Dichotomous role of integrin‐β5 in lung endothelial cells
Dichotomous role of integrin‐β5 in lung endothelial cells
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Publisher
United States: John Wiley & Sons, Inc
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Language
English
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Publisher
United States: John Wiley & Sons, Inc
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Contents
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, and impaired migration. The mechanisms leading to a...
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Full title
Dichotomous role of integrin‐β5 in lung endothelial cells
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TN_cdi_doaj_primary_oai_doaj_org_article_7fa0178ec4104c688ee2af64722585df
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7fa0178ec4104c688ee2af64722585df
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ISSN
2045-8940,2045-8932
E-ISSN
2045-8940
DOI
10.1002/pul2.12156
