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The International Journal of Biochemistry & Cell Biology|March 18, 2014
Genetics of cystic fibrosis: CFTR mutation classifications toward genotype-based CF therapiesPascale Fanen, Adeline Wohlhuter-Haddad, Alexandre Hinzpeter
International Journal of Molecular Sciences|October 13, 2021
Structure-Based Understanding of ABCA3 VariantsMarion Onnée, Pascale Fanen, Isabelle Callebaut, et al.
Biochemical Pharmacology|August 7, 2024
ABC transporters involved in respiratory and cholestatic diseases: From rare to very rare monogenic diseasesMounia Lakli, Marion Onnée, Thomas Carrez, et al.
Frontiers in Physiology|June 20, 2022
The Impact of Air Pollution on the Course of Cystic Fibrosis: A ReviewMarion Blayac, Patrice Coll, Valérie Urbach, et al.
American Journal of Physiology. Cell Physiology|March 7, 2002
Distribution of ClC-2 chloride channel in rat and human epithelial tissuesJoanna Lipecka, Moëz Bali, Annick Thomas, et al.
The Journal of Biological Chemistry|September 25, 2007
Modulation of epithelial sodium channel trafficking and function by sodium 4-phenylbutyrate in human nasal epithelial cellsVirginie Prulière-Escabasse, Carole Planès, Estelle Escudier, et al.
International Journal of Molecular Sciences|April 30, 2021
Small Hsps as Therapeutic Targets of Cystic Fibrosis Transmembrane Conductance Regulator ProteinStéphanie Simon, Abdel Aissat, Fanny Degrugillier, et al.
Annals of Thoracic Medicine|August 16, 2017
The most frequent ABCA3 nonsense mutation -p.Tyr1515* (Y1515X) causing lethal neonatal respiratory failure in a term neonateAlNashmi AlAnazi, Ralph Epaud, Humariya Heena, et al.
American Journal of Physiology. Cell Physiology|June 10, 2005
Cell-specific posttranscriptional regulation of CFTR gene expression via influence of MAPK cascades on 3'UTR part of transcriptsMaryvonne Baudouin-Legros, Alexandre Hinzpeter, Amandine Jaulmes, et al.
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