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Dendritic Cell Subsets and Effector Function in Idiopathic and Connective Tissue Disease-Associated Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a cardiopulmonary disease characterized by an incurable condition of the pulmonary vasculature, leading to increased pulmonary vascular resistance, elevated pulmonary arterial pressure resulting in progressive right ventricular failure and ultimately death. P...

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Detalhes bibliográficos
Publicado no:Front Immunol
Main Authors: van Uden, Denise, Boomars, Karin, Kool, Mirjam
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6349774/
https://ncbi.nlm.nih.gov/pubmed/30723471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2019.00011
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