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3 Results
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miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR ‐101 that regulate WISP1 expressionJournal of Pathology, 2021, 253 (2), pp.186-197. ⟨10.1002/path.5571⟩
Journal articles
hal-03234350v1
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Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR geneJournal of Cystic Fibrosis, 2019, 18 (4), pp.468-475. ⟨10.1016/j.jcf.2018.10.012⟩
Journal articles
hal-02400710v1
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Splicing mutations in the CFTR gene as therapeutic targetsGene Therapy, In press, ⟨10.1038/s41434-022-00347-0⟩
Journal articles
hal-03686178v1
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