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Items: 1 to 20 of 21

1.

FOXP2 variation in great ape populations offers insight into the evolution of communication skills.

Staes N, Sherwood CC, Wright K, de Manuel M, Guevara EE, Marques-Bonet T, Krützen M, Massiah M, Hopkins WD, Ely JJ, Bradley BJ.

Sci Rep. 2017 Dec 4;7(1):16866. doi: 10.1038/s41598-017-16844-x.

2.

The FOXP2-Driven Network in Developmental Disorders and Neurodegeneration.

Oswald F, Klöble P, Ruland A, Rosenkranz D, Hinz B, Butter F, Ramljak S, Zechner U, Herlyn H.

Front Cell Neurosci. 2017 Jul 26;11:212. doi: 10.3389/fncel.2017.00212. eCollection 2017.

3.

To transduce a zebra finch: interrogating behavioral mechanisms in a model system for speech.

Heston JB, White SA.

J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2017 Sep;203(9):691-706. doi: 10.1007/s00359-017-1153-0. Epub 2017 Mar 7.

4.

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

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

J Neurodev Disord. 2016 Nov 28;8:44. doi: 10.1186/s11689-016-9177-2. eCollection 2016.

5.

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development.

Mueller KL, Murray JC, Michaelson JJ, Christiansen MH, Reilly S, Tomblin JB.

PLoS One. 2016 Apr 11;11(4):e0152576. doi: 10.1371/journal.pone.0152576. eCollection 2016.

6.

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.

7.

Recent Advances in the Genetics of Vocal Learning.

Condro MC, White SA.

Comp Cogn Behav Rev. 2014;9:75-98.

8.

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.

9.

FOXP2.

Nudel R, Newbury DF.

Wiley Interdiscip Rev Cogn Sci. 2013 Sep;4(5):547-560. doi: 10.1002/wcs.1247. Epub 2013 Aug 13. Review.

10.

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.

Peter B, Raskind WH, Matsushita M, Lisowski M, Vu T, Berninger VW, Wijsman EM, Brkanac Z.

J Neurodev Disord. 2011 Mar;3(1):39-49. doi: 10.1007/s11689-010-9065-0. Epub 2010 Nov 9.

11.

Genetic advances in the study of speech and language disorders.

Newbury DF, Monaco AP.

Neuron. 2010 Oct 21;68(2):309-20. doi: 10.1016/j.neuron.2010.10.001. Review.

12.

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

Tolosa A, Sanjuán J, Dagnall AM, Moltó MD, Herrero N, de Frutos R.

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

13.

Striatal FoxP2 is actively regulated during songbird sensorimotor learning.

Teramitsu I, Poopatanapong A, Torrisi S, White SA.

PLoS One. 2010 Jan 6;5(1):e8548. doi: 10.1371/journal.pone.0008548.

14.

Conservation and diversity of Foxp2 expression in muroid rodents: functional implications.

Campbell P, Reep RL, Stoll ML, Ophir AG, Phelps SM.

J Comp Neurol. 2009 Jan 1;512(1):84-100. doi: 10.1002/cne.21881.

15.

Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells.

Fujita E, Tanabe Y, Shiota A, Ueda M, Suwa K, Momoi MY, Momoi T.

Proc Natl Acad Sci U S A. 2008 Feb 26;105(8):3117-22. doi: 10.1073/pnas.0712298105. Epub 2008 Feb 19.

16.

CAG-encoded polyglutamine length polymorphism in the human genome.

Butland SL, Devon RS, Huang Y, Mead CL, Meynert AM, Neal SJ, Lee SS, Wilkinson A, Yang GS, Yuen MM, Hayden MR, Holt RA, Leavitt BR, Ouellette BF.

BMC Genomics. 2007 May 22;8:126.

17.

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.

Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K.

Am J Hum Genet. 2006 Nov;79(5):965-72. Epub 2006 Sep 27.

18.

FoxP2 regulation during undirected singing in adult songbirds.

Teramitsu I, White SA.

J Neurosci. 2006 Jul 12;26(28):7390-4.

19.

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

Shu W, Cho JY, Jiang Y, Zhang M, Weisz D, Elder GA, Schmeidler J, De Gasperi R, Sosa MA, Rabidou D, Santucci AC, Perl D, Morrisey E, Buxbaum JD.

Proc Natl Acad Sci U S A. 2005 Jul 5;102(27):9643-8. Epub 2005 Jun 27.

20.

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.

MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE.

Am J Hum Genet. 2005 Jun;76(6):1074-80. Epub 2005 Apr 22.

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