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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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Detaylı Bibliyografya
Yayımlandı:Front Immunol
Asıl Yazarlar: van Uden, Denise, Boomars, Karin, Kool, Mirjam
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2019
Konular:
Online Erişim: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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