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J-GLOBAL ID：202002228418646816   Reference number：20A0590670

Transcription and Beyond: Delineating FOXG1 Function in Cortical Development and Disorders

転写とそれを超えて:皮質発達と障害におけるFoxg1機能の描写【JST・京大機械翻訳】

Author (7)： Hou Pei-Shan (Laboratory for Developmental Biology, Department of Biology, Faculty of Education and Integrated Arts and Sciences, Waseda University, Tokyo, Japan) ,  Hou Pei-Shan (Institute of Anatomy and Cell Biology, School of Medicine, National Yang-Ming University, Taipei, Taiwan) ,  hAilin Darren O (Department of Molecular Embryology, Institute of Anatomy and Cell Biology, Medical Faculty, University of Freiburg, Freiburg, Germany) ,  Vogel Tanja (Department of Molecular Embryology, Institute of Anatomy and Cell Biology, Medical Faculty, University of Freiburg, Freiburg, Germany) ,  Vogel Tanja (Center for Basics in NeuroModulation (NeuroModul Basics), Faculty of Medicine, University of Freiburg, Freiburg, Germany) ,  Hanashima Carina (Laboratory for Developmental Biology, Department of Biology, Faculty of Education and Integrated Arts and Sciences, Waseda University, Tokyo, Japan) ,  Hanashima Carina (Department of Integrative Bioscience and Biomedical Engineering, Graduate School of Advanced Science and Engineering, Waseda University Center for Advanced Biomedical Sciences, Tokyo, Japan)
Material： Frontiers in Cellular Neuroscience (Web)
Volume： 14  Page： 35  Publication year： 2020 
JST Material Number： U7064A  ISSN： 1662-5102  Document type： Article
Article type： 文献レビュー  Country of issue： Switzerland (CHE)  Language： ENGLISH (EN)

Abstract/Point： Forkhead Box G1 (FOXG1) is a m...

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Thesaurus term： Rett Syndrome ,  Mammalia ,  Mutation ,  transcription factor ,  cerebral cortex ,  spectrum ,  human ,  schizophrenia ,  redundancy (property) ,  *cortex ,  Microcephaly ,  gene expression ,  gene ,  pathogenesis ,  neuropathy ,  Vertebrata ,  telencephalon ,  molecular genetic phenomenon

Author keywords (7)： FOXG1 ,  cortical development ,  FOXG1 syndrome ,  transcription factor ,  posttranscriptional regulation ,  cellular reprogramming ,  cortical organoid

JST classification (4)： Basic neurology  (GN01020W) ,  Nervous system diseases  (GN03000O) ,  Biological function  (EB03040U) ,  Gene expression  (EC02040Q)

Reference (102)：

• Adesina A. M., Nguyen Y., Guanaratne P., Pulliam J., Lopez-Terrada D., Margolin J., et al. (2007). FOXG1 is overexpressed in hepatoblastoma. Hum. Pathol. 38, 400-409. doi: 10.1016/j.humpath.2006.09.003
• Aguiar D. P., Sghari S., Creuzet S. (2014). The facial neural crest controls fore- and midbrain patterning by regulating Foxg1 expression through Smad1 activity. Development 141, 2494-2505. doi: 10.1242/dev.101790
• Ahlgren S., Vogt P., Bronner-Fraser M. (2003). Excess FoxG1 causes overgrowth of the neural tube. J. Neurobiol. 57, 337-349. doi: 10.1002/neu.10287
• Allou L., Lambert L., Amsallem D., Bieth E., Edery P., Destrée A., et al. (2012). 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements. Eur. J. Hum. Genet. 20, 1216-1223. doi: 10.1038/ejhg.2012.127
• Ariani F., Hayek G., Rondinella D., Artuso R., Mencarelli M. A., Spanhol-Rosseto A., et al. (2008). FOXG1 is responsible for the congenital variant of Rett syndrome. Am. J. Hum. Genet. 83, 89-93. doi: 10.1016/j.ajhg.2008.05.015

Terms in the title (4)： 転写 ,  皮質発達 ,  障害 ,  FOXG1