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Frontiers in Pediatrics|February 3, 2023
Deciphering an isolated lung phenotype of NKX2-1 frameshift pathogenic variantCéline Delestrain, Abdel Aissat, Elodie Nattes, et al.
International Journal of Molecular Sciences|July 12, 2020
Phosphorylation of the Chaperone-Like HspB5 Rescues Trafficking and Function of F508del-CFTRFanny Degrugillier, Abdel Aissat, Virginie Prulière-Escabasse, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 4, 2009
Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiatorsAntonella Caputo, Alexandre Hinzpeter, Emanuela Caci, et al.
British Journal of Clinical Pharmacology|November 12, 2020
Methylprednisolone pulse treatment improves ProSP-C trafficking in twins with SFTPC mutation: An isoform story?Céline Delestrain, Abdel Aissat, Stéphanie Simon, et al.
Stem Cell Research|May 21, 2026
Generation of two iPSC lines carrying two cystic fibrosis rare intronic mutations c.1585-1G>A and c.1680-886A>G in the CFTR gene of the parental line PCIi033-A using CRISPR/Cas toolsBenjamin Simonneau, Sandrine Baghdoyan, Michel Cailleret, et al.
Pediatric Pulmonology|November 3, 2022
Inherited pulmonary surfactant metabolism disorders in Argentina: Differences between patients with SFTPC and ABCA3 variantsJuan E Balinotti, Camila Mallie, Alberto Maffey, et al.
Stem Cell Research|March 12, 2026
CRISPR-Cas9 genome editing in the parental iPSC line PCIi033-A to introduce the homozygous mutation p.F508del (c.1521_1523del) in the CFTR geneBenjamin Simonneau, Sandrine Baghdoyan, Michel Cailleret, et al.
British Journal of Pharmacology|February 20, 2016
New use for an old drug: COX-independent anti-inflammatory effects of sulindac in models of cystic fibrosisJérémy Rocca, Sylvie Manin, Anne Hulin, et al.
British Journal of Pharmacology|October 3, 2002
Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07Olga Zegarra-Moran, Leila Romio, Chiara Folli, et al.
Stem Cell Research|June 3, 2026
Generation of two iPSC lines each carrying a stop codon mutation, c.366T > A (p.Y122X) and c.1657C > T (p.R553X), in the CFTR gene from the parental line PCIi033-A using CRISPR/Cas9Benjamin Simonneau, Stecy Mienanzambi, Sandrine Baghdoyan, et al.
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