| 1 | CDKN1C, IGF2, PHLDA2
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| Abundances of placental imprinted genes CDKN1C, PHLDA2 and IGF-2 are related to low birth weight and early catch-up growth in full-term infants born small for gestational age
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| Xing Y, Liu H, Cui Y, Wang X, Tong X.
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| PLoS One. Jun 13;14(6):e0218278. doi: 10.1371/journal.pone.0218278 2019
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| 2 | IGF2, PHLDA2
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| Placental expression of PHLDA2 and IGF2 in selective intrauterine growth restriction in monozygotic twins.
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| Chen J, Pan S, Hang L, Zhong M, Yu Y.
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| Int J Clin Exp Pathol. Feb 1;11(2):876-881. 2018
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| 3 | IGF2, MYOD1, PRDM16
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| Double Myod and Igf2 inactivation promotes brown adipose tissue development by increasing Prdm16 expression.
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| Borensztein M, Viengchareun S, Montarras D, Journot L, Binart N, Lombès M, Dandolo L.
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| FASEB J 26(11):4584-91. doi: 10.1096/fj.12-208496. Epub 2012 Aug 2.
2012
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| 4 | AKT1, IGF2
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| Akt1 and insulin-like growth factor 2 (Igf2) regulate placentation and fetal/postnatal development.
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| Kent LN, Ohboshi S, Soares MJ.
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| Int J Dev Biol 56(4):255-61. doi: 10.1387/ijdb.113407lk.
2012
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| 5 | IGF2, MYOD1, PRDM16, UCP1
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| Double Myod and Igf2 inactivation promotes brown adipose tissue development by increasing Prdm16 expression.
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| Borensztein M, Viengchareun S, Montarras D, Journot L, Binart N, Lombès M, Dandolo L.
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| FASEB J 26(11):4584-91. doi: 10.1096/fj.12-208496. Epub 2012 Aug 2.
2012
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| 6 | BWS, H19, IGF2, SRS11
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| Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
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| Nativio R, Sparago A, Ito Y, Weksberg R, Riccio A, Murrell A.
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| Hum Mol Genet 20(7):1363-74. Epub 2011 Jan 31.
2011
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| 7 | BWS, H19, IGF2, SRS11
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| Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders.
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| Demars J, Shmela ME, Rossignol S, Okabe J, Netchine I, Azzi S, Cabrol S, Le Caignec C, David A, Le Bouc Y, El-Osta A, Gicquel C.
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| Hum Mol Genet 19(5):803-14. Epub 2009 Dec 9.PMID: 20007505 2010
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| 8 | H19, IGF2, SRS11
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| Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes.
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| Bartholdi D, Krajewska-Walasek M, Ounap K, Gaspar H, Chrzanowska KH, Ilyana H, Kayserili H, Lurie IW, Schinzel A, Baumer A.
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| J Med Genet 46(3):192-7. Epub 2008 Dec 9.
2009
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| 9 | CXCL12, IGF2, PPBP
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| IGF2 modulates the microenvironment for osteoclastogenesis.
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| Nakao K, Aoyama M, Fukuoka H, Fujita M, Miyazawa K, Asai K, Goto S.
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| Biochem Biophys Res Commun 378(3):462-6. Epub 2008 Dec 3.
2009
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| 10 | BWS, CDKN1C, IGF2, SRS11
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| Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regions.
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| Bliek J, Snijder S, Maas SM, Polstra A, van der Lip K, Alders M, Knegt AC, Mannens MM.
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| Eur J Med Genet 52(6):404-8. Epub 2009 Sep 6.
2009
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| 11 | H19, IGF2
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| Hypomethylated and hypermethylated profiles of H19DMR are associated with the aberrant imprinting of IGF2 and H19 in human hepatocellular carcinoma.
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| Wu J, Qin Y, Li B, He WZ, Sun ZL.
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| Genomics 91(5):443-50. Epub 2008 Mar 20.
2008
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| 12 | IGF2, H19, RB, BWS
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| Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.
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| Cerrato F, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Rinaldi MM, Boccuto L, Neri G, Magnani C, D'Angelo P, Collini P, Perotti D, Sebastio G, Maher ER, Riccio A.
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| Hum Mol Genet 17(10):1427-35. Epub 2008 Feb 1. 2008
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| 13 | IGF2
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| Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer.
