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There are 1405 results for: content related to: MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions

  1. Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH

    Clinical Genetics

    Volume 84, Issue 1, July 2013, Pages: 31–36, M Rio, G Royer, S Gobin, MC de Blois, C Ozilou, A Bernheim, M Nizon, A Munnich, J-P Bonnefont, S Romana, M Vekemans, C Turleau and V Malan

    Article first published online : 4 NOV 2012, DOI: 10.1111/cge.12036

  2. Identification of rare copy number variants in high burden schizophrenia families

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 3, April 2013, Pages: 273–282, Maarten J. Van Den Bossche, Mojca Strazisar, Sophia Cammaerts, Anthony M. Liekens, Geert Vandeweyer, Veerle Depreeuw, Maria Mattheijssens, An-Sofie Lenaerts, Sonia De Zutter, Peter De Rijk, Bernard Sabbe and Jurgen Del-Favero

    Article first published online : 15 MAR 2013, DOI: 10.1002/ajmg.b.32146

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    Association study of myelin transcription factor 1-like polymorphisms with schizophrenia in Han Chinese population

    Genes, Brain and Behavior

    Volume 11, Issue 1, February 2012, Pages: 87–93, W. Li, X. Wang, J. Zhao, J. Lin, X.-Q. Song, Y. Yang, C. Jiang, B. Xiao, G. Yang, H.-X. Zhang and L.-X. Lv

    Article first published online : 19 OCT 2011, DOI: 10.1111/j.1601-183X.2011.00734.x

  4. Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problems

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 7, 1 April 2007, Pages: 746–751, Ying S. Zou, Daniel L. Van Dyke and Jay W. Ellison

    Article first published online : 7 MAR 2007, DOI: 10.1002/ajmg.a.31645

  5. Myelin transcription factor 1 (Myt1) of the oligodendrocyte lineage, along with a closely related CCHC zinc finger, is expressed in developing neurons in the mammalian central nervous system

    Journal of Neuroscience Research

    Volume 50, Issue 2, 15 October 1997, Pages: 272–290, Jin G. Kim, Regina C. Armstrong, Denes v. Agoston, Alexandra Robinsky, Claudia Wiese, James Nagle and Lynn D. Hudson

    Article first published online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-4547(19971015)50:2<272::AID-JNR16>3.0.CO;2-A

  6. Recurrent inverted duplication of 2p with terminal deletion in a patient with the classical phenotype of trisomy 2p23-pter

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 20, 15 October 2007, Pages: 2417–2422, Nicolas Gruchy, Marie-Line Jacquemont, Stanislas Lyonnet, Philippe Labrune, Imen El Kamel, Jean-Pierre Siffroi and Marie-France Portnoï

    Article first published online : 12 SEP 2007, DOI: 10.1002/ajmg.a.31931

  7. Cytogenetic and molecular characterization of a partial trisomy 2p arising from inverted duplication of 2p with terminal deletion of 2pter

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 11, November 2009, Pages: 2507–2512, Carlos A. Tirado, Samuel Henderson, Naseem Uddin, Ewa Stewart, Santha Iyer, Ian M. Ratner, Erin Matthews, Jeffrey Doolittle, Rolando Garcia, Federico Valdez, Stephanie Dallaire, Taylor Appleberry, Deborah Payne and Robert Collins

    Article first published online : 28 OCT 2009, DOI: 10.1002/ajmg.a.33080

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    Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: Interaction of its intracellular domain with Myt1l

    Developmental Neurobiology

    Volume 68, Issue 4, March 2008, Pages: 521–541, Franc Llorens, Vanesa Gil, Susana Iraola, Laura Carim-Todd, Eulàlia Martí, Xavier Estivill, Eduardo Soriano, José Antonio del Rio and Lauro Sumoy

    Article first published online : 10 JAN 2008, DOI: 10.1002/dneu.20607

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    Myt1 family recruits histone deacetylase to regulate neural transcription

    Journal of Neurochemistry

    Volume 93, Issue 6, June 2005, Pages: 1444–1453, Elena Romm, Joseph A. Nielsen, Jin G. Kim and Lynn D. Hudson

    Article first published online : 1 APR 2005, DOI: 10.1111/j.1471-4159.2005.03131.x

