PMC Links for GEO Profiles (Select 75160618) - PMC

Select item 99147391.

Increased Nuclear FOXP2 Is Related to Reduced Neural Stem Cell Number and Increased Neurogenesis in the Dorsal Telencephalon of Embryos of Diabetic Rats through Histamine H₁ Receptors

Diana Sarahi De la Merced-García, Ángel Sánchez-Barrera, Juan Hernández-Yonca, Ismael Mancilla, Guadalupe García-López, Néstor Fabián Díaz, Luis Ignacio Terrazas, Anayansi Molina-Hernández

Cells. 2023 Feb; 12(3): 510. Published online 2023 Feb 3. doi: 10.3390/cells12030510

PMCID:: PMC9914739

Abstract Article PDF–12M

Select item 67776912.

miR-134-5p/Foxp2/Syn1 is involved in cognitive impairment in an early vascular dementia rat model

Xin Liu, Ruilin Zhang, Zimei Wu, Wenwen Si, Zhenxing Ren, Saixia Zhang, Jianhong Zhou, Dongfeng Chen

Int J Mol Med. 2019 Nov; 44(5): 1729–1740. Published online 2019 Sep 5. doi: 10.3892/ijmm.2019.4331

PMCID:: PMC6777691

Abstract Article PDF–1.4M

Select item 43321503.

Proteomic analyses reveal distinct chromatin-associated and soluble transcription factor complexes

Xu Li, Wenqi Wang, Jiadong Wang, Anna Malovannaya, Yuanxin Xi, Wei Li, Rudy Guerra, David H Hawke, Jun Qin, Junjie Chen

Mol Syst Biol. 2015 Jan; 11(1): 775. Published online 2015 Jan 21. doi: 10.15252/msb.20145504

PMCID:: PMC4332150

Abstract Article PDF–2.8M

Select item 42394224.

Androgen Modulation of Foxp1 and Foxp2 in the Developing Rat Brain: Impact on Sex Specific Vocalization

J. Michael Bowers, Miguel Perez-Pouchoulen, Clinton R. Roby, Timothy E. Ryan, Margaret M. McCarthy

Endocrinology. 2014 Dec; 155(12): 4881–4894. Published online 2014 Sep 23. doi: 10.1210/en.2014-1486

PMCID:: PMC4239422

Abstract Article

Select item 42072295.

Investigating Protein-protein Interactions in Live Cells Using Bioluminescence Resonance Energy Transfer

Pelagia Deriziotis, Sarah A. Graham, Sara B. Estruch, Simon E. Fisher

J Vis Exp. 2014; (87): 51438. Published online 2014 May 26. doi: 10.3791/51438

PMCID:: PMC4207229

Abstract Article PDF–2.7M

Select item 37274426.

Foxp2 Mediates Sex Differences in Ultrasonic Vocalization by Rat Pups and Directs Order of Maternal Retrieval

J. Michael Bowers, Miguel Perez-Pouchoulen, N. Shalon Edwards, Margaret M. McCarthy

J Neurosci. 2013 Feb 20; 33(8): 3276–3283. doi: 10.1523/JNEUROSCI.0425-12.2013

PMCID:: PMC3727442

Abstract Article PDF–1.4M

Select item 32609157.

Imaging genetics of FOXP2 in dyslexia

Arndt Wilcke, Carolin Ligges, Jana Burkhardt, Michael Alexander, Christiane Wolf, Elfi Quente, Peter Ahnert, Per Hoffmann, Albert Becker, Bertram Müller-Myhsok, Sven Cichon, Johannes Boltze, Holger Kirsten

Eur J Hum Genet. 2012 Feb; 20(2): 224–229. Published online 2011 Sep 7. doi: 10.1038/ejhg.2011.160

Correction in:: Eur J Hum Genet. 2012 Jun; 20(6): 714.

PMCID:: PMC3260915

Abstract Article PDF–394K

Select item 31780598.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

Select item 30348299.

FoxP2 expression defines dorsolateral pontine neurons activated by sodium deprivation*

Joel C Geerling, Matthew K Stein, Rebecca L Miller, Jung-Won Shin, Paul A Gray, Arthur D Loewy

Brain Res. Author manuscript; available in PMC 2012 Feb 23.

Published in final edited form as: Brain Res. 2011 Feb 23; 1375: 19–27. Published online 2010 Nov 23. doi: 10.1016/j.brainres.2010.11.028

PMCID:: PMC3034829

Abstract Article PDF–2.8M

Select item 291857110.

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies

Amparo Tolosa, Julio Sanjuán, Adam M Dagnall, María D Moltó, Neus Herrero, Rosa de Frutos

BMC Med Genet. 2010; 11: 114. Published online 2010 Jul 22. doi: 10.1186/1471-2350-11-114

PMCID:: PMC2918571

Abstract Article PDF–915K

Select item 278457511.

