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A KRAB domain zinc finger protein in imprinting and disease.

Hirasawa R, Feil R.

Dev Cell. 2008 Oct;15(4):487-8. doi: 10.1016/j.devcel.2008.09.006.


Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.

Mackay DJ, Callaway JL, Marks SM, White HE, Acerini CL, Boonen SE, Dayanikli P, Firth HV, Goodship JA, Haemers AP, Hahnemann JM, Kordonouri O, Masoud AF, Oestergaard E, Storr J, Ellard S, Hattersley AT, Robinson DO, Temple IK.

Nat Genet. 2008 Aug;40(8):949-51. doi: 10.1038/ng.187. Epub 2008 Jul 11.


Human and mouse ZFP57 proteins are functionally interchangeable in maintaining genomic imprinting at multiple imprinted regions in mouse ES cells.

Takikawa S, Wang X, Ray C, Vakulenko M, Bell FT, Li X.

Epigenetics. 2013 Dec;8(12):1268-79. doi: 10.4161/epi.26544. Epub 2013 Oct 17.


Zinc finger protein ZFP57 requires its co-factor to recruit DNA methyltransferases and maintains DNA methylation imprint in embryonic stem cells via its transcriptional repression domain.

Zuo X, Sheng J, Lau HT, McDonald CM, Andrade M, Cullen DE, Bell FT, Iacovino M, Kyba M, Xu G, Li X.

J Biol Chem. 2012 Jan 13;287(3):2107-18. doi: 10.1074/jbc.M111.322644. Epub 2011 Dec 5.


A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints.

Li X, Ito M, Zhou F, Youngson N, Zuo X, Leder P, Ferguson-Smith AC.

Dev Cell. 2008 Oct;15(4):547-57. doi: 10.1016/j.devcel.2008.08.014.


Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57.

Bak M, Boonen SE, Dahl C, Hahnemann JM, Mackay DJ, Tümer Z, Grønskov K, Temple IK, Guldberg P, Tommerup N.

BMC Med Genet. 2016 Apr 14;17:29. doi: 10.1186/s12881-016-0292-4.


Extending the maternal-zygotic effect with genomic imprinting.

Li X.

Mol Hum Reprod. 2010 Sep;16(9):695-703. doi: 10.1093/molehr/gaq028. Epub 2010 Apr 9.


Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression.

Strogantsev R, Krueger F, Yamazawa K, Shi H, Gould P, Goldman-Roberts M, McEwen K, Sun B, Pedersen R, Ferguson-Smith AC.

Genome Biol. 2015 May 30;16:112. doi: 10.1186/s13059-015-0672-7.


No evidence for additional imprinting defects in Silver-Russell syndrome patients with maternal uniparental disomy 7 or 11p15 epimutation.

Schönherr N, Meyer E, Binder G, Wollmann HA, Eggermann T.

J Pediatr Endocrinol Metab. 2007 Dec;20(12):1329-31.


Transient neonatal diabetes, a disorder of imprinting.

Temple IK, Shield JP.

J Med Genet. 2002 Dec;39(12):872-5. Review.


Partners in imprinting: noncoding RNA and polycomb group proteins.

Wu HA, Bernstein E.

Dev Cell. 2008 Nov;15(5):637-8. doi: 10.1016/j.devcel.2008.10.008.


The Kruppel-associated box repressor domain can trigger de novo promoter methylation during mouse early embryogenesis.

Wiznerowicz M, Jakobsson J, Szulc J, Liao S, Quazzola A, Beermann F, Aebischer P, Trono D.

J Biol Chem. 2007 Nov 23;282(47):34535-41. Epub 2007 Sep 24.


Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitus.

Mackay DJ, Coupe AM, Shield JP, Storr JN, Temple IK, Robinson DO.

Hum Genet. 2002 Feb;110(2):139-44. Epub 2002 Jan 24.


Microarray-based DNA methylation analysis of imprinted loci in a patient with transient neonatal diabetes mellitus.

Martin-Subero JI, Bibikova M, Mackay D, Wickham-Garcia E, Sellami N, Richter J, Santer R, Caliebe A, Fan JB, Temple IK, Siebert R.

Am J Med Genet A. 2008 Dec 15;146A(24):3227-9. doi: 10.1002/ajmg.a.32577. No abstract available.


Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals.

Henckel A, Nakabayashi K, Sanz LA, Feil R, Hata K, Arnaud P.

Hum Mol Genet. 2009 Sep 15;18(18):3375-83. doi: 10.1093/hmg/ddp277. Epub 2009 Jun 10.


Functional analysis of a novel KRAB/C2H2 zinc finger protein Mipu1.

Jiang L, Tang D, Wang K, Zhang H, Yuan C, Duan D, Xiao X.

Biochem Biophys Res Commun. 2007 May 18;356(4):829-35. Epub 2007 Mar 5.


ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells.

Anvar Z, Cammisa M, Riso V, Baglivo I, Kukreja H, Sparago A, Girardot M, Lad S, De Feis I, Cerrato F, Angelini C, Feil R, Pedone PV, Grimaldi G, Riccio A.

Nucleic Acids Res. 2016 Feb 18;44(3):1118-32. doi: 10.1093/nar/gkv1059. Epub 2015 Oct 19.


The specification of imprints in mammals.

Hanna CW, Kelsey G.

Heredity (Edinb). 2014 Aug;113(2):176-83. doi: 10.1038/hdy.2014.54. Epub 2014 Jun 18. Review.


Profound phenotypic variation among mice deficient in the maintenance of genomic imprints.

Toppings M, Castro C, Mills PH, Reinhart B, Schatten G, Ahrens ET, Chaillet JR, Trasler JM.

Hum Reprod. 2008 Apr;23(4):807-18. doi: 10.1093/humrep/den009. Epub 2008 Feb 13.


Maternal and zygotic Zfp57 modulate NOTCH signaling in cardiac development.

Shamis Y, Cullen DE, Liu L, Yang G, Ng SF, Xiao L, Bell FT, Ray C, Takikawa S, Moskowitz IP, Cai CL, Yang X, Li X.

Proc Natl Acad Sci U S A. 2015 Apr 21;112(16):E2020-9. doi: 10.1073/pnas.1415541112. Epub 2015 Apr 6.

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