Single-cell transcriptomic profile of human pulmonary artery endothelial cells in health and pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is an insidious disease characterized by severe remodeling of the pulmonary vasculature caused in part by pathologic changes of endothelial cell functions. Although heterogeneity of endothelial cells across various vascular beds is well known, the diversity amon...

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Detalles Bibliográficos
Autores principales: Asosingh, Kewal, Comhair, Suzy, Mavrakis, Lori, Xu, Weiling, Horton, Dean, Taylor, Ian, Tkachenko, Svyatoslav, Hu, Bo, Erzurum, Serpil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289993/
https://www.ncbi.nlm.nih.gov/pubmed/34282213
http://dx.doi.org/10.1038/s41598-021-94163-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289993/
https://www.ncbi.nlm.nih.gov/pubmed/34282213
http://dx.doi.org/10.1038/s41598-021-94163-y

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