134 related articles for article (PubMed ID: 10341083)
1. Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice.
Blaydes SM; Elmore M; Yang T; Brannan CI
Mamm Genome; 1999 Jun; 10(6):549-55. PubMed ID: 10341083
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
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; 12(4):452-4. PubMed ID: 8630505
[TBL] [Abstract][Full Text] [Related]
7. In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit.
Schweizer J; Zynger D; Francke U
Hum Mol Genet; 1999 Apr; 8(4):555-66. PubMed ID: 10072422
[TBL] [Abstract][Full Text] [Related]
8. The mouse Snrpn minimal promoter and its human orthologue: activity and imprinting.
Hershko AY; Finberg Y; Kantor B; Shemer R; Razin A
Genes Cells; 2001 Nov; 6(11):967-75. PubMed ID: 11733034
[TBL] [Abstract][Full Text] [Related]
9. 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; 8(8):1357-64. PubMed ID: 10400982
[TBL] [Abstract][Full Text] [Related]
10. 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; 21(16):5426-36. PubMed ID: 11463825
[TBL] [Abstract][Full Text] [Related]
11. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern.
Shemer R; Birger Y; Riggs AD; Razin A
Proc Natl Acad Sci U S A; 1997 Sep; 94(19):10267-72. PubMed ID: 9294199
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A targeted deletion upstream of Snrpn does not result in an imprinting defect.
Peery EG; Elmore MD; Resnick JL; Brannan CI; Johnstone KA
Mamm Genome; 2007 Apr; 18(4):255-62. PubMed ID: 17514346
[TBL] [Abstract][Full Text] [Related]
14. Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.
Rodriguez-Jato S; Shan J; Khadake J; Heggestad AD; Ma X; Johnstone KA; Resnick JL; Yang TP
PLoS One; 2013; 8(2):e52390. PubMed ID: 23390487
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Imprinted expression of SNRPN in human preimplantation embryos.
Huntriss J; Daniels R; Bolton V; Monk M
Am J Hum Genet; 1998 Oct; 63(4):1009-14. PubMed ID: 9758597
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch.
Bielinska B; Blaydes SM; Buiting K; Yang T; Krajewska-Walasek M; Horsthemke B; Brannan CI
Nat Genet; 2000 May; 25(1):74-8. PubMed ID: 10802660
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
Kubota T; Sutcliffe JS; Aradhya S; Gillessen-Kaesbach G; Christian SL; Horsthemke B; Beaudet AL; Ledbetter DH
Am J Med Genet; 1996 Dec; 66(1):77-80. PubMed ID: 8957518
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
