Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome.

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Transcription-driven DNA methylation setting on the mouse Peg3 locus.Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.

P2860

Q48512714-22BB3943-D706-4211-97F7-C0EAD6901A52 Q55168613-DD64B4A3-BACB-435B-B5DD-AE6FAF76C111

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Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome.

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http://www.wikidata.org/entity/Q48251733

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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Blocked transcription through ...... g Beckwith-Wiedemann syndrome.

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Blocked transcription through ...... g Beckwith-Wiedemann syndrome.

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Item

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Blocked transcription through ...... g Beckwith-Wiedemann syndrome.

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Blocked transcription through ...... g Beckwith-Wiedemann syndrome.

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Blocked transcription through ...... g Beckwith-Wiedemann syndrome.

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Blocked transcription through ...... g Beckwith-Wiedemann syndrome.

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P1476

Blocked transcription through ...... g Beckwith-Wiedemann syndrome.

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P2093

Joanna C Hillman

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Kayla E Wilson

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Kristopher M Attwood

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Shilpa Pathak

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Sirinapa Sribenja

http://www.w3.org/2001/XMLSchema#string

Vir B Singh

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P2860

Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice

KDM1B is a histone H3K4 demethylase required to establish maternal genomic imprints

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

Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes

Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15

The human ASCL2 gene escaping genomic imprinting and its expression pattern

High sensitivity mapping of methylated cytosines

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

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1820-1830

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scholarly article

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10.1242/DEV.145136

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English

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144

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Michael J Higgins

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2017-04-20T00:00:00Z

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28428215

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5450836

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Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome.

about

P2860

P2860

Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932