Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus. - Wikidata - wikimedia - TriplyDB

Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus.

Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus.

http://www.wikidata.org/entity/Q34126322

about

Maintaining memory of silencing at imprinted differentially methylated regions New insights into establishment and maintenance of DNA methylation imprints in mammals The specification of imprints in mammals The origin and evolution of genomic imprinting and viviparity in mammals Epigenetic genome-wide association methylation in aging and longevity A Mouse Model for Imprinting of the Human Retinoblastoma Gene Angelman syndrome imprinting center encodes a transcriptional promoter.Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.Epigenetic characterization of the growth hormone gene identifies SmcHD1 as a regulator of autosomal gene clusters.Long noncoding RNAs in imprinting and X chromosome inactivation.Transcription and chromatin determinants of de novo DNA methylation timing in oocytes.Forced expression of DNA methyltransferases during oocyte growth accelerates the establishment of methylation imprints but not functional genomic imprinting.Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.Transcription driven somatic DNA methylation within the imprinted Gnas cluster Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model Deep sequencing and de novo assembly of the mouse oocyte transcriptome define the contribution of transcription to the DNA methylation landscape Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain.Dynamic changes in histone modifications precede de novo DNA methylation in oocytes.Non-Coding RNAs at the Gnas and Snrpn-Ube3a Imprinted Gene Loci and Their Involvement in Hereditary Disorders.RNAs of the human chromosome 15q11-q13 imprinted region Alternative promoters of Peg3 with maternal specificity.Antagonist Xist and Tsix co-transcription during mouse oogenesis and maternal Xist expression during pre-implantation development calls into question the nature of the maternal imprint on the X chromosome.Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation De novo DNA methylation in the male germ line occurs by default but is excluded at sites of H3K4 methylation.The landscape of DNA methylation amid a perfect storm of autism aetiologies.Epigenetic and transcriptional features of the novel human imprinted lncRNA GPR1AS suggest it is a functional ortholog to mouse Zdbf2linc Epigenetic regulation of genomic imprinting from germ line to preimplantation.Transgenerational epigenetic inheritance: adaptation through the germline epigenome?Establishment and functions of DNA methylation in the germline.Genetic Studies on Mammalian DNA Methyltransferases.A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome.Recommendations for the investigation of animal models of Prader-Willi syndrome.Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome.Transcription-driven DNA methylation setting on the mouse Peg3 locus.Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.

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P2860

Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus.

http://www.wikidata.org/entity/Q34126322

description

2011 nî lūn-bûn

@nan

2011 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

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2011年論文

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2011年论文

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name

Transcription is required to e ...... e and Angelman syndrome locus.

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Transcription is required to e ...... e and Angelman syndrome locus.

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P356

JOURNAL.PGEN.1002422

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P1476

Transcription is required to e ...... e and Angelman syndrome locus.

@en

P2093

Christopher R Futtner

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

Emily Y Smith

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

James L Resnick

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

Karen A Johnstone

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

Stormy J Chamberlain

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

P2860

An imprinted, mammalian bicistronic transcript encodes two independent proteins

UBE3A/E6-AP mutations cause Angelman syndrome

High sensitivity mapping of methylated cytosines

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

A mouse model for Prader-Willi syndrome imprinting-centre mutations

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion

A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA

Mechanisms of genomic imprinting.

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e1002422

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scholarly article

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10.1371/JOURNAL.PGEN.1002422

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12

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7

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P577

2011-12-29T00:00:00Z

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221744681

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P698

22242001

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P932

3248558

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