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Journal Abstract Search

272 related items for PubMed ID: 8841186

  • 1. 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; 14(2):163-70. PubMed ID: 8841186
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region.
    Sutcliffe JS, Nakao M, Christian S, Orstavik KH, Tommerup N, Ledbetter DH, Beaudet AL.
    Nat Genet; 1994 Sep; 8(1):52-8. PubMed ID: 7987392
    [Abstract] [Full Text] [Related]

  • 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; 28(3):232-40. PubMed ID: 11431693
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

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

  • 7. 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
    [No Abstract] [Full Text] [Related]

  • 8. 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 17; 6(3):387-95. PubMed ID: 9147641
    [Abstract] [Full Text] [Related]

  • 9. In and around SNRPN.
    Lalande M.
    Nat Genet; 1994 Sep 17; 8(1):5-7. PubMed ID: 7987391
    [No Abstract] [Full Text] [Related]

  • 10. Mouse imprinting defect mutations that model Angelman syndrome.
    Wu MY, Chen KS, Bressler J, Hou A, Tsai TF, Beaudet AL.
    Genesis; 2006 Jan 17; 44(1):12-22. PubMed ID: 16397868
    [Abstract] [Full Text] [Related]

  • 11. 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 17; 2(4):259-64. PubMed ID: 1303276
    [Abstract] [Full Text] [Related]

  • 12. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
    Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD.
    Am J Med Genet; 1997 Jan 20; 68(2):195-206. PubMed ID: 9028458
    [Abstract] [Full Text] [Related]

  • 13. 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 20; 8(2):337-43. PubMed ID: 9931342
    [Abstract] [Full Text] [Related]

  • 14. Methylation analysis at three different loci within the imprinted region of chromosome 15q11-13.
    Buchholz T, Jackson J, Smith A.
    Am J Med Genet; 1997 Oct 03; 72(1):117-9. PubMed ID: 9295088
    [No Abstract] [Full Text] [Related]

  • 15. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome.
    Reed ML, Leff SE.
    Nat Genet; 1994 Feb 03; 6(2):163-7. PubMed ID: 7512861
    [Abstract] [Full Text] [Related]

  • 16. 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 03; 9(10):788-93. PubMed ID: 9745031
    [Abstract] [Full Text] [Related]

  • 17. Imprint switch mechanism indicated by mutations in Prader-Willi and Angelman syndromes.
    Kelsey G, Reik W.
    Bioessays; 1997 May 03; 19(5):361-5. PubMed ID: 9174400
    [Abstract] [Full Text] [Related]

  • 18. 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 03; 58(2):335-46. PubMed ID: 8571960
    [Abstract] [Full Text] [Related]

  • 19. Structure and function of the human chromosome 15 imprinting center.
    Horsthemke B.
    J Cell Physiol; 1997 Nov 03; 173(2):237-41. PubMed ID: 9365529
    [Abstract] [Full Text] [Related]

  • 20. 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 03; 19(1):25-31. PubMed ID: 9590284
    [Abstract] [Full Text] [Related]

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