195 related articles for article (PubMed ID: 22652393)
21. 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]
22. 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]
23. 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]
24. Functions of Gtf2i and Gtf2ird1 in the developing brain: transcription, DNA binding and long-term behavioral consequences.
Kopp ND; Nygaard KR; Liu Y; McCullough KB; Maloney SE; Gabel HW; Dougherty JD
Hum Mol Genet; 2020 Jun; 29(9):1498-1519. PubMed ID: 32313931
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. 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]
28. 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]
29. Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development.
Palmer SJ; Tay ES; Santucci N; Cuc Bach TT; Hook J; Lemckert FA; Jamieson RV; Gunnning PW; Hardeman EC
Gene Expr Patterns; 2007 Feb; 7(4):396-404. PubMed ID: 17239664
[TBL] [Abstract][Full Text] [Related]
30. Essential role of the N-terminal region of TFII-I in viability and behavior.
Lucena J; Pezzi S; Aso E; Valero MC; Carreiro C; Dubus P; Sampaio A; Segura M; Barthelemy I; Zindel MY; Sousa N; Barbero JL; Maldonado R; Pérez-Jurado LA; Campuzano V
BMC Med Genet; 2010 Apr; 11():61. PubMed ID: 20403157
[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. Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.
Hirota H; Matsuoka R; Chen XN; Salandanan LS; Lincoln A; Rose FE; Sunahara M; Osawa M; Bellugi U; Korenberg JR
Genet Med; 2003; 5(4):311-21. PubMed ID: 12865760
[TBL] [Abstract][Full Text] [Related]
33. TFII-I gene family during tooth development: candidate genes for tooth anomalies in Williams syndrome.
Ohazama A; Sharpe PT
Dev Dyn; 2007 Oct; 236(10):2884-8. PubMed ID: 17823943
[TBL] [Abstract][Full Text] [Related]
34. An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism.
Edelmann L; Prosnitz A; Pardo S; Bhatt J; Cohen N; Lauriat T; Ouchanov L; González PJ; Manghi ER; Bondy P; Esquivel M; Monge S; Delgado MF; Splendore A; Francke U; Burton BK; McInnes LA
J Med Genet; 2007 Feb; 44(2):136-43. PubMed ID: 16971481
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. 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]
38. 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]
39. Consistent hypersocial behavior in mice carrying a deletion of
Martin LA; Iceberg E; Allaf G
Brain Behav; 2018 Jan; 8(1):e00895. PubMed ID: 29568691
[TBL] [Abstract][Full Text] [Related]
40. Motor function deficits in the 12 month-old female 5xFAD mouse model of Alzheimer's disease.
O'Leary TP; Robertson A; Chipman PH; Rafuse VF; Brown RE
Behav Brain Res; 2018 Jan; 337():256-263. PubMed ID: 28890389
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]