Analysis of Dll4 regulation reveals a combinatorial role for Sox and Notch in arterial development. - Wikidata - wikimedia - TriplyDB

Analysis of Dll4 regulation reveals a combinatorial role for Sox and Notch in arterial development.

Analysis of Dll4 regulation reveals a combinatorial role for Sox and Notch in arterial development.

http://www.wikidata.org/entity/Q37031888

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Zebrafish as an Emerging Model Organism to Study Angiogenesis in Development and Regeneration Choroid plexus in developmental and evolutionary perspective Context-specific interactions between Notch and ALK1 cannot explain ALK1-associated arteriovenous malformations.An Intronic Flk1 Enhancer Directs Arterial-Specific Expression via RBPJ-Mediated Venous Repression.Sox17 is indispensable for acquisition and maintenance of arterial identity O-GlcNAc on NOTCH1 EGF repeats regulates ligand-induced Notch signaling and vascular development in mammals A Snail1/Notch1 signalling axis controls embryonic vascular development.The endothelial transcription factor ERG mediates Angiopoietin-1-dependent control of Notch signalling and vascular stability.SoxF factors and Notch regulate nr2f2 gene expression during venous differentiation in zebrafish Sox7 is regulated by ETV2 during cardiovascular development Decoding the regulatory network of early blood development from single-cell gene expression measurements.FGF signalling restricts haematopoietic stem cell specification via modulation of the BMP pathway.Delta-like 4 mRNA is regulated by adjacent natural antisense transcripts SMAD1 and SMAD5 Expression Is Coordinately Regulated by FLI1 and GATA2 during Endothelial Development.Cardiovascular Patterning as Determined by Hemodynamic Forces and Blood Vessel Genetics.Sox7, Sox17, and Sox18 Cooperatively Regulate Vascular Development in the Mouse Retina.Fast revascularization of the injured area is essential to support zebrafish heart regeneration.Pharmacological targeting of the transcription factor SOX18 delays breast cancer in mice.Mapping cell type-specific transcriptional enhancers using high affinity, lineage-specific Ep300 bioChIP-seq.Regulation of signaling interactions and receptor endocytosis in growing blood vessels.An arterial-specific enhancer of the human endothelin converting enzyme 1 (ECE1) gene is synergistically activated by Sox17, FoxC2, and Etv2.Lipid rafts: integrated platforms for vascular organization offering therapeutic opportunities.Molecular controls of arterial morphogenesis.SoxF factors induce Notch1 expression via direct transcriptional regulation during early arterial development.Sox17-mediated maintenance of fetal intra-aortic hematopoietic cell clusters.MEF2 transcription factors are key regulators of sprouting angiogenesis.LDB2 regulates the expression of DLL4 through the formation of oligomeric complexes in endothelial cells.Notch Signaling in Development, Tissue Homeostasis, and Disease.ALK1 signaling in development and disease: new paradigms.Dynamic regulation of VEGF-inducible genes by an ERK/ERG/p300 transcriptional network.Differential tissue specific, temporal and spatial expression patterns of the Aggrecan gene is modulated by independent enhancer elements.A novel reporter allele for monitoring Dll4 expression within the embryonic and adult mouse.Live imaging of wound angiogenesis reveals macrophage orchestrated vessel sprouting and regression.

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Analysis of Dll4 regulation reveals a combinatorial role for Sox and Notch in arterial development.

http://www.wikidata.org/entity/Q37031888

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on July 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

Analysis of Dll4 regulation re ...... Notch in arterial development.

@en

Analysis of Dll4 regulation re ...... Notch in arterial development.

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type

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Analysis of Dll4 regulation re ...... Notch in arterial development.

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Analysis of Dll4 regulation re ...... Notch in arterial development.

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prefLabel

Analysis of Dll4 regulation re ...... Notch in arterial development.

@en

Analysis of Dll4 regulation re ...... Notch in arterial development.

@nl

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PNAS.1300805110

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Proceedings of the National Academy of Sciences of the United States of America

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Analysis of Dll4 regulation re ...... Notch in arterial development.

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Benjamin Davies

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George Bou-Gharios

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Indrika Ratnayaka

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Ke Liu

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Luis Sanchez-Del-Campo

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Martin Fritzsche

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Natalia Sacilotto

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Philip Pinheiro

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Roger Patient

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Sarah De Val

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P2860

Transcriptional Regulatory Elements in the Human Genome

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox transcription factor gene families

Histone modifications at human enhancers reflect global cell-type-specific gene expression

Haploinsufficient lethality and formation of arteriovenous malformations in Notch pathway mutants

Redundant roles of Sox17 and Sox18 in early cardiovascular development of mouse embryos

The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development

ER71 acts downstream of BMP, Notch, and Wnt signaling in blood and vessel progenitor specification

Dosage-sensitive requirement for mouse Dll4 in artery development

The Wnt/beta-catenin pathway modulates vascular remodeling and specification by upregulating Dll4/Notch signaling

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scholarly article

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10.1073/PNAS.1300805110

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29

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110

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Colin R. Goding

Philipp W Becker

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2013-07-01T00:00:00Z

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244482670

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23818617

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