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Journal Abstract Search

141 related items for PubMed ID: 8634700

  • 1. Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci.
    Kawame H, Gartler SM, Hansen RS.
    Hum Mol Genet; 1995 Dec; 4(12):2287-93. PubMed ID: 8634700
    [Abstract] [Full Text] [Related]

  • 2. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome.
    Reed ML, Leff SE.
    Nat Genet; 1994 Feb; 6(2):163-7. PubMed ID: 7512861
    [Abstract] [Full Text] [Related]

  • 3. Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.
    Glenn CC, Saitoh S, Jong MT, Filbrandt MM, Surti U, Driscoll DJ, Nicholls RD.
    Am J Hum Genet; 1996 Feb; 58(2):335-46. PubMed ID: 8571960
    [Abstract] [Full Text] [Related]

  • 4. Methylation status of imprinting centers for H19/IGF2 and SNURF/SNRPN in primate embryonic stem cells.
    Mitalipov S, Clepper L, Sritanaudomchai H, Fujimoto A, Wolf D.
    Stem Cells; 2007 Mar; 25(3):581-8. PubMed ID: 17170068
    [Abstract] [Full Text] [Related]

  • 5. Association of acetylated histones with paternally expressed genes in the Prader--Willi deletion region.
    Fulmer-Smentek SB, Francke U.
    Hum Mol Genet; 2001 Mar 15; 10(6):645-52. PubMed ID: 11230184
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 12(4):452-4. PubMed ID: 8630505
    [Abstract] [Full Text] [Related]

  • 7. Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting.
    Szabó PE, Mann JR.
    Genes Dev; 1995 Aug 01; 9(15):1857-68. PubMed ID: 7649473
    [Abstract] [Full Text] [Related]

  • 8. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).
    Nakao M, Sutcliffe JS, Durtschi B, Mutirangura A, Ledbetter DH, Beaudet AL.
    Hum Mol Genet; 1994 Feb 01; 3(2):309-15. PubMed ID: 8004100
    [Abstract] [Full Text] [Related]

  • 9. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
    Zeschnigk M, Schmitz B, Dittrich B, Buiting K, Horsthemke B, Doerfler W.
    Hum Mol Genet; 1997 Mar 01; 6(3):387-95. PubMed ID: 9147641
    [Abstract] [Full Text] [Related]

  • 10. Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region.
    Gunaratne PH, Nakao M, Ledbetter DH, Sutcliffe JS, Chinault AC.
    Genes Dev; 1995 Apr 01; 9(7):808-20. PubMed ID: 7705658
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.
    White LM, Rogan PK, Nicholls RD, Wu BL, Korf B, Knoll JH.
    Am J Hum Genet; 1996 Aug 15; 59(2):423-30. PubMed ID: 8755930
    [Abstract] [Full Text] [Related]

  • 13. The human/mouse imprinted genes IGF2, H19, SNRPN and ZNF127 map to two conserved autosomal clusters in a marsupial.
    Toder R, Wilcox SA, Smithwick M, Graves JA.
    Chromosome Res; 1996 Jun 15; 4(4):295-300. PubMed ID: 8817070
    [Abstract] [Full Text] [Related]

  • 14. Expression of H19 does not influence the timing of replication of the Igf2/H19 imprinted region.
    Windham CQ, Jones PA.
    Dev Genet; 1997 Jun 15; 20(1):29-35. PubMed ID: 9094209
    [Abstract] [Full Text] [Related]

  • 15. Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.
    Squire JA, Li M, Perlikowski S, Fei YL, Bayani J, Zhang ZM, Weksberg R.
    Genomics; 2000 May 01; 65(3):234-42. PubMed ID: 10857747
    [Abstract] [Full Text] [Related]

  • 16. Asynchronous replication timing of imprinted loci is independent of DNA methylation, but consistent with differential subnuclear localization.
    Gribnau J, Hochedlinger K, Hata K, Li E, Jaenisch R.
    Genes Dev; 2003 Mar 15; 17(6):759-73. PubMed ID: 12651894
    [Abstract] [Full Text] [Related]

  • 17. Maintenance of imprinting of the insulin-like growth factor II gene (IGF2) and the small nuclear ribonucleoprotein polypeptide N gene (SNRPN) in the human uterus and leiomyoma.
    Hashimoto K, Azuma C, Kamiura S, Koyama M, Nobunaga T, Tokugawa Y, Kimura T, Kubota Y, Sawai K, Saji F.
    Gynecol Obstet Invest; 1996 Mar 15; 41(1):50-4. PubMed ID: 8821886
    [Abstract] [Full Text] [Related]

  • 18. DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1.
    Gregory RI, Randall TE, Johnson CA, Khosla S, Hatada I, O'Neill LP, Turner BM, Feil R.
    Mol Cell Biol; 2001 Aug 15; 21(16):5426-36. PubMed ID: 11463825
    [Abstract] [Full Text] [Related]

  • 19. Development of a monkey model for the study of primate genomic imprinting.
    Fujimoto A, Mitalipov SM, Clepper LL, Wolf DP.
    Mol Hum Reprod; 2005 Jun 15; 11(6):413-22. PubMed ID: 15908455
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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