Lipidomic alterations in human saliva from cystic fibrosis patients

Abstract Cystic fibrosis is a hereditary metabolic disorder characterized by impaired traffic of chloride ions and water through membranes of the respiratory and gastrointestinal, that causes inadequate hydration of airway surfaces, dehydrated mucous secretions and a high-sodium chloride sweat. Alth...

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Bibliographic Details
Main Authors: Marianna Caterino, Roberta Fedele, Vincenzo Carnovale, Alice Castaldo, Monica Gelzo, Paola Iacotucci, Margherita Ruoppolo, Giuseppe Castaldo
Format: Article
Language:English
Published: Nature Portfolio 2023-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-24429-6