Inhibition of hyaluronan synthesis attenuates pulmonary hypertension associated with lung fibrosis

BACKGROUND AND PURPOSE: Group III pulmonary hypertension (PH) is a highly lethal and widespread lung disorder that is a common complication in idiopathic pulmonary fibrosis (IPF) where it is considered to be the single most significant predictor of mortality. While increased levels of hyaluronan hav...

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Detaylı Bibliyografya
Yayımlandı:Br J Pharmacol
Asıl Yazarlar: Collum, Scott D, Chen, Ning‐Yuan, Hernandez, Adriana M, Hanmandlu, Ankit, Sweeney, Heather, Mertens, Tinne C J, Weng, Tingting, Luo, Fayong, Molina, Jose G, Davies, Jonathan, Horan, Ian P, Morrell, Nick W, Amione‐Guerra, Javier, Al‐Jabbari, Odeaa, Youker, Keith, Sun, Wenchao, Rajadas, Jayakumar, Bollyky, Paul L, Akkanti, Bindu H, Jyothula, Soma, Sinha, Neeraj, Guha, Ashrith, Karmouty‐Quintana, Harry
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2017
Konular:
Research Papers
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5595757/
https://ncbi.nlm.nih.gov/pubmed/28688167
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bph.13947
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