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There are 17316 results for: content related to: Hypothesis: Dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders

  1. Allelic specificity of Ube3a Expression In The Mouse Brain During Postnatal Development

    Journal of Comparative Neurology

    Volume 522, Issue 8, 01 June 2014, Pages: 1874–1896, Matthew C. Judson, Jason O. Sosa-Pagan, Wilmer A. Del Cid, Ji Eun Han and Benjamin D. Philpot

    Version of Record online : 3 APR 2014, DOI: 10.1002/cne.23507

  2. Genomic imprinting in the development and evolution of psychotic spectrum conditions

    Biological Reviews

    Volume 83, Issue 4, November 2008, Pages: 441–493, Bernard Crespi

    Version of Record online : 9 SEP 2008, DOI: 10.1111/j.1469-185X.2008.00050.x

  3. Subcellular organization of UBE3A in neurons

    Journal of Comparative Neurology

    Alain C. Burette, Matthew C. Judson, Susan Burette, Kristen D. Phend, Benjamin D. Philpot and Richard J. Weinberg

    Version of Record online : 11 JUL 2016, DOI: 10.1002/cne.24063

  4. A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

    American Journal of Medical Genetics Part A

    Volume 131A, Issue 1, 15 November 2004, Pages: 1–10, Yong-hui Jiang, Trilochan Sahoo, Ron C. Michaelis, Dani Bercovich, Jan Bressler, Catherine D. Kashork, Qian Liu, Lisa G. Shaffer, Richard J. Schroer, David W. Stockton, Richard S. Spielman, Roger E. Stevenson and Arthur L. Beaudet

    Version of Record online : 8 SEP 2004, DOI: 10.1002/ajmg.a.30297

  5. Neuronal chromatin dynamics of imprinting in development and disease

    Journal of Cellular Biochemistry

    Volume 112, Issue 2, February 2011, Pages: 365–373, Karen N. Leung, Stormy J. Chamberlain, Marc Lalande and Janine M. LaSalle

    Version of Record online : 25 JAN 2011, DOI: 10.1002/jcb.22958

  6. Autism spectrum disorders: The quest for genetic syndromes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 327–366, Dimitrios I. Zafeiriou, Athina Ververi, Vaios Dafoulis, Efrosini Kalyva and Euthymia Vargiami

    Version of Record online : 3 MAY 2013, DOI: 10.1002/ajmg.b.32152

  7. Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS

    American Journal of Medical Genetics Part A

    Volume 125A, Issue 2, 1 March 2004, Pages: 167–172, Megan P. Hitchins, Sarah Rickard, Fatima Dhalla, Bert B.A. de Vries, Robin Winter, Marcus E. Pembrey and Sue Malcolm

    Version of Record online : 31 JUL 2003, DOI: 10.1002/ajmg.a.20343

  8. You have free access to this content
    HECT-type E3 ubiquitin ligases in nerve cell development and synapse physiology

    FEBS Letters

    Volume 589, Issue 14, June 22, 2015, Pages: 1635–1643, Mateusz Cyryl Ambrozkiewicz and Hiroshi Kawabe

    Version of Record online : 13 MAY 2015, DOI: 10.1016/j.febslet.2015.05.009

  9. You have free access to this content
    15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes

    Human Mutation

    Volume 36, Issue 7, July 2015, Pages: 689–693, Abdul Noor, Lucie Dupuis, Kirti Mittal, Anath C. Lionel, Christian R. Marshall, Stephen W. Scherer, Tracy Stockley, John B. Vincent, Roberto Mendoza-Londono and Dimitri J. Stavropoulos

    Version of Record online : 11 JUN 2015, DOI: 10.1002/humu.22800

  10. Mouse models of autism spectrum disorders: The challenge for behavioral genetics

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 142C, Issue 1, 15 February 2006, Pages: 40–51, Sheryl S. Moy, Jessica J. Nadler, Terry R. Magnuson and Jacqueline N. Crawley

    Version of Record online : 17 JAN 2006, DOI: 10.1002/ajmg.c.30081

  11. You have full text access to this OnlineOpen article
    The Interstitial Duplication 15q11.2-q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature

