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 *

170 related articles for article (PubMed ID: 21684252)

  • 1. FOXP2 promotes the nuclear translocation of POT1, but FOXP2(R553H), mutation related to speech-language disorder, partially prevents it.
    Tanabe Y; Fujita E; Momoi T
    Biochem Biophys Res Commun; 2011 Jul; 410(3):593-6. PubMed ID: 21684252
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 353(4):869-74. PubMed ID: 17196932
    [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. 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]  

  • 5. The medaka FoxP2, a homologue of human language gene FOXP2, has a diverged structure and function.
    Itakura T; Chandra A; Yang Z; Xue X; Wang B; Kimura W; Hikosaka K; Inohaya K; Kudo A; Uezato T; Miura N
    J Biochem; 2008 Mar; 143(3):407-16. PubMed ID: 18079162
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Structural analysis of disease-causing mutations in the P-subfamily of forkhead transcription factors.
    Banerjee-Basu S; Baxevanis AD
    Proteins; 2004 Mar; 54(4):639-47. PubMed ID: 14997560
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 418(6900):869-72. PubMed ID: 12192408
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional genetic analysis of mutations implicated in a human speech and language disorder.
    Vernes SC; Nicod J; Elahi FM; Coventry JA; Kenny N; Coupe AM; Bird LE; Davies KE; Fisher SE
    Hum Mol Genet; 2006 Nov; 15(21):3154-67. PubMed ID: 16984964
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unravelling neurogenetic networks implicated in developmental language disorders.
    Vernes SC; Fisher SE
    Biochem Soc Trans; 2009 Dec; 37(Pt 6):1263-9. PubMed ID: 19909259
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interaction of the Arabidopsis E2F and DP proteins confers their concomitant nuclear translocation and transactivation.
    Kosugi S; Ohashi Y
    Plant Physiol; 2002 Mar; 128(3):833-43. PubMed ID: 11891240
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PTOP interacts with POT1 and regulates its localization to telomeres.
    Liu D; Safari A; O'Connor MS; Chan DW; Laegeler A; Qin J; Songyang Z
    Nat Cell Biol; 2004 Jul; 6(7):673-80. PubMed ID: 15181449
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nuclear transport of Ras-associated tumor suppressor proteins: different transport receptor binding specificities for arginine-rich nuclear targeting signals.
    Kumari G; Singhal PK; Rao MR; Mahalingam S
    J Mol Biol; 2007 Apr; 367(5):1294-311. PubMed ID: 17320110
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FOXP2: novel exons, splice variants, and CAG repeat length stability.
    Bruce HA; Margolis RL
    Hum Genet; 2002 Aug; 111(2):136-44. PubMed ID: 12189486
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.
    Roll P; Vernes SC; Bruneau N; Cillario J; Ponsole-Lenfant M; Massacrier A; Rudolf G; Khalife M; Hirsch E; Fisher SE; Szepetowski P
    Hum Mol Genet; 2010 Dec; 19(24):4848-60. PubMed ID: 20858596
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Aberrant expression of the neuronal transcription factor FOXP2 in neoplastic plasma cells.
    Campbell AJ; Lyne L; Brown PJ; Launchbury RJ; Bignone P; Chi J; Roncador G; Lawrie CH; Gatter KC; Kusec R; Banham AH
    Br J Haematol; 2010 Apr; 149(2):221-30. PubMed ID: 20096010
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Human p32 is a novel FOXC1-interacting protein that regulates FOXC1 transcriptional activity in ocular cells.
    Huang L; Chi J; Berry FB; Footz TK; Sharp MW; Walter MA
    Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5243-9. PubMed ID: 18676636
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.