Disease-specific platelet signaling defects in idiopathic pulmonary arterial hypertension

Idiopathic pulmonary arterial hypertension (IPAH) is a rapidly progressive disease with several treatment options. Long-term mortality remains high with great heterogeneity in treatment response. Even though most of the pathology of IPAH is observed in the lung, there is systemic involvement. Platel...

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Vydáno v:Am J Physiol Lung Cell Mol Physiol
Hlavní autoři: Aulak, Kulwant S., Al Abdi, Sami, Li, Ling, Crabb, Jack S., Ghosh, Arnab, Willard, Belinda, Stuehr, Dennis J., Crabb, John W., Dweik, Raed A., Tonelli, Adriano R.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Physiological Society 2021
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8174825/
https://ncbi.nlm.nih.gov/pubmed/33596129
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00500.2020
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