Metabotropic glutamate receptor 5 responses dictate differentiation of neural progenitors to NMDA-responsive cells in fragile X syndrome

    Developmental Neurobiology

    Venkat Swaroop Achuta, Heli Grym, Noora Putkonen, Verna Louhivuori, Virve Kärkkäinen, Jari Koistinaho, Laurent Roybon and Maija L. Castrén

    Version of Record online : 28 JUL 2016, DOI: 10.1002/dneu.22419

  3. You have full text access to this OnlineOpen article
    The effect of an mGluR5 inhibitor on procedural memory and avoidance discrimination impairments in Fmr1 KO mice

    Genes, Brain and Behavior

    Volume 11, Issue 3, April 2012, Pages: 325–331, M. F. Vinueza Veloz, R. A. M. Buijsen, R. Willemsen, A. Cupido, L. W. J. Bosman, S. K. E. Koekkoek, J. W. Potters, B. A. Oostra and C. I. De Zeeuw

    Version of Record online : 19 JAN 2012, DOI: 10.1111/j.1601-183X.2011.00763.x

  4. Increased coupling of caveolin-1 and estrogen receptor α contributes to the fragile X syndrome

    Annals of Neurology

    Volume 77, Issue 4, April 2015, Pages: 618–636, Qi Yang, Le Yang, Kun Zhang, Yan-Yan Guo, Shui-Bing Liu, Yu-Mei Wu, Xiao-Qiang Li, Qian Song, Min Zhuo and Ming-Gao Zhao

    Version of Record online : 26 FEB 2015, DOI: 10.1002/ana.24358

  5. You have full text access to this OnlineOpen article
    c-Jun N-terminal kinase regulates mGluR-dependent expression of post-synaptic FMRP target proteins

    Journal of Neurochemistry

    Volume 127, Issue 6, December 2013, Pages: 772–781, Travis L. Schmit, James A. Dowell, Margaret E. Maes and Michael Wilhelm

    Version of Record online : 24 OCT 2013, DOI: 10.1111/jnc.12453

  6. You have free access to this content
    Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice

    The Journal of Physiology

    Volume 587, Issue 4, February 2009, Pages: 787–804, Yair Pilpel, Aleksander Kolleker, Sven Berberich, Melanie Ginger, Andreas Frick, Edwin Mientjes, Ben A. Oostra and Peter H. Seeburg

    Version of Record online : 13 FEB 2009, DOI: 10.1113/jphysiol.2008.160929

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    Extinction of an instrumental response: a cognitive behavioral assay in Fmr1 knockout mice

    Genes, Brain and Behavior

    Volume 13, Issue 5, June 2014, Pages: 451–458, M. S. Sidorov, D. D. Krueger, M. Taylor, E. Gisin, E. K. Osterweil and M. F. Bear

    Version of Record online : 30 APR 2014, DOI: 10.1111/gbb.12137

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    The FMR1 gene and fragile X-associated tremor/ataxia syndrome

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 6, 5 September 2009, Pages: 782–798, J.R. Brouwer, R. Willemsen and B.A. Oostra

    Version of Record online : 22 DEC 2008, DOI: 10.1002/ajmg.b.30910

  9. You have full text access to this OnlineOpen article
    Increasing our understanding of human cognition through the study of fragile X syndrome

    Developmental Neurobiology

    Volume 74, Issue 2, February 2014, Pages: 147–177, Denise Cook, Erin Nuro and Keith K. Murai

    Version of Record online : 30 JUL 2013, DOI: 10.1002/dneu.22096

  10. CGG repeat in the FMR1 gene: size matters

    Clinical Genetics

    Volume 80, Issue 3, September 2011, Pages: 214–225, R Willemsen, J Levenga and BA Oostra

    Version of Record online : 30 JUN 2011, DOI: 10.1111/j.1399-0004.2011.01723.x

  11. You have free access to this content
    Fragile X syndrome: From protein function to therapy

    American Journal of Medical Genetics Part A

    Volume 161, Issue 11, November 2013, Pages: 2809–2821, Claudia Bagni and Ben A. Oostra

