BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 25995468)

  • 1. Enhanced procedural learning of speech sound categories in a genetic variant of FOXP2.
    Chandrasekaran B; Yi HG; Blanco NJ; McGeary JE; Maddox WT
    J Neurosci; 2015 May; 35(20):7808-12. PubMed ID: 25995468
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FOXP2 variation modulates functional hemispheric asymmetries for speech perception.
    Ocklenburg S; Arning L; Gerding WM; Epplen JT; Güntürkün O; Beste C
    Brain Lang; 2013 Sep; 126(3):279-84. PubMed ID: 23911943
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance.
    Schreiweis C; Bornschein U; Burguière E; Kerimoglu C; Schreiter S; Dannemann M; Goyal S; Rea E; French CA; Puliyadi R; Groszer M; Fisher SE; Mundry R; Winter C; Hevers W; Pääbo S; Enard W; Graybiel AM
    Proc Natl Acad Sci U S A; 2014 Sep; 111(39):14253-8. PubMed ID: 25225386
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. No association between common genetic variation in FOXP2 and language impairment in schizophrenia.
    McCarthy NS; Clark ML; Jablensky A; Badcock JC
    Psychiatry Res; 2019 Jan; 271():590-597. PubMed ID: 30554107
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FoxP2 in song-learning birds and vocal-learning mammals.
    Webb DM; Zhang J
    J Hered; 2005; 96(3):212-6. PubMed ID: 15618302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria.
    Turner SJ; Hildebrand MS; Block S; Damiano J; Fahey M; Reilly S; Bahlo M; Scheffer IE; Morgan AT
    Am J Med Genet A; 2013 Sep; 161A(9):2321-6. PubMed ID: 23918746
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Behavior-linked FoxP2 regulation enables zebra finch vocal learning.
    Heston JB; White SA
    J Neurosci; 2015 Feb; 35(7):2885-94. PubMed ID: 25698728
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Monoallelic expression of the human FOXP2 speech gene.
    Adegbola AA; Cox GF; Bradshaw EM; Hafler DA; Gimelbrant A; Chess A
    Proc Natl Acad Sci U S A; 2015 Jun; 112(22):6848-54. PubMed ID: 25422445
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Language gene].
    Takahashi H
    Rinsho Shinkeigaku; 2006 Nov; 46(11):848-50. PubMed ID: 17432197
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Foxp2 mutations impair auditory-motor association learning.
    Kurt S; Fisher SE; Ehret G
    PLoS One; 2012; 7(3):e33130. PubMed ID: 22412993
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Modified sound-evoked brainstem potentials in Foxp2 mutant mice.
    Kurt S; Groszer M; Fisher SE; Ehret G
    Brain Res; 2009 Sep; 1289():30-6. PubMed ID: 19596273
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FOXP2 and the role of cortico-basal ganglia circuits in speech and language evolution.
    Enard W
    Curr Opin Neurobiol; 2011 Jun; 21(3):415-24. PubMed ID: 21592779
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Incidental learning of sound categories is impaired in developmental dyslexia.
    Gabay Y; Holt LL
    Cortex; 2015 Dec; 73():131-43. PubMed ID: 26409017
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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. PubMed ID: 17999362
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interaction between MAOA and FOXP2 in association with autism and verbal communication in a Korean population.
    Park Y; Won S; Nam M; Chung JH; Kwack K
    J Child Neurol; 2014 Dec; 29(12):NP207-11. PubMed ID: 24356376
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.