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There are 3169 results for: content related to: Noncoding RNAs in mental retardation

  1. RNAs of the human chromosome 15q11-q13 imprinted region

    Wiley Interdisciplinary Reviews: RNA

    Volume 4, Issue 2, March/April 2013, Pages: 155–166, Stormy J. Chamberlain

    Article first published online : 3 DEC 2012, DOI: 10.1002/wrna.1150

  2. 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

    Article first published online : 25 JAN 2011, DOI: 10.1002/jcb.22958

  3. Mechanisms and brain specific consequences of genomic imprinting in Prader-Willi and Angelman syndromes

    Gene Function & Disease

    Volume 2, Issue 1, August 2001, Pages: 7–25, Axel Schumacher

    Article first published online : 21 AUG 2001, DOI: 10.1002/1438-826X(20018)2:1<7::AID-GNFD7>3.0.CO;2-N

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

    Biological Reviews

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

    Article first published online : 9 SEP 2008, DOI: 10.1111/j.1469-185X.2008.00050.x

  5. You have full text access to this OnlineOpen article
    The emerging landscape of small nucleolar RNAs in cell biology

    Wiley Interdisciplinary Reviews: RNA

    Volume 6, Issue 4, July/August 2015, Pages: 381–397, Fabien Dupuis-Sandoval, Mikaël Poirier and Michelle S. Scott

    Article first published online : 16 APR 2015, DOI: 10.1002/wrna.1284

  6. You have free access to this content
    Non-coding RNAs in imprinted gene clusters

    Biology of the Cell

    Volume 100, Issue 3, March 2008, Pages: 149–166, Hélène Royo and Jérôme Cavaillé

    Article first published online : 9 JAN 2012, DOI: 10.1042/BC20070126

  7. Prader–Willi syndrome and Angelman syndrome

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

    Volume 154C, Issue 3, 15 August 2010, Pages: 365–376, Karin Buiting

    Article first published online : 20 AUG 2010, DOI: 10.1002/ajmg.c.30273

  8. Processing of snoRNAs as a new source of regulatory non-coding RNAs

    BioEssays

    Volume 35, Issue 1, January 2013, Pages: 46–54, Marina Falaleeva and Stefan Stamm

    Article first published online : 26 NOV 2012, DOI: 10.1002/bies.201200117

  9. 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

    Article first published online : 7 JUN 2002, DOI: 10.1002/ajmg.10498

  10. Imprinting in Prader–Willi and Angelman syndromes

    Standard Article

    Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics

    Bernhard Horsthemke and Karin Buiting

    Published Online : 15 NOV 2005, DOI: 10.1002/047001153X.g103214

  11. 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

    Article first published online : 31 JUL 2003, DOI: 10.1002/ajmg.a.20343

  12. 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

    Article first published online : 3 MAY 2013, DOI: 10.1002/ajmg.b.32152

  13. Genome-wide small noncoding RNA profiling of pediatric high-grade gliomas reveals deregulation of several miRNAs, identifies downregulation of snoRNA cluster HBII-52 and delineates H3F3A and TP53 mutant-specific miRNAs and snoRNAs

    International Journal of Cancer

    Prerana Jha, Rahul Agrawal, Pankaj Pathak, Anupam Kumar, Suvendu Purkait, Supriyo Mallik, Vaishali Suri, Mehar Chand Sharma, Deepak Gupta, Ashish Suri, B.S. Sharma, P.K. Julka, Ritu Kulshreshtha and Chitra Sarkar

    Article first published online : 3 JUN 2015, DOI: 10.1002/ijc.29610

  14. 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

    Article first published online : 3 APR 2014, DOI: 10.1002/cne.23507

  15. 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

    Article first published online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32364

  16. You have free access to this content
    Angelman syndrome caused by an identical familial 1,487-kb deletion

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 1, 1 January 2007, Pages: 98–101, Kanako Sato, Mie Iwakoshi, Osamu Shimokawa, Haruya Sakai, Tohru Ohta, Shinji Saitoh, Noriko Miyake, Norio Niikawa, Naoki Harada, Hirotomo Saitsu, Takeshi Mizuguchi and Naomichi Matsumoto

    Article first published online : 6 DEC 2006, DOI: 10.1002/ajmg.a.31550

  17. Association study of the 15q11-q13 maternal expression domain in Japanese autistic patients

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 7, 5 October 2008, Pages: 1008–1012, Chieko Kato, Mamoru Tochigi, Jun Ohashi, Shinko Koishi, Yuki Kawakubo, Kenji Yamamoto, Hideo Matsumoto, Ohiko Hashimoto, Soo-Yung Kim, Keiichiro Watanabe, Yukiko Kano, Eiji Nanba, Nobumasa Kato and Tsukasa Sasaki

    Article first published online : 9 JAN 2008, DOI: 10.1002/ajmg.b.30690

  18. Whole genome microarray analysis of gene expression in Prader–Willi syndrome

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 5, 1 March 2007, Pages: 430–442, Douglas C. Bittel, Nataliya Kibiryeva, Susan M. Sell, Theresa V. Strong and Merlin G. Butler

    Article first published online : 18 JAN 2007, DOI: 10.1002/ajmg.a.31606

  19. You have full text access to this OnlineOpen article
    Box C/D snoRNP catalysed methylation is aided by additional pre-rRNA base-pairing

    The EMBO Journal

    Volume 30, Issue 12, June 15, 2011, Pages: 2420–2430, Robert Willem van Nues, Sander Granneman, Grzegorz Kudla, Katherine Elizabeth Sloan, Matthew Chicken, David Tollervey and Nicholas James Watkins

    Article first published online : 10 MAY 2011, DOI: 10.1038/emboj.2011.148

  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

    Article first published online : 6 AUG 2014, DOI: 10.1002/ajmg.a.36704