Proteomic Analysis Reveals Differential Expression Profiles in Idiopathic Pulmonary Fibrosis Cell Lines

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, irreversible lung disorder of unknown cause. This disease is characterized by profibrotic activation of resident pulmonary fibroblasts resulting in aberrant deposition of extracellular matrix (ECM) proteins. However, although much is kno...

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Detalles Bibliográficos
Autores principales: Velázquez-Enríquez, Juan Manuel, Ramírez-Hernández, Alma Aurora, Navarro, Luis Manuel Sánchez, Reyes-Avendaño, Itayetzi, González-García, Karina, Jiménez-Martínez, Cristian, Castro-Sánchez, Luis, Sánchez-Chino, Xariss Miryam, Vásquez-Garzón, Verónica Rocío, Baltiérrez-Hoyos, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105114/
https://www.ncbi.nlm.nih.gov/pubmed/35563422
http://dx.doi.org/10.3390/ijms23095032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105114/
https://www.ncbi.nlm.nih.gov/pubmed/35563422
http://dx.doi.org/10.3390/ijms23095032

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