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There are 6189 results for: content related to: FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome

  1. Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 395–403, R De Filippis, L Pancrazi, K Bjørgo, A Rosseto, T Kleefstra, E Grillo, A Panighini, F Cardarelli, I Meloni, F Ariani, MA Mencarelli, J Hayek, A Renieri, M Costa and F Mari

    Article first published online : 13 DEC 2011, DOI: 10.1111/j.1399-0004.2011.01810.x

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    Foxg1 is required for proper separation and formation of sensory cristae during inner ear development

    Developmental Dynamics

    Volume 238, Issue 11, November 2009, Pages: 2725–2734, Chan Ho Hwang, Antonio Simeone, Eseng Lai and Doris K. Wu

    Article first published online : 19 OCT 2009, DOI: 10.1002/dvdy.22111

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    Foxg1 is required for morphogenesis and histogenesis of the mammalian inner ear

    Developmental Dynamics

    Volume 235, Issue 9, September 2006, Pages: 2470–2482, Sarah Pauley, Eseng Lai and Bernd Fritzsch

    Article first published online : 11 MAY 2006, DOI: 10.1002/dvdy.20839

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    The role of sensory organs and the forebrain for the development of the craniofacial shape as revealed by Foxg1-cre-mediated microRNA loss

    genesis

    Volume 49, Issue 4, April 2011, Pages: 326–341, Jennifer Kersigo, Alex D'Angelo, Brian D. Gray, Garrett A. Soukup and Bernd Fritzsch

    Article first published online : 1 APR 2011, DOI: 10.1002/dvg.20714

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    FoxG1 Interacts with Bmi1 to Regulate Self-Renewal and Tumorigenicity of Medulloblastoma Stem Cells

    STEM CELLS

    Volume 31, Issue 7, July 2013, Pages: 1266–1277, Branavan Manoranjan, Xin Wang, Robin M. Hallett, Chitra Venugopal, Stephen C. Mack, Nicole McFarlane, Sara M. Nolte, Katrin Scheinemann, Thorsteinn Gunnarsson, John A. Hassell, Michael D. Taylor, Cathy Lee, Joanna Triscott, Colleen M. Foster, Christopher Dunham, Cynthia Hawkins, Sandra E. Dunn and Sheila K. Singh

    Article first published online : 5 JUL 2013, DOI: 10.1002/stem.1401

  6. Epilepsy and outcome in FOXG1-related disorders

    Epilepsia

    Volume 55, Issue 8, August 2014, Pages: 1292–1300, Laurie E. Seltzer, Mandy Ma, Sohnee Ahmed, Mary Bertrand, William B. Dobyns, James Wheless and Alex R. Paciorkowski

    Article first published online : 16 MAY 2014, DOI: 10.1111/epi.12648

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    Fibroblast growth factor signaling in development of the cerebral cortex

    Development, Growth & Differentiation

    Volume 51, Issue 3, April 2009, Pages: 299–323, Tomoko Iwata and Robert F. Hevner

    Article first published online : 30 MAR 2009, DOI: 10.1111/j.1440-169X.2009.01104.x

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    Emx2 and Foxg1 Inhibit Gliogenesis and Promote Neuronogenesis

    STEM CELLS

    Volume 28, Issue 7, July 2010, Pages: 1206–1218, Marco Brancaccio, Chiara Pivetta, Marilena Granzotto, Carol Filippis and Antonello Mallamaci

    Article first published online : 18 MAY 2010, DOI: 10.1002/stem.443

  9. FoxG1 haploinsufficiency results in impaired neurogenesis in the postnatal hippocampus and contextual memory deficits

    Hippocampus

    Volume 16, Issue 10, October 2006, Pages: 875–890, Lijian Shen, Hyung-Song Nam, Ping Song, Holly Moore and Stewart A. Anderson

    Article first published online : 28 AUG 2006, DOI: 10.1002/hipo.20218

  10. You have full text access to this OnlineOpen article
    The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development

    Developmental Dynamics

    Volume 243, Issue 9, September 2014, Pages: 1055–1066, Ethan D. Sperry, Elizabeth A. Hurd, Mark A. Durham, Elyse N. Reamer, Adam B. Stein and Donna M. Martin