  10. An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld–Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1318–1321, Feng Li, Denise A.S. Batista, Irene Maumenee and Tao Wang

    Article first published online : 13 APR 2010, DOI: 10.1002/ajmg.a.33355

  11. Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 479–486, Carla Sustek D'Angelo, Ilana Kohl, Monica Castro Varela, Cláudia Irene Emílio de Castro, Chong Ae Kim, Débora Romeo Bertola, Charles Marques Lourenço, Ana Beatriz Alvarez Perez and Celia Priszkulnik Koiffmann

    Article first published online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35761

  12. Forward engineering neuronal diversity using direct reprogramming

    The EMBO Journal

    Volume 34, Issue 11, 3 June 2015, Pages: 1445–1455, Rachel K Tsunemoto, Kevin T Eade, Joel W Blanchard and Kristin K Baldwin

    Article first published online : 23 APR 2015, DOI: 10.15252/embj.201591402

  13. Selective Expression of a Subset of Neuronal Genes in Oligodendroglioma with Chromosome 1p Loss

    Brain Pathology

    Volume 14, Issue 1, January 2004, Pages: 34–42, Akitake Mukasa, Keisuke Ueki, Xijin Ge, Shumpei Ishikawa, Takafumi Ide, Takamitsu Fujimaki, Ryo Nishikawa, Akio Asai, Takaaki Kirino and Hiroyuki Aburatani

    Article first published online : 5 APR 2006, DOI: 10.1111/j.1750-3639.2004.tb00495.x

  14. An unbalanced half-cryptic translocation involving the 6q subtelomeric region and 2p25.3 in a child with mental retardation: uses and limitations of fluorescence insitu hybridization

    Clinical Genetics

    Volume 55, Issue 4, April 1999, Pages: 265–268 , JR Batanian and MI Hussain

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550409.x

  15. PRENATAL DIAGNOSIS OF PARTIAL MONOSOMY 3p AND PARTIAL TRISOMY 2p IN A FETUS ASSOCIATED WITH SHORTENING OF THE LONG BONES AND A SINGLE UMBILICAL ARTERY

    Prenatal Diagnosis

    Volume 16, Issue 3, March 1996, Pages: 270–275, CHIH-PING CHEN, FEN-FEN LIU, SHEAU-WEN JAN, SHUAN-PEI LIN and CHUNG-CHI LAN

    Article first published online : 5 MAY 1999, DOI: 10.1002/(SICI)1097-0223(199603)16:3<270::AID-PD836>3.0.CO;2-0

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    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

    Article first published online : 19 DEC 2014, DOI: 10.1002/ajmg.b.32284

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    Spatiotemporal expression pattern of Myt/NZF family zinc finger transcription factors during mouse nervous system development

    Developmental Dynamics

    Volume 243, Issue 4, April 2014, Pages: 588–600, Fumio Matsushita, Toshiki Kameyama, Yuzo Kadokawa and Tohru Marunouchi

    Article first published online : 19 DEC 2013, DOI: 10.1002/dvdy.24091

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    Convergent functional genomics of genome-wide association data for bipolar disorder: Comprehensive identification of candidate genes, pathways and mechanisms

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 2, 5 March 2009, Pages: 155–181, H. Le-Niculescu, S.D. Patel, M. Bhat, R. Kuczenski, S.V. Faraone, M.T. Tsuang, F.J. McMahon, N.J. Schork, J.I. Nurnberger Jr. and A.B. Niculescu III

    Article first published online : 21 NOV 2008, DOI: 10.1002/ajmg.b.30887

  19. Induced neuronal reprogramming

    Journal of Comparative Neurology

    Volume 522, Issue 12, 15 August 2014, Pages: 2877–2886, Cheen Euong Ang and Marius Wernig

    Article first published online : 21 MAY 2014, DOI: 10.1002/cne.23620

  20. You have full text access to this OnlineOpen article
    Probing disorders of the nervous system using reprogramming approaches

    The EMBO Journal

    Volume 34, Issue 11, 3 June 2015, Pages: 1456–1477, Justin K Ichida and Evangelos Kiskinis

    Article first published online : 29 APR 2015, DOI: 10.15252/embj.201591267