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| Ito Y, Koessler T, Ibrahim AE, Rai S, Vowler SL, Abu-Amero S, Silva AL, Maia AT, Huddleston JE, Uribe-Lewis S, Woodfine K, Jagodic M, Nativio R, Dunning A, Moore G, Klenova E, Bingham S, Pharoah PD, Brenton JD, Beck S, Sandhu MS, Murrell A.
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| Hum Mol Genet 17(17):2633-43. Epub 2008 Jun 9.
2008
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| 14 | IGF2
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| IGF-2 and FLT-1/VEGF-R1 mRNA levels reveal distinctions and similarities between congenital and common infantile hemangioma.
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| Picard A, Boscolo E, Khan ZA, Bartch TC, Mulliken JB, Vazquez MP, Bischoff J.
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| Pediatr Res 63(3):263-7.
2008
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| 15 | IGF2, SRS11
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| Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas.
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| Yamazawa K, Kagami M, Nagai T, Kondoh T, Onigata K, Maeyama K, Hasegawa T, Hasegawa Y, Yamazaki T, Mizuno S, Miyoshi Y, Miyagawa S, Horikawa R, Matsuoka K, Ogata T.
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| J Mol Med 86(10):1171-81. Epub 2008 Jul 8.
2008
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| 16 | IGF2, BWS, WT1
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| Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesis.
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| Algar EM, St Heaps L, Darmanian A, Dagar V, Prawitt D, Peters GB, Collins F.
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| Cancer Res 67(5):2360-5. Epub 2007 Feb 26. 2007
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| 17 | 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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| 18 | IGF2
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| Duplication of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephroma of the cellular or mixed type.
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| Watanabe N, Haruta M, Soejima H, Fukushi D, Yokomori K, Nakadate H, Okita H, Hata JI, Fukuzawa M, Kaneko Y.
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| Genes Chromosomes Cancer 46(10):929-35. 2007
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| 19 | IGF2
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| Enhanced sensitivity to IGF-II signaling links loss of imprinting of IGF2 to increased cell proliferation and tumor risk.
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| Kaneda A, Wang CJ, Cheong R, Timp W, Onyango P, Wen B, Iacobuzio-Donahue CA, Ohlsson R, Andraos R, Pearson MA, Sharov AA, Longo DL, Ko MS, Levchenko A, Feinberg AP.
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| Proc Natl Acad Sci U S A 104(52):20926-31. Epub 2007 Dec 17. 2007
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| 20 | IGF2R, IGF2
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| Insulin-like growth factor 2 (IGF2) and IGF2 receptor gene variants are associated with fetal growth.
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| Kaku K, Osada H, Seki K, Sekiya S.
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| Acta Paediatr 96(3):363-7. 2007
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| 21 | IGF2
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| Loss of imprinting of insulin-like growth factor II is associated with increased risk of proximal colon cancer.
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| Liou JM, Wu MS, Lin JT, Wang HP, Huang SP, Chiu HM, Lee YC, Lin YB, Shun CT, Liang JT.
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| Eur J Cancer 43(8):1276-82. Epub 2007 Mar 26.
2007
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| 22 | IGF2
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| Insulin-like growth factor-II regulates the 12-lipoxygenase gene expression and promotes cell proliferation in human keratinocytes via the extracellular regulatory kinase and phosphatidylinositol 3-kinase pathways.
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| Yoo H, Kim SJ, Kim Y, Lee H, Kim TY.
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| Int J Biochem Cell Biol 39(6):1248-59. Epub 2007 Apr 20.
2007
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| 23 | IGF2
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| Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human.
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| Monk D, Sanches R, Arnaud P, Apostolidou S, Hills FA, Abu-Amero S, Murrell A, Friess H, Reik W, Stanier P, Constancia M, Moore GE.
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| Hum Mol Genet 15(8):1259-69. Epub 2006 Mar 10. 2006
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| 24 | H19, IGF2, IH
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| Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies.
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| Shuman C, Smith AC, Steele L, Ray PN, Clericuzio C, Zackai E, Parisi MA, Meadows AT, Kelly T, Tichauer D, Squire JA, Sadowski P, Weksberg R.
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| Am J Med Genet A 140(14):1497-503. 2006
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| 25 | IGF2
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| Loss of imprinting and promoter usage of the IGF2 in laryngeal squamous cell carcinoma.
