Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a rare disorder associated with high morbidity and mortality despite currently available treatments. We compared the phosphoproteome of lung tissue from subjects with idiopathic PAH (iPAH) obtained at the time of lung transplant with control lung tissue. The...

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Detalles Bibliográficos
Autores principales: Sitapara, Ravikumar, Lam, TuKiet T., Gandjeva, Aneta, Tuder, Rubin M., Zisman, Lawrence S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711668/
https://www.ncbi.nlm.nih.gov/pubmed/34966541
http://dx.doi.org/10.1177/20458940211031109

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711668/
https://www.ncbi.nlm.nih.gov/pubmed/34966541
http://dx.doi.org/10.1177/20458940211031109

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