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There are 7066193 results for: content related to: Lay abstracts

  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. You have free access to this content
    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

  3. 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

  4. 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

  5. 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

  6. You have free access to this content
    Reduction of BDNF expression in Fmr1 knockout mice worsens cognitive deficits but improves hyperactivity and sensorimotor deficits

    Genes, Brain and Behavior

    Volume 11, Issue 5, July 2012, Pages: 513–523, M. Uutela, J. Lindholm, V. Louhivuori, H. Wei, L. M. Louhivuori, A. Pertovaara, K. Åkerman, E. Castrén and M. L. Castrén

    Version of Record online : 11 APR 2012, DOI: 10.1111/j.1601-183X.2012.00784.x

  7. 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

  8. Indicators of anxiety and depression in women with the fragile X premutation: assessment of a clinical sample

    Journal of Intellectual Disability Research

    Volume 54, Issue 7, July 2010, Pages: 597–610, A. Lachiewicz, D. Dawson, G. Spiridigliozzi, M. Cuccaro, M. Lachiewicz and A. McConkie-Rosell

    Version of Record online : 14 JUN 2010, DOI: 10.1111/j.1365-2788.2010.01290.x

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    Altered anxiety-related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome

    Genes, Brain and Behavior

    Volume 4, Issue 7, October 2005, Pages: 420–430, C. M. Spencer, O. Alekseyenko, E. Serysheva, L. A. Yuva-Paylor and R. Paylor

    Version of Record online : 16 FEB 2005, DOI: 10.1111/j.1601-183X.2005.00123.x

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    Regulating fragile X gene transcription in the brain and beyond

    Journal of Cellular Physiology

    Volume 205, Issue 2, November 2005, Pages: 170–175, Jae H. Lim, Anne B. Booker and Justin R. Fallon

    Version of Record online : 13 MAY 2005, DOI: 10.1002/jcp.20401

  11. You have free access to this content
    Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells

    STEM CELLS

    Meng Li, Huashan Zhao, Gene E. Ananiev, Michael T. Musser, Kathryn H. Ness, Dianne L. Maglaque, Krishanu Saha, Anita Bhattacharyya and Xinyu Zhao

    Version of Record online : 27 JUL 2016, DOI: 10.1002/stem.2463

  12. You have free access to this content
    A phenotypic and molecular characterization of the fmr1-tm1Cgr Fragile X mouse

    Genes, Brain and Behavior

    Volume 3, Issue 6, December 2004, Pages: 337–359, Q. J. Yan, P. K. Asafo-Adjei, H. M. Arnold, R. E. Brown and R. P. Bauchwitz

    Version of Record online : 15 JUL 2004, DOI: 10.1111/j.1601-183X.2004.00087.x

  13. Males but not females show differences in calbindin immunoreactivity in the dorsal thalamus of the mouse model of fragile X syndrome

    Journal of Comparative Neurology

    Volume 521, Issue 4, 1 March 2013, Pages: 894–911, Rosa M. Giráldez-Pérez, M. Nieves Ávila, Mónica Feijóo-Cuaresma, Raúl Heredia, Yolanda De Diego-Otero, M. Ángeles Real and Salvador Guirado

    Version of Record online : 22 JAN 2013, DOI: 10.1002/cne.23209

  14. Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses

    Autism Research

    Volume 4, Issue 1, February 2011, Pages: 40–56, Corinne M. Spencer, Olga Alekseyenko, Shannon M. Hamilton, Alexia M. Thomas, Ekaterina Serysheva, Lisa A. Yuva-Paylor and Richard Paylor

    Version of Record online : 25 JAN 2011, DOI: 10.1002/aur.168

  15. You have free access to this content
    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

  16. GABAB receptor-mediated feed-forward circuit dysfunction in the mouse model of fragile X syndrome

    The Journal of Physiology

    Volume 593, Issue 22, 15 November 2015, Pages: 5009–5024, Sarah Wahlstrom-Helgren and Vitaly A. Klyachko

    Version of Record online : 2 OCT 2015, DOI: 10.1113/JP271190

  17. 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

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    Dampened dopamine-mediated neuromodulation in prefrontal cortex of fragile X mice

    The Journal of Physiology

    Volume 591, Issue 4, February 2013, Pages: 1133–1143, Kush Paul, Deepa V. Venkitaramani and Charles L. Cox

    Version of Record online : 8 JAN 2013, DOI: 10.1113/jphysiol.2012.241067

  19. Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 5, July 2012, Pages: 549–559, Jessica Ezzell Hunter, Mary Leslie, Gloria Novak, Debra Hamilton, Lisa Shubeck, Krista Charen, Ann Abramowitz, Michael P. Epstein, Adriana Lori, Elisabeth Binder, Joseph F. Cubells and Stephanie L. Sherman

    Version of Record online : 9 MAY 2012, DOI: 10.1002/ajmg.b.32061

  20. 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