Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts. - Test2 - elhamkhani - TriplyDB

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

http://www.wikidata.org/entity/Q33582189

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Anatomy of a blastocyst: cell behaviors driving cell fate choice and morphogenesis in the early mouse embryo Transcription factor AP-2γ is a core regulator of tight junction biogenesis and cavity formation during mouse early embryogenesis.PBX1 genomic pioneer function drives ERα signaling underlying progression in breast cancer.Initiation of trophectoderm lineage specification in mouse embryos is independent of Cdx2.Transcriptional regulators of the trophoblast lineage in mammals with hemochorial placentation.Evidence that transcription factor AP-2γ is not required for Oct4 repression in mouse blastocysts.Adaptive mechanisms controlling uterine spiral artery remodeling during the establishment of pregnancy.Transcription factor AP-2γ induces early Cdx2 expression and represses HIPPO signaling to specify the trophectoderm lineage.The Efficient Derivation of Trophoblast Cells from Porcine In Vitro Fertilized and Parthenogenetic Blastocysts and Culture with ROCK Inhibitor Y-27632.The Evolutionarily Conserved C-terminal Domains in the Mammalian Retinoblastoma Tumor Suppressor Family Serve as Dual Regulators of Protein Stability and Transcriptional Potency.Epigenetic silencing of Oct4 by a complex containing SUV39H1 and Oct4 pseudogene lncRNA.Derivation and characterization of embryonic stem cells lines derived from transgenic Fischer 344 and Dark Agouti rats.Transcriptional networks driving enhancer function in the CFTR gene.BRG1 Governs Nanog Transcription in Early Mouse Embryos and Embryonic Stem Cells via Antagonism of Histone H3 Lysine 9/14 Acetylation Maternal Cdx2 is dispensable for mouse development.Genetic mouse embryo assay: improving performance and quality testing for assisted reproductive technology (ART) with a functional bioassay.Creation of trophectoderm, the first epithelium, in mouse preimplantation development.Stress induces AMPK-dependent loss of potency factors Id2 and Cdx2 in early embryos and stem cells [corrected].Epigenetic control of cell fate in mouse blastocysts: the role of covalent histone modifications and chromatin remodeling.Epigenesis and plasticity of mouse trophoblast stem cells.ATP-dependent chromatin remodeling during mammalian development.Transcriptional reprogramming and chromatin remodeling accompanies Oct4 and Nanog silencing in mouse trophoblast lineage.NonO binds to the CpG island of oct4 promoter and functions as a transcriptional activator of oct4 gene expression.Trophoblast stem cells.Geminin escapes degradation in G1 of mouse pluripotent cells and mediates the expression of Oct4, Sox2, and Nanog Comparison of three differential mouse blastocyst staining methods.Making the first decision: lessons from the mouse.Chromatin Remodelling Proteins and Cell Fate Decisions in Mammalian Preimplantation Development.ARID1A, a component of SWI/SNF chromatin remodeling complexes, is required for porcine embryo development.Cell reprogramming. Histone chaperone ASF1A is required for maintenance of pluripotency and cellular reprogramming.Cdx2 Regulates Gene Expression through Recruitment of Brg1-associated Switch-Sucrose Non-fermentable (SWI-SNF) Chromatin Remodeling Activity.Functional characterization of CDX2 during bovine preimplantation development in vitro.Expression patterns of Oct4, Cdx2, Tead4, and Yap1 proteins during blastocyst formation in embryos of the marsupial, Monodelphis domestica Wagner.Intestinal regulation of suppression of tumorigenicity 14 (ST14) and serine peptidase inhibitor, Kunitz type -1 (SPINT1) by transcription factor CDX2 The States of Pluripotency: Pluripotent Lineage Development in the Embryo and in the Dish

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Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

http://www.wikidata.org/entity/Q33582189

description

2010 nî lūn-bûn

@nan

2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի մայիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

@wuu

name

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@ast

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@en

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@nl

type

label

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@ast

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@en

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@nl

prefLabel

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@ast

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@en

Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@nl

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JOURNAL.PONE.0010622

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Brg1 is required for Cdx2-mediated repression of Oct4 expression in mouse blastocysts.

@en

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Catherine A Wilson

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

Jason G Knott

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

Kai Wang

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

R William Henry

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

Satyaki Sengupta

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P2860

Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4

A novel nuclear receptor corepressor complex, N-CoR, contains components of the mammalian SWI/SNF complex and the corepressor KAP-1

Cdx2 is required for correct cell fate specification and differentiation of trophectoderm in the mouse blastocyst

Uncovering early response of gene regulatory networks in ESCs by systematic induction of transcription factors

The Hippo signaling pathway components Lats and Yap pattern Tead4 activity to distinguish mouse trophectoderm from inner cell mass

A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes

Physical and functional interaction of DNA methyltransferase 3A with Mbd3 and Brg1 in mouse lymphosarcoma cells

Interaction between Oct3/4 and Cdx2 determines trophectoderm differentiation

Promotion of trophoblast stem cell proliferation by FGF4

Global mapping of DNA methylation in mouse promoters reveals epigenetic reprogramming of pluripotency genes.

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