Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
about
Genome-wide and parental allele-specific analysis of CTCF and cohesin DNA binding in mouse brain reveals a tissue-specific binding pattern and an association with imprinted differentially methylated regionsMammalian-specific genomic functions: Newly acquired traits generated by genomic imprinting and LTR retrotransposon-derived genes in mammalsGenetic and molecular analyses of PEG10 reveal new aspects of genomic organization, transcription and translationA Prevalence of Imprinted Genes within the Total Transcriptomes of Human Tissues and Cells.Variations of X chromosome inactivation occur in early passages of female human embryonic stem cellsGender influences monoallelic expression of ATP10A in human brainTelomeric NAP1L4 and OSBPL5 of the KCNQ1 cluster, and the DECORIN gene are not imprinted in human trophoblast stem cells.Long non-coding RNA modifies chromatin: epigenetic silencing by long non-coding RNAs.Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.Genetic and epigenetic instability in human pluripotent stem cells.Variable imprinting of the MEST gene in human preimplantation embryos.Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader-Willi syndrome.Allele-biased expression in differentiating human neurons: implications for neuropsychiatric disordersStability of XIST repression in relation to genomic imprinting following global genome demethylation in a human cell line.The effects of culture on genomic imprinting profiles in human embryonic and fetal mesenchymal stem cells.Identifying and validating a combined mRNA and microRNA signature in response to imatinib treatment in a chronic myeloid leukemia cell line.Dynamic expression patterns of imprinted genes in human embryonic stem cells following prolonged passaging and differentiation.Derivation of primordial germ cells from human embryonic and induced pluripotent stem cells is significantly improved by coculture with human fetal gonadal cells.Human primordial germ cell commitment in vitro associates with a unique PRDM14 expression profile.Loss of non-coding RNA expression from the DLK1-DIO3 imprinted locus correlates with reduced neural differentiation potential in human embryonic stem cell lines.Novel Human Embryonic Stem Cell Regulators Identified by Conserved and Distinct CpG Island Methylation State.No Evidence for a Parent-of-Origin Specific Differentially Methylated Region Linked to RASGRF1.Recurrent variations in DNA methylation in human pluripotent stem cells and their differentiated derivatives.Transcriptional differences between rhesus embryonic stem cells generated from in vitro and in vivo derived embryos.Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage.mRNA Levels of Imprinted Genes in Bovine In Vivo Oocytes, Embryos and Cross Species Comparisons with Humans, Mice and Pigs.Differentiation of neural lineage cells from human pluripotent stem cells.Epigenetic alteration of imprinted genes during neural differentiation of germline-derived pluripotent stem cells.A sensitive functional assay reveals frequent loss of genomic imprinting in human placenta.The epigenome in pluripotency and differentiation.Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivatives.Universal cardiac induction of human pluripotent stem cells in two and three-dimensional formats: implications for in vitro maturation."The good into the pot, the bad into the crop!"--a new technology to free stem cells from feeder cells.Genome-wide analysis identifies changes in histone retention and epigenetic modifications at developmental and imprinted gene loci in the sperm of infertile men.Single nucleotide polymorphisms in the imprinted bovine insulin-like growth factor 2 receptor gene (IGF2R) are associated with body size traits in Irish Holstein-Friesian cattle.In Vitro Modeling of Human Germ Cell Development Using Pluripotent Stem Cells.Status of genomic imprinting in epigenetically distinct pluripotent stem cells.A Novel Variant with Positive Natural Selection Influenced Hb A2 Levels in Chinese Individuals with β-Thalassemia.
P2860
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P2860
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@ast
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@en
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@nl
type
label
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@ast
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@en
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@nl
prefLabel
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@ast
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@en
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@nl
P2093
P2860
P356
P1433
P1476
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
@en
P2093
Alexandra Thurston
Cinzia Allegrucci
Dorien Ward-van Oostwaard
Helen Priddle
Kee-Pyo Kim
Lorraine Young
P2860
P304
P356
10.1101/GR.6609207
P407
P577
2007-12-01T00:00:00Z