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Journal Abstract Search

89 related items for PubMed ID: 9070929

  • 1. Identification of novel exons 3' to the human SNRPN gene.
    Buiting K, Dittrich B, Endele S, Horsthemke B.
    Genomics; 1997 Feb 15; 40(1):132-7. PubMed ID: 9070929
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  • 2. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome.
    Reed ML, Leff SE.
    Nat Genet; 1994 Feb 15; 6(2):163-7. PubMed ID: 7512861
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  • 3. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene.
    Dittrich B, Buiting K, Korn B, Rickard S, Buxton J, Saitoh S, Nicholls RD, Poustka A, Winterpacht A, Zabel B, Horsthemke B.
    Nat Genet; 1996 Oct 15; 14(2):163-70. PubMed ID: 8841186
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  • 4. The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.
    Bressler J, Tsai TF, Wu MY, Tsai SF, Ramirez MA, Armstrong D, Beaudet AL.
    Nat Genet; 2001 Jul 15; 28(3):232-40. PubMed ID: 11431693
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  • 6. Detection of imprinting mutations in Angelman syndrome using a probe for exon alpha of SNRPN.
    Beuten J, Sutcliffe JS, Casey BM, Beaudet AL, Hennekam RC, Willems PJ.
    Am J Med Genet; 1996 May 17; 63(2):414-5. PubMed ID: 8725798
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  • 7. Maternal and paternal genomes function independently in mouse ova in establishing expression of the imprinted genes Snrpn and Igf2r: no evidence for allelic trans-sensing and counting mechanisms.
    Szabó PE, Mann JR.
    EMBO J; 1996 Nov 15; 15(22):6018-25. PubMed ID: 8947024
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  • 8. Structure and function correlations at the imprinted mouse Snrpn locus.
    Gabriel JM, Gray TA, Stubbs L, Saitoh S, Ohta T, Nicholls RD.
    Mamm Genome; 1998 Oct 15; 9(10):788-93. PubMed ID: 9745031
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  • 9. The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A.
    Runte M, Hüttenhofer A, Gross S, Kiefmann M, Horsthemke B, Buiting K.
    Hum Mol Genet; 2001 Nov 01; 10(23):2687-700. PubMed ID: 11726556
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  • 10. Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.
    Landers M, Bancescu DL, Le Meur E, Rougeulle C, Glatt-Deeley H, Brannan C, Muscatelli F, Lalande M.
    Nucleic Acids Res; 2004 Nov 01; 32(11):3480-92. PubMed ID: 15226413
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  • 15. Mouse imprinting defect mutations that model Angelman syndrome.
    Wu MY, Chen KS, Bressler J, Hou A, Tsai TF, Beaudet AL.
    Genesis; 2006 Jan 01; 44(1):12-22. PubMed ID: 16397868
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  • 16. Visualization of transcription-dependent association of imprinted genes with the nuclear matrix.
    Kagotani K, Nabeshima H, Kohda A, Nakao M, Taguchi H, Okumura K.
    Exp Cell Res; 2002 Apr 01; 274(2):189-96. PubMed ID: 11900479
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  • 17. The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion.
    Färber C, Dittrich B, Buiting K, Horsthemke B.
    Hum Mol Genet; 1999 Feb 01; 8(2):337-43. PubMed ID: 9931342
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  • 18. Epigenetic heterogeneity at imprinted loci in normal populations.
    Sakatani T, Wei M, Katoh M, Okita C, Wada D, Mitsuya K, Meguro M, Ikeguchi M, Ito H, Tycko B, Oshimura M.
    Biochem Biophys Res Commun; 2001 May 25; 283(5):1124-30. PubMed ID: 11355889
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  • 19. Changes in expression of imprinted genes following treatment of human cancer cell lines with non-mutagenic or mutagenic carcinogens.
    Shibui T, Higo Y, Tsutsui TW, Uchida M, Oshimura M, Barrett JC, Tsutsui T.
    Int J Oncol; 2008 Aug 25; 33(2):351-60. PubMed ID: 18636156
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  • 20. Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.
    Cooper PR, Smilinich NJ, Day CD, Nowak NJ, Reid LH, Pearsall RS, Reece M, Prawitt D, Landers J, Housman DE, Winterpacht A, Zabel BU, Pelletier J, Weissman BE, Shows TB, Higgins MJ.
    Genomics; 1998 Apr 01; 49(1):38-51. PubMed ID: 9570947
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