Evidence of Dysfunction of Endothelial Progenitors in Pulmonary Arterial Hypertension

Rationale: Severe pulmonary arterial hypertension (PAH) is characterized by the formation of plexiform lesions and concentric intimal fibrosis in small pulmonary arteries. The origin of cells contributing to these vascular lesions is uncertain. Endogenous endothelial progenitor cells are potential c...

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Détails bibliographiques
Auteurs principaux: Toshner, Mark, Voswinckel, Robert, Southwood, Mark, Al-Lamki, Rafia, Howard, Luke S. G., Marchesan, Denis, Yang, Jun, Suntharalingam, Jay, Soon, Elaine, Exley, Andrew, Stewart, Susan, Hecker, Markus, Zhu, Zhenping, Gehling, Ursula, Seeger, Werner, Pepke-Zaba, Joanna, Morrell, Nicholas W.
Format: Artigo
Langue:Inglês
Publié: American Thoracic Society 2009
Sujets:
G. Pulmonary Vascular Disease
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2778151/
https://ncbi.nlm.nih.gov/pubmed/19628780
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.200810-1662OC
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