261 related articles for article (PubMed ID: 10780788)
1. WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog.
de Luis O; Valero MC; Jurado LA
Eur J Hum Genet; 2000 Mar; 8(3):215-22. PubMed ID: 10780788
[TBL] [Abstract][Full Text] [Related]
2. Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome.
Osborne LR; Campbell T; Daradich A; Scherer SW; Tsui LC
Genomics; 1999 Apr; 57(2):279-84. PubMed ID: 10198167
[TBL] [Abstract][Full Text] [Related]
3. WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network.
Cairo S; Merla G; Urbinati F; Ballabio A; Reymond A
Hum Mol Genet; 2001 Mar; 10(6):617-27. PubMed ID: 11230181
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
Valero MC; de Luis O; Cruces J; Pérez Jurado LA
Genomics; 2000 Oct; 69(1):1-13. PubMed ID: 11013070
[TBL] [Abstract][Full Text] [Related]
6. A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome.
Tassabehji M; Carette M; Wilmot C; Donnai D; Read AP; Metcalfe K
Eur J Hum Genet; 1999; 7(7):737-47. PubMed ID: 10573005
[TBL] [Abstract][Full Text] [Related]
7. Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.
Osborne LR; Martindale D; Scherer SW; Shi XM; Huizenga J; Heng HH; Costa T; Pober B; Lew L; Brinkman J; Rommens J; Koop B; Tsui LC
Genomics; 1996 Sep; 36(2):328-36. PubMed ID: 8812460
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region.
Wang YK; Pérez-Jurado LA; Francke U
Genomics; 1998 Mar; 48(2):163-70. PubMed ID: 9521869
[TBL] [Abstract][Full Text] [Related]
10. A novel human gene FKBP6 is deleted in Williams syndrome.
Meng X; Lu X; Morris CA; Keating MT
Genomics; 1998 Sep; 52(2):130-7. PubMed ID: 9782077
[TBL] [Abstract][Full Text] [Related]
11. TBL2, a novel transducin family member in the WBS deletion: characterization of the complete sequence, genomic structure, transcriptional variants and the mouse ortholog.
Pérez Jurado LA; Wang YK; Francke U; Cruces J
Cytogenet Cell Genet; 1999; 86(3-4):277-84. PubMed ID: 10575226
[TBL] [Abstract][Full Text] [Related]
12. A novel human gene, WSTF, is deleted in Williams syndrome.
Lu X; Meng X; Morris CA; Keating MT
Genomics; 1998 Dec; 54(2):241-9. PubMed ID: 9828126
[TBL] [Abstract][Full Text] [Related]
13. A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK.
Pérez Jurado LA; Wang YK; Peoples R; Coloma A; Cruces J; Francke U
Hum Mol Genet; 1998 Mar; 7(3):325-34. PubMed ID: 9466987
[TBL] [Abstract][Full Text] [Related]
14. The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region.
Hoogenraad CC; Eussen BH; Langeveld A; van Haperen R; Winterberg S; Wouters CH; Grosveld F; De Zeeuw CI; Galjart N
Genomics; 1998 Nov; 53(3):348-58. PubMed ID: 9799601
[TBL] [Abstract][Full Text] [Related]
15. Identification of additional transcripts in the Williams-Beuren syndrome critical region.
Merla G; Ucla C; Guipponi M; Reymond A
Hum Genet; 2002 May; 110(5):429-38. PubMed ID: 12073013
[TBL] [Abstract][Full Text] [Related]
16. Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome.
Wang YK; Spörle R; Paperna T; Schughart K; Francke U
Genomics; 1999 Apr; 57(2):235-48. PubMed ID: 10198163
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes.
Meng X; Lu X; Li Z; Green ED; Massa H; Trask BJ; Morris CA; Keating MT
Hum Genet; 1998 Nov; 103(5):590-9. PubMed ID: 9860302
[TBL] [Abstract][Full Text] [Related]
19. The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3.
Merla G; Howald C; Antonarakis SE; Reymond A
Hum Mol Genet; 2004 Jul; 13(14):1505-14. PubMed ID: 15163635
[TBL] [Abstract][Full Text] [Related]
20. Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion.
Robinson WP; Waslynka J; Bernasconi F; Wang M; Clark S; Kotzot D; Schinzel A
Genomics; 1996 May; 34(1):17-23. PubMed ID: 8661020
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
