Role of the PI3K/AKT pathway in modulating cytoskeleton rearrangements and phenotype switching in rat pulmonary arterial vascular smooth muscle cells
Z Fan, C Li, C Qin, L Xie, X Wang, Z Gao… - DNA and Cell …, 2014 - liebertpub.com
Pulmonary arterial smooth muscle cell (PASMC) phenotype switching, which is
characterized by changes in smooth muscle (SM)-specific gene expression, contributes to …
characterized by changes in smooth muscle (SM)-specific gene expression, contributes to …
[PDF][PDF] Pulmonary hypertension in idiopathic pulmonary fibrosis
Pulmonary hypertension (PH) is a common in patients with idiopathic pulmonary fibrosis
(IPF) referred for transplantation. When present, PH is associated with increased mortality …
(IPF) referred for transplantation. When present, PH is associated with increased mortality …
Sinus venosus adaptation models prolonged cardiovascular disease and reveals insights into evolutionary transitions of the vertebrate heart
JT Gafranek, E D'Aniello, P Ravisankar… - Nature …, 2023 - nature.com
How two-chambered hearts in basal vertebrates have evolved from single-chamber hearts
found in ancestral chordates remains unclear. Here, we show that the teleost sinus venosus …
found in ancestral chordates remains unclear. Here, we show that the teleost sinus venosus …
Role of oral sildenafil in severe pulmonary arterial hypertension: clinical efficacy and dose response relationship
BACKGROUND: Sildenafil (phosphodiesterase type 5 inhibitor) has been shown to be
effective in pulmonary arterial hypertension (PAH). We evaluated the efficacy and safety of …
effective in pulmonary arterial hypertension (PAH). We evaluated the efficacy and safety of …
DPP-4 inhibition: А novel therapeutic approach to the treatment of pulmonary hypertension?
M Anderluh, G Kocic, K Tomovic, H Kocic… - Pharmacology & …, 2019 - Elsevier
Pulmonary hypertension (PH) is a progressive disorder characterized by alterations of the
vascular structure and function in the lungs. Despite the success in its stabilisation by …
vascular structure and function in the lungs. Despite the success in its stabilisation by …
Deficiency of lung antioxidants in idiopathic pulmonary arterial hypertension
FA Masri, SAA Comhair… - Clinical and …, 2008 - Wiley Online Library
Idiopathic pulmonary arterial hypertension (IPAH) is associated with lower levels of the
pulmonary vasodilator nitric oxide (NO) and its biochemical reaction products (nitrite [NO2−] …
pulmonary vasodilator nitric oxide (NO) and its biochemical reaction products (nitrite [NO2−] …
Hypoxia induces downregulation of PPAR-γ in isolated pulmonary arterial smooth muscle cells and in rat lung via transforming growth factor-β signaling
K Gong, D Xing, P Li, B Aksut… - … of Physiology-Lung …, 2011 - journals.physiology.org
Chronic hypoxia activates transforming growth factor-β (TGF-β) signaling and leads to
pulmonary vascular remodeling. Pharmacological activation of peroxisome proliferator …
pulmonary vascular remodeling. Pharmacological activation of peroxisome proliferator …
Metabolic alterations in cardiopulmonary vascular dysfunction
Cardiovascular diseases (CVD) are the leading cause of death worldwide. CVD comprise a
range of diseases affecting the functionality of the heart and blood vessels, including acute …
range of diseases affecting the functionality of the heart and blood vessels, including acute …
[HTML][HTML] Pulmonary artery remodeling in transposition of the great arteries: relevance for neoaortic root dilatation
S Lalezari, MG Hazekamp, MM Bartelings… - The Journal of thoracic …, 2003 - Elsevier
OBJECTIVE: Transposition of the great arteries is currently treated by performing the arterial
switch operation. Dilatation of the neoaortic root is a late complication with unknown cause …
switch operation. Dilatation of the neoaortic root is a late complication with unknown cause …
Chemical and biological assessment of metal organic frameworks (MOFs) in pulmonary cells and in an acute in vivo model: relevance to pulmonary arterial …
NA Mohamed, RP Davies, PD Lickiss… - Pulmonary …, 2017 - journals.sagepub.com
Pulmonary arterial hypertension (PAH) is a progressive and debilitating condition. Despite
promoting vasodilation, current drugs have a therapeutic window within which they are …
promoting vasodilation, current drugs have a therapeutic window within which they are …