Lipidomic alterations in human saliva from cystic fibrosis patients

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. Although the...

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Detalles Bibliográficos
Autores principales: Caterino, Marianna, Fedele, Roberta, Carnovale, Vincenzo, Castaldo, Alice, Gelzo, Monica, Iacotucci, Paola, Ruoppolo, Margherita, Castaldo, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837121/
https://www.ncbi.nlm.nih.gov/pubmed/36635275
http://dx.doi.org/10.1038/s41598-022-24429-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837121/
https://www.ncbi.nlm.nih.gov/pubmed/36635275
http://dx.doi.org/10.1038/s41598-022-24429-6

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