These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

400 related articles for article (PubMed ID: 8004100)

  • 1. 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; 3(2):309-15. PubMed ID: 8004100
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 18(3):546-52. PubMed ID: 8307564
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 9(10):788-93. PubMed ID: 9745031
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. 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; 2(12):1991-4. PubMed ID: 8111365
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 2(12):2001-5. PubMed ID: 8111367
    [TBL] [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; 6(3):387-95. PubMed ID: 9147641
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndrome.
    White HE; Durston VJ; Harvey JF; Cross NC
    Clin Chem; 2006 Jun; 52(6):1005-13. PubMed ID: 16574761
    [TBL] [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; 2(4):259-64. PubMed ID: 1303276
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [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; 8(2):337-43. PubMed ID: 9931342
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. Methylation-sensitive high-resolution melting-curve analysis of the SNRPN gene as a diagnostic screen for Prader-Willi and Angelman syndromes.
    White HE; Hall VJ; Cross NC
    Clin Chem; 2007 Nov; 53(11):1960-2. PubMed ID: 17890436
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 63(2):414-5. PubMed ID: 8725798
    [No Abstract]   [Full Text] [Related]  

  • 19. The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A.
    Runte M; Hüttenhofer A; Gross S; Kiefmann M; Horsthemke B; Buiting K
    Hum Mol Genet; 2001 Nov; 10(23):2687-700. PubMed ID: 11726556
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 20.