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There are 5125 results for: content related to: MECP2 promoter methylation and X chromosome inactivation in autism

  1. Differential distribution of the MeCP2 splice variants in the postnatal mouse brain

    Journal of Comparative Neurology

    Volume 501, Issue 4, 1 April 2007, Pages: 526–542, Joanna M. Dragich, Yong-Hwan Kim, Arthur P. Arnold and N. Carolyn Schanen

    Article first published online : 2 FEB 2007, DOI: 10.1002/cne.21264

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    Evidence for abnormal early development in a mouse model of Rett syndrome

    Genes, Brain and Behavior

    Volume 6, Issue 3, April 2007, Pages: 277–286, M. Santos, A. Silva-Fernandes, P. Oliveira, Nuno Sousa and Patrícia Maciel

    Article first published online : 17 JUL 2006, DOI: 10.1111/j.1601-183X.2006.00258.x

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    Disease Modeling Using Embryonic Stem Cells: MeCP2 Regulates Nuclear Size and RNA Synthesis in Neurons


    Volume 30, Issue 10, October 2012, Pages: 2128–2139, Morteza Yazdani, Rubén Deogracias, Jacky Guy, Raymond A. Poot, Adrian Bird and Yves-Alain Barde

    Article first published online : 20 SEP 2012, DOI: 10.1002/stem.1180

  4. Excitation/inhibition imbalance and impaired synaptic inhibition in hippocampal area CA3 of Mecp2 knockout mice


    Volume 25, Issue 2, February 2015, Pages: 159–168, Gaston Calfa, Wei Li, John M. Rutherford and Lucas Pozzo-Miller

    Article first published online : 25 SEP 2014, DOI: 10.1002/hipo.22360

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    MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits

    Genes, Brain and Behavior

    Volume 12, Issue 7, October 2013, Pages: 732–740, L. R. Schaevitz, N. B. Gómez, D. P. Zhen and J. E. Berger-Sweeney

    Article first published online : 26 AUG 2013, DOI: 10.1111/gbb.12070

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    Disruption of MeCP2 attenuates circadian rhythm in CRISPR/Cas9-based Rett syndrome model mouse

    Genes to Cells

    Yoshiki Tsuchiya, Yoichi Minami, Yasuhiro Umemura, Hitomi Watanabe, Daisuke Ono, Wataru Nakamura, Tomoyuki Takahashi, Sato Honma, Gen Kondoh, Toyojiro Matsuishi and Kazuhiro Yagita

    Article first published online : 12 OCT 2015, DOI: 10.1111/gtc.12305

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    Developmental abnormalities of cortical interneurons precede symptoms onset in a mouse model of Rett syndrome

    Journal of Neurochemistry

    Volume 131, Issue 1, October 2014, Pages: 115–127, Giulio Srubek Tomassy, Noemi Morello, Eleonora Calcagno and Maurizio Giustetto

    Article first published online : 5 AUG 2014, DOI: 10.1111/jnc.12803

  8. Mutations in MECP2 exon 1 in classical rett patients disrupt MECP2_e1 transcription, but not transcription of MECP2_e2

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 2, March 2012, Pages: 210–216, Peter J. Gianakopoulos, Yuzhi Zhang, Nela Pencea, Marija Orlic-Milacic, Kirti Mittal, Christian Windpassinger, Sara-Jane White, Peter M. Kroisel, Eva W.C. Chow, Carol J. Saunders, Berge A. Minassian and John B. Vincent

    Article first published online : 27 DEC 2011, DOI: 10.1002/ajmg.b.32015

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    Differential methylation of the micro-RNA 7b gene targets postnatal maturation of murine neuronal Mecp2 gene expression

    Developmental Neurobiology

    Volume 74, Issue 4, April 2014, Pages: 407–425, Yongjun Chen, Bo-Chul Shin, Shanthie Thamotharan and Sherin U. Devaskar

    Article first published online : 9 DEC 2013, DOI: 10.1002/dneu.22126

  10. The Behavioral Phenotype in MECP2 Duplication Syndrome: A Comparison With Idiopathic Autism

    Autism Research

    Volume 6, Issue 1, February 2013, Pages: 42–50, Sarika U. Peters, Rachel J. Hundley, Amy K. Wilson, Zachary Warren, Alison Vehorn, Claudia M.B. Carvalho, James R. Lupski and Melissa B. Ramocki

    Article first published online : 20 NOV 2012, DOI: 10.1002/aur.1262

  11. The MECP2 duplication syndrome

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1079–1088, Melissa B. Ramocki, Y. Jane Tavyev and Sarika U. Peters

