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There are 5808 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

    Version of Record 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

    Version of Record 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

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

  4. 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

  5. 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

    Version of Record online : 1 JUN 2005, DOI: 10.1002/mrdd.1410010405

  6. 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

    Version of Record online : 15 DEC 2014, DOI: 10.1002/mgg3.128

  7. Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing

    Human Mutation

    Volume 38, Issue 3, March 2017, Pages: 324–331, Simon Ardui, Valerie Race, Alena Zablotskaya, Matthew S. Hestand, Hilde Van Esch, Koenraad Devriendt, Gert Matthijs and Joris R. Vermeesch

    Version of Record online : 17 JAN 2017, DOI: 10.1002/humu.23150

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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

  9. 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

    Version of Record online : 22 MAY 2012, DOI: 10.1002/ajmg.b.32065

  10. Screening and instability of FMR1 alleles in a prospective sample of 24,449 mother–newborn pairs from the general population

    Clinical Genetics

    Volume 76, Issue 6, December 2009, Pages: 511–523, S Lévesque, C Dombrowski, M-L Morel, R Rehel, J-S Côté, J Bussières, K Morgan and F Rousseau

    Version of Record online : 23 OCT 2009, DOI: 10.1111/j.1399-0004.2009.01237.x

  11. 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

    Version of Record online : 18 JUN 2008, DOI: 10.1002/ajmg.b.30803

  12. 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

  13. 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

    Version of Record online : 15 AUG 2013, DOI: 10.1002/ajmg.a.36123

  14. Transcription of the FMR1 gene in individuals with fragile X syndrome

    American Journal of Medical Genetics

    Volume 97, Issue 3, Autumn (Fall) 2000, Pages: 195–203, Flora Tassone, Randi J. Hagerman, Winston D. Chamberlain and Paul J. Hagerman

    Version of Record online : 12 JAN 2001, DOI: 10.1002/1096-8628(200023)97:3<195::AID-AJMG1037>3.0.CO;2-R

  15. 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

    Version of Record online : 13 DEC 2012, DOI: 10.1002/ajmg.a.35680

  16. 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

    Version of Record online : 23 SEP 2005, DOI: 10.1002/ajmg.b.30241

  17. 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

    Version of Record online : 15 JAN 2010, DOI: 10.1002/ajmg.a.33213

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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

    Version of Record online : 21 MAY 2012, DOI: 10.1111/j.1528-1167.2012.03486.x

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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

    Version of Record online : 2 JAN 2012, DOI: 10.1111/j.1469-1809.2011.00696.x

  20. 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

    Version of Record online : 6 DEC 2006, DOI: 10.1002/ajmg.a.31559