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There are 1873 results for: content related to: The fragile X gene and its function

  1. 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

  2. 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

  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

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    Fragile X Syndrome: The FMR1 CGG Repeat Distribution Among World Populations

    Annals of Human Genetics

    Volume 76, Issue 2, March 2012, Pages: 178–191, Emmanuel Peprah

    Version of Record online : 21 DEC 2011, DOI: 10.1111/j.1469-1809.2011.00694.x

  5. 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

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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

  7. 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

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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

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    CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome

    Journal of Neurochemistry

    Volume 107, Issue 6, December 2008, Pages: 1671–1682, Judith R. Brouwer, Karin Huizer, Lies-Anne Severijnen, Renate K. Hukema, Robert F. Berman, Ben A. Oostra and Rob Willemsen

    Version of Record online : 21 OCT 2008, DOI: 10.1111/j.1471-4159.2008.05747.x

  10. Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: A case report and review of the literature

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 10, 15 May 2008, Pages: 1358–1367, Bradford Coffee, Morna Ikeda, Dejan B. Budimirovic, Lawrence N. Hjelm, Walter E. Kaufmann and Stephen T. Warren

    Version of Record online : 15 APR 2008, DOI: 10.1002/ajmg.a.32261

  11. The FRAXopathies: Definition, overview, and update

    American Journal of Medical Genetics Part A

    Volume 155, Issue 8, August 2011, Pages: 1803–1816, Filomena Pirozzi, Elisabetta Tabolacci and Giovanni Neri

    Version of Record online : 7 JUL 2011, DOI: 10.1002/ajmg.a.34113

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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

  13. Decreased home cage movement and oromotor impairments in adult Fmr1-KO mice

    Genes, Brain and Behavior

    S. J. Bonasera, T. R. Chaudoin, E. H. Goulding, M. Mittek and A. Dunaevsky

    Version of Record online : 29 MAR 2017, DOI: 10.1111/gbb.12374

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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

  15. Fragile X–associated tremor/ataxia syndrome

    Annals of the New York Academy of Sciences

    Volume 1338, Issue 1, March 2015, Pages: 58–70, Paul J. Hagerman and Randi J. Hagerman

    Version of Record online : 26 JAN 2015, DOI: 10.1111/nyas.12693

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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

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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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    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

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    Male and female Fmr1 knockout mice on C57 albino background exhibit spatial learning and memory impairments

    Genes, Brain and Behavior

    Volume 9, Issue 6, August 2010, Pages: 562–574, K. B. Baker, S. P. Wray, R. Ritter, S. Mason, T. H. Lanthorn and K.V. Savelieva

    Version of Record online : 6 APR 2010, DOI: 10.1111/j.1601-183X.2010.00585.x

  20. Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X male

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 13, 1 July 2006, Pages: 1463–1471, Xiao-Dong Han, Berkley R. Powell, Judith L. Phalin and Farid F. Chehab

    Version of Record online : 7 JUN 2006, DOI: 10.1002/ajmg.a.31291