    Article first published online : 2 APR 2010, DOI: 10.1002/ajmg.a.33184

  12. MECP2 coding sequence and 3′UTR variation in 172 unrelated autistic patients

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 4, 5 June 2007, Pages: 475–483, Ana M. Coutinho, Guiomar Oliveira, Cécile Katz, Jinong Feng, Jin Yan, Chunmei Yang, Carla Marques, Assunção Ataíde, Teresa S. Miguel, Luís Borges, Joana Almeida, Catarina Correia, António Currais, Celeste Bento, Luísa Mota-Vieira, Teresa Temudo, Mónica Santos, Patrícia Maciel, Steve S. Sommer and Astrid M. Vicente

    Article first published online : 10 APR 2007, DOI: 10.1002/ajmg.b.30490

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    The increase in body weight induced by lack of methyl CpG binding protein-2 is associated with altered leptin signalling in the hypothalamus

    Experimental Physiology

    Volume 99, Issue 9, 1 September 2014, Pages: 1229–1240, Rodrigo Torres-Andrade, Rodrigo Moldenhauer, Noemí Gutierrez-Bertín, Jessica Soto-Covasich, Cristian Mancilla-Medina, Carolina Ehrenfeld and Bredford Kerr

    Article first published online : 29 JUL 2014, DOI: 10.1113/expphysiol.2014.079798

  14. Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome

    Annals of Neurology

    Volume 66, Issue 6, December 2009, Pages: 771–782, Melissa B. Ramocki, Sarika U. Peters, Y. Jane Tavyev, Feng Zhang, Claudia M. B. Carvalho, Christian P. Schaaf, Ronald Richman, Ping Fang, Daniel G. Glaze, James R. Lupski and Huda Y. Zoghbi

    Article first published online : 26 MAR 2009, DOI: 10.1002/ana.21715

  15. Aminoglycoside-mediated partial suppression of MECP2 nonsense mutations responsible for Rett syndrome in vitro

    Journal of Neuroscience Research

    Volume 88, Issue 11, 15 August 2010, Pages: 2316–2324, Andreea C. Popescu, Elena Sidorova, Guangming Zhang and James H. Eubanks

    Article first published online : 13 APR 2010, DOI: 10.1002/jnr.22409

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    Variants within MECP2, a key transcription regulator, are associated with increased susceptibility to lupus and differential gene expression in patients with systemic lupus erythematosus

    Arthritis & Rheumatism

    Volume 60, Issue 4, April 2009, Pages: 1076–1084, Ryan Webb, Jonathan D. Wren, Matlock Jeffries, Jennifer A. Kelly, Kenneth M. Kaufman, Yuhong Tang, Mark Barton Frank, Joan Merrill, Robert P. Kimberly, Jeffrey C. Edberg, Rosalind Ramsey-Goldman, Michelle Petri, John D. Reveille, Graciela S. Alarcón, Luis M. Vilá, Marta E. Alarcón-Riquelme, Judith A. James, Timothy J. Vyse, Kathy L. Moser, Patrick M. Gaffney, Gary S. Gilkeson, John B. Harley and Amr H. Sawalha

    Article first published online : 30 MAR 2009, DOI: 10.1002/art.24360

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    Increasing brain serotonin corrects CO2 chemosensitivity in methyl-CpG-binding protein 2 (Mecp2)-deficient mice

    Experimental Physiology

    Volume 98, Issue 3, March 2013, Pages: 842–849, Marie A. Toward, Ana P. Abdala, Sharon J. Knopp, Julian F. R. Paton and John M. Bissonnette

    Article first published online : 20 FEB 2013, DOI: 10.1113/expphysiol.2012.069872

  18. Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 7, July 2013, Pages: 1638–1646, Christopher A. Chapleau, Jane Lane, Susan M. Kirwin, Carolyn Schanen, Kathy M.B. Vinette, Danielle Stubbolo, Patrick MacLeod and Alan K. Percy

    Article first published online : 21 MAY 2013, DOI: 10.1002/ajmg.a.35979

  19. Affective dysfunction in a mouse model of Rett syndrome: Therapeutic effects of environmental stimulation and physical activity

    Developmental Neurobiology

    Mari A. Kondo, Laura J. Gray, Gregory J. Pelka, Sook-Kwan Leang, John Christodoulou, Patrick P. L. Tam and Anthony J. Hannan

    Article first published online : 23 JUN 2015, DOI: 10.1002/dneu.22308

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    Early postnatal behavioral changes in the Mecp2-308 truncation mouse model of Rett syndrome

    Genes, Brain and Behavior

    Volume 9, Issue 2, March 2010, Pages: 213–223, B. De Filippis, L. Ricceri and G. Laviola

    Article first published online : 2 NOV 2009, DOI: 10.1111/j.1601-183X.2009.00551.x