    Version of Record online : 24 SEP 2013, DOI: 10.1002/ajmg.a.36241

  12. Fragile X syndrome therapy: to respond or not to respond may be a matter of methylation

    Clinical Genetics

    Volume 79, Issue 6, June 2011, Pages: 508–510, MA Pouladi

    Version of Record online : 20 APR 2011, DOI: 10.1111/j.1399-0004.2011.01663.x

  13. NMDA receptor hypofunction in the dentate gyrus and impaired context discrimination in adult Fmr1 knockout mice

    Hippocampus

    Volume 22, Issue 2, February 2012, Pages: 241–254, Brennan D. Eadie, Jesse Cushman, Timal S. Kannangara, Michael S. Fanselow and Brian R. Christie

    Version of Record online : 3 NOV 2010, DOI: 10.1002/hipo.20890

  14. You have free access to this content
    Lithium treatment alleviates impaired cognition in a mouse model of fragile X syndrome

    Genes, Brain and Behavior

    Volume 12, Issue 7, October 2013, Pages: 723–731, M. K. King and R. S. Jope

    Version of Record online : 29 AUG 2013, DOI: 10.1111/gbb.12071

  15. Pathways to Drug Development for Autism Spectrum Disorders

    Clinical Pharmacology & Therapeutics

    Volume 91, Issue 2, February 2012, Pages: 189–200, D R Hampson, S Gholizadeh and L K K Pacey

    Version of Record online : 28 DEC 2011, DOI: 10.1038/clpt.2011.245

  16. Prepulse inhibition in fragile X syndrome: Feasibility, reliability, and implications for treatment

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 4, 5 June 2009, Pages: 545–553, David Hessl, Elizabeth Berry-Kravis, Lisa Cordeiro, Jennifer Yuhas, Edward M. Ornitz, Aaron Campbell, Elizabeth Chruscinski, Crystal Hervey, James M. Long and Randi J. Hagerman

    Version of Record online : 10 SEP 2008, DOI: 10.1002/ajmg.b.30858

  17. Analysis of Fmr1 Deletion in a Subpopulation of Post-Mitotic Neurons in Mouse Cortex and Hippocampus

    Autism Research

    Volume 7, Issue 1, February 2014, Pages: 60–71, Anahita Amiri, Efrain Sanchez-Ortiz, Woosung Cho, Shari G. Birnbaum, Jing Xu, Renée M. McKay and Luis F. Parada

    Version of Record online : 9 JAN 2014, DOI: 10.1002/aur.1342

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    Identification of Fragile X Syndrome Specific Molecular Markers in Human Fibroblasts: A Useful Model to Test the Efficacy of Therapeutic Drugs

    Human Mutation

    Volume 35, Issue 12, December 2014, Pages: 1485–1494, Daman Kumari, Aditi Bhattacharya, Jeffrey Nadel, Kristen Moulton, Nicole M. Zeak, Anne Glicksman, Carl Dobkin, David J. Brick, Philip H. Schwartz, Carolyn B. Smith, Eric Klann and Karen Usdin

    Version of Record online : 24 NOV 2014, DOI: 10.1002/humu.22699

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    Concise Review: Fragile X Proteins in Stem Cell Maintenance and Differentiation

    STEM CELLS

    Volume 32, Issue 7, July 2014, Pages: 1724–1733, Yue Li and Xinyu Zhao

    Version of Record online : 17 JUN 2014, DOI: 10.1002/stem.1698

  20. You have free access to this content
    Fragile X mental retardation protein is required for chemically-induced long-term potentiation of the hippocampus in adult mice

    Journal of Neurochemistry

    Volume 111, Issue 3, November 2009, Pages: 635–646, Yuze Shang, Hansen Wang, Valentina Mercaldo, Xiangyao Li, Tao Chen and Min Zhuo

    Version of Record online : 30 JUL 2009, DOI: 10.1111/j.1471-4159.2009.06314.x