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Select item 103603951.

FOXG1 targets BMP repressors and cell cycle inhibitors in human neural progenitor cells

Nuwan C Hettige, Peter Fleming, Amelia Semenak, Xin Zhang, Huashan Peng, Marc-Daniel Hagel, Jean-François Théroux, Ying Zhang, Anjie Ni, Malvin Jefri, Lilit Antonyan, Shaima Alsuwaidi, Andreas Schuppert, Patrick S Stumpf, Carl Ernst

Hum Mol Genet. 2023 Aug 1; 32(15): 2511–2522. Published online 2023 May 22. doi: 10.1093/hmg/ddad089

PMCID:: PMC10360395

Abstract Article PDF–1.2M

Select item 98317212.

A comprehensive analysis of the FOX family for predicting kidney renal clear cell carcinoma prognosis and the oncogenic role of FOXG1

Wenjie Yang, Hualin Chen, Lin Ma, Jie Dong, Mengchao Wei, Xiaoqiang Xue, Yingjie Li, Zhaoheng Jin, Weifeng Xu, Zhigang Ji

Aging (Albany NY) 2022 Dec 31; 14(24): 10107–10124. Published online 2022 Dec 29. doi: 10.18632/aging.204448

PMCID:: PMC9831721

Abstract Article PDF–1.7M

Select item 92876703.

Zika virus induces FOXG1 nuclear displacement and downregulation in human neural progenitors

Giulia Lottini, Matteo Baggiani, Giulia Chesi, Beatrice D’Orsi, Paola Quaranta, Michele Lai, Laura Pancrazi, Marco Onorati, Mauro Pistello, Giulia Freer, Mario Costa

Stem Cell Reports. 2022 Jul 12; 17(7): 1683–1698. Published online 2022 Jun 16. doi: 10.1016/j.stemcr.2022.05.008

PMCID:: PMC9287670

Abstract Article PDF–5.4M

Select item 90401784.

FOXG1 dose tunes cell proliferation dynamics in human forebrain progenitor cells

Nuwan C. Hettige, Huashan Peng, Hanrong Wu, Xin Zhang, Volodymyr Yerko, Ying Zhang, Malvin Jefri, Vincent Soubannier, Gilles Maussion, Shaima Alsuwaidi, Anjie Ni, Cecilia Rocha, Jeyashree Krishnan, Vincent McCarty, Lilit Antonyan, Andreas Schuppert, Gustavo Turecki, Edward A. Fon, Thomas M. Durcan, Carl Ernst

Stem Cell Reports. 2022 Mar 8; 17(3): 475–488. Published online 2022 Feb 10. doi: 10.1016/j.stemcr.2022.01.010

PMCID:: PMC9040178

Abstract Article PDF–3.3M

Select item 87807395.

Paving Therapeutic Avenues for FOXG1 Syndrome: Untangling Genotypes and Phenotypes from a Molecular Perspective

Ipek Akol, Fabian Gather, Tanja Vogel

Int J Mol Sci. 2022 Jan; 23(2): 954. Published online 2022 Jan 16. doi: 10.3390/ijms23020954

PMCID:: PMC8780739

Abstract Article PDF–1.5M

Select item 86856246.

Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region

Xin (Cynthia) Ye, Nicole M Roslin, Andrew D Paterson, Christopher J Lyons, Victor Pegado, Phillip Richmond, Casper Shyr, Oriol Fornes, XiaoHua Han, Michelle Higginson, Colin J Ross, Deborah Giaschi, Cheryl Gregory-Evans, Millan S Patel, Wyeth W Wasserman

J Med Genet. 2022 Jan; 59(1): 46–55. Published online 2020 Nov 30. doi: 10.1136/jmedgenet-2020-107226

PMCID:: PMC8685624

Abstract Article PDF–3.4M

Select item 86154217.

Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephaly

Han Na Jang, Taeho Kim, Ah Young Jung, Beom Hee Lee, Mi-Sun Yum, Tae-Sung Ko

Medicine (Baltimore) 2021 Nov 24; 100(47): e27949. Published online 2021 Nov 24. doi: 10.1097/MD.0000000000027949

PMCID:: PMC8615421

Abstract Article PDF–1.1M

Select item 82991998.

FOXG1 improves mitochondrial function and promotes the progression of nasopharyngeal carcinoma

Huajun Xi, Zhengxiang He, Cao Lv

Mol Med Rep. 2021 Sep; 24(3): 651. Published online 2021 Jul 14. doi: 10.3892/mmr.2021.12290

PMCID:: PMC8299199

Abstract Article PDF–7.6M

Select item 63899849.

Precisely controlling endogenous protein dosage in hPSCs and derivatives to model FOXG1 syndrome

Wenliang Zhu, Boya Zhang, Mengqi Li, Fan Mo, Tingwei Mi, Yihui Wu, Zhaoqian Teng, Qi Zhou, Wei Li, Baoyang Hu

Nat Commun. 2019; 10: 928. Published online 2019 Feb 25. doi: 10.1038/s41467-019-08841-7

PMCID:: PMC6389984

Abstract Article PDF–6.4M

Select item 583904510.

Regulatory variants of FOXG1 in the context of its topological domain organisation

Mana M Mehrjouy, Ana Carolina S. Fonseca, Nadja Ehmke, Giorgio Paskulin, Antonio Novelli, Francesco Benedicenti, Maria Antonietta Mencarelli, Alessandra Renieri, Tiffany Busa, Chantal Missirian, Claus Hansen, Kikue Terada Abe, Carlos Eduardo Speck-Martins, Angela M. Vianna-Morgante, Mads Bak, Niels Tommerup

Eur J Hum Genet. 2018 Feb; 26(2): 186–196. Published online 2017 Dec 30. doi: 10.1038/s41431-017-0011-4

PMCID:: PMC5839045

Abstract Article PDF–1.5M

Select item 557584611.

Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation

Qingping Zhang, Jiaping Wang, Jiarui Li, Xinhua Bao, Ying Zhao, Xiaoying Zhang, Liping Wei, Xiru Wu

BMC Med Genet. 2017; 18: 96. Published online 2017 Aug 29. doi: 10.1186/s12881-017-0455-y

PMCID:: PMC5575846

Abstract Article PDF–439K

Select item 552261712.

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B. Dobyns

J Med Genet. Author manuscript; available in PMC 2017 Jul 22.

Published in final edited form as: J Med Genet. 2011 Jun; 48(6): 396–406. Published online 2011 Mar 25. doi: 10.1136/jmg.2010.087528

PMCID:: PMC5522617

Abstract Article PDF–1.3M

Select item 532053913.

hBfl-1/hNOXA Interaction Studies Provide New Insights on the Role of Bfl-1 in Cancer Cell Resistance and for the Design of Novel Anticancer Agents

Elisa Barile, Guya D. Marconi, Surya K. De, Carlo Baggio, Luca Gambini, Ahmed F. Salem, Manoj K. Kashyap, Januario E. Castro, Thomas J. Kipps, Maurizio Pellecchia

ACS Chem Biol. 2017 Feb 17; 12(2): 444–455. Published online 2016 Nov 18. doi: 10.1021/acschembio.6b00962

PMCID:: PMC5320539

Abstract Article PDF–5.5M

Select item 486224414.

Delineation of the movement disorders associated with FOXG1 mutations

Apostolos Papandreou, Ruth B. Schneider, Erika F. Augustine, Joanne Ng, Kshitij Mankad, Esther Meyer, Amy McTague, Adeline Ngoh, Cheryl Hemingway, Robert Robinson, Sophia M. Varadkar, Maria Kinali, Vincenzo Salpietro, Margaret C. O'Driscoll, S. Nigel Basheer, Richard I. Webster, Shekeeb S. Mohammad, Shpresa Pula, Marian McGowan, Natalie Trump, Lucy Jenkins, Frances Elmslie, Richard H. Scott, Jane A. Hurst, Belen Perez-Duenas, Alexander R. Paciorkowski, Manju A. Kurian

Neurology. 2016 May 10; 86(19): 1794–1800. doi: 10.1212/WNL.0000000000002585

PMCID:: PMC4862244

Abstract Article PDF–282K

Select item 471720415.

