These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
253 related articles for article (PubMed ID: 17035521)
21. 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. PubMed ID: 15877281 [TBL] [Abstract][Full Text] [Related]
22. Striatal FoxP2 is actively regulated during songbird sensorimotor learning. Teramitsu I; Poopatanapong A; Torrisi S; White SA PLoS One; 2010 Jan; 5(1):e8548. PubMed ID: 20062527 [TBL] [Abstract][Full Text] [Related]
23. The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration. Padovani A; Cosseddu M; Premi E; Archetti S; Papetti A; Agosti C; Bigni B; Cerini C; Paghera B; Bellelli G; Borroni B J Alzheimers Dis; 2010; 22(3):923-31. PubMed ID: 20858950 [TBL] [Abstract][Full Text] [Related]
24. [The FoxP2 gene makes humans speak and birds twitter]. Rochefort C Med Sci (Paris); 2008 Nov; 24(11):906-7. PubMed ID: 19038086 [No Abstract] [Full Text] [Related]
25. FoxP2 regulation during undirected singing in adult songbirds. Teramitsu I; White SA J Neurosci; 2006 Jul; 26(28):7390-4. PubMed ID: 16837586 [TBL] [Abstract][Full Text] [Related]
26. 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; 24(13):3152-63. PubMed ID: 15056695 [TBL] [Abstract][Full Text] [Related]
27. Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability. Murugan M; Harward S; Scharff C; Mooney R Neuron; 2013 Dec; 80(6):1464-76. PubMed ID: 24268418 [TBL] [Abstract][Full Text] [Related]
28. The songbird as a model for the generation and learning of complex sequential behaviors. Fee MS; Scharff C ILAR J; 2010; 51(4):362-77. PubMed ID: 21131713 [TBL] [Abstract][Full Text] [Related]
29. FOXP genes, neural development, speech and language disorders. Takahashi H; Takahashi K; Liu FC Adv Exp Med Biol; 2009; 665():117-29. PubMed ID: 20429420 [TBL] [Abstract][Full Text] [Related]
30. 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]
31. CNTNAP2 is a direct FoxP2 target in vitro and in vivo in zebra finches: complex regulation by age and activity. Adam I; Mendoza E; Kobalz U; Wohlgemuth S; Scharff C Genes Brain Behav; 2017 Jul; 16(6):635-642. PubMed ID: 28488276 [TBL] [Abstract][Full Text] [Related]
32. Language fMRI abnormalities associated with FOXP2 gene mutation. Liégeois F; Baldeweg T; Connelly A; Gadian DG; Mishkin M; Vargha-Khadem F Nat Neurosci; 2003 Nov; 6(11):1230-7. PubMed ID: 14555953 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. FoxP2 protein decreases at a specific region in the chick midbrain after hatching. Bessho C; Yamada S; Tanida T; Tanaka M Neurosci Lett; 2023 Mar; 800():137119. PubMed ID: 36773927 [TBL] [Abstract][Full Text] [Related]
35. Neocerebellar Crus I Abnormalities Associated with a Speech and Language Disorder Due to a Mutation in FOXP2. Argyropoulos GPD; Watkins KE; Belton-Pagnamenta E; Liégeois F; Saleem KS; Mishkin M; Vargha-Khadem F Cerebellum; 2019 Jun; 18(3):309-319. PubMed ID: 30460543 [TBL] [Abstract][Full Text] [Related]
36. Differential Song Deficits after Lentivirus-Mediated Knockdown of FoxP1, FoxP2, or FoxP4 in Area X of Juvenile Zebra Finches. Norton P; Barschke P; Scharff C; Mendoza E J Neurosci; 2019 Dec; 39(49):9782-9796. PubMed ID: 31641053 [TBL] [Abstract][Full Text] [Related]
38. 7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder. Rieger M; Krumbiegel M; Reuter MS; Schützenberger A; Reis A; Zweier C Am J Med Genet A; 2020 Nov; 182(11):2737-2741. PubMed ID: 32885567 [TBL] [Abstract][Full Text] [Related]
39. Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review. Che F; Li C; Zhang L; Qian C; Mo L; Li B; Wu H; Wang L; Yang Y J Appl Genet; 2024 May; 65(2):367-373. PubMed ID: 38418803 [TBL] [Abstract][Full Text] [Related]
40. Recruitment of FoxP2-expressing neurons to area X varies during song development. Rochefort C; He X; Scotto-Lomassese S; Scharff C Dev Neurobiol; 2007 May; 67(6):809-17. PubMed ID: 17443826 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]