B4GALT1 as a New Biomarker of Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a disease characterized by progressive scarring of the lung that involves the pulmonary interstitium. The disease may rapidly progress, leading to respiratory failure, and the long-term survival is poor. There are no accurate biomarkers available so far. Our ai...

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Detalles Bibliográficos
Autores principales: De Vitis, Claudia, D’Ascanio, Michela, Sacconi, Andrea, Pizzirusso, Dario, Salvati, Valentina, Mancini, Massimiliano, Scafetta, Giorgia, Cirombella, Roberto, Ascenzi, Francesca, Bruschini, Sara, Esposito, Antonella, Castelli, Silvia, Salvucci, Claudia, Teodonio, Leonardo, Sposato, Bruno, Catizone, Angela, Di Napoli, Arianna, Vecchione, Andrea, Ciliberto, Gennaro, Sciacchitano, Salvatore, Ricci, Alberto, Mancini, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738382/
https://www.ncbi.nlm.nih.gov/pubmed/36499368
http://dx.doi.org/10.3390/ijms232315040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738382/
https://www.ncbi.nlm.nih.gov/pubmed/36499368
http://dx.doi.org/10.3390/ijms232315040

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