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| Grbesa I, Ivkic M, Pegan B, Gall-Troselj K.
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| Cancer Lett 238(2):224-9. Epub 2005 Aug 18. 2006
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| 26 | CTCF, H19, IGF2, BWS, WT1
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| Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor.
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| Prawitt D, Enklaar T, Gartner-Rupprecht B, Spangenberg C, Oswald M, Lausch E, Schmidtke P, Reutzel D, Fees S, Lucito R, Korzon M, Brozek I, Limon J, Housman DE, Pelletier J, Zabel B.
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| Proc Natl Acad Sci U S A 102(11):4085-90. Epub 2005 Mar 2. 2005
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| 27 | PLAG1, IGF2
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| Amplification and overexpression of the IGF2 regulator PLAG1 in hepatoblastoma.
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| Zatkova A, Rouillard JM, Hartmann W, Lamb BJ, Kuick R, Eckart M, von Schweinitz D, Koch A, Fonatsch C, Pietsch T, Hanash SM, Wimmer K.
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| Genes Chromosomes Cancer 39(2):126-37. 2004
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| 28 | TRPM5, INS, DMR1, KCNQ1OT1, IGF2, BWS
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| The KCNQ1OT1 promoter, a key regulator of genomic imprinting in human chromosome 11p15.5.
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| Du M, Zhou W, Beatty LG, Weksberg R, Sadowski PD.
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| Genomics 84(2):288-300. 2004
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| 29 | BWS, IGF2, H19
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| Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.
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| Sparago A, Cerrato F, Vernucci M, Ferrero GB, Silengo MC, Riccio A.
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| Nat Genet 36(9):958-60. Epub 2004 Aug 15. 2004
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| 30 | IGF2, BWS
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| An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype.
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| Murrell A, Heeson S, Cooper WN, Douglas E, Apostolidou S, Moore GE, Maher ER, Reik W.
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| Hum Mol Genet 13(2):247-55. Epub 2003 Nov 25. 2004
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| 31 | IGF2
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| Genomic imprinting of IGF2 is maintained in infantile hemangioma despite its high level of expression.
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| Yu Y, Wylie-Sears J, Boscolo E, Mulliken JB, Bischoff J.
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| Mol Med 10(7-12):117-23. 2004
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| 32 | IGF2
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| Loss of IGF2 imprinting: a potential marker of colorectal cancer risk.
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| Cui H, Cruz-Correa M, Giardiello FM, Hutcheon DF, Kafonek DR, Brandenburg S, Wu Y, He X, Powe NR, Feinberg AP.
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| Science 299(5613):1753-5. 2003
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| 33 | CDKN1C, H19, IGF2, KCNQ1OT1, SLC22A18, PHLDA2, BWS
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| Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development.
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| Weksberg R, Smith AC, Squire J, Sadowski P.
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| Hum Mol Genet 12 Spec No 1:R61-8. 2003
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| 34 | IGF2, INS
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| Evidence of multiple causal sites affecting weight in the IGF2-INS-TH region of human chromosome 11.
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| Gu D, O'Dell SD, Chen Xh XH, Miller GJ, Day IM.
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| Hum Genet 110(2):173-81. 2002
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| 35 | H19, IGF2, KCNQ1
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| A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator.
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| Kanduri C, Fitzpatrick G, Mukhopadhyay R, Kanduri M, Lobanenkov V, Higgins M, Ohlsson R.
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| J Biol Chem 277(20):18106-10. 2002
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| 36 | IGF2
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| Placental-specific IGF-II is a major modulator of placental and fetal growth.
|
| Constancia M, Hemberger M, Hughes J, Dean W, Ferguson-Smith A, Fundele R, Stewart F, Kelsey G, Fowden A, Sibley C, Reik W.
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| Nature 417(6892):945-8. 2002
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| 37 | IGF2
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| Loss of genomic imprinting of insulin-like growth factor 2 is strongly associated with cellular proliferation in normal hematopoietic cells.
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| Hofmann WK, Takeuchi S, Frantzen MA, Hoelzer D, Koeffler HP.
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| Exp Hematol 30(4):318-23. 2002
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| 38 | IGF2
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| Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer.
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| Nakagawa H, Chadwick RB, Peltomaki P, Plass C, Nakamura Y, de La Chapelle A.
