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There are 1798 results for: content related to: Sequence analysis of 17 NRXN1 deletions

  1. A novel Foxn1eGFP/+ mouse model identifies Bmp4-induced maintenance of Foxn1 expression and thymic epithelial progenitor populations

    European Journal of Immunology

    Volume 47, Issue 2, February 2017, Pages: 291–304, Marco Barsanti, Joanna M. C. Lim, Michael L. Hun, Natalie Lister, Kahlia Wong, Maree V. Hammett, Ailin Lepletier, Richard L. Boyd, Antonietta Giudice and Ann P. Chidgey

    Version of Record online : 7 DEC 2016, DOI: 10.1002/eji.201646553

  2. Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 4, June 2014, Pages: 303–313, Abdul Noor, Anath C. Lionel, Sarah Cohen-Woods, Narges Moghimi, James Rucker, Alanna Fennell, Bhooma Thiruvahindrapuram, Liana Kaufman, Bryan Degagne, John Wei, Sagar V. Parikh, Pierandrea Muglia, Julia Forte, Stephen W. Scherer, James L. Kennedy, Wei Xu, Peter McGuffin, Anne Farmer, John Strauss and John B. Vincent

    Version of Record online : 3 APR 2014, DOI: 10.1002/ajmg.b.32232

  3. You have full text access to this OnlineOpen article
    FOXN1 in thymus organogenesis and development

    European Journal of Immunology

    Volume 46, Issue 8, August 2016, Pages: 1826–1837, Harsh Jayesh Vaidya, Alberto Briones Leon and C. Clare Blackburn

    Version of Record online : 12 AUG 2016, DOI: 10.1002/eji.201545814

  4. 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

  5. Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 388–403, Frédérique Béna, Damien L. Bruno, Mats Eriksson, Conny van Ravenswaaij-Arts, Zornitza Stark, Trijnie Dijkhuizen, Erica Gerkes, Stefania Gimelli, Devika Ganesamoorthy, Ann Charlotte Thuresson, Audrey Labalme, Marianne Till, Frédéric Bilan, Laurent Pasquier, Alain Kitzis, Christele Dubourgm, Massimiliano Rossi, Armand Bottani, Maryline Gagnebin, Damien Sanlaville, Brigitte Gilbert-Dussardier, Michel Guipponi, Arie van Haeringen, Marjolein Kriek, Claudia Ruivenkamp, Stylianos E. Antonarakis, Britt Marie Anderlid, Howard R. Slater and Jacqueline Schoumans

    Version of Record online : 26 MAR 2013, DOI: 10.1002/ajmg.b.32148

  6. You have full text access to this Open Access content
    Declining expression of a single epithelial cell-autonomous gene accelerates age-related thymic involution

    Aging Cell

    Volume 9, Issue 3, June 2010, Pages: 347–357, Liguang Sun, Jianfei Guo, Robert Brown, Takashi Amagai, Yong Zhao and Dong-Ming Su

    Version of Record online : 12 FEB 2010, DOI: 10.1111/j.1474-9726.2010.00559.x

  7. Msx2 and Foxn1 regulate nail homeostasis


    Volume 49, Issue 6, June 2011, Pages: 449–459, Jing Cai and Liang Ma

    Version of Record online : 31 MAY 2011, DOI: 10.1002/dvg.20744

  8. You have free access to this content
    Induction of sulfiredoxin expression and reduction of peroxiredoxin hyperoxidation by the neuroprotective Nrf2 activator 3H-1,2-dithiole-3-thione

    Journal of Neurochemistry

    Volume 107, Issue 2, October 2008, Pages: 533–543, Francesc X. Soriano, Frédéric Léveillé, Sofia Papadia, Larry G. Higgins, James Varley, Paul Baxter, John D. Hayes and Giles E. Hardingham

    Version of Record online : 29 AUG 2008, DOI: 10.1111/j.1471-4159.2008.05648.x

  9. You have free access to this content
    DL4-mediated Notch signaling is required for the development of fetal αβ and γδ T cells

    European Journal of Immunology

    Volume 43, Issue 11, November 2013, Pages: 2845–2853, Isabel Ferrero, Ute Koch, Stephanie Claudinot, Stéphanie Favre, Freddy Radtke, Sanjiv A. Luther and H. R. MacDonald

    Version of Record online : 25 AUG 2013, DOI: 10.1002/eji.201343527

  10. Genetic dissection of thymus development in mouse and zebrafish

    Immunological Reviews

    Volume 195, Issue 1, October 2003, Pages: 15–27, Thomas Boehm, Conrad C. Bleul and Michael Schorpp

