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There are 4586 results for: content related to: Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics

  1. Evolutionary conservation and conversion of Foxg1 function in brain development

    Development, Growth & Differentiation

    Volume 59, Issue 4, May 2017, Pages: 258–269, Takuma Kumamoto and Carina Hanashima

    Version of Record online : 5 JUN 2017, DOI: 10.1111/dgd.12367

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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

    Version of Record online : 11 MAY 2006, DOI: 10.1002/dvdy.20839

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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

    Version of Record online : 5 JUL 2013, DOI: 10.1002/stem.1401

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    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

    Version of Record online : 16 MAY 2014, DOI: 10.1111/epi.12648

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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

    Version of Record online : 18 MAY 2010, DOI: 10.1002/stem.443

  6. Excess FoxG1 causes overgrowth of the neural tube

    Journal of Neurobiology

    Volume 57, Issue 3, December 2003, Pages: 337–349, Sara Ahlgren, Peter Vogt and Marianne Bronner-Fraser

    Version of Record online : 8 OCT 2003, DOI: 10.1002/neu.10287

  7. FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome

    Clinical Genetics

    Volume 82, Issue 6, December 2012, Pages: 569–573, S Takahashi, N Matsumoto, A Okayama, N Suzuki, A Araki, K Okajima, H Tanaka and A Miyamoto

    Version of Record online : 16 DEC 2011, DOI: 10.1111/j.1399-0004.2011.01819.x

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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

    Version of Record online : 1 APR 2011, DOI: 10.1002/dvg.20714

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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

    Version of Record online : 19 OCT 2009, DOI: 10.1002/dvdy.22111

  10. 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

    Version of Record online : 28 AUG 2006, DOI: 10.1002/hipo.20218

  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

    Version of Record online : 4 AUG 2009, DOI: 10.1111/j.1749-6632.2009.04372.x

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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

    Version of Record online : 30 MAR 2009, DOI: 10.1111/j.1440-169X.2009.01104.x

  13. Low FoxG1 and high Olig-2 labelling indices define a prognostically favourable subset in isocitrate dehydrogenase (IDH)-mutant gliomas

    Neuropathology and Applied Neurobiology

    S. Schäfer, F. Behling, M. Skardelly, M. Koch, I. Ott, F. Paulsen, G. Tabatabai and J. Schittenhelm

    Version of Record online : 23 NOV 2017, DOI: 10.1111/nan.12447

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    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

    Version of Record online : 29 SEP 2014, DOI: 10.1111/epi.12800

  15. 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

    Version of Record online : 16 AUG 2013, DOI: 10.1002/ajmg.a.36170

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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

    Version of Record online : 23 MAY 2014, DOI: 10.1002/stem.1673

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    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

    Version of Record online : 20 JAN 2015, DOI: 10.1002/hep.27491

  18. 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

    Version of Record online : 7 NOV 2006, DOI: 10.1002/glia.20456

  19. West syndrome associated with mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14

    American Journal of Medical Genetics Part A

    Volume 155, Issue 10, October 2011, Pages: 2584–2588, Jun Tohyama, Toshiyuki Yamamoto, Kana Hosoki, Keisuke Nagasaki, Noriyuki Akasaka, Tsukasa Ohashi, Yu Kobayashi and Shinji Saitoh

    Version of Record online : 9 SEP 2011, DOI: 10.1002/ajmg.a.34224

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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

    Version of Record online : 7 DEC 2010, DOI: 10.1002/humu.21422