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Items: 1 to 20 of 80

1.

Methylation profile of SNRPN gene and its correlation with weight and chronological age.

Carobin NV, Rubatino FV, Freitas ML, de Oliveira VT, Pietra RX, Bosco AA, Jehee FS.

Genet Mol Res. 2015 Oct 29;14(4):13791-8. doi: 10.4238/2015.October.28.41.

2.

Serum SmD autoantibody proteomes are clonally restricted and share variable-region peptides.

Al Kindi MA, Chataway TK, Gilada GA, Jackson MW, Goldblatt FM, Walker JG, Colella AD, Gordon TP.

J Autoimmun. 2015 Feb;57:77-81. doi: 10.1016/j.jaut.2014.12.005.

PMID:
25577500
3.

Effect of small nuclear ribonucleoprotein-associated polypeptide N on the proliferation of medulloblastoma cells.

Jing J, Zhao Y, Wang C, Zhao Q, Liang Q, Wang S, Ma J.

Mol Med Rep. 2015 May;11(5):3337-43. doi: 10.3892/mmr.2015.3148.

4.

Modulation of alternative splicing by expression of small nuclear ribonucleoprotein polypeptide N.

Lee MS, Lin YS, Deng YF, Hsu WT, Shen CC, Cheng YH, Huang YT, Li C.

FEBS J. 2014 Dec;281(23):5194-207. doi: 10.1111/febs.13059.

5.

Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites.

Chen Y, Liu YJ, Pei YF, Yang TL, Deng FY, Liu XG, Li DY, Deng HW.

Obesity (Silver Spring). 2011 Jun;19(6):1229-34. doi: 10.1038/oby.2010.323.

6.

Variable methylation of the imprinted gene, SNRPN, supports a relationship between intracranial germ cell tumours and neural stem cells.

Lee SH, Appleby V, Jeyapalan JN, Palmer RD, Nicholson JC, Sottile V, Gao E, Coleman N, Scotting PJ.

J Neurooncol. 2011 Feb;101(3):419-28. doi: 10.1007/s11060-010-0275-9.

PMID:
20582452
7.

Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos.

Geuns E, De Rycke M, Van Steirteghem A, Liebaers I.

Hum Mol Genet. 2003 Nov 15;12(22):2873-9.

8.
10.

Prader-Willi syndrome is caused by disruption of the SNRPN gene.

Kuslich CD, Kobori JA, Mohapatra G, Gregorio-King C, Donlon TA.

Am J Hum Genet. 1999 Jan;64(1):70-6.

11.

Identification of novel exons 3' to the human SNRPN gene.

Buiting K, Dittrich B, Endele S, Horsthemke B.

Genomics. 1997 Feb 15;40(1):132-7.

PMID:
9070929
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.

PMID:
8841186
13.

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome.

Reed ML, Leff SE.

Nat Genet. 1994 Feb;6(2):163-7.

PMID:
7512861
14.
15.

In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients.

Mayo S, Monfort S, Roselló M, Oltra S, Orellana C, Martínez F.

Biomed Res Int. 2015;2015:341986. doi: 10.1155/2015/341986.

16.

Methylation pattern of methylene tetrahydrofolate reductase and small nuclear ribonucleoprotein polypeptide N promoters in oligoasthenospermia: a case-control study.

Botezatu A, Socolov R, Socolov D, Iancu IV, Anton G.

Reprod Biomed Online. 2014 Feb;28(2):225-31. doi: 10.1016/j.rbmo.2013.10.010.

PMID:
24365028
17.

Behavioral phenotype in adults with Prader-Willi syndrome.

Sinnema M, Einfeld SL, Schrander-Stumpel CT, Maaskant MA, Boer H, Curfs LM.

Res Dev Disabil. 2011 Mar-Apr;32(2):604-12. doi: 10.1016/j.ridd.2010.12.014.

18.

CpG methylation analysis of the MEG3 and SNRPN imprinted genes in acute myeloid leukemia and myelodysplastic syndromes.

Benetatos L, Hatzimichael E, Dasoula A, Dranitsaris G, Tsiara S, Syrrou M, Georgiou I, Bourantas KL.

Leuk Res. 2010 Feb;34(2):148-53. doi: 10.1016/j.leukres.2009.06.019.

PMID:
19595458
19.

Mechanisms of imprinting of the Prader-Willi/Angelman region.

Horsthemke B, Wagstaff J.

Am J Med Genet A. 2008 Aug 15;146A(16):2041-52. doi: 10.1002/ajmg.a.32364. Review.

PMID:
18627066
20.

Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter.

Maina EN, Webb T, Soni S, Whittington J, Boer H, Clarke D, Holland A.

J Hum Genet. 2007;52(4):297-307.

PMID:
17262171
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