Phenotypic complementation establishes requirements for specific POU domain and generic transactivation function of Oct-3/4 in embryonic stem cells.
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P1343
Notch promotes neural lineage entry by pluripotent embryonic stem cells.Differences between cellular and molecular profiles of induced pluripotent stem cells generated from mouse embryonic fibroblastsUse of altered-specificity binding Oct-4 suggests an absence of pluripotent cell-specific cofactor usageEx uno plures: molecular designs for embryonic pluripotencyIntercellular interactions, position, and polarity in establishing blastocyst cell lineages and embryonic axesE-cadherin-coated plates maintain pluripotent ES cells without colony formationPOU-V factors antagonize maternal VegT activity and beta-Catenin signaling in Xenopus embryosThe NuRD component Mbd3 is required for pluripotency of embryonic stem cellsAnteriorization of neural fate by inhibitor of beta-catenin and T cell factor (ICAT), a negative regulator of Wnt signalingCsn3 gene is regulated by all-trans retinoic acid during neural differentiation in mouse P19 cellsReverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiationKlf4 cooperates with Oct3/4 and Sox2 to activate the Lefty1 core promoter in embryonic stem cellsRecombination signal sequence-binding protein Jkappa alters mesodermal cell fate decisions by suppressing cardiomyogenesis.Extra-embryonic endoderm cells derived from ES cells induced by GATA factors acquire the character of XEN cells.Rex1/Zfp42 is dispensable for pluripotency in mouse ES cellsAngiogenesis in differentiated placental multipotent mesenchymal stromal cells is dependent on integrin alpha5beta1.The hypoxic microenvironment maintains glioblastoma stem cells and promotes reprogramming towards a cancer stem cell phenotype.Oct-4 controls cell-cycle progression of embryonic stem cells.Auto-regulation of the Sohlh1 gene by the SOHLH2/SOHLH1/SP1 complex: implications for early spermatogenesis and oogenesis.TIF1beta regulates the pluripotency of embryonic stem cells in a phosphorylation-dependent manner.Recruitment of Oct4 protein to UV-damaged chromatin in embryonic stem cellsImproved cloning efficiency and developmental potential in bovine somatic cell nuclear transfer with the oosight imaging system.On the origin of POU5F1.Secreted cerberus1 as a marker for quantification of definitive endoderm differentiation of the pluripotent stem cells.Kinetics of drug selection systems in mouse embryonic stem cellsSuccessful reprogramming of epiblast stem cells by blocking nuclear localization of β-cateninDual roles of Oct4 in the maintenance of mouse P19 embryonal carcinoma cells: as negative regulator of Wnt/β-catenin signaling and competence provider for Brachyury induction.Evolutionarily conserved role of nucleostemin: controlling proliferation of stem/progenitor cells during early vertebrate development.Construction and applications of exon-trapping gene-targeting vectors with a novel strategy for negative selection.Differentiation of embryonic stem cells is induced by GATA factorsHow are pluripotent cells captured in culture?Dental follicle stem cells in bone regeneration on titanium implantsGtsf1l and Gtsf2 Are Specifically Expressed in Gonocytes and Spermatids but Are Not Essential for Spermatogenesis.Isolation and biological characterization of chicken amnion epithelial cells.Chromatin-prebound Crm1 recruits Nup98-HoxA9 fusion to induce aberrant expression of Hox cluster genes.A Role for MOSPD1 in Mesenchymal Stem Cell Proliferation and Differentiation.Critical POU domain residues confer Oct4 uniqueness in somatic cell reprogramming.A membrane-associated β-catenin/Oct4 complex correlates with ground-state pluripotency in mouse embryonic stem cellsA defined Oct4 level governs cell state transitions of pluripotency entry and differentiation into all embryonic lineagesWnt3a-dependent and -independent protein interaction networks of chromatin-bound β-catenin in mouse embryonic stem cells.
P2860
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P2860
Phenotypic complementation establishes requirements for specific POU domain and generic transactivation function of Oct-3/4 in embryonic stem cells.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Phenotypic complementation est ...... t-3/4 in embryonic stem cells.
@en
Phenotypic complementation est ...... t-3/4 in embryonic stem cells.
@nl
type
label
Phenotypic complementation est ...... t-3/4 in embryonic stem cells.
@en
Phenotypic complementation est ...... t-3/4 in embryonic stem cells.
@nl
prefLabel
Phenotypic complementation est ...... t-3/4 in embryonic stem cells.
@en
Phenotypic complementation est ...... t-3/4 in embryonic stem cells.
@nl
P2093
P2860
P1476
Phenotypic complementation est ...... ct-3/4 in embryonic stem cells
@en
P2093
Austin G Smith
Hitoshi Niwa
Shinji Masui
P2860
P304
P356
10.1128/MCB.22.5.1526-1536.2002
P407
P4510
P577
2002-03-01T00:00:00Z