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There are 4772 results for: content related to: Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature

  1. Investigation of NRXN1 deletions: Clinical and molecular characterization

    American Journal of Medical Genetics Part A

    Volume 161, Issue 4, April 2013, Pages: 717–731, Mindy Preston Dabell, Jill A. Rosenfeld, Patricia Bader, Luis F. Escobar, Dima El-Khechen, Stephanie E. Vallee, Mary Beth Palko Dinulos, Cynthia Curry, Jamie Fisher, Raymond Tervo, Mark C. Hannibal, Kiana Siefkas, Philip R. Wyatt, Lauren Hughes, Rosemarie Smith, Sara Ellingwood, Yves Lacassie, Tracy Stroud, Sandra A. Farrell, Pedro A. Sanchez-Lara, Linda M. Randolph, Dmitriy Niyazov, Cathy A. Stevens, Cheri Schoonveld, David Skidmore, Sara MacKay, Judith H. Miles, Manikum Moodley, Adam Huillet, Nicholas J. Neill, Jay W. Ellison, Blake C. Ballif and Lisa G. Shaffer

    Version of Record online : 12 MAR 2013, DOI: 10.1002/ajmg.a.35780

  2. Sequence analysis of 17 NRXN1 deletions

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 1, January 2014, Pages: 52–61, Louise Kristine Enggaard Hoeffding, Thomas Hansen, Andrés Ingason, Linh Doung, Johan H. Thygesen, Rikke S. Møller, Niels Tommerup, George Kirov, Dan Rujescu, Lars A. Larsen and Thomas Werge

    Version of Record online : 25 SEP 2013, DOI: 10.1002/ajmg.b.32204

    Corrected by:

    Erratum: Erratum: Sequence analysis of 17 NRXN1 deletions

    Vol. 165, Issue 3, 261, Version of Record online: 12 MAR 2014

  3. Copy number variation plays an important role in clinical epilepsy

    Annals of Neurology

    Volume 75, Issue 6, June 2014, Pages: 943–958, Heather Olson, Yiping Shen, Jennifer Avallone, Beth R. Sheidley, Rebecca Pinsky, Ann M. Bergin, Gerard T. Berry, Frank H. Duffy, Yaman Eksioglu, David J. Harris, Fuki M. Hisama, Eugenia Ho, Mira Irons, Christina M. Jacobsen, Philip James, Sanjeev Kothare, Omar Khwaja, Jonathan Lipton, Tobias Loddenkemper, Jennifer Markowitz, Kiran Maski, J. Thomas Megerian, Edward Neilan, Peter C. Raffalli, Michael Robbins, Amy Roberts, Eugene Roe, Caitlin Rollins, Mustafa Sahin, Dean Sarco, Alison Schonwald, Sharon E. Smith, Janet Soul, Joan M. Stoler, Masanori Takeoka, Wen-Han Tan, Alcy R. Torres, Peter Tsai, David K. Urion, Laura Weissman, Robert Wolff, Bai-Lin Wu, David T. Miller and Annapurna Poduri

    Version of Record online : 13 JUN 2014, DOI: 10.1002/ana.24178

  4. You have free access to this content
    Optogenetic manipulation of neural and non-neural functions

    Development, Growth & Differentiation

    Volume 55, Issue 4, May 2013, Pages: 474–490, Hiromu Yawo, Toshifumi Asano, Seiichiro Sakai and Toru Ishizuka

    Version of Record online : 4 APR 2013, DOI: 10.1111/dgd.12053

  5. You have full text access to this OnlineOpen article
    Burkholderia genome mining for nonribosomal peptide synthetases reveals a great potential for novel siderophores and lipopeptides synthesis

    MicrobiologyOpen

    Volume 5, Issue 3, June 2016, Pages: 512–526, Qassim Esmaeel, Maude Pupin, Nam Phuong Kieu, Gabrielle Chataigné, Max Béchet, Jovana Deravel, François Krier, Monica Höfte, Philippe Jacques and Valérie Leclère

    Version of Record online : 5 APR 2016, DOI: 10.1002/mbo3.347

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    Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome

    British Journal of Haematology

    Volume 142, Issue 6, September 2008, Pages: 934–945, Ken C. Lo, Jane Chalker, Sabine Strehl, Michael Neat, Owen Smith, Nicole Dastugue, Lyndal Kearney, Shai Izraeli, Helena Kempski and John K. Cowell

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1365-2141.2008.07280.x

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    Chr4, a Schizosaccharomyces pombe homologue of the Saccharomyces cerevisiae Chs4p/Skt5p protein, is related to septum formation and is required for the proper localization of Chs2

    Yeast

    Volume 21, Issue 12, September 2004, Pages: 1005–1019, Yasuhiro Matsuo, Yoshinori Matsuura, Katsunori Tanaka, Hideyuki Matsuda and Makoto Kawamukai

    Version of Record online : 27 SEP 2004, DOI: 10.1002/yea.1145

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    WONOEP appraisal: Optogenetic tools to suppress seizures and explore the mechanisms of epileptogenesis

    Epilepsia

    Volume 55, Issue 11, November 2014, Pages: 1693–1702, Laura Mantoan Ritter, Peyman Golshani, Koji Takahashi, Suzie Dufour, Taufik Valiante and Merab Kokaia

