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There are 13285 results for: content related to: Association of an activity-enhancing variant of IRAK1 and an MECP2–IRAK1 haplotype with increased susceptibility to rheumatoid arthritis

  1. MECP2 deletions and genotype–phenotype correlation in Rett syndrome

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 23, 1 December 2007, Pages: 2775–2784, Elisa Scala, Ilaria Longo, Federica Ottimo, Caterina Speciale, Katia Sampieri, Eleni Katzaki, Rosangela Artuso, Maria Antonietta Mencarelli, Tatiana D'Ambrogio, Giuseppina Vonella, Michele Zappella, Giuseppe Hayek, Agatino Battaglia, Francesca Mari, Alessandra Renieri and Francesca Ariani

    Version of Record online : 29 OCT 2007, DOI: 10.1002/ajmg.a.32002

  2. 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

  3. 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

  4. You have full text access to this OnlineOpen article
    In sickness and in health: the role of methyl-CpG binding protein 2 in the central nervous system

    European Journal of Neuroscience

    Volume 33, Issue 9, May 2011, Pages: 1563–1574, Sol Díaz de León-Guerrero, Gustavo Pedraza-Alva and Leonor Pérez-Martínez

    Version of Record online : 1 APR 2011, DOI: 10.1111/j.1460-9568.2011.07658.x

  5. De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features

    Clinical Genetics

    Volume 78, Issue 2, August 2010, Pages: 175–180, P Makrythanasis, I Moix, S Gimelli, J Fluss, K Aliferis, SE Antonarakis, MA Morris, F Béna and A Bottani

    Version of Record online : 5 JAN 2010, DOI: 10.1111/j.1399-0004.2010.01371.x

  6. Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 6, June 2012, Pages: 1285–1291, Jennifer N. Sanmann, Danielle L. Bishay, Lois J. Starr, Carla A. Bell, Diane L. Pickering, Jadd M. Stevens, Stephen G. Kahler, Ann Haskins Olney, G. Bradley Schaefer and Warren G. Sanger

    Version of Record online : 11 MAY 2012, DOI: 10.1002/ajmg.a.35347

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    Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism

    Genes, Brain and Behavior

    Volume 7, Issue 7, October 2008, Pages: 754–760, C. S. Loat, S. Curran, C. M. Lewis, , J. Duvall, D. Geschwind, P. Bolton and I. W. Craig,

    Version of Record online : 2 JUN 2008, DOI: 10.1111/j.1601-183X.2008.00414.x

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    Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis

    EMBO reports

    Volume 10, Issue 12, December 2009, Pages: 1327–1333, Giorgia Bracaglia, Barbara Conca, Anna Bergo, Laura Rusconi, Zhaolan Zhou, Michael E Greenberg, Nicoletta Landsberger, Silvia Soddu and Charlotte Kilstrup-Nielsen

    Version of Record online : 9 OCT 2009, DOI: 10.1038/embor.2009.217

  9. 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

  10. The role of oxidative stress in Rett syndrome: an overview

    Annals of the New York Academy of Sciences

    Volume 1259, Issue 1, July 2012, Pages: 121–135, Claudio De Felice, Cinzia Signorini, Silvia Leoncini, Alessandra Pecorelli, Thierry Durand, Giuseppe Valacchi, Lucia Ciccoli and Joussef Hayek

    Version of Record online : 3 JUL 2012, DOI: 10.1111/j.1749-6632.2012.06611.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

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

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    Inhibition of miR-15a Promotes BDNF Expression and Rescues Dendritic Maturation Deficits in MeCP2-Deficient Neurons


    Volume 33, Issue 5, May 2015, Pages: 1618–1629, Yu Gao, Juan Su, Weixiang Guo, Eric D. Polich, Daniel P. Magyar, Yina Xing, Hongda Li, Richard D. Smrt, Qiang Chang and Xinyu Zhao

    Version of Record online : 23 APR 2015, DOI: 10.1002/stem.1950

  13. The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1

    Autism Research

    Volume 5, Issue 6, December 2012, Pages: 385–397, Holly N. Cukier, Joycelyn M. Lee, Deqiong Ma, Juan I. Young, Vera Mayo, Brittany L. Butler, Sandhya S. Ramsook, Joseph A. Rantus, Alexander J. Abrams, Patrice L. Whitehead, Harry H. Wright, Ruth K. Abramson, Jonathan L. Haines, Michael L. Cuccaro, Margaret A. Pericak-Vance and John R. Gilbert

    Version of Record online : 10 OCT 2012, DOI: 10.1002/aur.1251

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    MeCP2 preferentially binds to methylated linker DNA in the absence of the terminal tail of histone H3 and independently of histone acetylation

    FEBS Letters

    Volume 582, Issue 7, April 02, 2008, Pages: 1157–1162, Toyotaka Ishibashi, Anita A. Thambirajah and Juan Ausió

    Version of Record online : 11 MAR 2008, DOI: 10.1016/j.febslet.2008.03.005

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    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

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

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    Electroclinical pattern in MECP2 duplication syndrome: Eight new reported cases and review of literature


    Volume 53, Issue 7, July 2012, Pages: 1146–1155, Aglaia Vignoli, Renato Borgatti, Angela Peron, Claudio Zucca, Lucia Ballarati, Clara Bonaglia, Melissa Bellini, Lucio Giordano, Romina Romaniello, Maria Francesca Bedeschi, Roberta Epifanio, Silvia Russo, Rossella Caselli, Daniela Giardino, Francesca Darra, Francesca La Briola, Giuseppe Banderali and Maria Paola Canevini

    Version of Record online : 11 MAY 2012, DOI: 10.1111/j.1528-1167.2012.03501.x

  17. Brain region-specific expression of Fxyd1, an Mecp2 target gene, is regulated by epigenetic mechanisms

    Journal of Neuroscience Research

    Volume 89, Issue 6, June 2011, Pages: 840–851, Fatima Banine, Valerie Matagne, Larry S. Sherman and Sergio R. Ojeda

    Version of Record online : 10 MAR 2011, DOI: 10.1002/jnr.22608

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    MeCP2 deficiency is associated with impaired microtubule stability

    FEBS Letters

    Volume 587, Issue 2, January 16, 2013, Pages: 245–253, Chloé Delépine, Juliette Nectoux, Nadia Bahi-Buisson, Jamel Chelly and Thierry Bienvenu

    Version of Record online : 10 DEC 2012, DOI: 10.1016/j.febslet.2012.11.033

  19. 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