Altered expression of neuropeptides in FoxG1-null heterozygous mutant mice

Elisa Frullanti, Sonia Amabile, Maria Grazia Lolli, Anna Bartolini, Gabriella Livide, Elisa Landucci, Francesca Mari, Flora M Vaccarino, Francesca Ariani, Luca Massimino, Alessandra Renieri, Ilaria Meloni

Eur J Hum Genet. 2016 Feb; 24(2): 252–257. Published online 2015 May 13. doi: 10.1038/ejhg.2015.79

PMCID:: PMC4717204

Abstract Article PDF–685K

Select item 471561916.

Familial Recurrences of FOXG1-Related Disorder: Evidence for Mosaicism

Kelly Q. McMahon, Apostolos Papandreou, Mandy Ma, Brenda J. Barry, Ghayda M. Mirzaa, William B. Dobyns, Richard H. Scott, Natalie Trump, Manju A. Kurian, Alex R. Paciorkowski

Am J Med Genet A. Author manuscript; available in PMC 2016 Dec 1.

Published in final edited form as: Am J Med Genet A. 2015 Dec; 167(12): 3096–3102. Published online 2015 Sep 14. doi: 10.1002/ajmg.a.37353

PMCID:: PMC4715619

Abstract Article PDF–347K

Select item 451901617.

FOXG1-dependent dysregulation of GABA/glutamate neuron differentiation in autism spectrum disorders

Jessica Mariani, Gianfilippo Coppola, Ping Zhang, Alexej Abyzov, Lauren Provini, Livia Tomasini, Mariangela Amenduni, Anna Szekely, Dean Palejev, Michael Wilson, Mark Gerstein, Elena Grigorenko, Katarzyna Chawarska, Kevin Pelphrey, James Howe, Flora M. Vaccarino

Cell. Author manuscript; available in PMC 2016 Jul 16.

Published in final edited form as: Cell. 2015 Jul 16; 162(2): 375–390. doi: 10.1016/j.cell.2015.06.034

PMCID:: PMC4519016

Abstract Article PDF–2.9M

Select item 426546118.

Epilepsy and outcome in FOXG1-related disorders

Laurie E. Seltzer, Mandy Ma, Sohnee Ahmed, Mary Bertrand, William B. Dobyns, James Wheless, Alex R. Paciorkowski

Epilepsia. Author manuscript; available in PMC 2015 Aug 1.

Published in final edited form as: Epilepsia. 2014 Aug; 55(8): 1292–1300. Published online 2014 May 16. doi: 10.1111/epi.12648

PMCID:: PMC4265461

Abstract Article PDF–442K

Select item 383108519.

Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12

Christophe Goubau, Koen Devriendt, Nathalie Van der Aa, An Crepel, Dagmar Wieczorek, Tjitske Kleefstra, Marjolein H Willemsen, Anita Rauch, Andreas Tzschach, Thomy de Ravel, Peter Leemans, Chris Van Geet, Gunnar Buyse, Kathleen Freson

Eur J Hum Genet. 2013 Dec; 21(12): 1349–1355. Published online 2013 May 1. doi: 10.1038/ejhg.2013.86

PMCID:: PMC3831085

Abstract Article PDF–868K

Select item 364138420.

14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype

Carolyn J Ellaway, Gladys Ho, Elisa Bettella, Alisa Knapman, Felicity Collins, Anna Hackett, Fiona McKenzie, Artur Darmanian, Gregory B Peters, Kerry Fagan, John Christodoulou

Eur J Hum Genet. 2013 May; 21(5): 522–527. Published online 2012 Sep 12. doi: 10.1038/ejhg.2012.208

PMCID:: PMC3641384

Abstract Article PDF–512K

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