HSP47: A Therapeutic Target in Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by a progressive decline in lung function and poor prognosis. The deposition of the extracellular matrix (ECM) by myofibroblasts contributes to the stiffening of lung tissue and impaired oxygen exchange in IPF. Type I collag...

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Detalles Bibliográficos
Autores principales: Sakamoto, Noriho, Okuno, Daisuke, Tokito, Takatomo, Yura, Hirokazu, Kido, Takashi, Ishimoto, Hiroshi, Tanaka, Yoshimasa, Mukae, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525413/
https://www.ncbi.nlm.nih.gov/pubmed/37760828
http://dx.doi.org/10.3390/biomedicines11092387

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525413/
https://www.ncbi.nlm.nih.gov/pubmed/37760828
http://dx.doi.org/10.3390/biomedicines11092387

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