Citations for
1AP1G1, MEG3
MEG3 promotes liver cancer by activating PI3K/AKT pathway through regulating AP1G1 2019PMID:
Sun Y, Cao FL, Qu LL, Wang ZM, Liu XY.
Eur Rev Med Pharmacol Sci. Feb;23(4):1459-1467. doi: 10.26355/eurrev_201902_17103. 2019
2MEG3, SNRPD2
Nuclear retention element recruits U1 snRNP components to restrain spliced lncRNAs in the nucleus
Azam S, Hou S, Zhu B, Wang W, Hao T, Bu X, Khan M, Lei H.
RNA Biol. Aug;16(8):1001-1009. doi: 10.1080/15476286.2019.1620061. Epub 2019 Jun 4. 2019
3DIO3, MEF2A, MEG3
MEF2A regulates the Gtl2-Dio3 microRNA mega-cluster to modulate WNT signaling in skeletal muscle regeneration.
Snyder CM, Rice AL, Estrella NL, Held A, Kandarian SC, Naya FJ.
Development 140(1):31-42. doi: 10.1242/dev.081851. Epub 2012 Nov 15. 2013
4DLK1, MEG3, UPD14P
Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype.
Kagami M, Kato F, Matsubara K, Sato T, Nishimura G, Ogata T.
Eur J Hum Genet 20(9):928-32. doi: 10.1038/ejhg.2012.26. Epub 2012 Feb 22. 2012
5DLK1, MEG3
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.
Wallace C, Smyth DJ, Maisuria-Armer M, Walker NM, Todd JA, Clayton DG.
Nat Genet 42(1):68-71. Epub 2009 Dec 6.PMID: 19966805 2010
6MEG3, SNRPN
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 34(2):148-53.PMID: 19595458 2010
7MEG3
Selective loss of MEG3 expression and intergenic differentially methylated region hypermethylation in the MEG3/DLK1 locus in human clinically nonfunctioning pituitary adenomas.
Gejman R, Batista DL, Zhong Y, Zhou Y, Zhang X, Swearingen B, Stratakis CA, Hedley-Whyte ET, Klibanski A.
J Clin Endocrinol Metab 93(10):4119-25. Epub 2008 Jul 15. 2008
8IGF2, MEST, IPW, SNRPN, PEG3, MEG3, KCNQ1OT1
Status of genomic imprinting in human embryonic stem cells as revealed by a large cohort of independently derived and maintained lines.
Rugg-Gunn PJ, Ferguson-Smith AC, Pedersen RA.
Hum Mol Genet 16 Spec No 2:R243-51. 2007
9CTCF, MEG3
Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32.
Rosa AL, Wu YQ, Kwabi-Addo B, Coveler KJ, Reid Sutton V, Shaffer LG.
Chromosome Res 13(8):809-18. Epub 2005 Dec 8. 2005
10MEG3, MEG8
The callipyge locus: evidence for the trans interaction of reciprocally imprinted genes.
Georges M, Charlier C, Cockett N.
Trends Genet 19(5):248-52. Review. 2003
11DLK1, MEG3, SNORD113-1, SNORD113-2, SNORD113-3, SNORD113-4, SNORD113-5, SNORD113-6, SNORD113-7, SNORD113-8, SNORD113@, TRCD0, TRCD1, TRCD2, UPD14M, UPD14P
Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region.
Cavaille J, Seitz H, Paulsen M, Ferguson-Smith AC, Bachellerie JP.
Hum Mol Genet 11(13):1527-38. 2002
12DLK1, MEG3, MEG8, RTL1
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8.
Charlier C, Segers K, Wagenaar D, Karim L, Berghmans S, Jaillon O, Shay T, Weissenbach J, Cockett N, Gyapay G, Georges M.
Genome Res 11(5):850-62. 2001
13DLK1, MEG3
Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region.
Paulsen M, Takada S, Youngson NA, Benchaib M, Charlier C, Segers K, Georges M, Ferguson-Smith AC.
Genome Res 11(12):2085-94. 2001
14MEG3
Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.
Miyoshi N, Wagatsuma H, Wakana S, Shiroishi T, Nomura M, Aisaka K, Kohda T, Surani MA, Kaneko-Ishino T, Ishino F.
Genes Cells 5(3):211-20. 2000
15MEG3, UPD14M
Parental origin effects in human trisomy for chromosome 14q: implications for genomic imprinting.
Georgiades P, Chierakul C, Ferguson-Smith AC.
J Med Genet 35(10):821-4. 1998