… Furthermore, Masson’s trichrome staining of lung sections to evaluate fibrotic lesions
showed that recurrent LPS exposure led to prominent pulmonary fibrosis, and this fibrosis was …

… Amplification parameters consisted of initial denaturation at 95C for 10 min followed by 40
cycles of denaturation at 95C for 15 s and annealing and extension at 60C for 1 min. Relative …

The heritable form of pulmonary arterial hypertension (PAH) is typically caused by a mutation
in bone morphogenic protein receptor type 2 (BMPR2), and mice expressing Bmpr2 …

Background— Pulmonary arterial hypertension (PAH) is a proliferative disease of the
pulmonary vasculature that preferentially affects women. Estrogens such as the metabolite 16α-…

Pulmonary hypertension (PH) complicating chronic parenchymal lung disease, such as
idiopathic pulmonary fibrosis, results in significant morbidity and mortality. Since the hypoxia-…

… atrium (RA), right ventricle (RV) and pulmonary artery (PA, frames 1–2), left atrium (LA), left
ventricle (LV), aorta (AO, frames 3–4), then to the normally supplied intraventricular septum (S…

… from the dataset that map to the pathway divided by the total number of molecules that map
to the canonical pathways (indicated by the orange line and boxes), and (2) Fisher’s exact …

… The use, distribution or reproduction in other forums is permitted, provided the original
author(s) and the copyright owner are credited and that the original publication in this journal is …

… For measurements of activated TGF-β1, a 1:1 dilution of media to serum-free Dulbecco’s
modification of Eagle’s medium (DMEM, Corning CellGro) was prepared, and for …

BACKGROUND: Pulmonary hypertension (PH) in heart failure with preserved ejection
fraction (HFpEF) is a common and highly morbid syndrome, but mechanisms driving PH-HFpEF …