Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
about
REX-1 expression and p38 MAPK activation status can determine proliferation/differentiation fates in human mesenchymal stem cellsRex1 (Zfp42) null mice show impaired testicular function, abnormal testis morphology, and aberrant gene expressionDNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2Pluripotency Factors on Their Lineage MoveLong nonoding RNAs in the X-inactivation centerRex1/Zfp42 as an epigenetic regulator for genomic imprintingGenetic exploration of the exit from self-renewal using haploid embryonic stem cellsRegulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell PotencyTranscriptional signature and memory retention of human-induced pluripotent stem cellsTracking the embryonic stem cell transition from ground state pluripotency.Transcriptome profiling of spinal muscular atrophy motor neurons derived from mouse embryonic stem cellsPluripotency factors in embryonic stem cells regulate differentiation into germ layers.Demarcation of stable subpopulations within the pluripotent hESC compartment.Stress-induced enzyme activation primes murine embryonic stem cells to differentiate toward the first extraembryonic lineageKinetics of drug selection systems in mouse embryonic stem cellsAnalysis of Rex1 (zfp42) function in embryonic stem cell differentiation.Epigenetic landscapes explain partially reprogrammed cells and identify key reprogramming genes.How are pluripotent cells captured in culture?A panel of induced pluripotent stem cells from chimpanzees: a resource for comparative functional genomics.In Vivo Chromatin Targets of the Transcription Factor Yin Yang 2 in Trophoblast Stem Cells.Releasing the break on X chromosome inactivation: Rnf12/RLIM targets REX1 for degradation.Development and Validation of a Rex1-RFP Potency Activity Reporter Assay That Quantifies Stress-Forced Potency Loss in Mouse Embryonic Stem Cells.The pluripotency-associated gene Dppa4 is dispensable for embryonic stem cell identity and germ cell development but essential for embryogenesis.Regulation of stem cell pluripotency and differentiation involves a mutual regulatory circuit of the NANOG, OCT4, and SOX2 pluripotency transcription factors with polycomb repressive complexes and stem cell microRNAs.Direct Conversion of Human Fibroblasts into Neural Progenitors Using Transcription Factors Enriched in Human ESC-Derived Neural Progenitors.Do all roads lead to Oct4? the emerging concepts of induced pluripotency.Mapping the route from naive pluripotency to lineage specification.Directed differentiation of human embryonic stem cells to interrogate the cardiac gene regulatory networkExpression of endogenous retroviruses is negatively regulated by the pluripotency marker Rex1/Zfp42.Embryonic stem cell factors undifferentiated transcription factor-1 (UFT-1) and reduced expression protein-1 (REX-1) are widely expressed in human skin and may be involved in cutaneous differentiation but not in stem cell fate determination.RNF12 initiates X-chromosome inactivation by targeting REX1 for degradation.Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells.Membrane translocation of t-SNARE protein syntaxin-4 abrogates ground-state pluripotency in mouse embryonic stem cells.Microarray analyses of otospheres derived from the cochlea in the inner ear identify putative transcription factors that regulate the characteristics of otospheres.Functional analysis of Rex1 during preimplantation developmentDifferentiation of Human Pluripotent Stem Cells into Mesodermal and Ectodermal Derivatives Is Independent of the Type of Isogenic Reprogrammed Somatic Cells.The C-terminal region of Xpc is dispensable for the transcriptional activity of Oct3/4 in mouse embryonic stem cells.Reduction of pluripotent gene expression in murine embryonic stem cells exposed to mechanical loading or Cyclo RGD peptide.Effect of High Hydrostatic Pressure Applied Before Cryopreservation on the Survival Rate and Quality of Porcine Mesenchymal Stem Cells After Thawing.Induction of differentiation by down-regulation of Nanog and Rex-1 in cord blood derived unrestricted somatic stem cells.
P2860
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P2860
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
description
2008 nî lūn-bûn
@nan
2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
@ast
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
@en
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells.
@nl
type
label
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
@ast
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
@en
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells.
@nl
prefLabel
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
@ast
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
@en
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells.
@nl
P2093
P2860
P356
P1476
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
@en
P2093
Hitoshi Niwa
Kadue Takahashi
Satoshi Ohtsuka
Shinji Masui
P2860
P2888
P356
10.1186/1471-213X-8-45
P577
2008-04-24T00:00:00Z
P6179
1021174828