Role of epidermal growth factor inhibition in experimental pulmonary hypertension.
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Therapeutic efficacy of TBC3711 in monocrotaline-induced pulmonary hypertensionEnhanced depolarization-induced pulmonary vasoconstriction following chronic hypoxia requires EGFR-dependent activation of NAD(P)H oxidase 2Calpain mediates pulmonary vascular remodeling in rodent models of pulmonary hypertension, and its inhibition attenuates pathologic features of diseaseInvolvement of mast cells in monocrotaline-induced pulmonary hypertension in rats.Platelet-derived growth factor receptor-β and epidermal growth factor receptor in pulmonary vasculature of systemic sclerosis-associated pulmonary arterial hypertension versus idiopathic pulmonary arterial hypertension and pulmonary veno-occlusive dEffects of chrysin (5,7-dihydroxyflavone) on vascular remodeling in hypoxia-induced pulmonary hypertension in ratsHypoxic pulmonary hypertension in mice with constitutively active platelet-derived growth factor receptor-β.Hyperplastic Growth of Pulmonary Artery Smooth Muscle Cells from Subjects with Pulmonary Arterial Hypertension Is Activated through JNK and p38 MAPK.A Critical Role of the mTOR/eIF2α Pathway in Hypoxia-Induced Pulmonary Hypertension.The H2S-generating enzymes cystathionine β-synthase and cystathionine γ-lyase play a role in vascular development during normal lung alveolarization.IGF-1 signaling in neonatal hypoxia-induced pulmonary hypertension: Role of epigenetic regulation.Trigeminal nerve injury ErbB3/ErbB2 promotes mechanical hypersensitivity.Signal transduction in the development of pulmonary arterial hypertensionA critical role for p130Cas in the progression of pulmonary hypertension in humans and rodents.Inhalation of the BK(Ca)-opener NS1619 attenuates right ventricular pressure and improves oxygenation in the rat monocrotaline model of pulmonary hypertension.Mechanisms of disease: pulmonary arterial hypertension.Update on pulmonary vascular diseases 2010.Imatinib mesylate for the treatment of pulmonary arterial hypertension.Anticipated classes of new medications and molecular targets for pulmonary arterial hypertensionSmooth muscle cell hypertrophy, proliferation, migration and apoptosis in pulmonary hypertension.Novel and emerging therapies for pulmonary hypertension.Endothelial nanomedicine for the treatment of pulmonary disease.Pathways and Drugs in Pulmonary Arterial Hypertension - Focus on the Role of Endothelin Receptor Antagonists.Novel investigational therapies for treating pulmonary arterial hypertension.Targeted elimination of activated hepatic stellate cells by an anti-epidermal growth factor-receptor single chain fragment variable antibody-tumor necrosis factor-related apoptosis-inducing ligand (scFv425-sTRAIL).The first Keystone Symposia Conference on pulmonary vascular isease and right ventricular dysfunction: Current concepts and future therapies.Csk/Src/EGFR signaling regulates migration of myofibroblasts and alveolarization.Fluorofenidone attenuates vascular remodeling in hypoxia-induced pulmonary hypertension of rats.Altered Redox Balance in the Development of Chronic Hypoxia-induced Pulmonary Hypertension.Complexity of macrophage migration inhibitory factor (MIF) and other angiogenic biomarkers profiling in pulmonary arterial hypertension.Finally, Progress in Pulmonary Hypertension Associated with Heart Failure with Preserved Ejection Fraction.Translational Advances in the Field of Pulmonary Hypertension. From Cancer Biology to New Pulmonary Arterial Hypertension Therapeutics. Targeting Cell Growth and Proliferation Signaling Hubs.Mouse Genome-Wide Association Study of Preclinical Group II Pulmonary Hypertension Identifies Epidermal Growth Factor Receptor.Redox regulation of epidermal growth factor receptor signaling during the development of pulmonary hypertension.Hypoxia enhances platelet-derived growth factor signaling in the pulmonary vasculature by down-regulation of protein tyrosine phosphatases.Sex differences in pulmonary arterial hypertension: role of infection and autoimmunity in the pathogenesis of disease.Hypoxic-induction of arginase II requires EGF-mediated EGFR activation in human pulmonary microvascular endothelial cells.Inhibition of Shp2 ameliorates monocrotaline-induced pulmonary arterial hypertension in ratsLow plasma stem cell factor combined with high transforming growth factor-α identifies high-risk patients in pulmonary arterial hypertension
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P2860
Role of epidermal growth factor inhibition in experimental pulmonary hypertension.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Role of epidermal growth factor inhibition in experimental pulmonary hypertension.
@en
Role of epidermal growth factor inhibition in experimental pulmonary hypertension.
@nl
type
label
Role of epidermal growth factor inhibition in experimental pulmonary hypertension.
@en
Role of epidermal growth factor inhibition in experimental pulmonary hypertension.
@nl
prefLabel
Role of epidermal growth factor inhibition in experimental pulmonary hypertension.
@en
Role of epidermal growth factor inhibition in experimental pulmonary hypertension.
@nl
P2093
P2860
P50
P1476
Role of epidermal growth factor inhibition in experimental pulmonary hypertension
@en
P2093
Aleksandra Tretyn
Bhola Kumar Dahal
Djuro Kosanovic
Gamal-Andre Banat
Rio Dumitrascu
Robert Voswinckel
Teodora Cornitescu
P2860
P304
P356
10.1164/RCCM.200811-1682OC
P407
P50
P577
2009-10-22T00:00:00Z