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Aleksander Edelman

Showing results (51-60 of 108) with videos related to

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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Proteomics techniques for cystic fibrosis researchMónica Roxo-Rosa, Noëlie Davezac, Noura Bensalem, et al.
Cellular and Molecular Life Sciences : CMLS|October 7, 2024
Novel gain-of-function mutants identify a critical region within CFTR membrane-spanning domain 2 controlling cAMP-dependent and ATP-independent channel activationSolène Castanier, Ahmad Elbahnsi, Benoit Chevalier, et al.
American Journal of Respiratory and Critical Care Medicine|February 15, 2005
Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotesIsabelle Sermet-Gaudelus, Michèle Déchaux, Benoît Vallée, et al.
International Journal of Molecular Sciences|September 15, 2020
Urinary Exosomes of Patients with Cystic Fibrosis Unravel CFTR-Related Renal DiseaseSebastien Gauthier, Iwona Pranke, Vincent Jung, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 20, 2025
CFTR correctors potentiate gating mutants causing cystic fibrosisSolène Castanier, Ahmad Elbahnsi, Benoit Chevalier, et al.
Plos One|November 7, 2009
A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patientsIda Chiara Guerrera, Giuseppe Astarita, Jean-Philippe Jais, et al.
Pediatric Research|November 1, 2002
Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutationIsabelle Sermet-Gaudelus, Benoit Vallée, Ilse Urbin, et al.
Thorax|August 10, 2017
<i>Pseudomonas aeruginosa</i> LasB protease impairs innate immunity in mice and humans by targeting a lung epithelial cystic fibrosis transmembrane regulator-IL-6-antimicrobial-repair pathwayVinciane Saint-Criq, Bérengère Villeret, Fabien Bastaert, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Measurement of halide efflux from cultured and primary airway epithelial cells using fluorescence indicatorsFelix Munkonge, Eric W F W Alton, Charlotte Andersson, et al.
Plos One|June 30, 2009
Peroxiredoxin 6 fails to limit phospholipid peroxidation in lung from Cftr-knockout mice subjected to oxidative challengeStéphanie Trudel, Mairead Kelly, Janine Fritsch, et al.
Pageof 11

Showing results (51-60 of 108) with videos related to

Sort By:
Pageof 11
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Proteomics techniques for cystic fibrosis researchMónica Roxo-Rosa, Noëlie Davezac, Noura Bensalem, et al.
Cellular and Molecular Life Sciences : CMLS|October 7, 2024
Novel gain-of-function mutants identify a critical region within CFTR membrane-spanning domain 2 controlling cAMP-dependent and ATP-independent channel activationSolène Castanier, Ahmad Elbahnsi, Benoit Chevalier, et al.
American Journal of Respiratory and Critical Care Medicine|February 15, 2005
Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotesIsabelle Sermet-Gaudelus, Michèle Déchaux, Benoît Vallée, et al.
International Journal of Molecular Sciences|September 15, 2020
Urinary Exosomes of Patients with Cystic Fibrosis Unravel CFTR-Related Renal DiseaseSebastien Gauthier, Iwona Pranke, Vincent Jung, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 20, 2025
CFTR correctors potentiate gating mutants causing cystic fibrosisSolène Castanier, Ahmad Elbahnsi, Benoit Chevalier, et al.
Plos One|November 7, 2009
A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patientsIda Chiara Guerrera, Giuseppe Astarita, Jean-Philippe Jais, et al.
Pediatric Research|November 1, 2002
Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutationIsabelle Sermet-Gaudelus, Benoit Vallée, Ilse Urbin, et al.
Thorax|August 10, 2017
<i>Pseudomonas aeruginosa</i> LasB protease impairs innate immunity in mice and humans by targeting a lung epithelial cystic fibrosis transmembrane regulator-IL-6-antimicrobial-repair pathwayVinciane Saint-Criq, Bérengère Villeret, Fabien Bastaert, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Measurement of halide efflux from cultured and primary airway epithelial cells using fluorescence indicatorsFelix Munkonge, Eric W F W Alton, Charlotte Andersson, et al.
Plos One|June 30, 2009
Peroxiredoxin 6 fails to limit phospholipid peroxidation in lung from Cftr-knockout mice subjected to oxidative challengeStéphanie Trudel, Mairead Kelly, Janine Fritsch, et al.
Pageof 11