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Journal Abstract Search

407 related items for PubMed ID: 7849716

  • 1. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.
    Wevrick R, Kerns JA, Francke U.
    Hum Mol Genet; 1994 Oct; 3(10):1877-82. PubMed ID: 7849716
    [Abstract] [Full Text] [Related]

  • 2. Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
    Saitoh S, Buiting K, Rogan PK, Buxton JL, Driscoll DJ, Arnemann J, König R, Malcolm S, Horsthemke B, Nicholls RD.
    Proc Natl Acad Sci U S A; 1996 Jul 23; 93(15):7811-5. PubMed ID: 8755558
    [Abstract] [Full Text] [Related]

  • 3. 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 23; 12(4):452-4. PubMed ID: 8630505
    [Abstract] [Full Text] [Related]

  • 4. 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 23; 66(3):848-58. PubMed ID: 10712201
    [Abstract] [Full Text] [Related]

  • 5. 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 23; 3(4):321-32. PubMed ID: 9237260
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.
    Wevrick R, Francke U.
    Hum Mol Genet; 1997 Feb 28; 6(2):325-32. PubMed ID: 9063754
    [Abstract] [Full Text] [Related]

  • 8. Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient.
    Greger V, Woolf E, Lalande M.
    Hum Mol Genet; 1993 Jul 28; 2(7):921-4. PubMed ID: 8364575
    [Abstract] [Full Text] [Related]

  • 9. 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 28; 3(2):309-15. PubMed ID: 8004100
    [Abstract] [Full Text] [Related]

  • 10. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
    Christian SL, Robinson WP, Huang B, Mutirangura A, Line MR, Nakao M, Surti U, Chakravarti A, Ledbetter DH.
    Am J Hum Genet; 1995 Jul 28; 57(1):40-8. PubMed ID: 7611294
    [Abstract] [Full Text] [Related]

  • 11. 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 28; 1(6):417-25. PubMed ID: 1363801
    [Abstract] [Full Text] [Related]

  • 12. Functional imprinting and epigenetic modification of the human SNRPN gene.
    Glenn CC, Porter KA, Jong MT, Nicholls RD, Driscoll DJ.
    Hum Mol Genet; 1993 Dec 28; 2(12):2001-5. PubMed ID: 8111367
    [Abstract] [Full Text] [Related]

  • 13. Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome.
    Tsai TF, Jiang YH, Bressler J, Armstrong D, Beaudet AL.
    Hum Mol Genet; 1999 Aug 28; 8(8):1357-64. PubMed ID: 10400982
    [Abstract] [Full Text] [Related]

  • 14. The imprinting box of the Prader-Willi/Angelman syndrome domain.
    Shemer R, Hershko AY, Perk J, Mostoslavsky R, Tsuberi B, Cedar H, Buiting K, Razin A.
    Nat Genet; 2000 Dec 28; 26(4):440-3. PubMed ID: 11101841
    [Abstract] [Full Text] [Related]

  • 15. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.
    Buiting K, Dittrich B, Gross S, Lich C, Färber C, Buchholz T, Smith E, Reis A, Bürger J, Nöthen MM, Barth-Witte U, Janssen B, Abeliovich D, Lerer I, van den Ouweland AM, Halley DJ, Schrander-Stumpel C, Smeets H, Meinecke P, Malcolm S, Gardner A, Lalande M, Nicholls RD, Friend K, Schulze A, Matthijs G, Kokkonen H, Hilbert P, Van Maldergem L, Glover G, Carbonell P, Willems P, Gillessen-Kaesbach G, Horsthemke B.
    Am J Hum Genet; 1998 Jul 28; 63(1):170-80. PubMed ID: 9634532
    [Abstract] [Full Text] [Related]

  • 16. Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain.
    Brant JO, Riva A, Resnick JL, Yang TP.
    Epigenetics; 2014 Nov 28; 9(11):1540-56. PubMed ID: 25482058
    [Abstract] [Full Text] [Related]

  • 17. 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 28; 6(3):387-95. PubMed ID: 9147641
    [Abstract] [Full Text] [Related]

  • 18. A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene.
    Mutirangura A, Jayakumar A, Sutcliffe JS, Nakao M, McKinney MJ, Buiting K, Horsthemke B, Beaudet AL, Chinault AC, Ledbetter DH.
    Genomics; 1993 Dec 28; 18(3):546-52. PubMed ID: 8307564
    [Abstract] [Full Text] [Related]

  • 19. Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities.
    Muralidhar B, Marney A, Butler MG.
    Genet Med; 1999 Dec 28; 1(4):141-5. PubMed ID: 11258349
    [Abstract] [Full Text] [Related]

  • 20. Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene.
    Buiting K, Dittrich B, Gross S, Greger V, Lalande M, Robinson W, Mutirangura A, Ledbetter D, Horsthemke B.
    Hum Mol Genet; 1993 Dec 28; 2(12):1991-4. PubMed ID: 8111365
    [Abstract] [Full Text] [Related]

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