1 | CEBPA, MEST, PPARG, SOX6
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| The transcription factor SOX6 contributes to the developmental origins of obesity by promoting adipogenesis.
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| Leow SC, Poschmann J, Too PG, Yin J, Joseph R, McFarlane C, Dogra S, Shabbir A, Ingham PW, Prabhakar S, Leow MK, Lee YS, Ng KL, Chong YS, Gluckman PD, Stünkel W.
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| Development Mar 15;143(6):950-61. doi: 10.1242/dev.131573. Epub 2016 Feb 18 2016
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2 | COPG2, MEST, TSGA14
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| Methylation and Expression Analyses of the 7q Autism Susceptibility Locus Genes MEST, COPG2, and TSGA14 in Human and Anthropoid Primate Cortices.
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| Schneider E, Mayer S, El Hajj N, Jensen LR, Kuss AW, Zischler H, Kondova I, Bontrop RE, Navarro B, Fuchs E, Zechner U, Haaf T.
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| Cytogenet Genome Res ytogenet Genome Res. 2012 Mar 24. [Epub ahead of print]
2012
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3 | MEST, SRS7
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| Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome features.
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| Eggermann T, Spengler S, Begemann M, Binder G, Buiting K, Albrecht B, Spranger S.
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| Clin Genet 81(3):298-300. doi: 10.1111/j.1399-0004.2011.01719.x. Epub 2011 Dec 28. No abstract available.
2012
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4 | COPG2, MEST
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| Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2.
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| MacIsaac JL, Bogutz AB, Morrissy AS, Lefebvre L.
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| Nucleic Acids Res 40(4):1523-35. Epub 2011 Nov 3.
2012
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5 | LRP6, MEST
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| Mest/Peg1 inhibits Wnt signalling through regulation of LRP6 glycosylation.
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| Jung H, Lee SK, Jho EH.
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| Biochem J 436(2):263-9.
2011
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6 | MEST
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| DNA methylation imprinting marks and DNA methyltransferase expression in human spermatogenic cell stages.
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| Marques CJ, João Pinho M, Carvalho F, Bièche I, Barros A, Sousa M.
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| Epigenetics 6(11). [Epub ahead of print]
2011
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7 | MEST
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| Imprinting and expression status of isoforms 1 and 2 of PEG1/MEST gene in uterine leiomyoma.
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| Moon YS, Park SK, Kim HT, Lee TS, Kim JH, Choi YS.
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| Gynecol Obstet Invest 70(2):120-5. Epub 2010 Mar 26.
2010
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8 | MEST
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| Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia.
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| Marques CJ, Costa P, Vaz B, Carvalho F, Fernandes S, Barros A, Sousa M.
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| Mol Hum Reprod 14(2):67-74. Epub 2008 Jan 4.
2008
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9 | MEST
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| Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST.
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| Kagami M, Nagai T, Fukami M, Yamazawa K, Ogata T.
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| J Assist Reprod Genet 24(4):131-6. Epub 2007 Feb 16. 2007
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10 | 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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11 | GRB10, MEST, SRS7
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| Detection of maternal uniparental disomy at the two imprinted genes on chromosome 7, GRB10 and PEG1/MEST, in a Silver-Russell syndrome patient using methylation-specific PCR assays.
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| Kim Y, Kim SS, Kim G, Park S, Park IS, Yoo HW.
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| Clin Genet 67(3):267-9. No abstract available. 2005
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12 | MEST
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| Promoter switch: a novel mechanism causing biallelic PEG1/MEST expression in invasive breast cancer.
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| Pedersen IS, Dervan P, McGoldrick A, Harrison M, Ponchel F, Speirs V, Isaacs JD, Gorey T, McCann A.
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| Hum Mol Genet 11(12):1449-53. 2002
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13 | MEST
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| An imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoa.
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| Li T, Vu TH, Lee KO, Yang Y, Nguyen CV, Bui HQ, Zeng ZL, Nguyen BT, Hu JF, Murphy SK, Jirtle RL, Hoffman AR.
