Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 103

1.

Sox-Oct motifs contribute to maintenance of the unmethylated H19 ICR in YAC transgenic mice.

Sakaguchi R, Okamura E, Matsuzaki H, Fukamizu A, Tanimoto K.

Hum Mol Genet. 2013 Nov 15;22(22):4627-37. doi: 10.1093/hmg/ddt311. Epub 2013 Jul 2.

PMID:
23821645
2.

CTCF binding is not the epigenetic mark that establishes post-fertilization methylation imprinting in the transgenic H19 ICR.

Matsuzaki H, Okamura E, Fukamizu A, Tanimoto K.

Hum Mol Genet. 2010 Apr 1;19(7):1190-8. doi: 10.1093/hmg/ddp589. Epub 2010 Jan 4.

PMID:
20047949
3.

The H19 imprinting control region mediates preimplantation imprinted methylation of nearby sequences in yeast artificial chromosome transgenic mice.

Okamura E, Matsuzaki H, Sakaguchi R, Takahashi T, Fukamizu A, Tanimoto K.

Mol Cell Biol. 2013 Feb;33(4):858-71. doi: 10.1128/MCB.01003-12. Epub 2012 Dec 10.

4.

Synthetic DNA fragments bearing ICR cis elements become differentially methylated and recapitulate genomic imprinting in transgenic mice.

Matsuzaki H, Okamura E, Kuramochi D, Ushiki A, Hirakawa K, Fukamizu A, Tanimoto K.

Epigenetics Chromatin. 2018 Jun 29;11(1):36. doi: 10.1186/s13072-018-0207-z.

5.

Oct4/Sox2 binding sites contribute to maintaining hypomethylation of the maternal igf2/h19 imprinting control region.

Zimmerman DL, Boddy CS, Schoenherr CS.

PLoS One. 2013 Dec 6;8(12):e81962. doi: 10.1371/journal.pone.0081962. eCollection 2013.

6.

A randomly integrated transgenic H19 imprinting control region acquires methylation imprinting independently of its establishment in germ cells.

Matsuzaki H, Okamura E, Shimotsuma M, Fukamizu A, Tanimoto K.

Mol Cell Biol. 2009 Sep;29(17):4595-603. doi: 10.1128/MCB.00275-09. Epub 2009 Jun 22.

7.

The chicken HS4 insulator element does not protect the H19 ICR from differential DNA methylation in yeast artificial chromosome transgenic mouse.

Okamura E, Matsuzaki H, Fukamizu A, Tanimoto K.

PLoS One. 2013 Sep 4;8(9):e73925. doi: 10.1371/journal.pone.0073925. eCollection 2013.

8.

Tissue-specific insulator function at H19/Igf2 revealed by deletions at the imprinting control region.

Ideraabdullah FY, Thorvaldsen JL, Myers JA, Bartolomei MS.

Hum Mol Genet. 2014 Dec 1;23(23):6246-59. doi: 10.1093/hmg/ddu344. Epub 2014 Jul 2.

9.

A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.

Higashimoto K, Jozaki K, Kosho T, Matsubara K, Fuke T, Yamada D, Yatsuki H, Maeda T, Ohtsuka Y, Nishioka K, Joh K, Koseki H, Ogata T, Soejima H.

Clin Genet. 2014 Dec;86(6):539-44. doi: 10.1111/cge.12318. Epub 2013 Dec 4.

PMID:
24299031
10.

Sequences in the H19 ICR that are transcribed as small RNA in oocytes are dispensable for methylation imprinting in YAC transgenic mice.

Takahashi T, Matsuzaki H, Tomizawa S, Okamura E, Ichiyanagi T, Fukamizu A, Sasaki H, Tanimoto K.

Gene. 2012 Oct 15;508(1):26-34. doi: 10.1016/j.gene.2012.07.062. Epub 2012 Aug 4.

PMID:
22890135
11.

CTCF maintains differential methylation at the Igf2/H19 locus.

Schoenherr CJ, Levorse JM, Tilghman SM.

Nat Genet. 2003 Jan;33(1):66-9. Epub 2002 Dec 2.

PMID:
12461525
12.

Genomic imprinting recapitulated in the human beta-globin locus.

Tanimoto K, Shimotsuma M, Matsuzaki H, Omori A, Bungert J, Engel JD, Fukamizu A.

Proc Natl Acad Sci U S A. 2005 Jul 19;102(29):10250-5. Epub 2005 Jul 8.

13.

Mutation of a single CTCF target site within the H19 imprinting control region leads to loss of Igf2 imprinting and complex patterns of de novo methylation upon maternal inheritance.

Pant V, Kurukuti S, Pugacheva E, Shamsuddin S, Mariano P, Renkawitz R, Klenova E, Lobanenkov V, Ohlsson R.

Mol Cell Biol. 2004 Apr;24(8):3497-504.

14.
15.

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
16.

IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch.

Li T, Vu TH, Ulaner GA, Littman E, Ling JQ, Chen HL, Hu JF, Behr B, Giudice L, Hoffman AR.

Mol Hum Reprod. 2005 Sep;11(9):631-40. Epub 2005 Oct 11.

PMID:
16219628
17.

Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome.

Nativio R, Sparago A, Ito Y, Weksberg R, Riccio A, Murrell A.

Hum Mol Genet. 2011 Apr 1;20(7):1363-74. doi: 10.1093/hmg/ddr018. Epub 2011 Jan 31.

18.

Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality.

Lee DH, Singh P, Tsark WM, Szabó PE.

PLoS One. 2010 Sep 8;5(9):e12630. doi: 10.1371/journal.pone.0012630.

19.

Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.

Poole RL, Leith DJ, Docherty LE, Shmela ME, Gicquel C, Splitt M, Temple IK, Mackay DJ.

Eur J Hum Genet. 2012 Feb;20(2):240-3. doi: 10.1038/ejhg.2011.166. Epub 2011 Aug 24.

20.

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.

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.

Hum Mol Genet. 2010 Mar 1;19(5):803-14. doi: 10.1093/hmg/ddp549. Epub 2009 Dec 9.

PMID:
20007505

Supplemental Content

Support Center