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