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There are 1697 results for: content related to: Clinical significance of the ubiquitin ligase UBE3C in hepatocellular carcinoma revealed by exome sequencing

  1. You have free access to this content
    Autoubiquitination of the 26S Proteasome on Rpn13 Regulates Breakdown of Ubiquitin Conjugates

    The EMBO Journal

    Volume 33, Issue 10, 16 May 2014, Pages: 1159–1176, Henrike C Besche, Zhe Sha, Nikolay V Kukushkin, Andreas Peth, Eva-Maria Hock, Woong Kim, Steven Gygi, Juan A Gutierrez, Hua Liao, Lawrence Dick and Alfred L Goldberg

    Version of Record online : 8 MAY 2014, DOI: 10.1002/embj.201386906

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    Alterations in mRNA expression and protein products following spinal cord injury in humans

    The Journal of Physiology

    Volume 579, Issue 3, March 2007, Pages: 877–892, Maria L. Urso, Yi-Wen Chen, Angus G. Scrimgeour, Patrick C. Lee, K. Francis Lee and Priscilla M. Clarkson

    Version of Record online : 14 MAR 2007, DOI: 10.1113/jphysiol.2006.118042

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    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

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    Hepatology highlights


    Volume 59, Issue 6, June 2014, Pages: 2059–2061, Jean-François Dufour

    Version of Record online : 28 MAY 2014, DOI: 10.1002/hep.27166

  5. 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

  6. 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

  7. Bioinformatic analyses and conceptual synthesis of evidence linking ZNF804A to risk for schizophrenia and bipolar disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 1, January 2015, Pages: 14–35, Jonathan L. Hess, Thomas P. Quinn, Schahram Akbarian and Stephen J. Glatt

    Version of Record online : 19 DEC 2014, DOI: 10.1002/ajmg.b.32284

  8. 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

  9. Impaired Neurite Contact Guidance in Ubiquitin Ligase E3a (Ube3a)-Deficient Hippocampal Neurons on Nanostructured Substrates

    Advanced Healthcare Materials

    Volume 5, Issue 7, April 6, 2016, Pages: 850–862, I. Tonazzini, S. Meucci, G. M. Van Woerden, Y. Elgersma and M. Cecchini

    Version of Record online : 4 FEB 2016, DOI: 10.1002/adhm.201500815

  10. Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 8, August 2010, Pages: 1994–2001, Sarika U. Peters, Lynne M. Bird, Virginia Kimonis, Daniel G. Glaze, Lina M. Shinawi, Terry Jo Bichell, Rene Barbieri-Welge, Mark Nespeca, Irina Anselm, Susan Waisbren, Erica Sanborn, Qin Sun, William E. O'Brien, Arthur L. Beaudet and Carlos A. Bacino

    Version of Record online : 15 JUL 2010, DOI: 10.1002/ajmg.a.33509

  11. 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

  12. You have full text access to this OnlineOpen article
    Perturbed proteostasis in autism spectrum disorders

    Journal of Neurochemistry

    Susana R. Louros and Emily K. Osterweil

    Version of Record online : 4 AUG 2016, DOI: 10.1111/jnc.13723

  13. 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

  14. 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

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    Angelman syndrome: Current understanding and research prospects


    Volume 50, Issue 11, November 2009, Pages: 2331–2339, Bernard Dan

    Version of Record online : 23 OCT 2009, DOI: 10.1111/j.1528-1167.2009.02311.x

  16. 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

  17. 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

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    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

  19. Molecular and clinical characterization of Angelman syndrome in Chinese patients

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 273–277, J.-L. Bai, Y.-J. Qu, Y.-W. Jin, H. Wang, Y.-L. Yang, Y.-W. Jiang, X.-Y. Yang, L.-P. Zou and F. Song

    Version of Record online : 23 APR 2013, DOI: 10.1111/cge.12155

  20. Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2873–2878, Yukiko Kuroda, Ikuko Ohashi, Toshiyuki Saito, Jun-Ichi Nagai, Kazumi Ida, Takuya Naruto, Takahito Wada and Kenji Kurosawa

    Version of Record online : 6 AUG 2014, DOI: 10.1002/ajmg.a.36704