BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 22198572)

  • 21. GTF2IRD2 is located in the Williams-Beuren syndrome critical region 7q11.23 and encodes a protein with two TFII-I-like helix-loop-helix repeats.
    Makeyev AV; Erdenechimeg L; Mungunsukh O; Roth JJ; Enkhmandakh B; Ruddle FH; Bayarsaihan D
    Proc Natl Acad Sci U S A; 2004 Jul; 101(30):11052-7. PubMed ID: 15243160
    [TBL] [Abstract][Full Text] [Related]  

  • 22. GTF2IRD1 regulates transcription by binding an evolutionarily conserved DNA motif 'GUCE'.
    Thompson PD; Webb M; Beckett W; Hinsley T; Jowitt T; Sharrocks AD; Tassabehji M
    FEBS Lett; 2007 Mar; 581(6):1233-42. PubMed ID: 17346708
    [TBL] [Abstract][Full Text] [Related]  

  • 23. An In Vivo Gain-of-Function Screen Identifies the Williams-Beuren Syndrome Gene GTF2IRD1 as a Mammary Tumor Promoter.
    Huo Y; Su T; Cai Q; Macara IG
    Cell Rep; 2016 Jun; 15(10):2089-2096. PubMed ID: 27239038
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Extensive characterization of a Williams syndrome murine model shows Gtf2ird1-mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior.
    Nygaard KR; Maloney SE; Swift RG; McCullough KB; Wagner RE; Fass SB; Garbett K; Mirnics K; Veenstra-VanderWeele J; Dougherty JD
    Genes Brain Behav; 2023 Aug; 22(4):e12853. PubMed ID: 37370259
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulation.
    Carmona-Mora P; Widagdo J; Tomasetig F; Canales CP; Cha Y; Lee W; Alshawaf A; Dottori M; Whan RM; Hardeman EC; Palmer SJ
    Hum Genet; 2015 Oct; 134(10):1099-115. PubMed ID: 26275350
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23.
    Franke Y; Peoples RJ; Francke U
    Cytogenet Cell Genet; 1999; 86(3-4):296-304. PubMed ID: 10575229
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular basis of Williams-Beuren syndrome: TFII-I regulated targets involved in craniofacial development.
    Makeyev AV; Bayarsaihan D
    Cleft Palate Craniofac J; 2011 Jan; 48(1):109-16. PubMed ID: 20500075
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A transcriptomic study of Williams-Beuren syndrome associated genes in mouse embryonic stem cells.
    De Cegli R; Iacobacci S; Fedele A; Ballabio A; di Bernardo D
    Sci Data; 2019 Nov; 6(1):262. PubMed ID: 31695049
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Innate frequency-discrimination hyperacuity in Williams-Beuren syndrome mice.
    Davenport CM; Teubner BJW; Han SB; Patton MH; Eom TY; Garic D; Lansdell BJ; Shirinifard A; Chang TC; Klein J; Pruett-Miller SM; Blundon JA; Zakharenko SS
    Cell; 2022 Oct; 185(21):3877-3895.e21. PubMed ID: 36152627
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Regulation of alternative splicing of Gtf2ird1 and its impact on slow muscle promoter activity.
    Tay ES; Guven KL; Subramaniam N; Polly P; Issa LL; Gunning PW; Hardeman EC
    Biochem J; 2003 Sep; 374(Pt 2):359-67. PubMed ID: 12780350
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Myg1-deficient mice display alterations in stress-induced responses and reduction of sex-dependent behavioural differences.
    Philips MA; Abramov U; Lilleväli K; Luuk H; Kurrikoff K; Raud S; Plaas M; Innos J; Puussaar T; Kõks S; Vasar E
    Behav Brain Res; 2010 Feb; 207(1):182-95. PubMed ID: 19818808
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays.
    Dai L; Bellugi U; Chen XN; Pulst-Korenberg AM; Järvinen-Pasley A; Tirosh-Wagner T; Eis PS; Graham J; Mills D; Searcy Y; Korenberg JR
    Am J Med Genet A; 2009 Mar; 149A(3):302-14. PubMed ID: 19205026
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.
    Ferrero GB; Howald C; Micale L; Biamino E; Augello B; Fusco C; Turturo MG; Forzano S; Reymond A; Merla G
    Eur J Hum Genet; 2010 Jan; 18(1):33-8. PubMed ID: 19568270
    [TBL] [Abstract][Full Text] [Related]  

  • 34. GTF2IRD2 from the Williams-Beuren critical region encodes a mobile-element-derived fusion protein that antagonizes the action of its related family members.
    Palmer SJ; Taylor KM; Santucci N; Widagdo J; Chan YK; Yeo JL; Adams M; Gunning PW; Hardeman EC
    J Cell Sci; 2012 Nov; 125(Pt 21):5040-50. PubMed ID: 22899722
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.
    Kopp ND; Parrish PCR; Lugo M; Dougherty JD; Kozel BA
    Mol Genet Genomic Med; 2018 Sep; 6(5):749-765. PubMed ID: 30008175
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Williams-Beuren syndrome: a challenge for genotype-phenotype correlations.
    Tassabehji M
    Hum Mol Genet; 2003 Oct; 12 Spec No 2():R229-37. PubMed ID: 12952863
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Enhanced endocrine response to novel environment stress and lack of corticosterone circadian rhythm in staggerer (Rora sg/sg) mutant mice.
    Frédéric F; Chianale C; Oliver C; Mariani J
    J Neurosci Res; 2006 Jun; 83(8):1525-32. PubMed ID: 16555296
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Reduced exploration, increased anxiety, and altered social behavior: Autistic-like features of euchromatin histone methyltransferase 1 heterozygous knockout mice.
    Balemans MC; Huibers MM; Eikelenboom NW; Kuipers AJ; van Summeren RC; Pijpers MM; Tachibana M; Shinkai Y; van Bokhoven H; Van der Zee CE
    Behav Brain Res; 2010 Mar; 208(1):47-55. PubMed ID: 19896504
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development.
    Enkhmandakh B; Makeyev AV; Erdenechimeg L; Ruddle FH; Chimge NO; Tussie-Luna MI; Roy AL; Bayarsaihan D
    Proc Natl Acad Sci U S A; 2009 Jan; 106(1):181-6. PubMed ID: 19109438
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder.
    Segura-Puimedon M; Sahún I; Velot E; Dubus P; Borralleras C; Rodrigues AJ; Valero MC; Valverde O; Sousa N; Herault Y; Dierssen M; Pérez-Jurado LA; Campuzano V
    Hum Mol Genet; 2014 Dec; 23(24):6481-94. PubMed ID: 25027326
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.