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Your search keyword '"Chevalier, Benoit"' showing total 47 results

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1. Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and airway epithelial cells

4. Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children

5. Role of KCNK3 Dysfunction in Dasatinib-associated PAH and Endothelial Cell Dysfunction

6. Beyond Kaftrio : mechanistic insights to maximize N1303K-CFTR rescue

9. Keratin 8 is a scaffolding and regulatory protein of ERAD complexes

10. Role of KCNK3 Dysfunction in Dasatinib-associated Pulmonary Arterial Hypertension and Endothelial Cell Dysfunction.

11. Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epithelium

14. New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation

15. Author Correction: New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation

16. Targeting different binding sites in the CFTR structures allows to synergistically potentiate channel activity

18. Theratyping cystic fibrosis patients to guide elexacaftor/tezacaftor/ivacaftor out-of-label prescription

19. The U UGA C sequence provides a favorable context to ELX-02 induced CFTR readthrough

20. Design of Crotoxin-Based Peptides with Potentiator Activity Targeting the ΔF508NBD1 Cystic Fibrosis Transmembrane Conductance Regulator

22. Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forward

23. Keratin 8 is a scaffolding and regulatory protein of ERAD complexes

24. Cloning and variation of ground state intestinal stem cells

26. CFTR corrector efficacy is associated with occupancy of distinct binding sites

27. Quand t'es une queen

28. Prime editing functionally corrects cystic fibrosis-causing CFTRmutations in human organoids and airway epithelial cells

31. The “one airway, one disease” concept in light of Th2 inflammation

35. Cisvariants identified in F508del complex alleles modulate CFTR channel rescue by small molecules

36. Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons

37. Late Breaking Abstract - The “one airway, one disease” concept at the light of Th2 inflammation

38. <italic>Cis</italic> variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules.

39. Mo1861 Cloning and Variation of Ground State Intestinal Stem Cells

41. Identification of Keratinocyte Growth Factor as a Target of microRNA-155 in Lung Fibroblasts: Implication in Epithelial-Mesenchymal Interactions

43. Schistosomoses

47. Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules.

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