    Autism Research

    Volume 6, Issue 4, August 2013, Pages: 268–279, Nora Urraca, Julie Cleary, Victoria Brewer, Eniko K. Pivnick, Kathryn McVicar, Ronald L. Thibert, N. Carolyn Schanen, Carmen Esmer, Dustin Lamport and Lawrence T. Reiter

    Version of Record online : 14 MAR 2013, DOI: 10.1002/aur.1284

  12. Novel UBE3A mutations causing Angelman syndrome: Different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 3, March 2009, Pages: 343–348, Cristina Camprubí, Miriam Guitart, Elisabeth Gabau, Maria Dolors Coll, Sergi Villatoro, Silvestre Oltra, Monica Roselló, Irene Ferrer, Sandra Monfort, Carmen Orellana and Francisco Martínez

    Version of Record online : 11 FEB 2009, DOI: 10.1002/ajmg.a.32659

  13. Discordant phenotypes in first cousins with UBE3A frameshift mutation

    American Journal of Medical Genetics Part A

    Volume 127A, Issue 3, 15 June 2004, Pages: 258–262, G.A. Molfetta, M.V.R. Muñoz, A.C. Santos, W.A. Silva, J. Wagstaff and J.M. Pina-Neto

    Version of Record online : 5 MAR 2004, DOI: 10.1002/ajmg.a.20723

  14. UBE3A gene mutations in finnish Angelman syndrome patients detected by conformation sensitive gel electrophoresis

    American Journal of Medical Genetics Part A

    Volume 126A, Issue 3, 30 April 2004, Pages: 248–252, Katrin Rapakko, Hannaleena Kokkonen and Jaakko Leisti

    Version of Record online : 26 NOV 2003, DOI: 10.1002/ajmg.a.20587

  15. Syndromes and epistemology II: Is autism a polygenic disorder?

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 17, 1 September 2008, Pages: 2203–2212, Gene S. Fisch

    Version of Record online : 29 JUL 2008, DOI: 10.1002/ajmg.a.32438

  16. Mechanisms of imprinting of the Prader–Willi/Angelman region

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 16, 15 August 2008, Pages: 2041–2052, Bernhard Horsthemke and Joseph Wagstaff

    Version of Record online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32364

  17. Familial interstitial 570 kbp deletion of the UBE3A gene region causing Angelman syndrome but not Prader-Willi syndrome

    American Journal of Medical Genetics

    Volume 111, Issue 3, 15 August 2002, Pages: 233–237, Joachim Bürger, Denise Horn, Holger Tönnies, Heidemarie Neitzel and André Reis

    Version of Record online : 7 JUN 2002, DOI: 10.1002/ajmg.10498

  18. Region-specific impairments in striatal synaptic transmission and impaired instrumental learning in a mouse model of Angelman syndrome

    European Journal of Neuroscience

    Volume 39, Issue 6, March 2014, Pages: 1018–1025, Volodya Hayrapetyan, Stephen Castro, Tatyana Sukharnikova, Chunxiu Yu, Xinyu Cao, Yong-Hui Jiang and Henry H. Yin

    Version of Record online : 13 DEC 2013, DOI: 10.1111/ejn.12442

  19. UBE3A regulates MC1R expression: a link to hypopigmentation in Angelman syndrome

    Pigment Cell & Melanoma Research

    Volume 24, Issue 5, October 2011, Pages: 944–952, Daren Low and Ken-Shiung Chen

    Version of Record online : 27 JUL 2011, DOI: 10.1111/j.1755-148X.2011.00884.x

  20. Mutation Update for UBE3A Variants in Angelman Syndrome

    Human Mutation

    Volume 35, Issue 12, December 2014, Pages: 1407–1417, Bekim Sadikovic, Priscilla Fernandes, Victor Wei Zhang, Patricia A. Ward, Irene Miloslavskaya, William Rhead, Richard Rosenbaum, Robert Gin, Benjamin Roa and Ping Fang

    Version of Record online : 24 NOV 2014, DOI: 10.1002/humu.22687