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Human Genetics|March 4, 2005
A neutral variant involved in a complex CFTR allele contributes to a severe cystic fibrosis phenotypeJérôme Clain, Jacqueline Lehmann-Che, Emmanuelle Girodon, et al.
FEBS Letters|February 5, 2004
Altered channel gating mechanism for CFTR inhibition by a high-affinity thiazolidinone blockerAlessandro Taddei, Chiara Folli, Olga Zegarra-Moran, et al.
Biochimica Et Biophysica Acta|February 13, 2008
CSN5 binds to misfolded CFTR and promotes its degradationGaëlle Tanguy, Loïc Drévillon, Nicole Arous, et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma|September 23, 2020
Association analysis of the surfactant protein-C gene to childhood asthmaMalek Nefzi, Imen Wahabi, Sondess Hadj Fredj, et al.
Pediatric Allergy, Immunology, and Pulmonology|September 19, 2022
Variable Expression of Lung Disease Due to a Novel Homozygous <i>ABCA3</i> VariantSamia Hamouda, Alix de Becdelièvre, Salma Ben Ameur, et al.
Plos One|April 13, 2011
COMMD1-mediated ubiquitination regulates CFTR traffickingLoïc Drévillon, Gaëlle Tanguy, Alexandre Hinzpeter, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|September 14, 2004
TGF-beta 1 downregulates CFTR expression and function in nasal polyps of non-CF patientsVirginie Prulière-Escabasse, Pascale Fanen, Anne Catherine Dazy, et al.
The International Journal of Biochemistry & Cell Biology|July 30, 2013
COMMD1 modulates noxious inflammation in cystic fibrosisAlix de Becdelièvre, Jérémy Rocca, Abdel Aissat, et al.
European Journal of Human Genetics : EJHG|March 16, 2017
Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotypeCéline Delestrain, Stéphanie Simon, Abdel Aissat, et al.
Proteomics|November 6, 2004
Global proteomic approach unmasks involvement of keratins 8 and 18 in the delivery of cystic fibrosis transmembrane conductance regulator (CFTR)/deltaF508-CFTR to the plasma membraneNoélie Davezac, Danielle Tondelier, Joanna Lipecka, et al.
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