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There are 7211 results for: content related to: The Fragile X Protein binds m RNA s involved in cancer progression and modulates metastasis formation

  1. You have full text access to this OnlineOpen article
    A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function

    EMBO Molecular Medicine

    Volume 7, Issue 4, April 2015, Pages: 423–437, Zeynep Okray, Celine EF de Esch, Hilde Van Esch, Koen Devriendt, Annelies Claeys, Jiekun Yan, Jelle Verbeeck, Guy Froyen, Rob Willemsen, Femke MS de Vrij and Bassem A Hassan

    Version of Record online : 18 FEB 2015, DOI: 10.15252/emmm.201404576

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    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

  3. You have full text access to this OnlineOpen article
    Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes

    EMBO Molecular Medicine

    Volume 7, Issue 12, December 2015, Pages: 1565–1579, Beata Stepniak, Anne Kästner, Giulia Poggi, Marina Mitjans, Martin Begemann, Annette Hartmann, Sandra Van der Auwera, Farahnaz Sananbenesi, Dilja Krueger-Burg, Gabriela Matuszko, Cornelia Brosi, Georg Homuth, Henry Völzke, Fritz Benseler, Claudia Bagni, Utz Fischer, Alexander Dityatev, Hans-Jörgen Grabe, Dan Rujescu, Andre Fischer and Hannelore Ehrenreich

    Version of Record online : 26 NOV 2015, DOI: 10.15252/emmm.201505696

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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

  5. 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

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    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

  7. Fragile X-Linked Mental Retardation

    Standard Article

    Reviews in Cell Biology and Molecular Medicine

    Ilse Gantois, R. Frank Kooy and Ben A. Oostra

    Published Online : 15 SEP 2006, DOI: 10.1002/3527600906.mcb.200300051

  8. FMR1 gene and fragile X syndrome

    American Journal of Medical Genetics

    Volume 97, Issue 2, Summer 2000, Pages: 153–163, Barbara Bardoni, Jean-Louis Mandel and Gene S. Fisch

    Version of Record online : 28 NOV 2000, DOI: 10.1002/1096-8628(200022)97:2<153::AID-AJMG7>3.0.CO;2-M

  9. Increased transient Na+ conductance and action potential output in layer 2/3 prefrontal cortex neurons of the fmr1−/y mouse

    The Journal of Physiology

    Volume 595, Issue 13, 1 July 2017, Pages: 4431–4448, Brandy N. Routh, Rahul K. Rathour, Michael E. Baumgardner, Brian E. Kalmbach, Daniel Johnston and Darrin H. Brager

    Version of Record online : 23 MAY 2017, DOI: 10.1113/JP274258

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    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

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    A normal genetic variation modulates synaptic MMP-9 protein levels and the severity of schizophrenia symptoms

    EMBO Molecular Medicine

    Volume 9, Issue 8, August 2017, Pages: 1100–1116, Katarzyna Lepeta, Katarzyna J Purzycka, Katarzyna Pachulska-Wieczorek, Marina Mitjans, Martin Begemann, Behnam Vafadari, Krystian Bijata, Ryszard W Adamiak, Hannelore Ehrenreich, Magdalena Dziembowska and Leszek Kaczmarek

    Version of Record online : 16 JUN 2017, DOI: 10.15252/emmm.201707723

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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

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    Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells

    STEM CELLS

    Volume 35, Issue 1, January 2017, Pages: 158–169, 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

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    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

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    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

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    High-Throughput Screening to Identify Compounds That Increase Fragile X Mental Retardation Protein Expression in Neural Stem Cells Differentiated From Fragile X Syndrome Patient-Derived Induced Pluripotent Stem Cells

    STEM CELLS Translational Medicine

    Volume 4, Issue 7, July 2015, Pages: 800–808, Daman Kumari, Manju Swaroop, Noel Southall, Wenwei Huang, Wei Zheng and Karen Usdin

    Version of Record online : 21 MAY 2015, DOI: 10.5966/sctm.2014-0278

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    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

  18. 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

  19. 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