    Version of Record online : 10 SEP 2003, DOI: 10.1034/j.1600-065X.2003.00070.x

  11. The influence of genes on “positive valence systems” constructs: A systematic review

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 1, January 2016, Pages: 92–110, Jonathan L. Hess, Daniel M. Kawaguchi, Kayla E. Wagner, Stephen V. Faraone and Stephen J. Glatt

    Version of Record online : 14 SEP 2015, DOI: 10.1002/ajmg.b.32382

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    Early development of the thymus in Xenopus laevis

    Developmental Dynamics

    Volume 242, Issue 2, February 2013, Pages: 164–178, Young-Hoon Lee, Allison Williams, Chang-Soo Hong, Youngjae You, Makoto Senoo and Jean-Pierre Saint-Jeannet

    Version of Record online : 5 DEC 2012, DOI: 10.1002/dvdy.23905

  13. You have full text access to this OnlineOpen article
    Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 4, June 2010, Pages: 937–947, Michael S.L. Ching, Yiping Shen, Wen-Hann Tan, Shafali S. Jeste, Eric M. Morrow, Xiaoli Chen, Nahit M. Mukaddes, Seung-Yun Yoo, Ellen Hanson, Rachel Hundley, Christina Austin, Ronald E. Becker, Gerard T. Berry, Katherine Driscoll, Elizabeth C. Engle, Sandra Friedman, James F. Gusella, Fuki M. Hisama, Mira B. Irons, Tina Lafiosca, Elaine LeClair, David T. Miller, Michael Neessen, Jonathan D. Picker, Leonard Rappaport, Cynthia M. Rooney, Dean P. Sarco, Joan M. Stoler, Christopher A. Walsh, Robert R. Wolff, Ting Zhang, Ramzi H. Nasir, Bai-Lin Wu and on behalf of the Children's Hospital Boston Genotype Phenotype Study Group

    Version of Record online : 7 APR 2010, DOI: 10.1002/ajmg.b.31063

  14. T cells affect central and peripheral noradrenergic mechanisms and neurotrophin concentration in the spleen and hypothalamus

    Annals of the New York Academy of Sciences

    Volume 1261, Issue 1, July 2012, Pages: 18–25, Jamela Jouda, Johannes Wildmann, Martin Schäfer, Eduardo Roggero, Hugo O. Besedovsky and Adriana del Rey

    Version of Record online : 23 JUL 2012, DOI: 10.1111/j.1749-6632.2012.06642.x

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    Two novel AP2/ERF domain proteins interact with cis-element VWRE for wound-induced expression of the Tobacco tpoxN1 gene

    The Plant Journal

    Volume 50, Issue 6, June 2007, Pages: 1079–1092, Katsutomo Sasaki, Ichiro Mitsuhara, Shigemi Seo, Hiroyuki Ito, Hirokazu Matsui and Yuko Ohashi

    Version of Record online : 3 MAY 2007, DOI: 10.1111/j.1365-313X.2007.03111.x

  16. Foxn1 and Mmp-9 expression in intact skin and during excisional wound repair in young, adult, and old C57Bl/6 mice

    Wound Repair and Regeneration

    Volume 25, Issue 2, March/April 2017, Pages: 248–259, Marta M. Kopcewicz, Anna Kur-Piotrowska, Joanna Bukowska, Jeffrey M. Gimble and Barbara Gawronska-Kozak

    Version of Record online : 19 APR 2017, DOI: 10.1111/wrr.12524

  17. Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 3, April 2012, Pages: 354–358, Linh Duong, Laura L. Klitten, Rikke S. Møller, Andrés Ingason, Klaus D. Jakobsen, Celina Skjødt, Michael Didriksen, Helle Hjalgrim, Thomas Werge and Niels Tommerup

    Version of Record online : 15 FEB 2012, DOI: 10.1002/ajmg.b.32036

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    Phosphorylation of ATXN1 at Ser776 in the cerebellum

    Journal of Neurochemistry

    Volume 110, Issue 2, July 2009, Pages: 675–686, Nathan D. Jorgensen, J. Michael Andresen, Sara Lagalwar, Ben Armstrong, Sam Stevens, Courtney E. Byam, Lisa A. Duvick, Shaojuan Lai, Paymaan Jafar-Nejad, Huda Y. Zoghbi, H. Brent Clark and Harry T. Orr

    Version of Record online : 15 MAY 2009, DOI: 10.1111/j.1471-4159.2009.06164.x

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    Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy


    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

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    Electron transport to nitrogenase in Rhodospirillum rubrum: Identification of a new fdxN gene encoding the primary electron donor to nitrogenase

    FEMS Microbiology Letters

    Volume 245, Issue 2, April 2005, Pages: 345–351, Tomas Edgren and Stefan Nordlund

    Version of Record online : 9 JAN 2006, DOI: 10.1016/j.femsle.2005.03.024