<p>Light microscopy demonstrating immunohistochemical p65+ (pink)-staining in vascular cells in diseased pulmonary arteries in lung sections from pulmonary arterial hypertension (PAH) subjects. Pulmonary arterial endothelial cells show intense staining for p65+ as indicated with a black arrow (A and B). Pulmonary arterial smooth muscle cells (PASMC) stain positive for nuclear p65+ (black arrow) and p65-stain negative (unfilled arrow) (C). Results representative of those from 12 PAH subjects. Magnification x200.</p
ABSTRACT: The respective abundance of circulating endothelial cells and endothelial progenitor cells...
International audienceIdiopathic pulmonary arterial hypertension (IPAH) is a complex disease associa...
Background—Congenital heart disease can be complicated by pulmonary arterial hypertension (PAH), the...
<p>Macrophages (CD68+ cells, brown) are seen surrounding a diseased pulmonary artery in a post-trans...
<p>(A) Overall p65+ was increased in pulmonary arterial endothelial cells (EC) (62.3±2.9 vs. 14.4±3....
To assess activation of the inflammatory transcription factor NF-kappa B (NF-κB) in human idiopathic...
Objectives: To assess activation of the inflammatory transcription factor NF-kappa B (NF-kB) in huma...
To assess activation of the inflammatory transcription factor NF-kappa B (NF-κB) in human idiopathic...
<p>A) Representative images of NFATc3 (red) and smooth muscle alpha-actin (blue) immunostaining of l...
Pulmonary arterial hypertension (PAH) is a syndrome of dyspnea, fatigue, chest pain and syncope defi...
<p>A to C show pulmonary muscular arteries from Case 17 with intimal fibrotic changes and moderate m...
RATIONALE: Severe pulmonary arterial hypertension (PAH) is characterized by the formation of plexifo...
Pulmonary arterial hypertension (PAH) is a rare multifactorial disease characterized by abnormal hig...
<p><b>A–C</b> Confocal immunofluorescence images show phosphorylation of the NF-κB p65 subunit in lu...
(A) Representative merged immunofluorescence (IF) images of optical sections and Z-stacks obtained b...
ABSTRACT: The respective abundance of circulating endothelial cells and endothelial progenitor cells...
International audienceIdiopathic pulmonary arterial hypertension (IPAH) is a complex disease associa...
Background—Congenital heart disease can be complicated by pulmonary arterial hypertension (PAH), the...
<p>Macrophages (CD68+ cells, brown) are seen surrounding a diseased pulmonary artery in a post-trans...
<p>(A) Overall p65+ was increased in pulmonary arterial endothelial cells (EC) (62.3±2.9 vs. 14.4±3....
To assess activation of the inflammatory transcription factor NF-kappa B (NF-κB) in human idiopathic...
Objectives: To assess activation of the inflammatory transcription factor NF-kappa B (NF-kB) in huma...
To assess activation of the inflammatory transcription factor NF-kappa B (NF-κB) in human idiopathic...
<p>A) Representative images of NFATc3 (red) and smooth muscle alpha-actin (blue) immunostaining of l...
Pulmonary arterial hypertension (PAH) is a syndrome of dyspnea, fatigue, chest pain and syncope defi...
<p>A to C show pulmonary muscular arteries from Case 17 with intimal fibrotic changes and moderate m...
RATIONALE: Severe pulmonary arterial hypertension (PAH) is characterized by the formation of plexifo...
Pulmonary arterial hypertension (PAH) is a rare multifactorial disease characterized by abnormal hig...
<p><b>A–C</b> Confocal immunofluorescence images show phosphorylation of the NF-κB p65 subunit in lu...
(A) Representative merged immunofluorescence (IF) images of optical sections and Z-stacks obtained b...
ABSTRACT: The respective abundance of circulating endothelial cells and endothelial progenitor cells...
International audienceIdiopathic pulmonary arterial hypertension (IPAH) is a complex disease associa...
Background—Congenital heart disease can be complicated by pulmonary arterial hypertension (PAH), the...