PubMed for id: 346171

Year	Number of Results
1993	1
1994	1
2002	1
2004	1
2005	1
2008	2
2009	2
2011	3
2012	1
2013	4
2014	3
2015	1
2016	1
2018	2
2019	3
2020	2
2021	2
2022	2
2024	0

1

The role of ZFP57 and additional KRAB-zinc finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbances.

Monteagudo-Sánchez A, Hernandez Mora JR, Simon C, Burton A, Tenorio J, Lapunzina P, Clark S, Esteller M, Kelsey G, López-Siguero JP, de Nanclares GP, Torres-Padilla ME, Monk D. Monteagudo-Sánchez A, et al. Nucleic Acids Res. 2020 Nov 18;48(20):11394-11407. doi: 10.1093/nar/gkaa837. Nucleic Acids Res. 2020. PMID: 33053156 Free PMC article.

2

ZFP57 suppress proliferation of breast cancer cells through down-regulation of MEST-mediated Wnt/β-catenin signalling pathway.

Chen L, Wu X, Xie H, Yao N, Xia Y, Ma G, Qian M, Ge H, Cui Y, Huang Y, Wang S, Zheng M. Chen L, et al. Cell Death Dis. 2019 Feb 20;10(3):169. doi: 10.1038/s41419-019-1335-5. Cell Death Dis. 2019. PMID: 30787268 Free PMC article.

3

The Embryonic Stem Cell-Specific Transcription Factor ZFP57 Promotes Liver Metastasis of Colorectal Cancer.

Shoji Y, Takamura H, Ninomiya I, Fushida S, Tada Y, Yokota T, Ohta T, Koide H. Shoji Y, et al. J Surg Res. 2019 May;237:22-29. doi: 10.1016/j.jss.2018.11.014. Epub 2019 Jan 22. J Surg Res. 2019. PMID: 30694787

4

Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?

Sparago A, Cerrato F, Riccio A. Sparago A, et al. Clin Epigenetics. 2018 Feb 21;10:23. doi: 10.1186/s13148-018-0454-7. eCollection 2018. Clin Epigenetics. 2018. PMID: 29484033 Free PMC article.

5

Fine mapping genetic determinants of the highly variably expressed MHC gene ZFP57.

Plant K, Fairfax BP, Makino S, Vandiedonck C, Radhakrishnan J, Knight JC. Plant K, et al. Eur J Hum Genet. 2014 Apr;22(4):568-71. doi: 10.1038/ejhg.2013.244. Epub 2013 Nov 6. Eur J Hum Genet. 2014. PMID: 24193346 Free PMC article.

6

Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57 gene.

Boyraz M, Ulucan K, Taşkın N, Akçay T, Flanagan SE, Mackay DJ. Boyraz M, et al. J Clin Res Pediatr Endocrinol. 2013;5(2):125-8. doi: 10.4274/Jcrpe.928. J Clin Res Pediatr Endocrinol. 2013. PMID: 23748067 Free PMC article.

7

No evidence for pathogenic variants or maternal effect of ZFP57 as the cause of Beckwith-Wiedemann Syndrome.

Boonen SE, Hahnemann JM, Mackay D, Tommerup N, Brøndum-Nielsen K, Tümer Z, Grønskov K. Boonen SE, et al. Eur J Hum Genet. 2012 Jan;20(1):119-21. doi: 10.1038/ejhg.2011.140. Epub 2011 Aug 24. Eur J Hum Genet. 2012. PMID: 21863059 Free PMC article.

8

Screening for genomic variants in ZFP57 in Silver-Russell syndrome patients with 11p15 epimutations.

Spengler S, Gogiel M, Schönherr N, Binder G, Eggermann T. Spengler S, et al. Eur J Med Genet. 2009 Nov-Dec;52(6):415-6. doi: 10.1016/j.ejmg.2009.07.005. Epub 2009 Jul 24. Eur J Med Genet. 2009. PMID: 19632365

9

The stem cell transcription factor ZFP57 induces IGF2 expression to promote anchorage-independent growth in cancer cells.

Tada Y, Yamaguchi Y, Kinjo T, Song X, Akagi T, Takamura H, Ohta T, Yokota T, Koide H. Tada Y, et al. Oncogene. 2015 Feb 5;34(6):752-60. doi: 10.1038/onc.2013.599. Epub 2014 Jan 27. Oncogene. 2015. PMID: 24469060

10

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. Takikawa S, et al. Epigenetics. 2013 Dec;8(12):1268-79. doi: 10.4161/epi.26544. Epub 2013 Oct 17. Epigenetics. 2013. PMID: 24135613 Free PMC article.

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