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106 related items for PubMed ID: 7705658

  • 1. 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]

  • 2. 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 01; 2(4):265-9. PubMed ID: 1303277
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  • 3. [Prader-Willi syndrome and genomic imprinting].
    Wang W, Wang DF, Cui YF, Ni JH, Dong ZY, Fu MF, Fu HM, Lu GQ, Chen FS.
    Zhonghua Er Ke Za Zhi; 2003 Jun 01; 41(6):453-6. PubMed ID: 14749005
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  • 4. 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 01; 12(4):452-4. PubMed ID: 8630505
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  • 5. 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]

  • 6. 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 01; 8(1):52-8. PubMed ID: 7987392
    [Abstract] [Full Text] [Related]

  • 7. A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes.
    Chotai KA, Payne SJ.
    J Med Genet; 1998 Jun 01; 35(6):472-5. PubMed ID: 9643288
    [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 01; 6(3):387-95. PubMed ID: 9147641
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 2(4):259-64. PubMed ID: 1303276
    [Abstract] [Full Text] [Related]

  • 10. Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci.
    Kawame H, Gartler SM, Hansen RS.
    Hum Mol Genet; 1995 Dec 01; 4(12):2287-93. PubMed ID: 8634700
    [Abstract] [Full Text] [Related]

  • 11. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.
    Wevrick R, Kerns JA, Francke U.
    Hum Mol Genet; 1994 Oct 01; 3(10):1877-82. PubMed ID: 7849716
    [Abstract] [Full Text] [Related]

  • 12. The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse.
    MacDonald HR, Wevrick R.
    Hum Mol Genet; 1997 Oct 01; 6(11):1873-8. PubMed ID: 9302265
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 6(1):41-6. PubMed ID: 8136833
    [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 01; 26(4):440-3. PubMed ID: 11101841
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  • 18. 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 01; 85(5):630-40. PubMed ID: 15820315
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