    Version of Record online : 9 OCT 2014, DOI: 10.1111/epi.12804

  9. The retrotrapezoid nucleus stimulates breathing by releasing glutamate in adult conscious mice

    European Journal of Neuroscience

    Volume 42, Issue 6, September 2015, Pages: 2271–2282, Benjamin B. Holloway, Kenneth E. Viar, Ruth L. Stornetta and Patrice G. Guyenet

    Version of Record online : 23 JUL 2015, DOI: 10.1111/ejn.12996

  10. Opsin spectral sensitivity determines the effectiveness of optogenetic termination of ventricular fibrillation in the human heart: a simulation study

    The Journal of Physiology

    Thomas V. Karathanos, Jason D. Bayer, Dafang Wang, Patrick M. Boyle and Natalia A. Trayanova

    Version of Record online : 24 APR 2016, DOI: 10.1113/JP271739

  11. Somatic mutations in the notch, NF-KB, PIK3CA, and hedgehog pathways in human breast cancers

    Genes, Chromosomes and Cancer

    Volume 51, Issue 5, May 2012, Pages: 480–489, Xiang Jiao, Laura D. Wood, Monica Lindman, Sian Jones, Phillip Buckhaults, Kornelia Polyak, Saraswati Sukumar, Hannah Carter, Dewey Kim, Rachel Karchin and Tobias Sjöblom

    Version of Record online : 3 FEB 2012, DOI: 10.1002/gcc.21935

  12. Genome Wide Copy Number Abnormalities in Pediatric Medulloblastomas as Assessed by Array Comparative Genome Hybridization

    Brain Pathology

    Volume 17, Issue 3, July 2007, Pages: 282–296, Ken C. Lo, Michael R. Rossi, Charles G. Eberhart and John K. Cowell

    Version of Record online : 23 APR 2007, DOI: 10.1111/j.1750-3639.2007.00072.x

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    Human alpha- and beta-NRXN1 isoforms rescue behavioral impairments of Caenorhabditis elegans neurexin-deficient mutants

    Genes, Brain and Behavior

    Volume 12, Issue 4, June 2013, Pages: 453–464, F. Calahorro and M. Ruiz-Rubio

    Version of Record online : 20 MAY 2013, DOI: 10.1111/gbb.12046

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    Aggression in non-human vertebrates: Genetic mechanisms and molecular pathways

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 5, July 2016, Pages: 603–640, Florian Freudenberg, Hector Carreño Gutierrez, Antonia M. Post, Andreas Reif and William H. J. Norton

    Version of Record online : 18 AUG 2015, DOI: 10.1002/ajmg.b.32358

  15. Array CGH analysis of pediatric medulloblastomas

    Genes, Chromosomes and Cancer

    Volume 45, Issue 3, March 2006, Pages: 290–303, Michael R. Rossi, Jeffrey Conroy, Devin McQuaid, Norma J. Nowak, James T. Rutka and John K. Cowell

    Version of Record online : 30 NOV 2005, DOI: 10.1002/gcc.20292

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    Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy

    Epilepsia

    Volume 54, Issue 2, February 2013, Pages: 256–264, Rikke S. Møller, Yvonne G. Weber, Laura L. Klitten, Holger Trucks, Hiltrud Muhle, Wolfram S. Kunz, Heather C. Mefford, Andre Franke, Monika Kautza, Peter Wolf, Dieter Dennig, Stefan Schreiber, Ina-Maria Rückert, H.-Erich Wichmann, Jan P. Ernst, Claudia Schurmann, Hans J. Grabe, Niels Tommerup, Ulrich Stephani, Holger Lerche, Helle Hjalgrim, Ingo Helbig, Thomas Sander and EPICURE Consortium

    Version of Record online : 7 JAN 2013, DOI: 10.1111/epi.12078

    Corrected by:

    Erratum: Erratum

    Vol. 54, Issue 12, 2232, Version of Record online: 4 DEC 2013

  17. A Murine Toolbox for Imaging the Neurovascular Unit

    Microcirculation

    Volume 22, Issue 3, April 2015, Pages: 168–182, David A. Hartmann, Robert G. Underly, Ashley N. Watson and Andy Y. Shih

    Version of Record online : 9 APR 2015, DOI: 10.1111/micc.12176

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    Characteristics of 2p15-p16.1 microdeletion syndrome: Review and description of two additional patients

    Congenital Anomalies

    Volume 55, Issue 3, August 2015, Pages: 125–132, Keiko Shimojima, Nobuhiko Okamoto and Toshiyuki Yamamoto

    Version of Record online : 26 JUL 2015, DOI: 10.1111/cga.12112

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    Glutamate receptor δ1 induces preferentially inhibitory presynaptic differentiation of cortical neurons by interacting with neurexins through cerebellin precursor protein subtypes

    Journal of Neurochemistry

    Volume 121, Issue 5, June 2012, Pages: 705–716, Misato Yasumura, Tomoyuki Yoshida, Sung-Jin Lee, Takeshi Uemura, Jae-Yeol Joo and Masayoshi Mishina

    Version of Record online : 23 JAN 2012, DOI: 10.1111/j.1471-4159.2011.07631.x

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    The use of mouse models to unravel genetic architecture of physical activity: a review

    Genes, Brain and Behavior

    Volume 13, Issue 1, January 2014, Pages: 87–103, E. Kostrzewa and M. J. Kas

    Version of Record online : 31 OCT 2013, DOI: 10.1111/gbb.12091