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Journal Abstract Search

252 related items for PubMed ID: 11779826

  • 1. Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.
    DeSilva U, Elnitski L, Idol JR, Doyle JL, Gan W, Thomas JW, Schwartz S, Dietrich NL, Beckstrom-Sternberg SM, McDowell JC, Blakesley RW, Bouffard GG, Thomas PJ, Touchman JW, Miller W, Green ED.
    Genome Res; 2002 Jan; 12(1):3-15. PubMed ID: 11779826
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  • 3. Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.
    DeSilva U, Massa H, Trask BJ, Green ED.
    Genome Res; 1999 May; 9(5):428-36. PubMed ID: 10330122
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  • 5. Divergent human and mouse orthologs of a novel gene (WBSCR15/Wbscr15) reside within the genomic interval commonly deleted in Williams syndrome.
    Doyle JL, DeSilva U, Miller W, Green ED.
    Cytogenet Cell Genet; 2000 May; 90(3-4):285-90. PubMed ID: 11124535
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  • 6. Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5.
    Wilson MD, Riemer C, Martindale DW, Schnupf P, Boright AP, Cheung TL, Hardy DM, Schwartz S, Scherer SW, Tsui LC, Miller W, Koop BF.
    Nucleic Acids Res; 2001 Mar 15; 29(6):1352-65. PubMed ID: 11239002
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  • 8. Williams-Beuren syndrome: genes and mechanisms.
    Francke U.
    Hum Mol Genet; 1999 Mar 15; 8(10):1947-54. PubMed ID: 10469848
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  • 9. 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 01; 73(1):20-7. PubMed ID: 11352562
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  • 10. 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 01; 7(3):325-34. PubMed ID: 9466987
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  • 11. 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 01; 103(5):590-9. PubMed ID: 9860302
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  • 12. 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 01; 12(7):551-60. PubMed ID: 15100712
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  • 13. 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 01; 8(3):215-22. PubMed ID: 10780788
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  • 18. Comparative genomic sequence analysis of the Williams syndrome region (LIMK1-RFC2) of human chromosome 7q11.23.
    Martindale DW, Wilson MD, Wang D, Burke RD, Chen X, Duronio V, Koop BF.
    Mamm Genome; 2000 Oct 01; 11(10):890-8. PubMed ID: 11003705
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