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Items: 1 to 20 of 79


A genome-integrated massively parallel reporter assay reveals DNA sequence determinants of cis-regulatory activity in neural cells.

Maricque BB, Dougherty JD, Cohen BA.

Nucleic Acids Res. 2017 Feb 28;45(4):e16. doi: 10.1093/nar/gkw942. No abstract available.


MicroRNAs as regulators and mediators of forkhead box transcription factors function in human cancers.

Li C, Zhang K, Chen J, Chen L, Wang R, Chu X.

Oncotarget. 2017 Feb 14;8(7):12433-12450. doi: 10.18632/oncotarget.14015. Review.


A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice.

Chabout J, Sarkar A, Patel SR, Radden T, Dunson DB, Fisher SE, Jarvis ED.

Front Behav Neurosci. 2016 Oct 20;10:197. eCollection 2016.


Lessons to be learned: how a comprehensive neurobiological framework of atypical reading development can inform educational practice.

Ozernov-Palchik O, Yu X, Wang Y, Gaab N.

Curr Opin Behav Sci. 2016 Aug;10:45-58. Epub 2016 May 19.


Early neuroimaging markers of FOXP2 intragenic deletion.

LiƩgeois FJ, Hildebrand MS, Bonthrone A, Turner SJ, Scheffer IE, Bahlo M, Connelly A, Morgan AT.

Sci Rep. 2016 Oct 13;6:35192. doi: 10.1038/srep35192.


Evolution of language: Lessons from the genome.

Fisher SE.

Psychon Bull Rev. 2017 Feb;24(1):34-40. doi: 10.3758/s13423-016-1112-8.


Sumoylation in Synaptic Function and Dysfunction.

Schorova L, Martin S.

Front Synaptic Neurosci. 2016 Apr 28;8:9. doi: 10.3389/fnsyn.2016.00009. eCollection 2016. Review.


Salivary FOXP2 expression and oral feeding success in premature infants.

Zimmerman E, Maki M, Maron J.

Cold Spring Harb Mol Case Stud. 2016 Jan;2(1):a000554. doi: 10.1101/mcs.a000554.


FOXP2 gene deletion and infant feeding difficulties: a case report.

Zimmerman E, Maron JL.

Cold Spring Harb Mol Case Stud. 2016 Jan;2(1):a000547. doi: 10.1101/mcs.a000547.


The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers.

Estruch SB, Graham SA, Deriziotis P, Fisher SE.

Sci Rep. 2016 Feb 12;6:20911. doi: 10.1038/srep20911.


Human-specific increase of dopaminergic innervation in a striatal region associated with speech and language: A comparative analysis of the primate basal ganglia.

Raghanti MA, Edler MK, Stephenson AR, Wilson LJ, Hopkins WD, Ely JJ, Erwin JM, Jacobs B, Hof PR, Sherwood CC.

J Comp Neurol. 2016 Jul 1;524(10):2117-29. doi: 10.1002/cne.23937. Epub 2015 Dec 29.


Retinoic Acid Signaling: A New Piece in the Spoken Language Puzzle.

van Rhijn JR, Vernes SC.

Front Psychol. 2015 Nov 26;6:1816. doi: 10.3389/fpsyg.2015.01816. eCollection 2015.


The language faculty that wasn't: a usage-based account of natural language recursion.

Christiansen MH, Chater N.

Front Psychol. 2015 Aug 27;6:1182. doi: 10.3389/fpsyg.2015.01182. eCollection 2015. Review.


The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21WAF1/CIP1 in 143B Osteosarcoma Cell Growth Arrest.

Gascoyne DM, Spearman H, Lyne L, Puliyadi R, Perez-Alcantara M, Coulton L, Fisher SE, Croucher PI, Banham AH.

PLoS One. 2015 Jun 2;10(6):e0128513. doi: 10.1371/journal.pone.0128513. eCollection 2015.


Association Study between the CD157/BST1 Gene and Autism Spectrum Disorders in a Japanese Population.

Yokoyama S, Al Mahmuda N, Munesue T, Hayashi K, Yagi K, Yamagishi M, Higashida H.

Brain Sci. 2015 May 20;5(2):188-200. doi: 10.3390/brainsci5020188.


Neural FoxP2 and FoxP1 expression in the budgerigar, an avian species with adult vocal learning.

Hara E, Perez JM, Whitney O, Chen Q, White SA, Wright TF.

Behav Brain Res. 2015 Apr 15;283:22-9. doi: 10.1016/j.bbr.2015.01.017. Epub 2015 Jan 16.


Differential FoxP2 and FoxP1 expression in a vocal learning nucleus of the developing budgerigar.

Whitney O, Voyles T, Hara E, Chen Q, White SA, Wright TF.

Dev Neurobiol. 2015 Jul;75(7):778-90. doi: 10.1002/dneu.22247. Epub 2014 Nov 26.


FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways.

Devanna P, Middelbeek J, Vernes SC.

Front Cell Neurosci. 2014 Sep 26;8:305. doi: 10.3389/fncel.2014.00305. eCollection 2014.


Multiple microRNAs regulate human FOXP2 gene expression by targeting sequences in its 3' untranslated region.

Fu L, Shi Z, Luo G, Tu W, Wang X, Fang Z, Li X.

Mol Brain. 2014 Oct 1;7:71. doi: 10.1186/s13041-014-0071-0.


De novo TBR1 mutations in sporadic autism disrupt protein functions.

Deriziotis P, O'Roak BJ, Graham SA, Estruch SB, Dimitropoulou D, Bernier RA, Gerdts J, Shendure J, Eichler EE, Fisher SE.

Nat Commun. 2014 Sep 18;5:4954. doi: 10.1038/ncomms5954.

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