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There are 9320 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. 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

    Article first published online : 1 APR 2011, DOI: 10.1111/j.1460-9568.2011.07658.x

  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

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

  3. 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

    Article first published online : 29 OCT 2007, DOI: 10.1002/ajmg.a.32002

  4. You have free access to this content
    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

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

  5. Altered microtubule dynamics in Mecp2-deficient astrocytes

    Journal of Neuroscience Research

    Volume 90, Issue 5, May 2012, Pages: 990–998, Juliette Nectoux, Cedrick Florian, Chloe Delepine, Nadia Bahi-Buisson, Malik Khelfaoui, Sophie Reibel, Jamel Chelly and Thierry Bienvenu

    Article first published online : 18 JAN 2012, DOI: 10.1002/jnr.23001

  6. You have free access to this content
    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

    Article first published online : 9 OCT 2009, DOI: 10.1038/embor.2009.217

  7. 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

  8. You have free access to this content
    Temporal and Regional Alterations in NMDA Receptor Expression in Mecp2-Null Mice

    The Anatomical Record

    Volume 294, Issue 10, October 2011, Pages: 1624–1634, Mary E. Blue, Walter E. Kaufmann, Joseph Bressler, Charlotte Eyring, Cliona O'driscoll, Sakkubai Naidu and Michael V. Johnston

    Article first published online : 8 SEP 2011, DOI: 10.1002/ar.21380

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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

  10. 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

  11. 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

    Article first published online : 3 JUL 2012, DOI: 10.1111/j.1749-6632.2012.06611.x

  12. Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient mice

    Journal of Neuroscience Research

    Volume 88, Issue 7, 15 May 2010, Pages: 1500–1509, Jean-Christophe Roux, Nicolas Panayotis, Emmanuelle Dura and Laurent Villard

    Article first published online : 8 DEC 2009, DOI: 10.1002/jnr.22312

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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

  14. 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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    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,

    Article first published online : 2 JUN 2008, DOI: 10.1111/j.1601-183X.2008.00414.x

  16. 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

    Article first published online : 10 MAR 2011, DOI: 10.1002/jnr.22608

  17. 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

  18. 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

    Article first published online : 11 MAY 2012, DOI: 10.1002/ajmg.a.35347

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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

  20. 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

    Article first published online : 10 OCT 2012, DOI: 10.1002/aur.1251