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| J Biol Chem 277(16):13518-27. Epub 2002 Jan 30. 2002
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14 | GRB10, MEST, NOS3, SERPINE1, UPD7M
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| Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA.
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| Hannula K, Lipsanen-Nyman M, Scherer SW, Holmberg C, Hoglund P, Kere J.
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| Genomics 73(1):1-9. 2001
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15 | IGF2, MEST
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| Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma.
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| Kohda M, Hoshiya H, Katoh M, Tanaka I, Masuda R, Takemura T, Fujiwara M, Oshimura M.
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| Mol Carcinog 31(4):184-91. 2001
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16 | MEST
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| Isoform-specific imprinting of the human PEG1/MEST gene.
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| Kosaki K, Kosaki R, Craigen WJ, Matsuo N.
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| Am J Hum Genet 66(1):309-12. No abstract available. 2000
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17 | CATR1, CPA2, MEST
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| Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32.
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| Hayashida S, Yamasaki K, Asada Y, Soeda E, Niikawa N, Kishino T.
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| Genomics 66(2):221-5. 2000
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18 | MEST
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| Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis.
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| Kerjean A, Dupont JM, Vasseur C, Le Tessier D, Cuisset L, Paldi A, Jouannet P, Jeanpierre M.
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| Hum Mol Genet 9(14):2183-7. 2000
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19 | COPG2, COPG2IT1, MEST
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| The novel gene, gamma2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting.
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| Yamasaki K, Hayashida S, Miura K, Masuzaki H, Ishimaru T, Niikawa N, Kishino T.
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| Genomics 68(3):330-5. 2000
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20 | COPG2, MEST
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| gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome.
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| Blagitko N, Schulz U, Schinzel AA, Ropers HH, Kalscheuer VM.
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| Hum Mol Genet 8(13):2387-96 1999
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21 | MEST
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| Frequent loss of imprinting of PEG1/MEST in invasive breast cancer.
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| Pedersen IS, Dervan PA, Broderick D, Harrison M, Miller N, Delany E, O'Shea D, Costello P, McGoldrick A, Keating G, Tobin B, Gorey T, McCann A.
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| Cancer Res 59(21):5449-51 1999
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22 | MEST, SRS7, UPD7M
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| Evidence against a major role of PEG1/MEST in Silver-Russell syndrome.
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| Riesewijk AM, et al.
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| Eur J Hum Genet 6 : 114-120. 1998
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23 | MEST
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| Human PEG1/MEST, an imprinted gene on chromosome 7.
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| Kobayashi S, Kohda T, Miyoshi N, Kuroiwa Y, Aisaka K, Tsutsumi O, Kaneko-Ishino T, Ishino F.
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| Hum Mol Genet 6(5):781-6. 1997
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24 | MEST, MESTR1, MESTR2
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| Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses.
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| Riesewijk AM, Hu L, Schulz U, Tariverdian G, Hoglund P, Kere J, Ropers HH, Kalscheuer VM.
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| Genomics 42(2):236-44. 1997
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25 | MEST
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| Genomic structure and parent-of-origin-specific methylation of Peg1.
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| Lefebvre L, Viville S, Barton SC, Ishino F, Surani MA.
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| Hum Mol Genet 6(11):1907-15. 1997
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26 | MEST, UPD7M
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| PEG1 expression in maternal uniparental disomy 7.
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| Cuisset L, Le Stunff C, Dupont JM, Vasseur C, Cartigny M, Despert F, Delpech M, Bougnere P, Jeanpierre M.
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| Ann Genet 40(4):211-5. 1997
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27 | MEST
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| Genomic imprinting and chromosomal localization of the human MEST gene.
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| Nishita Y, et al.
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| Genomics 36 : 539-542. 1996
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28 | MEST
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| Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization.
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| Kaneko-Ishino T, et al.
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| Nat Genet 11 : 52-54. 1995
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