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Similar articles for PubMed (Select 22577095)

1.

Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndrome.

Higashimoto K, Nakabayashi K, Yatsuki H, Yoshinaga H, Jozaki K, Okada J, Watanabe Y, Aoki A, Shiozaki A, Saito S, Koide K, Mukai T, Hata K, Soejima H.

Am J Med Genet A. 2012 Jul;158A(7):1670-5. doi: 10.1002/ajmg.a.35335. Epub 2012 May 10.

PMID:
22577095
2.

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

Gaston V, Le Bouc Y, Soupre V, Burglen L, Donadieu J, Oro H, Audry G, Vazquez MP, Gicquel C.

Eur J Hum Genet. 2001 Jun;9(6):409-18.

3.

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

Sparago A, Cerrato F, Vernucci M, Ferrero GB, Silengo MC, Riccio A.

Nat Genet. 2004 Sep;36(9):958-60. Epub 2004 Aug 15.

PMID:
15314640
4.

Hypomethylation along with increased H19 expression in placentas from pregnancies complicated with fetal growth restriction.

Koukoura O, Sifakis S, Zaravinos A, Apostolidou S, Jones A, Hajiioannou J, Widschwendter M, Spandidos DA.

Placenta. 2011 Jan;32(1):51-7. doi: 10.1016/j.placenta.2010.10.017. Epub 2010 Dec 3.

PMID:
21129773
5.

Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome.

Lee BH, Kim GH, Oh TJ, Kim JH, Lee JJ, Choi SH, Lee JY, Kim JM, Choi IH, Kim YM, Choi JH, Yoo HW.

J Hum Genet. 2013 Sep;58(9):604-10. doi: 10.1038/jhg.2013.67. Epub 2013 Jun 27.

PMID:
23803580
6.

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.

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.

Hum Mol Genet. 2008 May 15;17(10):1427-35. doi: 10.1093/hmg/ddn031. Epub 2008 Feb 1.

7.

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS.

Bliek J, Maas SM, Ruijter JM, Hennekam RC, Alders M, Westerveld A, Mannens MM.

Hum Mol Genet. 2001 Mar 1;10(5):467-76.

8.

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Catchpoole D, Lam WW, Valler D, Temple IK, Joyce JA, Reik W, Schofield PN, Maher ER.

J Med Genet. 1997 May;34(5):353-9.

9.

Rapid detection of methylation change at H19 in human imprinting disorders using methylation-sensitive high-resolution melting.

Wojdacz TK, Dobrovic A, Algar EM.

Hum Mutat. 2008 Oct;29(10):1255-60. doi: 10.1002/humu.20779.

PMID:
18473334
10.

Beckwith-Wiedemann syndrome with placental chorangioma due to H19-differentially methylated region hypermethylation: a case report.

Aoki A, Shiozaki A, Sameshima A, Higashimoto K, Soejima H, Saito S.

J Obstet Gynaecol Res. 2011 Dec;37(12):1872-6. doi: 10.1111/j.1447-0756.2011.01654.x. Epub 2011 Sep 28.

PMID:
21955307
11.

Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.

Higashimoto K, Urano T, Sugiura K, Yatsuki H, Joh K, Zhao W, Iwakawa M, Ohashi H, Oshimura M, Niikawa N, Mukai T, Soejima H.

Am J Hum Genet. 2003 Oct;73(4):948-56. Epub 2003 Aug 29.

12.

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.

Am J Hum Genet. 2000 Mar;66(3):841-7.

13.

Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.

Squire JA, Li M, Perlikowski S, Fei YL, Bayani J, Zhang ZM, Weksberg R.

Genomics. 2000 May 1;65(3):234-42.

PMID:
10857747
14.

Placentas from pregnancies conceived by IVF/ICSI have a reduced DNA methylation level at the H19 and MEST differentially methylated regions.

Nelissen EC, Dumoulin JC, Daunay A, Evers JL, Tost J, van Montfoort AP.

Hum Reprod. 2013 Apr;28(4):1117-26. doi: 10.1093/humrep/des459. Epub 2013 Jan 22.

15.

Expression and methylation status of imprinted genes in placentas of deceased and live cloned transgenic calves.

Su JM, Yang B, Wang YS, Li YY, Xiong XR, Wang LJ, Guo ZK, Zhang Y.

Theriogenology. 2011 Apr 15;75(7):1346-59. doi: 10.1016/j.theriogenology.2010.11.045. Epub 2011 Feb 4.

PMID:
21295824
16.

Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae.

Guo L, Choufani S, Ferreira J, Smith A, Chitayat D, Shuman C, Uxa R, Keating S, Kingdom J, Weksberg R.

Dev Biol. 2008 Aug 1;320(1):79-91. doi: 10.1016/j.ydbio.2008.04.025. Epub 2008 Apr 27.

17.
18.

Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies.

Hiura H, Okae H, Miyauchi N, Sato F, Sato A, Van De Pette M, John RM, Kagami M, Nakai K, Soejima H, Ogata T, Arima T.

Hum Reprod. 2012 Aug;27(8):2541-8. doi: 10.1093/humrep/des197. Epub 2012 Jun 6.

19.

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.

Engel JR, Smallwood A, Harper A, Higgins MJ, Oshimura M, Reik W, Schofield PN, Maher ER.

J Med Genet. 2000 Dec;37(12):921-6.

20.

Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology.

Turan N, Katari S, Gerson LF, Chalian R, Foster MW, Gaughan JP, Coutifaris C, Sapienza C.

PLoS Genet. 2010 Jul 22;6(7):e1001033. doi: 10.1371/journal.pgen.1001033.

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