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Results: 1 to 20 of 120

1.

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.

Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ.

Brain. 2003 Nov;126(Pt 11):2455-62. Epub 2003 Jul 22.

PMID:
12876151
[PubMed - indexed for MEDLINE]
Free Article
2.

Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder.

Fujita E, Tanabe Y, Momoi MY, Momoi T.

Neurosci Lett. 2012 Jan 11;506(2):277-80. doi: 10.1016/j.neulet.2011.11.022. Epub 2011 Nov 22.

PMID:
22133810
[PubMed - indexed for MEDLINE]
3.

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.

Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA.

J Comp Neurol. 2003 May 26;460(2):266-79.

PMID:
12687690
[PubMed - indexed for MEDLINE]
4.

FOXP genes, neural development, speech and language disorders.

Takahashi H, Takahashi K, Liu FC.

Adv Exp Med Biol. 2009;665:117-29. Review.

PMID:
20429420
[PubMed - indexed for MEDLINE]
5.

Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum.

Takahashi K, Liu FC, Hirokawa K, Takahashi H.

J Neurosci Res. 2003 Jul 1;73(1):61-72.

PMID:
12815709
[PubMed - indexed for MEDLINE]
6.

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.

Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, Geschwind DH, Fisher SE.

Am J Hum Genet. 2007 Dec;81(6):1232-50. Epub 2007 Oct 31.

PMID:
17999362
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

FOXP2 as a molecular window into speech and language.

Fisher SE, Scharff C.

Trends Genet. 2009 Apr;25(4):166-77. doi: 10.1016/j.tig.2009.03.002. Epub 2009 Mar 21. Review.

PMID:
19304338
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
15877281
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction.

Teramitsu I, Kudo LC, London SE, Geschwind DH, White SA.

J Neurosci. 2004 Mar 31;24(13):3152-63.

PMID:
15056695
[PubMed - indexed for MEDLINE]
Free Article
10.

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.

Vernes SC, Oliver PL, Spiteri E, Lockstone HE, Puliyadi R, Taylor JM, Ho J, Mombereau C, Brewer A, Lowy E, Nicod J, Groszer M, Baban D, Sahgal N, Cazier JB, Ragoussis J, Davies KE, Geschwind DH, Fisher SE.

PLoS Genet. 2011 Jul;7(7):e1002145. doi: 10.1371/journal.pgen.1002145. Epub 2011 Jul 7.

PMID:
21765815
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Intracellular distribution of a speech/language disorder associated FOXP2 mutant.

Mizutani A, Matsuzaki A, Momoi MY, Fujita E, Tanabe Y, Momoi T.

Biochem Biophys Res Commun. 2007 Feb 23;353(4):869-74. Epub 2006 Dec 26.

PMID:
17196932
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
18287060
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.

Spiteri E, Konopka G, Coppola G, Bomar J, Oldham M, Ou J, Vernes SC, Fisher SE, Ren B, Geschwind DH.

Am J Hum Genet. 2007 Dec;81(6):1144-57. Epub 2007 Oct 31.

PMID:
17999357
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

A forkhead-domain gene is mutated in a severe speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP.

Nature. 2001 Oct 4;413(6855):519-23.

PMID:
11586359
[PubMed - indexed for MEDLINE]
15.

Molecular evolution of FOXP2, a gene involved in speech and language.

Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Pääbo S.

Nature. 2002 Aug 22;418(6900):869-72. Epub 2002 Aug 14.

PMID:
12192408
[PubMed - indexed for MEDLINE]
16.

[Language gene].

Takahashi H.

Rinsho Shinkeigaku. 2006 Nov;46(11):848-50. Japanese.

PMID:
17432197
[PubMed - indexed for MEDLINE]
17.

Generation of mice with a conditional Foxp2 null allele.

French CA, Groszer M, Preece C, Coupe AM, Rajewsky K, Fisher SE.

Genesis. 2007 Jul;45(7):440-6.

PMID:
17619227
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.

Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE.

Curr Biol. 2008 Mar 11;18(5):354-62. doi: 10.1016/j.cub.2008.01.060.

PMID:
18328704
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Foxp2 mutations impair auditory-motor association learning.

Kurt S, Fisher SE, Ehret G.

PLoS One. 2012;7(3):e33130. doi: 10.1371/journal.pone.0033130. Epub 2012 Mar 7.

PMID:
22412993
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Deciphering the genetic basis of speech and language disorders.

Fisher SE, Lai CS, Monaco AP.

Annu Rev Neurosci. 2003;26:57-80. Epub 2003 Jan 8. Review.

PMID:
12524432
[PubMed - indexed for MEDLINE]

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