Emerging findings indicate there is a vital cross-talk between gut microbiota and the lungs,
which is known as gut–lung axis. The gut disturbances in lung diseases including allergy …

The human gut microbiome represents a complex ecosystem contributing essential
functions to its host. Recent large-scale metagenomic studies have provided insights into its …

Cystic fibrosis (CF) is a heritable, multiorgan disease that impacts all tissues that normally
express cystic fibrosis transmembrane conductance regulator (CFTR) protein. While the …

Mass Spectrometry (MS) allows the analysis of proteins and peptides through a variety of
methods, such as Electrospray Ionization-Mass Spectrometry (ESI-MS) or Matrix-Assisted …

Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance
regulator (CFTR) gene. Next to progressive airway disease, CF is also associated with …

Intestinal dysbiosis has been observed in children with cystic fibrosis (CF), yet the functional
consequences are poorly understood. We investigated the functional capacity of intestinal …

Abstract Background and Aims Cystic Fibrosis (CF) is associated with gut dysbiosis, local
and systemic inflammation, and impaired immune function. Gut microbiota dysbiosis results …

Unipept (https://unipept. ugent. be) is a web application for metaproteome data analysis, with
an initial focus on tryptic-peptide-based biodiversity analysis of MS/MS samples. Because …

Most infants with cystic fibrosis (CF) have pancreatic exocrine insufficiency that results in
nutrient malabsorption and requires oral pancreatic enzyme replacement. Newborn …

Cystic fibrosis (CF) is a life-limiting autosomal recessive multisystem disease. While its
burden of morbidity and mortality is classically associated with pulmonary disease, CF also …