233 related articles for article (PubMed ID: 15014980)
1. SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome.
Runte M; Kroisel PM; Gillessen-Kaesbach G; Varon R; Horn D; Cohen MY; Wagstaff J; Horsthemke B; Buiting K
Hum Genet; 2004 May; 114(6):553-61. PubMed ID: 15014980
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.
Landers M; Bancescu DL; Le Meur E; Rougeulle C; Glatt-Deeley H; Brannan C; Muscatelli F; Lalande M
Nucleic Acids Res; 2004; 32(11):3480-92. PubMed ID: 15226413
[TBL] [Abstract][Full Text] [Related]
4. R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation.
Powell WT; Coulson RL; Gonzales ML; Crary FK; Wong SS; Adams S; Ach RA; Tsang P; Yamada NA; Yasui DH; Chédin F; LaSalle JM
Proc Natl Acad Sci U S A; 2013 Aug; 110(34):13938-43. PubMed ID: 23918391
[TBL] [Abstract][Full Text] [Related]
5. An imprinted, mammalian bicistronic transcript encodes two independent proteins.
Gray TA; Saitoh S; Nicholls RD
Proc Natl Acad Sci U S A; 1999 May; 96(10):5616-21. PubMed ID: 10318933
[TBL] [Abstract][Full Text] [Related]
6. Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells.
Haruta M; Meguro M; Sakamoto YK; Hoshiya H; Kashiwagi A; Kaneko Y; Mitsuya K; Oshimura M
J Hum Genet; 2005; 50(3):124-132. PubMed ID: 15744456
[TBL] [Abstract][Full Text] [Related]
7. Expression of the Snurf-Snrpn IC transcript in the oocyte and its putative role in the imprinting establishment of the mouse 7C imprinting domain.
Mapendano CK; Kishino T; Miyazaki K; Kondo S; Yoshiura KI; Hishikawa Y; Koji T; Niikawa N; Ohta T
J Hum Genet; 2006; 51(3):236-243. PubMed ID: 16429232
[TBL] [Abstract][Full Text] [Related]
8. Imprinting analysis of the mouse chromosome 7C region in DNMT1-null embryos.
Nakagaki A; Osanai H; Kishino T
Gene; 2014 Dec; 553(1):63-8. PubMed ID: 25300248
[TBL] [Abstract][Full Text] [Related]
9. Expression of SNURF-SNRPN upstream transcripts and epigenetic regulatory genes during human spermatogenesis.
Wawrzik M; Spiess AN; Herrmann R; Buiting K; Horsthemke B
Eur J Hum Genet; 2009 Nov; 17(11):1463-70. PubMed ID: 19471314
[TBL] [Abstract][Full Text] [Related]
10. Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells.
Tsai TF; Bressler J; Jiang YH; Beaudet AL
Genesis; 2003 Dec; 37(4):151-61. PubMed ID: 14666508
[TBL] [Abstract][Full Text] [Related]
11. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
Samaco RC; Hogart A; LaSalle JM
Hum Mol Genet; 2005 Feb; 14(4):483-92. PubMed ID: 15615769
[TBL] [Abstract][Full Text] [Related]
12. A novel deletion of SNURF/SNRPN exon 1 in a patient with Prader-Willi-like phenotype.
Cao Y; AlHumaidi SS; Faqeih EA; Pitel BA; Lundquist P; Aypar U
Eur J Med Genet; 2017 Aug; 60(8):416-420. PubMed ID: 28554868
[TBL] [Abstract][Full Text] [Related]
13. Mouse imprinting defect mutations that model Angelman syndrome.
Wu MY; Chen KS; Bressler J; Hou A; Tsai TF; Beaudet AL
Genesis; 2006 Jan; 44(1):12-22. PubMed ID: 16397868
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus.
Rodriguez-Jato S; Nicholls RD; Driscoll DJ; Yang TP
Nucleic Acids Res; 2005; 33(15):4740-53. PubMed ID: 16116039
[TBL] [Abstract][Full Text] [Related]
17. The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a.
Chamberlain SJ; Brannan CI
Genomics; 2001 May; 73(3):316-22. PubMed ID: 11350123
[TBL] [Abstract][Full Text] [Related]
18. Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region.
Cavaillé J; Seitz H; Paulsen M; Ferguson-Smith AC; Bachellerie JP
Hum Mol Genet; 2002 Jun; 11(13):1527-38. PubMed ID: 12045206
[TBL] [Abstract][Full Text] [Related]
19. Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region.
Le Meur E; Watrin F; Landers M; Sturny R; Lalande M; Muscatelli F
Dev Biol; 2005 Oct; 286(2):587-600. PubMed ID: 16126194
[TBL] [Abstract][Full Text] [Related]
20. An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript.
Rougeulle C; Cardoso C; Fontés M; Colleaux L; Lalande M
Nat Genet; 1998 May; 19(1):15-6. PubMed ID: 9590281
[No Abstract] [Full Text] [Related]
[Next] [New Search]
