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Journal Abstract Search

283 related items for PubMed ID: 8095339

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  • 2. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC, Driscoll DJ, Yang TP, Nicholls RD.
    Mol Hum Reprod; 1997 Apr; 3(4):321-32. PubMed ID: 9237260
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  • 4. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.
    Jiang YH, Wauki K, Liu Q, Bressler J, Pan Y, Kashork CD, Shaffer LG, Beaudet AL.
    BMC Genomics; 2008 Jan 28; 9():50. PubMed ID: 18226259
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  • 5. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region.
    Knoll JH, Cheng SD, Lalande M.
    Nat Genet; 1994 Jan 28; 6(1):41-6. PubMed ID: 8136833
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  • 8. Physical mapping studies at D15S10: implications for candidate gene identification in the Angelman syndrome/Prader-Willi syndrome chromosome region of 15q11-q13.
    Woodage T, Lindeman R, Deng ZM, Fimmel A, Smith A, Trent RJ.
    Genomics; 1994 Jan 01; 19(1):170-2. PubMed ID: 8188222
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  • 13. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.
    Lee S, Wevrick R.
    Am J Hum Genet; 2000 Mar 01; 66(3):848-58. PubMed ID: 10712201
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  • 15. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
    Kuwano A, Mutirangura A, Dittrich B, Buiting K, Horsthemke B, Saitoh S, Niikawa N, Ledbetter SA, Greenberg F, Chinault AC.
    Hum Mol Genet; 1992 Sep 01; 1(6):417-25. PubMed ID: 1363801
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  • 16. 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.
    Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM.
    Hum Mol Genet; 2007 Mar 15; 16(6):691-703. PubMed ID: 17339270
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  • 17. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
    Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Malcolm S, Pembrey ME, Nicholls RD.
    Am J Med Genet; 1993 Oct 01; 47(5):683-6. PubMed ID: 8266996
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  • 18. Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptor.
    Culiat CT, Stubbs L, Nicholls RD, Montgomery CS, Russell LB, Johnson DK, Rinchik EM.
    Proc Natl Acad Sci U S A; 1993 Jun 01; 90(11):5105-9. PubMed ID: 8389469
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  • 20. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
    Nicholls RD, Knepper JL.
    Annu Rev Genomics Hum Genet; 2001 Jun 01; 2():153-75. PubMed ID: 11701647
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