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There are 4070 results for: content related to: CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation

  1. You have free access to this content
    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

    Article first published online : 21 DEC 2011, DOI: 10.1111/j.1469-1809.2011.00694.x

  2. 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

    Article first published online : 7 JUN 2006, DOI: 10.1002/ajmg.a.31291

  3. 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

    Article first published online : 15 APR 2008, DOI: 10.1002/ajmg.a.32261

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    Abnormal dendrite and spine morphology in primary visual cortex in the CGG knock-in mouse model of the fragile X premutation

    Epilepsia

    Volume 53, Issue s1, June 2012, Pages: 150–160, Robert F. Berman, Karl D. Murray, Gloria Arque, Michael R. Hunsaker and H. Jürgen Wenzel

    Article first published online : 21 MAY 2012, DOI: 10.1111/j.1528-1167.2012.03486.x

  5. You have full text access to this OnlineOpen article
    Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population

    Molecular Genetics & Genomic Medicine

    Volume 3, Issue 3, May 2015, Pages: 172–181, Wen Huang, Qiuping Xia, Shiyu Luo, Hua He, Ting Zhu, Qian Du and Ranhui Duan

    Article first published online : 15 DEC 2014, DOI: 10.1002/mgg3.128

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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

    Article first published online : 22 DEC 2008, DOI: 10.1002/ajmg.b.30910

  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

    Article first published online : 30 JUN 2011, DOI: 10.1111/j.1399-0004.2011.01723.x

  8. Prevalence of CGG expansions of the FMR1 gene in a US population-based sample

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 5, July 2012, Pages: 589–597, Dr. Marsha Mailick Seltzer, Mei Wang Baker, Jinkuk Hong, Matthew Maenner, Jan Greenberg and Daniel Mandel

    Article first published online : 22 MAY 2012, DOI: 10.1002/ajmg.b.32065

  9. 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

  10. Risk of cognitive impairment in female premutation carriers of fragile X premutation: Analysis by means of robust segmented linear regression models

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 2, 5 March 2009, Pages: 262–270, Mónica Mínguez, Berta Ibáñez, Maria-Pilar Ribate, Feliciano Ramos, Eva García-Alegría, Aránzazu Fernández-Rivas, Eduardo Ruiz-Parra, Marisa Poch, Angel Alonso, Cristina Martinez-Bouzas, Elena Beristain and Maria-Isabel Tejada

    Article first published online : 18 JUN 2008, DOI: 10.1002/ajmg.b.30803

  11. 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

    Article first published online : 14 JUN 2010, DOI: 10.1111/j.1365-2788.2010.01290.x

  12. Maternal FMR1 premutation allele expansion and contraction in fraternal twins

    American Journal of Medical Genetics Part A

    Volume 161, Issue 10, October 2013, Pages: 2620–2625, Maria P. Alfaro, Melinda Cohen and Cindy L. Vnencak-Jones

    Article first published online : 15 AUG 2013, DOI: 10.1002/ajmg.a.36123

  13. Newborn screening and cascade testing for FMR1 mutations

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 59–69, Page L. Sorensen, Louise W. Gane, Mark Yarborough, Randi J. Hagerman and Flora Tassone

    Article first published online : 13 DEC 2012, DOI: 10.1002/ajmg.a.35680

  14. Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 139B, Issue 1, 5 November 2005, Pages: 115–121, David Hessl, Flora Tassone, Danuta Z. Loesch, Elizabeth Berry-Kravis, Maureen A. Leehey, Louise W. Gane, Ingrid Barbato, Cathlin Rice, Emma Gould, Deborah A. Hall, James Grigsby, Jacob A. Wegelin, Susan Harris, Foster Lewin, Dahlia Weinberg, Paul J. Hagerman and Randi J. Hagerman

    Article first published online : 23 SEP 2005, DOI: 10.1002/ajmg.b.30241

  15. Unexpected finding of a paternal premutation of the fragile X FMR1 gene in a female fetus of a premutation carrier mother

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 2, February 2010, Pages: 409–412, M. Grazia Pomponi, Roberta Pietrobono, Caterina Neri, Pietro Chiurazzi and Giovanni Neri

    Article first published online : 15 JAN 2010, DOI: 10.1002/ajmg.a.33213

  16. The fragile X mutation

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 1, Issue 4, 1995, Pages: 251–262, Georges Imbert and Dr. Jean-Louis Mandel

    Article first published online : 1 JUN 2005, DOI: 10.1002/mrdd.1410010405

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    Single Nucleotide Polymorphism and FMR1 CGG Repeat Instability in Two Basque Valleys

    Annals of Human Genetics

    Volume 76, Issue 2, March 2012, Pages: 110–120, Maitane Barasoain, Gorka Barrenetxea, Eduardo Ortiz-Lastra, Javier González, Iratxe Huerta, Mercedes Télez, Juan Manuel Ramírez, Amaia Domínguez, Paula Gurtubay, Begoña Criado and Isabel Arrieta

    Article first published online : 2 JAN 2012, DOI: 10.1111/j.1469-1809.2011.00696.x

  18. You have free access to this content
    Neuropathic features in fragile X premutation carriers

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 1, 1 January 2007, Pages: 19–26, Elizabeth Berry-Kravis, Christopher G. Goetz, Maureen A. Leehey, Randi J. Hagerman, Lin Zhang, Lexin Li, Danh Nguyen, Deborah A. Hall, Nicole Tartaglia, Jennifer Cogswell, Flora Tassone and Paul J. Hagerman

    Article first published online : 6 DEC 2006, DOI: 10.1002/ajmg.a.31559

  19. CGG repeat length correlates with age of onset of motor signs of the fragile X-associated tremor/ataxia syndrome (FXTAS)

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 4, 5 June 2007, Pages: 566–569, Flora Tassone, John Adams, Elizabeth M. Berry-Kravis, Susannah S. Cohen, Alfredo Brusco, Maureen A. Leehey, Lexin Li, Randi J. Hagerman and Paul J. Hagerman

    Article first published online : 10 APR 2007, DOI: 10.1002/ajmg.b.30482

  20. Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion

    Clinical Genetics

    Volume 87, Issue 2, February 2015, Pages: 173–178, D. Z. Loesch, M. Q. Bui, E. Hammersley, A. Schneider, E. Storey, P. Stimpson, T. Burgess, D. Francis, H. Slater, F. Tassone, R. J. Hagerman and D. Hessl

    Article first published online : 17 FEB 2014, DOI: 10.1111/cge.12347