Lipid analysis has been a crucial source of information in cystic fibrosis (CF). New methodologies for qualitative and quantitative lipidomics allow evaluation of a large number of samples, of special interest in patient screening for diagnostic and prognostic biological markers, as well as in cell physiology. In this chapter, two new complementary approaches are described: matrix-assisted laser desorption coupled to time of flight (MALDI-TOF-ClinProTools™) and liquid chromatography coupled to ion trap mass spectrometry (LC-MS( n )). MALDI-TOF-ClinProTools™ offers a large unbiased screening for the discovery of potential lipid alterations in diseased patients. LC-MS( n ) represents a state-of-the-art lipidomic tool for the identification an...
International audience: A consistent body of research has linked cystic fibrosis (CF) with variation...
In recent years, a number of drugs have been approved for the treatment of cystic fibrosis (CF). Amo...
AbstractObjectivesTo assess fatty acid (FA) profiles in whole blood of 90 cystic fibrosis patients (...
Lipid analysis has been a crucial source of information in cystic fibrosis (CF). New methodologies f...
The aim of this study was to search for lipid signatures in blood plasma from cystic fibrosis (CF) p...
AbstractLipid studies in the context of cystic fibrosis have been addressed from two perspectives: t...
Cystic fibrosis (CF) is associated with abnormal lipid metabolism. We have recently shown variations...
Cystic fibrosis (CF) is a genetic disease characterized by abnormal levels of essential fatty acids ...
Abstract Cystic fibrosis is a hereditary metabolic disorder characterized by impaired traffic of chl...
Since phosphatidylcholine (PC) is the most abundant phospholipid (PL) class in human serum, its conc...
BACKGROUND: An altered distribution of fatty acids in cells and tissues is found in patients with cy...
Mass spectrometry together with fast photochemical oxidation of proteins was utilized to study struc...
Background: An altered distribution of fatty acids in cells and tissues is found in patients with cy...
OBJECTIVES: To assess fatty acid (FA) profiles in whole blood of 90 cystic fibrosis patients (CF) an...
Objectives: To assess fatty acid (FA) profiles in whole blood of 90 cystic fibrosis patients (CF) an...
International audience: A consistent body of research has linked cystic fibrosis (CF) with variation...
In recent years, a number of drugs have been approved for the treatment of cystic fibrosis (CF). Amo...
AbstractObjectivesTo assess fatty acid (FA) profiles in whole blood of 90 cystic fibrosis patients (...
Lipid analysis has been a crucial source of information in cystic fibrosis (CF). New methodologies f...
The aim of this study was to search for lipid signatures in blood plasma from cystic fibrosis (CF) p...
AbstractLipid studies in the context of cystic fibrosis have been addressed from two perspectives: t...
Cystic fibrosis (CF) is associated with abnormal lipid metabolism. We have recently shown variations...
Cystic fibrosis (CF) is a genetic disease characterized by abnormal levels of essential fatty acids ...
Abstract Cystic fibrosis is a hereditary metabolic disorder characterized by impaired traffic of chl...
Since phosphatidylcholine (PC) is the most abundant phospholipid (PL) class in human serum, its conc...
BACKGROUND: An altered distribution of fatty acids in cells and tissues is found in patients with cy...
Mass spectrometry together with fast photochemical oxidation of proteins was utilized to study struc...
Background: An altered distribution of fatty acids in cells and tissues is found in patients with cy...
OBJECTIVES: To assess fatty acid (FA) profiles in whole blood of 90 cystic fibrosis patients (CF) an...
Objectives: To assess fatty acid (FA) profiles in whole blood of 90 cystic fibrosis patients (CF) an...
International audience: A consistent body of research has linked cystic fibrosis (CF) with variation...
In recent years, a number of drugs have been approved for the treatment of cystic fibrosis (CF). Amo...
AbstractObjectivesTo assess fatty acid (FA) profiles in whole blood of 90 cystic fibrosis patients (...