Laddar...

Transcriptomic analysis of pulmonary artery smooth muscle cells identifies new potential therapeutic targets for idiopathic pulmonary arterial hypertension

BACKGROUND AND PURPOSE: Pulmonary arterial hypertension (PAH, type 1 pulmonary hypertension) has a 3‐year survival of ~50% and is in need of new, effective therapies. In PAH, remodelling of the pulmonary artery (PA) increases pulmonary vascular resistance and can result in right heart dysfunction an...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Br J Pharmacol
Huvudupphovsmän: Gorr, Matthew W., Sriram, Krishna, Muthusamy, Abinaya, Insel, Paul A.
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2020
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7348089/
https://ncbi.nlm.nih.gov/pubmed/32337710
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bph.15074
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!