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85 related items for PubMed ID: 9878248

  • 1. Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion.
    Paperna T, Peoples R, Wang YK, Kaplan P, Francke U.
    Genomics; 1998 Dec 15; 54(3):453-9. PubMed ID: 9878248
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  • 2. 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 15; 57(2):235-48. PubMed ID: 10198163
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  • 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 15; 8(3):215-22. PubMed ID: 10780788
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  • 4. 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 01; 69(1):1-13. PubMed ID: 11013070
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  • 5. 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 15; 57(2):279-84. PubMed ID: 10198167
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  • 6. 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 Apr 15; 86(3-4):277-84. PubMed ID: 10575226
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  • 8. 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 Apr 15; 86(3-4):296-304. PubMed ID: 10575229
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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 15; 7(3):325-34. PubMed ID: 9466987
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  • 14. 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 15; 12(7):551-60. PubMed ID: 15100712
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  • 15. A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23.
    Wang YK, Samos CH, Peoples R, Pérez-Jurado LA, Nusse R, Francke U.
    Hum Mol Genet; 1997 Mar 15; 6(3):465-72. PubMed ID: 9147651
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  • 16. 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 01; 53(3):348-58. PubMed ID: 9799601
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  • 17. Clostridium perfringens enterotoxin utilizes two structurally related membrane proteins as functional receptors in vivo.
    Katahira J, Sugiyama H, Inoue N, Horiguchi Y, Matsuda M, Sugimoto N.
    J Biol Chem; 1997 Oct 17; 272(42):26652-8. PubMed ID: 9334247
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  • 18. Cloning, expression, and chromosomal mapping of the human 14-3-3gamma gene (YWHAG) to 7q11.23.
    Horie M, Suzuki M, Takahashi E, Tanigami A.
    Genomics; 1999 Sep 01; 60(2):241-3. PubMed ID: 10486217
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  • 19. Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome.
    Doll A, Grzeschik KH.
    Cytogenet Cell Genet; 2001 Sep 01; 95(1-2):20-7. PubMed ID: 11978965
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