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| Proc Natl Acad Sci U S A 98(2):591-6. 2001
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| 39 | IGF2, MEST
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| Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma.
|
| 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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| 40 | BWS, IGF2, KTWS1
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| Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
|
| Sperandeo MP, Ungaro P, Vernucci M, Pedone PV, Cerrato F, Perone L, Casola S, Cubellis MV, Bruni CB, Andria G, Sebastio G, Riccio A.
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| Am J Hum Genet 66(3):841-7. 2000
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| 41 | BWS, CDKN1C, H19, IGF2, NAP1L4
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| Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome.
|
| Catchpoole D, Smallwood AV, Joyce JA, Murrell A, Lam W, Tang T, Munroe D, Reik W, Schofield PN, Maher ER.
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| J Med Genet 37(3):212-5. No abstract available. 2000
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| 42 | IGF2, INS
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| Transmission ratio distortion at the INS-IGF2 VNTR.
|
| Eaves IA, et al.
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| Nat Genet 22(4):324-5. No abstract available 1999
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| 43 | H19, IGF2
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| Enhancer competition between H19 and Igf2 does not mediate their imprinting.
|
| Schmidt JV, et al.
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| Proc Natl Acad Sci U S A 96(17):9733-8 1999
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| 44 | IGF2, INS, MODY10
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| Associations of IGF2 apaI RFLP and INS VNTR class I allele size with obesity.
|
| O'Dell SD, et al.
|
| Eur J Hum Genet 7(7):821-7 1999
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| 45 | IGF2
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| Cloning of breakpoints in and downstream the IGF2 gene that are associated with overexpression of IGF2 transcripts in colorectal tumours.
|
| Hodzic D, Frey B, Marechal D, Scarcez T, Grooteclaes M, Winkler R.
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| Oncogene 18(33):4710-7 1999
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| 46 | H19, IGF2
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| Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma.
|
| el-Naggar AK, Lai S, Tucker SA, Clayman GL, Goepfert H, Hong WK, Huff V.
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| Oncogene 18(50):7063-9. 1999
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| 47 | CDKN1C, IGF2
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| Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome.
|
| Caspary T, Cleary MA, Perlman EJ, Zhang P, Elledge SJ, Tilghman SM.
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| Genes Dev 13(23):3115-24. 1999
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| 48 | H19, IGF2
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| Dissociation of IGF2 and H19 imprinting in human brain.
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| Pham NV, et al.
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| Brain Res 810 : 1-8. 1998
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| 49 | IGF2
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| IGF2 is parentally imprinted in human preimplantation embryos.
|
| Lighten AD, et al.
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| Nat Genet 15 : 122-123. 1997
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| 50 | IGF2
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| Loss of imprinting of human insulin-like growth factor II gene, IGF2, in acute myeloid leukemia.
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| Wu HK, et al.
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| Biochem Biophys Res Commun 231 : 466-472. 1997
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| 51 | IGF2, H19, WT2
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| Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.
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| Okamoto K, et al.
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| Proc Natl Acad Sci U S A 94 : 5367-5371. 1997
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| 52 | BWS, IGF2, H19
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| Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.
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| Joyce JA, Lam WK, Catchpoole DJ, Jenks P, Reik W, Maher ER, Schofield PN.
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| Hum Mol Genet 6(9):1543-8. 1997
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| 53 | IGF2
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| Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
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| Sun FL, Dean WL, Kelsey G, Allen ND, Reik W.
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| Nature 389(6653):809-15. 1997
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| 54 | IGF2
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| Novel splicing of an IGF2 polymorphic region in human adrenocortical carcinomas.
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| Gray SG, Kjellman M, Larsson C, Ekstrom TJ.
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| Biochem Biophys Res Commun 239(3):878-83. 1997
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| 55 | IGF2
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| Biallelic expression of the IGF2 gene in human breast disease.
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| McCann AH, et al.
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| Hum Mol Genet 5 : 1123-1127. 1996
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| 56 | BWS, H19, IGF2
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| Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.
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| Brown KW, et al.
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| Hum Mol Genet 5 : 2027-2032. 1996
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| 57 | BWS, H19, IGF2
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| Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain.
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| Reik W, et al.
