PD-L1 Expression in Patients with Idiopathic Pulmonary Fibrosis

Background: Idiopathic pulmonary fibrosis (IPF) is the most common and severe form within the group of idiopathic interstitial pneumonias. It is characterized by repetitive alveolar injury in genetically susceptible individuals and abnormal wound healing, leading to dysregulated bronchiolar prolifer...

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Detalles Bibliográficos
Autores principales: Kronborg-White, Sissel, Madsen, Line Bille, Bendstrup, Elisabeth, Poletti, Venerino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658518/
https://www.ncbi.nlm.nih.gov/pubmed/34884264
http://dx.doi.org/10.3390/jcm10235562

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658518/
https://www.ncbi.nlm.nih.gov/pubmed/34884264
http://dx.doi.org/10.3390/jcm10235562

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