360 related articles for article (PubMed ID: 15983371)
1. 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; 102(27):9643-8. PubMed ID: 15983371
[TBL] [Abstract][Full Text] [Related]
2. 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; 105(8):3117-22. PubMed ID: 18287060
[TBL] [Abstract][Full Text] [Related]
3. Temporal expression and mitochondrial localization of a Foxp2 isoform lacking the forkhead domain in developing Purkinje cells.
Tanabe Y; Fujiwara Y; Matsuzaki A; Fujita E; Kasahara T; Yuasa S; Momoi T
J Neurochem; 2012 Jul; 122(1):72-80. PubMed ID: 21985339
[TBL] [Abstract][Full Text] [Related]
4. Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity.
Fujita E; Tanabe Y; Imhof BA; Momoi MY; Momoi T
PLoS One; 2012; 7(1):e30151. PubMed ID: 22272290
[TBL] [Abstract][Full Text] [Related]
5. Specific expression of FOXP2 in cerebellum improves ultrasonic vocalization in heterozygous but not in homozygous Foxp2 (R552H) knock-in pups.
Fujita-Jimbo E; Momoi T
Neurosci Lett; 2014 Apr; 566():162-6. PubMed ID: 24607928
[TBL] [Abstract][Full Text] [Related]
6. A humanized version of Foxp2 affects ultrasonic vocalization in adult female and male mice.
von Merten S; Pfeifle C; Künzel S; Hoier S; Tautz D
Genes Brain Behav; 2021 Sep; 20(7):e12764. PubMed ID: 34342113
[TBL] [Abstract][Full Text] [Related]
7. A humanized version of Foxp2 does not affect ultrasonic vocalization in adult mice.
Hammerschmidt K; Schreiweis C; Minge C; Pääbo S; Fischer J; Enard W
Genes Brain Behav; 2015 Nov; 14(8):583-90. PubMed ID: 26250064
[TBL] [Abstract][Full Text] [Related]
8. 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; 506(2):277-80. PubMed ID: 22133810
[TBL] [Abstract][Full Text] [Related]
9. Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization.
Fröhlich H; Rafiullah R; Schmitt N; Abele S; Rappold GA
Hum Mol Genet; 2017 Apr; 26(8):1511-1521. PubMed ID: 28204507
[TBL] [Abstract][Full Text] [Related]
10. Region-specific Foxp2 deletions in cortex, striatum or cerebellum cannot explain vocalization deficits observed in spontaneous global knockouts.
Urbanus BHA; Peter S; Fisher SE; De Zeeuw CI
Sci Rep; 2020 Dec; 10(1):21631. PubMed ID: 33303861
[TBL] [Abstract][Full Text] [Related]
11. Ultrasonic vocalizations of adult male Foxp2-mutant mice: behavioral contexts of arousal and emotion.
Gaub S; Fisher SE; Ehret G
Genes Brain Behav; 2016 Feb; 15(2):243-59. PubMed ID: 26566793
[TBL] [Abstract][Full Text] [Related]
12. 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; 413(6855):519-23. PubMed ID: 11586359
[TBL] [Abstract][Full Text] [Related]
13. The structure of innate vocalizations in Foxp2-deficient mouse pups.
Gaub S; Groszer M; Fisher SE; Ehret G
Genes Brain Behav; 2010 Jun; 9(4):390-401. PubMed ID: 20132318
[TBL] [Abstract][Full Text] [Related]
14. Sumoylation of FOXP2 Regulates Motor Function and Vocal Communication Through Purkinje Cell Development.
Usui N; Co M; Harper M; Rieger MA; Dougherty JD; Konopka G
Biol Psychiatry; 2017 Feb; 81(3):220-230. PubMed ID: 27009683
[TBL] [Abstract][Full Text] [Related]
15. Ultrasonic vocalization changes and FOXP2 expression after experimental stroke.
Doran SJ; Trammel C; Benashaski SE; Venna VR; McCullough LD
Behav Brain Res; 2015 Apr; 283():154-61. PubMed ID: 25644653
[TBL] [Abstract][Full Text] [Related]
16. FOXP2 as a molecular window into speech and language.
Fisher SE; Scharff C
Trends Genet; 2009 Apr; 25(4):166-77. PubMed ID: 19304338
[TBL] [Abstract][Full Text] [Related]
17. 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; 18(5):354-62. PubMed ID: 18328704
[TBL] [Abstract][Full Text] [Related]
18. 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; 73(1):61-72. PubMed ID: 12815709
[TBL] [Abstract][Full Text] [Related]
19. Differential effects of Foxp2 disruption in distinct motor circuits.
French CA; Vinueza Veloz MF; Zhou K; Peter S; Fisher SE; Costa RM; De Zeeuw CI
Mol Psychiatry; 2019 Mar; 24(3):447-462. PubMed ID: 30108312
[TBL] [Abstract][Full Text] [Related]
20. FOXP2 is not a major susceptibility gene for autism or specific language impairment.
Newbury DF; Bonora E; Lamb JA; Fisher SE; Lai CS; Baird G; Jannoun L; Slonims V; Stott CM; Merricks MJ; Bolton PF; Bailey AJ; Monaco AP;
Am J Hum Genet; 2002 May; 70(5):1318-27. PubMed ID: 11894222
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]