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There are 5704 results for: content related to: RNA-binding proteins involved in RNA localization and their implications in neuronal diseases

  1. RNA-binding proteins in neurodegenerative disease: TDP-43 and beyond

    Wiley Interdisciplinary Reviews: RNA

    Volume 3, Issue 2, March/April 2012, Pages: 265–285, Keith A. Hanson, Sang Hwa Kim and Randal S. Tibbetts

    Version of Record online : 25 OCT 2011, DOI: 10.1002/wrna.111

  2. Autistic behavior in children with fragile X syndrome: Prevalence, stability, and the impact of FMRP

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 17, 1 September 2006, Pages: 1804–1813, Deborah D. Hatton, John Sideris, Martie Skinner, Jean Mankowski, Donald B. Bailey Jr, Jane Roberts and Penny Mirrett

    Version of Record online : 12 MAY 2006, DOI: 10.1002/ajmg.a.31286

  3. ADHD symptoms in children with FXS

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 21, 1 November 2006, Pages: 2275–2288, Kelly Sullivan, Deborah Hatton, Julie Hammer, John Sideris, Stephen Hooper, Peter Ornstein and Donald Bailey Jr.

    Version of Record online : 4 OCT 2006, DOI: 10.1002/ajmg.a.31388

  4. You have free access to this content
    Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndrome

    Genes, Brain and Behavior

    Volume 11, Issue 3, April 2012, Pages: 332–341, C. A. Hoeffer, E. Sanchez, R. J. Hagerman, Y. Mu, D. V. Nguyen, H. Wong, A. M. Whelan, R. S. Zukin, E. Klann and F. Tassone

    Version of Record online : 15 FEB 2012, DOI: 10.1111/j.1601-183X.2012.00768.x

  5. 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

  6. Early identification of autism in fragile X syndrome: a review

    Journal of Intellectual Disability Research

    Volume 57, Issue 9, September 2013, Pages: 803–814, L. M. McCary and J. E. Roberts

    Version of Record online : 14 SEP 2012, DOI: 10.1111/j.1365-2788.2012.01609.x

  7. Systematic mapping of fragile X granules in the mouse brain reveals a potential role for presynaptic FMRP in sensorimotor functions

    Journal of Comparative Neurology

    Volume 520, Issue 16, 1 November 2012, Pages: 3687–3706, Michael R. Akins, Hannah F. LeBlanc, Emily E. Stackpole, Eunice Chyung and Justin R. Fallon

    Version of Record online : 5 SEP 2012, DOI: 10.1002/cne.23123

  8. 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

  9. Phonological awareness and reading in boys with fragile X syndrome

    Journal of Child Psychology and Psychiatry

    Volume 56, Issue 1, January 2015, Pages: 30–39, Suzanne M. Adlof, Jessica Klusek, Svetlana V. Shinkareva, Marissa L. Robinson and Jane E. Roberts

    Version of Record online : 3 JUN 2014, DOI: 10.1111/jcpp.12267

  10. 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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    G-quadruplexes: Emerging roles in neurodegenerative diseases and the non-coding transcriptome

    FEBS Letters

    Volume 589, Issue 14, June 22, 2015, Pages: 1653–1668, Roberto Simone, Pietro Fratta, Stephen Neidle, Gary N. Parkinson and Adrian M. Isaacs

    Version of Record online : 13 MAY 2015, DOI: 10.1016/j.febslet.2015.05.003

  12. Cardiovascular indices of physiological arousal in boys with fragile X syndrome

    Developmental Psychobiology

    Volume 39, Issue 2, September 2001, Pages: 107–123, Jane E. Roberts, Maria L. Boccia, Donald B. Bailey Jr., Deborah D. Hatton and Martie Skinner

    Version of Record online : 31 AUG 2001, DOI: 10.1002/dev.1035

  13. Fragile X syndrome: an overview and update of the FMR1 gene

    Clinical Genetics

    Accepted manuscript online: 15 JUN 2017, Montserrat Mila, Maria Isabel Alvarez-Mora, Irene madrigal and Laia Rodriguez-Revenga

    DOI: 10.1111/cge.13075

  14. Human pathologies associated with defective RNA transport and localization in the nervous system

    Biology of the Cell

    Volume 99, Issue 11, November 2007, Pages: 649–661, Ralf Dahm and Paolo Macchi

    Version of Record online : 9 JAN 2012, DOI: 10.1042/BC20070045

  15. Chronological age, but not FMRP levels, predicts neuropsychological performance in girls with fragile X syndrome

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 5, 5 July 2006, Pages: 468–472, Amy A. Lightbody, Scott S. Hall and Allan L. Reiss

    Version of Record online : 1 JUN 2006, DOI: 10.1002/ajmg.b.30307

  16. Cognitive aspects of Fragile X syndrome

    Wiley Interdisciplinary Reviews: Cognitive Science

    Volume 5, Issue 4, July/August 2014, Pages: 501–508, Lillie B. Huddleston, Jeannie Visootsak and Stephanie L. Sherman

    Version of Record online : 29 MAY 2014, DOI: 10.1002/wcs.1296

  17. Mapping nonverbal IQ in young boys with fragile X syndrome

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 1, 1 January 2005, Pages: 25–32, Martie Skinner, Stephen Hooper, Deborah D. Hatton, Jane Roberts, Penny Mirrett, Jennifer Schaaf, Kelly Sullivan, Anne Wheeler and Donald B. Bailey Jr

    Version of Record online : 18 NOV 2004, DOI: 10.1002/ajmg.a.30353

  18. Expression of fragile X mental retardation-1 gene with nuclear export signal mutation changes the expression profiling of mouse cerebella immortal neuronal cell

    PROTEOMICS

    Volume 5, Issue 15, No. 15 October 2005, Pages: 3979–3990, LiPing Hu, YuTing Chen, Stefan Evers and Yan Shen

    Version of Record online : 30 AUG 2005, DOI: 10.1002/pmic.200401252

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    Role for metabotropic glutamate receptor 5 (mGluR5) in the pathogenesis of fragile X syndrome

    The Journal of Physiology

    Volume 586, Issue 6, March 2008, Pages: 1503–1508, Gül Dölen and Mark F. Bear

    Version of Record online : 17 MAR 2008, DOI: 10.1113/jphysiol.2008.150722

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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