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| Hum Mol Genet 4 : 2379-2385. 1995
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| 58 | H19, IGF2
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| Expression, promoter usage and parental imprinting status of insulin-like growth factor II (IGF2) in human hepatoblastoma : uncoupling of IGF2 and H19 imprinting.
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| Li X, et al.
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| Oncogene 11 : 221-229. 1995
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| 59 | IGF2
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| Transcribed dinucleotide repeat polymorphism in the IGF2 gene.
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| Rainier S, et al.
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| Hum Mol Genet 3 : 386. 1994
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| 60 | H19, IGF2, WT2
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| Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms'tumour.
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| Steenman MJC, et al.
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| Nat Genet 7 : 433-439. 1994
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| 61 | IGF2
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| Parental genomic imprinting of the human IGF2 gene.
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| Giannoukakis N, et al.
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| Nat Genet 4 : 98-101. 1993
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| 62 | IGF2, BWS
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| IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome.
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| Ohlsson R, et al.
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| Nat Genet 4 : 94-97. 1993
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| 63 | H19, IGF2
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| Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2.
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| Zemel S, et al.
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| Nat Genet 2 : 61-65. 1992
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| 64 | IGF2
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| Polymerase chain reaction (PCR) for detection of ApaI polymorphism at the insulin like growth factor II gene (IGF2).
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| Tadokoro K, et al.
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| Nucleic Acids Res 19 : 6967. 1991
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| 65 | IGF2
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| Ava II RFLP at the insulin-like growth factor II (IGF II) locus on chromosome 11.
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| Schneid H, Girard F, Binoux M, Le Bouc Y.
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| Nucleic Acids Res 17 : 466. 1989
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| 66 | IGF2
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| Insulin-like growth factor II and the riddle of tumor-induced hypoglycemia.
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| Axelrod L, Ron D.
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| N Engl J Med 319 : 1477-1479. 1988
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| 67 | IGF2
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| Synthesis and secretion of insulin-like growth factor II by a leiomyosarcoma with associated hypoglycemia.
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| Daughaday WH, Emanuele MA, Brooks MH, Barbato AL, Kapadia M, Rotwein P.
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| N Engl J Med 319 : 1434-1440. 1988
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| 68 | IGF2
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| ApaI and SstI RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.
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| Xiang K, et al.
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| Nucleic Acids Res 16 : 3599. 1988
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| 69 | IGF2
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| EcoRI RFLP in the human IGF II gene.
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| Nucleic Acids Res 16 : 2737. 1988
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| 70 | IGF2
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| BamHI RFLP at the insulin-like growth factor II (IGF2) locus on chromosome 11.
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| Nucleic Acids Res 15 : 7655. 1987
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| 71 | EGF, IGF1, IGF2
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| Human genes for insulin-like growth factors I and II and epidermal growth factor are located on 12q22-q24.1, 11p15, and 4q25-q27, respectively.
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| Morton CC, et al.
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| Cytogenet Cell Genet 41 : 245-249. 1986
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| 72 | IGF2
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| Regional assignment of IGF2 to distal 11p15.
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| (HGM8) Cytogenet Cell Genet 40 : 648-649. 1985
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| 73 | IGF2
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| Nucleotide sequences of cDNAs encoding precursors of human insulin-like growth factor II (IGF-II) and an IGF-II variant.
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| Jansen M, van Schaik FM, van Tol H, Van den Brande JL, Sussenbach JS.
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| FEBS Lett 179 : 243-246. 1985
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| 74 | IGF1, IGF2
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| The insulin-like growth factor-1 (IGF1) is encoded at 12q22-q24.1, and insulin-like growth factor-2 (IGF2) is at 11p15.
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| Morton C, et al.
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| (HGM8) Cytogenet Cell Genet 40 : 703. 1985
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| 75 | IGF1, IGF2
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| Sub-regional localization of human genes for insulin-like growth factors (IGF1) and II (IGF2) by in situ hybridization.
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| Yang-Feng TL, et al.
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| (HGM8) Cytogenet Cell Genet 40 : 782. 1985
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| 76 | IGF2
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| Chromosomal localization and preliminary characterization of the human gene encoding insulin-like growth factor II.
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| Hum Genet 69 : 170-173. 1985
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| 77 | EGF, IGF2
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| Human chromosomal mapping of genes for insulin-like growth factors I and II and epidermal growth factor.
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| Nature 310 : 781-784. 1984
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