Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing. - Wikidata - wikimedia - TriplyDB

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

http://www.wikidata.org/entity/Q37148001

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In Vitro Generation of Vascular Wall-Resident Multipotent Stem Cells of Mesenchymal Nature from Murine Induced Pluripotent Stem Cells.Autism spectrum disorders and disease modeling using stem cells.Long non-coding RNAs in ischemic stroke.A Comprehensive Atlas of E3 Ubiquitin Ligase Mutations in Neurological Disorders.New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome.Uncovering True Cellular Phenotypes: Using Induced Pluripotent Stem Cell-Derived Neurons to Study Early Insults in Neurodevelopmental Disorders.Subcellular organization of UBE3A in human cerebral cortex

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Corrigendum: Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

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Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

http://www.wikidata.org/entity/Q37148001

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 03 August 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

@en

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

@nl

type

label

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

@en

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

@nl

prefLabel

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

@en

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

@nl

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Scientific Reports

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Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing

@en

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Agnes Bankfalvi

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

Anika Neureiter

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

Hannah de Oliveira Kessler

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

Jana Stanurova

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Kristin Stolp

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Laura Steenpass

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Michaela Hiber

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

Roman Goetzke

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Corrigendum: Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

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UBE3A/E6-AP mutations cause Angelman syndrome

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

The specification of imprints in mammals

Residual expression of the reprogramming factors prevents differentiation of iPSC generated from human fibroblasts and cord blood CD34+ progenitors

Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a

Lentiviral vector design and imaging approaches to visualize the early stages of cellular reprogramming.

Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.

Protein transduction from retroviral Gag precursors

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.

Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model

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30792

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scholarly article

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10.1038/SREP30792

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6

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2016-08-03T00:00:00Z

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27484051

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4971516

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