Cargando…

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...

Descripción completa

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

Ejemplares similares

Impaired Ratio of Unsaturated to Saturated Non-Esterified Fatty Acids in Saliva from Patients with Cystic Fibrosis
por: Gelzo, Monica, et al.
Publicado: (2020)

Oxylipin profile in saliva from patients with cystic fibrosis reveals a balance between pro-resolving and pro-inflammatory molecules
por: Carnovale, Vincenzo, et al.
Publicado: (2022)

Salivary Cytokines and Airways Disease Severity in Patients with Cystic Fibrosis
por: Castaldo, Alice, et al.
Publicado: (2020)

Physical Activity Regulates TNFα and IL-6 Expression to Counteract Inflammation in Cystic Fibrosis Patients
por: Nigro, Ersilia, et al.
Publicado: (2021)

Cystic Fibrosis Patients with F508del/Minimal Function Genotype: Laboratory and Nutritional Evaluations after One Year of Elexacaftor/Tezacaftor/Ivacaftor Treatment
por: Carnovale, Vincenzo, et al.
Publicado: (2022)

TAS2R38 is a novel modifier gene in patients with cystic fibrosis
por: Castaldo, Alice, et al.
Publicado: (2020)

Adiponectin Expression Is Modulated by Long-Term Physical Activity in Adult Patients Affected by Cystic Fibrosis
por: Polito, Rita, et al.
Publicado: (2019)

Challenges in Metabolomics-Based Tests, Biomarkers Revealed by Metabolomic Analysis, and the Promise of the Application of Metabolomics in Precision Medicine
por: Di Minno, Alessandro, et al.
Publicado: (2022)

Extensive CFTR Gene Analysis Revealed a Higher Occurrence of Cystic Fibrosis Transmembrane Regulator-Related Disorders (CFTR-RD) among CF Carriers
por: Esposito, Maria Valeria, et al.
Publicado: (2020)

Impaired cholesterol metabolism in the mouse model of cystic fibrosis. A preliminary study
por: Amato, Felice, et al.
Publicado: (2021)

Lung Microbiome in Cystic Fibrosis
por: Scialo, Filippo, et al.
Publicado: (2021)

The Serum Metabolome of Moderate and Severe COVID-19 Patients Reflects Possible Liver Alterations Involving Carbon and Nitrogen Metabolism
por: Caterino, Marianna, et al.
Publicado: (2021)

Employment Status and Work Ability in Adults with Cystic Fibrosis
por: Leso, Veruscka, et al.
Publicado: (2021)

Prenatal Diagnosis of Cystic Fibrosis and Hemophilia: Incidental Findings and Weak Points
por: Comegna, Marika, et al.
Publicado: (2019)

Dysregulation of lipid metabolism and pathological inflammation in patients with COVID-19
por: Caterino, Marianna, et al.
Publicado: (2021)

Incidental late diagnosis of cystic fibrosis following AH1N1 influenza virus pneumonia: a case report
por: Iadevaia, Carlo, et al.
Publicado: (2017)

Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study
por: Maglione, Marco, et al.
Publicado: (2017)

Targeted Metabolomic Analysis of a Mucopolysaccharidosis IIIB Mouse Model Reveals an Imbalance of Branched-Chain Amino Acid and Fatty Acid Metabolism
por: De Pasquale, Valeria, et al.
Publicado: (2020)

COVIDomics: The Proteomic and Metabolomic Signatures of COVID-19
por: Costanzo, Michele, et al.
Publicado: (2022)

WS14.3 Virtual consultation in cystic fibrosis: an Italian experience
por: Carnovale, V., et al.
Publicado: (2021)

Proteomic and Bioinformatic Investigation of Altered Pathways in Neuroglobin-Deficient Breast Cancer Cells
por: Costanzo, Michele, et al.
Publicado: (2021)

Immunophenotyping of peripheral blood cells allows to discriminate MIS-C and Kawasaki disease
por: Castaldo, Alice, et al.
Publicado: (2022)

Dataset of a comparative proteomics experiment in a methylmalonyl-CoA mutase knockout HEK 293 cell model
por: Costanzo, Michele, et al.
Publicado: (2020)

Proteomics Reveals that Methylmalonyl-CoA Mutase Modulates Cell Architecture and Increases Susceptibility to Stress
por: Costanzo, Michele, et al.
Publicado: (2020)

Targeted lipidomics data of COVID-19 patients
por: Costanzo, Michele, et al.
Publicado: (2023)

Elevated sweat chloride test: is it always cystic fibrosis?
por: Cimbalo, C., et al.
Publicado: (2021)

Clinical expression of cystic fibrosis in a large cohort of Italian siblings
por: Terlizzi, Vito, et al.
Publicado: (2018)

Cystic Fibrosis-Screening Positive Inconclusive Diagnosis: Newborn Screening and Long-Term Follow-Up Permits to Early Identify Patients with CFTR-Related Disorders
por: Castaldo, Alice, et al.
Publicado: (2020)

MIS-C: A COVID-19-as sociated condition between hypoimmunity and hyperimmunity
por: Gelzo, Monica, et al.
Publicado: (2022)

Elexacaftor/Tezacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for the F508del Mutation and Advanced Lung Disease: A 48-Week Observational Study
por: Carnovale, Vincenzo, et al.
Publicado: (2022)

Cystic Fibrosis: Recent Insights into Inhaled Antibiotic Treatment and Future Perspectives
por: Taccetti, Giovanni, et al.
Publicado: (2021)

The Diagnosis of Cystic Fibrosis in Adult Age. Data from the Italian Registry
por: Padoan, Rita, et al.
Publicado: (2021)

Multi-Omics Studies Unveil Extraciliary Functions of BBS10 and Show Metabolic Aberrations Underlying Renal Disease in Bardet–Biedl Syndrome
por: Marchese, Emanuela, et al.
Publicado: (2022)

Gene Mutation in MicroRNA Target Sites of CFTR Gene: A Novel Pathogenetic Mechanism in Cystic Fibrosis?
por: Amato, Felice, et al.
Publicado: (2013)

Proteome data of neuroblastoma cells overexpressing Neuroglobin
por: Costanzo, Michele, et al.
Publicado: (2022)

Non-invasive tools for detection of liver disease in children and adolescents with cystic fibrosis
por: Tosco, Antonella, et al.
Publicado: (2021)

Saliva as a potential tool for cystic fibrosis diagnosis
por: Gonçalves, Aline Cristina, et al.
Publicado: (2013)

Microbiology of airway disease in a cohort of patients with Cystic Fibrosis
por: Lambiase, Antonietta, et al.
Publicado: (2006)

NGS Gene Panel Analysis Revealed Novel Mutations in Patients with Rare Congenital Diarrheal Disorders
por: Esposito, Maria Valeria, et al.
Publicado: (2021)

An Innovative Lipidomic Workflow to Investigate the Lipid Profile in a Cystic Fibrosis Cell Line
por: Dei Cas, Michele, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_rhbt13dfmc4ih0oovqsl0kr09p