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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 16984964)

  • 21. Human-specific transcriptional regulation of CNS development genes by FOXP2.
    Konopka G; Bomar JM; Winden K; Coppola G; Jonsson ZO; Gao F; Peng S; Preuss TM; Wohlschlegel JA; Geschwind DH
    Nature; 2009 Nov; 462(7270):213-7. PubMed ID: 19907493
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Phonological working memory and FOXP2.
    Schulze K; Vargha-Khadem F; Mishkin M
    Neuropsychologia; 2018 Jan; 108():147-152. PubMed ID: 29174050
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A Key Evolutionary Mutation Enhances DNA Binding of the FOXP2 Forkhead Domain.
    Morris G; Fanucchi S
    Biochemistry; 2016 Apr; 55(13):1959-67. PubMed ID: 26950495
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1.
    Saleem RA; Banerjee-Basu S; Berry FB; Baxevanis AD; Walter MA
    Hum Mol Genet; 2003 Nov; 12(22):2993-3005. PubMed ID: 14506133
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting
    Morison LD; Meffert E; Stampfer M; Steiner-Wilke I; Vollmer B; Schulze K; Briggs T; Braden R; Vogel A; Thompson-Lake D; Patel C; Blair E; Goel H; Turner S; Moog U; Riess A; Liegeois F; Koolen DA; Amor DJ; Kleefstra T; Fisher SE; Zweier C; Morgan AT
    J Med Genet; 2023 Jun; 60(6):597-607. PubMed ID: 36328423
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Multiple domains define the expression and regulatory properties of Foxp1 forkhead transcriptional repressors.
    Wang B; Lin D; Li C; Tucker P
    J Biol Chem; 2003 Jul; 278(27):24259-68. PubMed ID: 12692134
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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. PubMed ID: 17033973
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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. PubMed ID: 17999357
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. The DISC1 promoter: characterization and regulation by FOXP2.
    Walker RM; Hill AE; Newman AC; Hamilton G; Torrance HS; Anderson SM; Ogawa F; Derizioti P; Nicod J; Vernes SC; Fisher SE; Thomson PA; Porteous DJ; Evans KL
    Hum Mol Genet; 2012 Jul; 21(13):2862-72. PubMed ID: 22434823
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Early neuroimaging markers of FOXP2 intragenic deletion.
    Liégeois FJ; Hildebrand MS; Bonthrone A; Turner SJ; Scheffer IE; Bahlo M; Connelly A; Morgan AT
    Sci Rep; 2016 Oct; 6():35192. PubMed ID: 27734906
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.
    Han TU; Park J; Domingues CF; Moretti-Ferreira D; Paris E; Sainz E; Gutierrez J; Drayna D
    Neurobiol Dis; 2014 Sep; 69():23-31. PubMed ID: 24807205
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Effect of pH on the Structure and DNA Binding of the FOXP2 Forkhead Domain.
    Blane A; Fanucchi S
    Biochemistry; 2015 Jun; 54(25):4001-7. PubMed ID: 26055196
    [TBL] [Abstract][Full Text] [Related]  

  • 38. An Etiological Foxp2 Mutation Impairs Neuronal Gain in Layer VI Cortico-Thalamic Cells through Increased GABA
    Druart M; Groszer M; Le Magueresse C
    J Neurosci; 2020 Oct; 40(44):8543-8555. PubMed ID: 33020214
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Phenotype of FOXP2 haploinsufficiency in a mother and son.
    Rice GM; Raca G; Jakielski KJ; Laffin JJ; Iyama-Kurtycz CM; Hartley SL; Sprague RE; Heintzelman AT; Shriberg LD
    Am J Med Genet A; 2012 Jan; 158A(1):174-81. PubMed ID: 22106036
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.