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There are 6810 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

    Version of Record online : 2 FEB 2007, DOI: 10.1002/cne.21264

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

    STEM CELLS

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

    Version of Record online : 20 SEP 2012, DOI: 10.1002/stem.1180

  3. 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

    Version of Record online : 20 NOV 2012, DOI: 10.1002/aur.1262

  4. Hyperexcitability of Mesencephalic Trigeminal Neurons and Reorganization of Ion Channel Expression in a Rett Syndrome Model

    Journal of Cellular Physiology

    Volume 232, Issue 5, May 2017, Pages: 1151–1164, Max F. Oginsky, Ningren Cui, Weiwei Zhong, Christopher M. Johnson and Chun Jiang

    Version of Record online : 30 SEP 2016, DOI: 10.1002/jcp.25589

  5. 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

    Version of Record online : 2 APR 2010, DOI: 10.1002/ajmg.a.33184

  6. You have full text access to this OnlineOpen article
    MicroRNAs downregulated in neuropathic pain regulate MeCP2 and BDNF related to pain sensitivity

    FEBS Open Bio

    Volume 5, Issue 1, January 01, 2015, Pages: 733–740, Melissa T. Manners, Yuzhen Tian, Zhaolan Zhou and Seena K. Ajit

    Version of Record online : 31 AUG 2015, DOI: 10.1016/j.fob.2015.08.010

  7. 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

    Version of Record online : 10 APR 2007, DOI: 10.1002/ajmg.b.30490

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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

    Version of Record online : 26 AUG 2013, DOI: 10.1111/gbb.12070

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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

    Version of Record online : 17 JUL 2006, DOI: 10.1111/j.1601-183X.2006.00258.x

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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

    Version of Record online : 5 AUG 2014, DOI: 10.1111/jnc.12803

  11. 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

    Version of Record online : 27 DEC 2011, DOI: 10.1002/ajmg.b.32015

  12. You have full text access to this OnlineOpen article
    Mild expression differences of MECP2 influencing aggressive social behavior

    EMBO Molecular Medicine

    Volume 6, Issue 5, May 2014, Pages: 662–684, Martesa Tantra, Christian Hammer, Anne Kästner, Liane Dahm, Martin Begemann, Chiranjeevi Bodda, Kurt Hammerschmidt, Ina Giegling, Beata Stepniak, Aracely Castillo Venzor, Bettina Konte, Begun Erbaba, Annette Hartmann, Asieh Tarami, Walter Schulz-Schaeffer, Dan Rujescu, Ashraf U Mannan and Hannelore Ehrenreich

    Version of Record online : 20 MAR 2014, DOI: 10.1002/emmm.201303744

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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

    Version of Record online : 9 DEC 2013, DOI: 10.1002/dneu.22126

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

    Hippocampus

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

    Version of Record online : 25 SEP 2014, DOI: 10.1002/hipo.22360

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

    Genes to Cells

    Volume 20, Issue 12, December 2015, Pages: 992–1005, Yoshiki Tsuchiya, Yoichi Minami, Yasuhiro Umemura, Hitomi Watanabe, Daisuke Ono, Wataru Nakamura, Tomoyuki Takahashi, Sato Honma, Gen Kondoh, Toyojiro Matsuishi and Kazuhiro Yagita

    Version of Record online : 12 OCT 2015, DOI: 10.1111/gtc.12305

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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

    Version of Record online : 29 JUL 2014, DOI: 10.1113/expphysiol.2014.079798

  17. 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

    Version of Record online : 26 MAR 2009, DOI: 10.1002/ana.21715

  18. Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of rett syndrome: Evidence for disruption of neuronal networks

    Journal of Comparative Neurology

    Volume 514, Issue 3, 20 May 2009, Pages: 240–258, Pavel V. Belichenko, Elena E. Wright, Nadia P. Belichenko, Eliezer Masliah, Hong Hua Li, William C. Mobley and Uta Francke

    Version of Record online : 23 FEB 2009, DOI: 10.1002/cne.22009

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    Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes

    Journal of Cellular and Molecular Medicine

    Volume 14, Issue 7, July 2010, Pages: 1962–1974, J. Nectoux, Y. Fichou, H. Rosas-Vargas, N. Cagnard, N. Bahi-Buisson, P. Nusbaum, F. Letourneur, J. Chelly and T. Bienvenu

    Version of Record online : 19 AUG 2010, DOI: 10.1111/j.1582-4934.2010.01107.x

  20. 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

    Version of Record online : 13 APR 2010, DOI: 10.1002/jnr.22409