Dichotomous role of integrin‐β5 in lung endothelial cells

Pulmonary arterial hypertension (PAH) is a progressive, devastating disease, and its main histological manifestation is an occlusive pulmonary arteriopathy. One important functional component of PAH is aberrant endothelial cell (EC) function including apoptosis‐resistance, unchecked proliferation, a...

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Detalles Bibliográficos
Autores principales: Blanchard, Neil, Link, Patrick A., Farkas, Daniela, Harmon, Brennan, Hudson, Jaylen, Bogamuwa, Srimathi, Piper, Bryce, Authelet, Kayla, Cool, Carlyne D., Heise, Rebecca L., Freishtat, Robert, Farkas, Laszlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684688/
https://www.ncbi.nlm.nih.gov/pubmed/36438452
http://dx.doi.org/10.1002/pul2.12156

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684688/
https://www.ncbi.nlm.nih.gov/pubmed/36438452
http://dx.doi.org/10.1002/pul2.12156

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