Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter - Wikidata - wikimedia - TriplyDB

Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter

Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter

http://www.wikidata.org/entity/Q37347018

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Hematopoietic stem cell development, niches, and signaling pathways RUNX1 regulates the CD34 gene in haematopoietic stem cells by mediating interactions with a distal regulatory element ERG dependence distinguishes developmental control of hematopoietic stem cell maintenance from hematopoietic specification A Runx1-Smad6 rheostat controls Runx1 activity during embryonic hematopoiesis Cellular Reprogramming Using Defined Factors and MicroRNAs Concise review: programming human pluripotent stem cells into blood Specification and function of hemogenic endothelium during embryogenesis Genetic and Epigenetic Mechanisms That Maintain Hematopoietic Stem Cell Function Angiocrine functions of organ-specific endothelial cells Linkage between the mechanisms of thrombocytopenia and thrombopoiesis The development and maintenance of resident macrophages Ontogeny of Tissue-Resident Macrophages Lost in translation: pluripotent stem cell-derived hematopoiesis Hematopoiesis: from start to immune reconstitution potential Hematopoietic specification from human pluripotent stem cells: current advances and challenges toward de novo generation of hematopoietic stem cells.Transcription factor-mediated reprogramming toward hematopoietic stem cells A gene trap transposon eliminates haematopoietic expression of zebrafish Gfi1aa, but does not interfere with haematopoiesis.Adenosine signaling promotes hematopoietic stem and progenitor cell emergence.Epoxyeicosatrienoic acids enhance embryonic haematopoiesis and adult marrow engraftment.The RUNX1 +24 enhancer and P1 promoter identify a unique subpopulation of hematopoietic progenitor cells derived from human pluripotent stem cells Definitive Hematopoietic Multipotent Progenitor Cells Are Transiently Generated From Hemogenic Endothelial Cells in Human Pluripotent Stem Cells.Myeloid cells contribute to tumor lymphangiogenesis Gata2b is a restricted early regulator of hemogenic endothelium in the zebrafish embryo.Activation of the TGFβ pathway impairs endothelial to haematopoietic transition.Hematopoietic (stem) cell development - how divergent are the roads taken?The many faces of hematopoietic stem cell heterogeneity Receptor Signaling Directs Global Recruitment of Pre-existing Transcription Factors to Inducible Elements Stem Cells: Potential Therapy for Neonatal Injury?Modeling Human Bone Marrow Failure Syndromes Using Pluripotent Stem Cells and Genome Engineering Oceans of opportunity: exploring vertebrate hematopoiesis in zebrafish Vascular niche promotes hematopoietic multipotent progenitor formation from pluripotent stem cells Development of the renal arterioles.Three-dimensional cartography of hematopoietic clusters in the vasculature of whole mouse embryos.VEGF and FGF prime vascular tube morphogenesis and sprouting directed by hematopoietic stem cell cytokines.Gata2 cis-element is required for hematopoietic stem cell generation in the mammalian embryo.Endothelio-mesenchymal interaction controls runx1 expression and modulates the notch pathway to initiate aortic hematopoiesis Fusing VE-cadherin to α-catenin impairs fetal liver hematopoiesis and lymph but not blood vessel formation.Dynamic haematopoietic cell contribution to the developing and adult epicardium.Quiescence of adult oligodendrocyte precursor cells requires thyroid hormone and hypoxia to activate Runx1.A Src family kinase-Shp2 axis controls RUNX1 activity in megakaryocyte and T-lymphocyte differentiation.

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Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter

http://www.wikidata.org/entity/Q37347018

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 07 January 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Runx1 is required for the endo ...... transition but not thereafter

@en

Runx1 is required for the endo ...... transition but not thereafter.

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type

label

Runx1 is required for the endo ...... transition but not thereafter

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Runx1 is required for the endo ...... transition but not thereafter.

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prefLabel

Runx1 is required for the endo ...... transition but not thereafter

@en

Runx1 is required for the endo ...... transition but not thereafter.

@nl

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Runx1 is required for the endo ...... transition but not thereafter

@en

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Brandon M Zeigler

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

Elaine Dzierzak

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

Michael J Chen

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

Nancy A Speck

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

Tomomasa Yokomizo

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

P2860

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

Brachyury is required for elongation and vasculogenesis in the murine allantois

Characterization of purified intraembryonic hematopoietic stem cells as a tool to define their site of origin.

The emergence of hematopoietic stem cells is initiated in the placental vasculature in the absence of circulation.

Runx1 expression marks long-term repopulating hematopoietic stem cells in the midgestation mouse embryo.

Hematopoietic stem cells localize to the endothelial cell layer in the midgestation mouse aorta.

AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis.

A 5' element of the chicken beta-globin domain serves as an insulator in human erythroid cells and protects against position effect in Drosophila.

Progressive divergence of definitive haematopoietic stem cells from the endothelial compartment does not depend on contact with the foetal liver.

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887-891

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scholarly article

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10.1038/NATURE07619

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P433

7231

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457

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2009-01-07T00:00:00Z

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23764568

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1050657682

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19129762

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2744041

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