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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
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 |
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