190 related articles for article (PubMed ID: 21909369)
21. Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome.
Tipney HJ; Hinsley TA; Brass A; Metcalfe K; Donnai D; Tassabehji M
Eur J Hum Genet; 2004 Jul; 12(7):551-60. PubMed ID: 15100712
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Enhanced prefrontal serotonin 5-HT(1A) currents in a mouse model of Williams-Beuren syndrome with low innate anxiety.
Proulx E; Young EJ; Osborne LR; Lambe EK
J Neurodev Disord; 2010 Jun; 2(2):99-108. PubMed ID: 20585377
[TBL] [Abstract][Full Text] [Related]
25. New TFII-I family target genes involved in embryonic development.
Makeyev AV; Bayarsaihan D
Biochem Biophys Res Commun; 2009 Sep; 386(4):554-8. PubMed ID: 19527686
[TBL] [Abstract][Full Text] [Related]
26. SUMOylation of GTF2IRD1 regulates protein partner interactions and ubiquitin-mediated degradation.
Widagdo J; Taylor KM; Gunning PW; Hardeman EC; Palmer SJ
PLoS One; 2012; 7(11):e49283. PubMed ID: 23145142
[TBL] [Abstract][Full Text] [Related]
27. Identification of the TFII-I family target genes in the vertebrate genome.
Chimge NO; Makeyev AV; Ruddle FH; Bayarsaihan D
Proc Natl Acad Sci U S A; 2008 Jul; 105(26):9006-10. PubMed ID: 18579769
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome.
Durkin ME; Keck-Waggoner CL; Popescu NC; Thorgeirsson SS
Genomics; 2001 Apr; 73(1):20-7. PubMed ID: 11352562
[TBL] [Abstract][Full Text] [Related]
31. A 1.3-mb 7q11.23 atypical deletion identified in a cohort of patients with williams-beuren syndrome.
Delgado LM; Gutierrez M; Augello B; Fusco C; Micale L; Merla G; Pastene EA
Mol Syndromol; 2013 Mar; 4(3):143-7. PubMed ID: 23653586
[TBL] [Abstract][Full Text] [Related]
32. The contribution of CLIP2 haploinsufficiency to the clinical manifestations of the Williams-Beuren syndrome.
Vandeweyer G; Van der Aa N; Reyniers E; Kooy RF
Am J Hum Genet; 2012 Jun; 90(6):1071-8. PubMed ID: 22608712
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models.
Kopp N; McCullough K; Maloney SE; Dougherty JD
Hum Mol Genet; 2019 Oct; 28(20):3443-3465. PubMed ID: 31418010
[TBL] [Abstract][Full Text] [Related]
35. The transcription factor GTF2IRD1 regulates the topology and function of photoreceptors by modulating photoreceptor gene expression across the retina.
Masuda T; Zhang X; Berlinicke C; Wan J; Yerrabelli A; Conner EA; Kjellstrom S; Bush R; Thorgeirsson SS; Swaroop A; Chen S; Zack DJ
J Neurosci; 2014 Nov; 34(46):15356-68. PubMed ID: 25392503
[TBL] [Abstract][Full Text] [Related]
36. The early embryonic expression of TFII-I during mouse preimplantation development.
Enkhmandakh B; Bitchevaia N; Ruddle F; Bayarsaihan D
Gene Expr Patterns; 2004 Jan; 4(1):25-8. PubMed ID: 14678824
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. GTF2IRD1 in craniofacial development of humans and mice.
Tassabehji M; Hammond P; Karmiloff-Smith A; Thompson P; Thorgeirsson SS; Durkin ME; Popescu NC; Hutton T; Metcalfe K; Rucka A; Stewart H; Read AP; Maconochie M; Donnai D
Science; 2005 Nov; 310(5751):1184-7. PubMed ID: 16293761
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
