The embryonic mouse hindbrain as a qualitative and quantitative model for studying the molecular and cellular mechanisms of angiogenesis
about
Neuropilin 1 (NRP1) hypomorphism combined with defective VEGF-A binding reveals novel roles for NRP1 in developmental and pathological angiogenesisThe neuropilin 1 cytoplasmic domain is required for VEGF-A-dependent arteriogenesisNRP1 function and targeting in neurovascular development and eye diseaseVascularisation of the central nervous systemEgfl7 is differentially expressed in arteries and veins during retinal vascular development.Quantitative assessment of angiogenesis, perfused blood vessels and endothelial tip cells in the postnatal mouse brain.BMP-SMAD signalling output is highly regionalized in cardiovascular and lymphatic endothelial networks.Placental growth factor deficiency is associated with impaired cerebral vascular development in mice.Regulation of embryonic neurogenesis by germinal zone vasculature.FOXO1 couples metabolic activity and growth state in the vascular endothelium.Novel insights into the development and maintenance of the blood-brain barrier.Neuropilin regulation of angiogenesis.VEGF189 binds NRP1 and is sufficient for VEGF/NRP1-dependent neuronal patterning in the developing brain.Nogo-A regulates vascular network architecture in the postnatal brain.NRP1 Regulates CDC42 Activation to Promote Filopodia Formation in Endothelial Tip Cells.Podoplanin and CLEC-2 drive cerebrovascular patterning and integrity during development.Neuropilin 1 sequestration by neuropathogenic mutant glycyl-tRNA synthetase is permissive to vascular homeostasisIntracellular adenosine regulates epigenetic programming in endothelial cells to promote angiogenesis.MEF2 transcription factors are key regulators of sprouting angiogenesis.Fascin 1 is dispensable for developmental and tumour angiogenesis.Crypto-rhombomeres of the mouse medulla oblongata, defined by molecular and morphological features.The Mouse Hindbrain As a Model for Studying Embryonic Neurogenesis.MPDZ promotes DLL4-induced Notch signaling during angiogenesis.Elevated Expression of miR302-367 in Endothelial Cells Inhibits Developmental Angiogenesis via CDC42/CCND1 Mediated Signaling Pathways.
P2860
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P2860
The embryonic mouse hindbrain as a qualitative and quantitative model for studying the molecular and cellular mechanisms of angiogenesis
description
2013 nî lūn-bûn
@nan
2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
The embryonic mouse hindbrain ...... lar mechanisms of angiogenesis
@ast
The embryonic mouse hindbrain ...... lar mechanisms of angiogenesis
@en
type
label
The embryonic mouse hindbrain ...... lar mechanisms of angiogenesis
@ast
The embryonic mouse hindbrain ...... lar mechanisms of angiogenesis
@en
prefLabel
The embryonic mouse hindbrain ...... lar mechanisms of angiogenesis
@ast
The embryonic mouse hindbrain ...... lar mechanisms of angiogenesis
@en
P2093
P2860
P356
P1433
P1476
The embryonic mouse hindbrain ...... lar mechanisms of angiogenesis
@en
P2093
Alessandro Fantin
Alice Plein
Charlotte H Maden
Christiana Ruhrberg
Joaquim M Vieira
P2860
P2888
P304
P356
10.1038/NPROT.2013.015
P577
2013-02-01T00:00:00Z
P5875
P6179
1026501759