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Journal Abstract Search

338 related items for PubMed ID: 9590284

  • 1. A mouse model for Prader-Willi syndrome imprinting-centre mutations.
    Yang T, Adamson TE, Resnick JL, Leff S, Wevrick R, Francke U, Jenkins NA, Copeland NG, Brannan CI.
    Nat Genet; 1998 May; 19(1):25-31. PubMed ID: 9590284
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  • 2. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
    Schulze A, Hansen C, Skakkebaek NE, Brøndum-Nielsen K, Ledbeter DH, Tommerup N.
    Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505
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  • 5. 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; 28(3):232-40. PubMed ID: 11431693
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  • 6. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region.
    Leff SE, Brannan CI, Reed ML, Ozçelik T, Francke U, Copeland NG, Jenkins NA.
    Nat Genet; 1992 Dec; 2(4):259-64. PubMed ID: 1303276
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  • 7. Disruption of the mouse necdin gene results in early post-natal lethality.
    Gérard M, Hernandez L, Wevrick R, Stewart CL.
    Nat Genet; 1999 Oct; 23(2):199-202. PubMed ID: 10508517
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  • 8. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.
    Ozçelik T, Leff S, Robinson W, Donlon T, Lalande M, Sanjines E, Schinzel A, Francke U.
    Nat Genet; 1992 Dec; 2(4):265-9. PubMed ID: 1303277
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  • 11. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
    Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B.
    Nat Genet; 1995 Apr; 9(4):395-400. PubMed ID: 7795645
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  • 12. A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression.
    Cattanach BM, Barr JA, Evans EP, Burtenshaw M, Beechey CV, Leff SE, Brannan CI, Copeland NG, Jenkins NA, Jones J.
    Nat Genet; 1992 Dec; 2(4):270-4. PubMed ID: 1303278
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  • 13. Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
    Kubota T, Sutcliffe JS, Aradhya S, Gillessen-Kaesbach G, Christian SL, Horsthemke B, Beaudet AL, Ledbetter DH.
    Am J Med Genet; 1996 Dec 02; 66(1):77-80. PubMed ID: 8957518
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  • 14. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome.
    Reed ML, Leff SE.
    Nat Genet; 1994 Feb 02; 6(2):163-7. PubMed ID: 7512861
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  • 15. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
    Stefan M, Portis T, Longnecker R, Nicholls RD.
    Genomics; 2005 May 02; 85(5):630-40. PubMed ID: 15820315
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  • 16. Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome.
    Relkovic D, Doe CM, Humby T, Johnstone KA, Resnick JL, Holland AJ, Hagan JJ, Wilkinson LS, Isles AR.
    Eur J Neurosci; 2010 Jan 02; 31(1):156-64. PubMed ID: 20092561
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  • 17. Control elements within the PWS/AS imprinting box and their function in the imprinting process.
    Kantor B, Makedonski K, Green-Finberg Y, Shemer R, Razin A.
    Hum Mol Genet; 2004 Apr 01; 13(7):751-62. PubMed ID: 14962980
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  • 20. A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects.
    Johnstone KA, DuBose AJ, Futtner CR, Elmore MD, Brannan CI, Resnick JL.
    Hum Mol Genet; 2006 Feb 01; 15(3):393-404. PubMed ID: 16368707
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