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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Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2009
Assuntos:
G. Pulmonary Vascular Disease
Acesso em linha: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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