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

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

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

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

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2018年学术文章

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

@en

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

@nl

type

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

@en

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

@nl

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

@en

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

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Clinical epigenetics

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

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Flavia Cerrato

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

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

New insights into establishment and maintenance of DNA methylation imprints in mammals

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor.

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

A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome.

In embryonic stem cells, ZFP57/KAP1 recognize a methylated hexanucleotide to affect chromatin and DNA methylation of imprinting control regions

Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans.

The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.

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

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10.1186/S13148-018-0454-7

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