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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Detalles Bibliográficos
Autores principales: van Uden, Denise, Boomars, Karin, Kool, Mirjam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349774/
https://www.ncbi.nlm.nih.gov/pubmed/30723471
http://dx.doi.org/10.3389/fimmu.2019.00011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349774/
https://www.ncbi.nlm.nih.gov/pubmed/30723471
http://dx.doi.org/10.3389/fimmu.2019.00011

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