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Reference percentiles for FEV1 and BMI in European children and adults with c...
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Evidence for decline in the incidence of cystic fibrosis: a 35-year observati...
International audience -
Gα12 and Gα13 in cystic fibrosis : Role in F508del-CFTR degradation and in th...
F508del, the most frequent mutation found in cystic fibrosis (CF) population, impacts CFTR (Cystic Fibrosis Transmembrane conductance Regulator) trafficking and causes... -
Enzyme replacement therapy for pancreatic insufficiency: present and future.
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Combined Computational-Experimental Analyses of CFTR Exon Strength Uncover Pr...
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Folate-equipped nanolipoplexes mediated efficient gene transfer into human ep...
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Study of biological and antimicrobial properties of pyocyanine, redox-active ...
Pyocyanin (PYO) is a blue-green phenazin, specifically produced by the opportunistic bacterium Pseudomonas aeruginosa (Pa). Aerobic toxicity of PYO toward mammalian... -
Ancestral haplotype 8.1 in cystic fibrosis
Cystic fibrosis is an autosomic recessive disease due to mutations in the gene CFTR. There is a great phenotypic variability among patients with identical mutations... -
Bacteriophages therapy to treat Pseudomonas aeruginosa infections in Cystic F...
Repetitive antibiotic treatments against Pseudomonas aeruginosa in cystic fibrosis patients lead to the emergence of multi-resistant strains calling for new... -
Proposal of a quantitative PCR-based protocol for an optimal Pseudomonas aeru...
International audience -
The soluble innate immune receptor PTX3 is functionaly altered in cystic fibr...
The prototypic long pentraxin PTX3, a soluble pattern recognition receptor, plays an important role in innate defense against selected pathogens, by favoring their... -
Probiotics: A new way to fight bacterial pulmonary infections?
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Bone health in cystic fibrosis: use of oral biphosphonates
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The F508del mutation in cystic fibrosis transmembrane conductance regulator g...
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Nucleotide-binding domains of human Cystic Fibrosis Transmembrane Conductance...
The cystic fibrosis transmembrane conductance regulator (CFTR) protein is encoded by the gene that is defective in cystic fibrosis, the most common lethal inherited... -
Epidemiological study of infections causing Pseudomonas aeruginosa strains an...
The use of viruses of bacteria commonly called bacteriophages could constitute an efficient complement to antibiotics. During my PhD, I have characterized phages... -
Distribution in the cystic fibrosis context and ecology of the different spec...
The Pseudallescheria boydii / Scedosporium apiospermum species complex ranks second among the filamentous fungi isolated from sputum samples of patients with cystic... -
Enhanced F508del-CFTR channel activity ameliorates bone pathology in murine c...
International audience