    Article first published online : 10 JUL 2014, DOI: 10.1002/dvdy.24156

  11. The Role of Foxg1 in the Development of Neural Stem Cells of the Olfactory Epithelium

    Annals of the New York Academy of Sciences

    Volume 1170, Issue 1, July 2009, Pages: 21–27, Shimako Kawauchi, Rosaysela Santos, Joon Kim, Piper L. W. Hollenbeck, Richard C. Murray and Anne L. Calof

    Article first published online : 4 AUG 2009, DOI: 10.1111/j.1749-6632.2009.04372.x

  12. Sloppy paired 1/2 regulate glial cell fates by inhibiting Gcm Function

    Glia

    Volume 55, Issue 3, February 2007, Pages: 282–293, Soma Mondal, Stacey M. Ivanchuk, James T. Rutka and Gabrielle L. Boulianne

    Article first published online : 7 NOV 2006, DOI: 10.1002/glia.20456

  13. A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder

    Epilepsia

    Volume 55, Issue 11, November 2014, Pages: e116–e119, Gaetano Terrone, Thierry Bienvenu, David Germanaud, Marie-Anne Barthez-Carpentier, Bertrand Diebold, Catherine Delanoe, Sandrine Passemard and Stéphane Auvin

    Article first published online : 29 SEP 2014, DOI: 10.1111/epi.12800

  14. Dysregulation of FOXG1 pathway in a 14q12 microdeletion case

    American Journal of Medical Genetics Part A

    Volume 161, Issue 12, December 2013, Pages: 3072–3077, Olivier Perche, Georges Haddad, Arnaud Menuet, Patrick Callier, Mélanie Marcos, Sylvain Briault and Béatrice Laudier

    Article first published online : 16 AUG 2013, DOI: 10.1002/ajmg.a.36170

  15. Double-negative feedback loop between MicroRNA-422a and forkhead box (FOX)G1/Q1/E1 regulates hepatocellular carcinoma tumor growth and metastasis

    Hepatology

    Volume 61, Issue 2, February 2015, Pages: 561–573, Jin Zhang, Yun Yang, Tian Yang, Shengxian Yuan, Ruoyu Wang, Zeya Pan, Yuan Yang, Gang Huang, Fangming Gu, Beige Jiang, Chuan Lin and Weiping Zhou

    Article first published online : 20 JAN 2015, DOI: 10.1002/hep.27491

  16. Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome

    American Journal of Medical Genetics Part A

    Heather E. Olson, Dimira Tambunan, Christopher LaCoursiere, Marti Goldenberg, Rebecca Pinsky, Emilie Martin, Eugenia Ho, Omar Khwaja, Walter E. Kaufmann and Annapurna Poduri

    Article first published online : 25 APR 2015, DOI: 10.1002/ajmg.a.37132

  17. Genetic disorders associated with postnatal microcephaly

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 166, Issue 2, June 2014, Pages: 140–155, Laurie E. Seltzer and Alex R. Paciorkowski

    Article first published online : 16 MAY 2014, DOI: 10.1002/ajmg.c.31400

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    Synaptic plasticity and signaling in rett syndrome

    Developmental Neurobiology

    Volume 74, Issue 2, February 2014, Pages: 178–196, Grazia Della Sala and Tommaso Pizzorusso

    Article first published online : 20 OCT 2013, DOI: 10.1002/dneu.22114

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    A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localization

    Human Mutation

    Volume 32, Issue 2, February 2011, Pages: E2026–E2035, Tangui Le Guen, Yann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, François Rivier, Nathalie Boddaert, Bertrand Diebold, Delphine Héron, Jamel Chelly and Thierry Bienvenu

    Article first published online : 7 DEC 2010, DOI: 10.1002/humu.21422

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    Concise Review: Forkhead Pathway in the Control of Adult Neurogenesis

    STEM CELLS

    Volume 32, Issue 6, June 2014, Pages: 1398–1407, Emmanuelle C. Genin, Nicolas Caron, Renaud Vandenbosch, Laurent Nguyen and Brigitte Malgrange

    Article first published online : 23 MAY 2014, DOI: 10.1002/stem.1673