Smooth muscle protein 22alpha-mediated patchy deletion of Bmpr1a impairs cardiac contractility but protects against pulmonary vascular remodeling.
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Targeting BMP signalling in cardiovascular disease and anaemiaSM22alpha-targeted deletion of bone morphogenetic protein receptor 1A in mice impairs cardiac and vascular development, and influences organogenesisWhole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertensionGenetically manipulated mouse models of lung disease: potential and pitfallsBmp2 and Bmp4 exert opposing effects in hypoxic pulmonary hypertensionHemodynamic forces, vascular oxidative stress, and regulation of BMP-2/4 expressionMicroRNA-885-3p inhibits the growth of HT-29 colon cancer cell xenografts by disrupting angiogenesis via targeting BMPR1A and blocking BMP/Smad/Id1 signaling.ID family protein expression and regulation in hypoxic pulmonary hypertension.Bone Morphogenetic Protein (BMP) signaling in development and human diseasesActivation of the Wnt/planar cell polarity pathway is required for pericyte recruitment during pulmonary angiogenesis.Characterization of the isolated, ventilated, and instrumented mouse lung perfused with pulsatile flow.Wnt signaling activation in adipose progenitors promotes insulin-independent muscle glucose uptake.ProNGF, a cytokine induced after myocardial infarction in humans, targets pericytes to promote microvascular damage and activationPatchy deletion of Bmpr1a potentiates proximal pulmonary artery remodeling in mice exposed to chronic hypoxiaMolecular pathogenesis of pulmonary arterial hypertensionStructure and composition of pulmonary arteries, capillaries, and veins.Elastin insufficiency predisposes to elevated pulmonary circulatory pressures through changes in elastic artery structureTie2-mediated loss of peroxisome proliferator-activated receptor-gamma in mice causes PDGF receptor-beta-dependent pulmonary arterial muscularization.BMP signaling in vascular development and disease.Molecular pathogenesis and current pathology of pulmonary hypertension.Restoring BMPRII functions in pulmonary arterial hypertension: opportunities, challenges and limitations.Polygenic Causes of Congenital Diaphragmatic Hernia Produce Common Lung Pathologies.Involvement of BMPR2 in the protective effect of fluoxetine against monocrotaline-induced endothelial apoptosis in rats.Ectopic upregulation of membrane-bound IL6R drives vascular remodeling in pulmonary arterial hypertension
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P2860
Smooth muscle protein 22alpha-mediated patchy deletion of Bmpr1a impairs cardiac contractility but protects against pulmonary vascular remodeling.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 13 December 2007
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Smooth muscle protein 22alpha- ...... pulmonary vascular remodeling.
@en
Smooth muscle protein 22alpha- ...... pulmonary vascular remodeling.
@nl
type
label
Smooth muscle protein 22alpha- ...... pulmonary vascular remodeling.
@en
Smooth muscle protein 22alpha- ...... pulmonary vascular remodeling.
@nl
prefLabel
Smooth muscle protein 22alpha- ...... pulmonary vascular remodeling.
@en
Smooth muscle protein 22alpha- ...... pulmonary vascular remodeling.
@nl
P2093
P2860
P1433
P1476
Smooth muscle protein 22alpha- ...... pulmonary vascular remodeling.
@en
P2093
Ahmad Y Sheikh
Christophe Guignabert
Lingli Wang
Marlene Rabinovitch
Nesrine El-Bizri
Robert P Mecham
Russell H Knutsen
Sandra L Merklinger
Takashi Urashima
Tushar Desai
P2860
P304
P356
10.1161/CIRCRESAHA.107.161059
P577
2007-12-13T00:00:00Z