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

Sonja C Vernes, Kay D MacDermot, Anthony P Monaco, Simon E Fisher

Eur J Hum Genet. 2009 Oct; 17(10): 1354–1358. Published online 2009 Apr 8. doi: 10.1038/ejhg.2009.43

PMCID:: PMC2784575

Abstract Article PDF–265K

Select item 275640912.

A Functional Genetic Link between Distinct Developmental Language Disorders

Sonja C. Vernes, Dianne F. Newbury, Brett S. Abrahams, Laura Winchester, Jérôme Nicod, Matthias Groszer, Maricela Alarcón, Peter L. Oliver, Kay E. Davies, Daniel H. Geschwind, Anthony P. Monaco, Simon E. Fisher

N Engl J Med. Author manuscript; available in PMC 2009 Oct 3.

Published in final edited form as: N Engl J Med. 2008 Nov 27; 359(22): 2337–2345. Published online 2008 Nov 5. doi: 10.1056/NEJMoa0802828

PMCID:: PMC2756409

Abstract Article PDF–1.2M

Select item 268232913.

Generation of mice with a conditional Foxp2 null allele

Catherine A French, Matthias Groszer, Christopher Preece, Anne-Marie Coupe, Klaus Rajewsky, Simon E Fisher

Genesis. 2007 Jul; 45(7): 440–446. doi: 10.1002/dvg.20305

PMCID:: PMC2682329

Abstract Article PDF–845K

Select item 239625214.

Foxp2 Inhibits Nkx2.1-Mediated Transcription of SP-C via Interactions with the Nkx2.1 Homeodomain

Beiyun Zhou, Qian Zhong, Parviz Minoo, Changgong Li, David K. Ann, Baruch Frenkel, Edward E. Morrisey, Edward D. Crandall, Zea Borok

Am J Respir Cell Mol Biol. 2008 Jun; 38(6): 750–758. Published online 2008 Jan 31. doi: 10.1165/rcmb.2007-0350OC

PMCID:: PMC2396252

Abstract Article PDF–585K

Select item 231239015.

Maternal infection leads to abnormal gene regulation and brain atrophy in mouse offspring: Implications for genesis of neurodevelopmental disorders

S. Hossein Fatemi, Teri J. Reutiman, Timothy D. Folsom, Hao Huang, Kenichi Oishi, Susumu Mori, Donald F. Smee, David A. Pearce, Christine Winter, Reinhard Sohr, Georg Juckel

Schizophr Res. Author manuscript; available in PMC 2009 Feb 1.

Published in final edited form as: Schizophr Res. 2008 Feb; 99(1-3): 56–70. Published online 2008 Jan 9. doi: 10.1016/j.schres.2007.11.018

PMCID:: PMC2312390

Abstract Article PDF–1.0M

Select item 169855716.

Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia

Lars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, Jennifer Skaug, Kazuhiko Nakabayashi, Brenda Finucane, Danielle Hartung, Micheil Innes, Batsheva Kerem, Małgorzata J. Nowaczyk, Joseph Rivlin, Wendy Roberts, Lili Senman, Anne Summers, Peter Szatmari, Virginia Wong, John B. Vincent, Susan Zeesman, Lucy R. Osborne, Janis Oram Cardy, Juha Kere, Stephen W. Scherer, Katariina Hannula-Jouppi

Am J Hum Genet. 2006 Nov; 79(5): 965–972. Published online 2006 Sep 27. doi: 10.1086/508902

PMCID:: PMC1698557

Abstract Article PDF–358K

Select item 119644517.

Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

Kay D. MacDermot, Elena Bonora, Nuala Sykes, Anne-Marie Coupe, Cecilia S. L. Lai, Sonja C. Vernes, Faraneh Vargha-Khadem, Fiona McKenzie, Robert L. Smith, Anthony P. Monaco, Simon E. Fisher

Am J Hum Genet. 2005 Jun; 76(6): 1074–1080. Published online 2005 Apr 22. doi: 10.1086/430841

PMCID:: PMC1196445

Abstract Article PDF–135K

Select item 116051818.

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

Weiguo Shu, Julie Y. Cho, Yuhui Jiang, Minhua Zhang, Donald Weisz, Gregory A. Elder, James Schmeidler, Rita De Gasperi, Miguel A. Gama Sosa, Donald Rabidou, Anthony C. Santucci, Daniel Perl, Edward Morrisey, Joseph D. Buxbaum

Proc Natl Acad Sci U S A. 2005 Jul 5; 102(27): 9643–9648. Published online 2005 Jun 27. doi: 10.1073/pnas.0503739102

PMCID:: PMC1160518

Abstract Article PDF–600K

Select item 34378619.

Transcriptional and DNA Binding Activity of the Foxp1/2/4 Family Is Modulated by Heterotypic and Homotypic Protein Interactions

Shanru Li, Joel Weidenfeld, Edward E. Morrisey

Mol Cell Biol. 2004 Jan; 24(2): 809–822. doi: 10.1128/MCB.24.2.809-822.2004

PMCID:: PMC343786

Abstract Article PDF–420K

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