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 *

264 related articles for article (PubMed ID: 11352562)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects.
    Stumpo DJ; Eddy RL; Haley LL; Sait S; Shows TB; Lai WS; Young WS; Speer MC; Dehejia A; Polymeropoulos M; Blackshear PJ
    Genomics; 1998 Apr; 49(2):253-64. PubMed ID: 9598313
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genomic organization of the genes Gtf2ird1, Gtf2i, and Ncf1 at the mouse chromosome 5 region syntenic to the human chromosome 7q11.23 Williams syndrome critical region.
    Bayarsaihan D; Dunai J; Greally JM; Kawasaki K; Sumiyama K; Enkhmandakh B; Shimizu N; Ruddle FH
    Genomics; 2002 Jan; 79(1):137-43. PubMed ID: 11827466
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Transgene stability and features of rasH2 mice as an animal model for short-term carcinogenicity testing.
    Suemizu H; Muguruma K; Maruyama C; Tomisawa M; Kimura M; Hioki K; Shimozawa N; Ohnishi Y; Tamaoki N; Nomura T
    Mol Carcinog; 2002 May; 34(1):1-9. PubMed ID: 12112317
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. A postimplantation lethal mutation induced by transgene insertion on mouse chromosome 8.
    Pravtcheva DD; Wise TL
    Genomics; 1995 Dec; 30(3):529-44. PubMed ID: 8825640
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alterations in specific gene expression and focal neoplastic growth during spontaneous hepatocarcinogenesis in albumin-SV40 T antigen transgenic rats.
    Dragan YP; Sargent LM; Babcock K; Kinunen N; Pitot HC
    Mol Carcinog; 2004 Jul; 40(3):150-9. PubMed ID: 15224347
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome.
    Duba HC; Doll A; Neyer M; Erdel M; Mann C; Hammerer I; Utermann G; Grzeschik KH
    Eur J Hum Genet; 2002 Jun; 10(6):351-61. PubMed ID: 12080386
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.