E. Dreano

发表

Structure-guided combination therapy to potently improve the function of mutant CFTRs

A. Orth, P. McNamara, G. Lukács, 2018, Nature Medicine.

Another “String to the Bow” of PJ34, a Potent Poly(ADP-Ribose)Polymerase Inhibitor: An Antiplatelet Effect through P2Y12 Antagonism?

B. Palmier, C. Marchand-Leroux, I. Margaill, 2014, PloS one.

Elexacaftor/Tezacaftor/Ivacaftor alters branching morphogenesis of the mouse embryonic lung

C. Delacourt, Nicolas Houde, I. Sermet-Gaudelus, 2021, bioRxiv.

Impaired platelet activation and cAMP homeostasis in MRP 4-deficient mice Short title : MRP 4 controls platelet cAMP homeostasis

C. Denis, J. Hulot, A. Lompré, 2015 .

Impaired platelet activation and cAMP homeostasis in MRP4-deficient mice.

C. Denis, J. Hulot, A. Lompré, 2015, Blood.

MRP4 (ABCC4) as a potential pharmacologic target for cardiovascular disease.

J. Hulot, P. Gaussem, C. Bachelot-Loza, 2016, Pharmacological research.

Characterization of two rat models of cystic fibrosis—KO and F508del CFTR—Generated by Crispr‐Cas9

M. Bacchetta, J. Concordet, M. Chanson, 2019, Animal models and experimental medicine.

Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis

L. Touqui, J. Sallenave, X. Nassif, 2019, Scientific Reports.

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

O. Namy, P. Reix, L. Bidou, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Role of oculocerebrorenal syndrome of Lowe (OCRL) protein in megakaryocyte maturation, platelet production and functions: a study in patients with Lowe syndrome

C. Elie, R. Salomon, D. Baruch, 2021, British journal of haematology.

Isolation, cultivation, and application of primary respiratory epithelial cells obtained by nasal brushing, polyp samples, or lung explants

I. Sermet, D. Downey, L. Galietta, 2022, STAR protocols.

Elexacaftor/Tezacaftor/Ivacaftor Disrupts Respiratory Tract Development in a Murine Fetal Lung Explant Model

C. Delacourt, Nicolas Houde, I. Sermet-Gaudelus, 2022, American journal of respiratory cell and molecular biology.

Airway Surface Liquid pH Regulation in Airway Epithelium Current Understandings and Gaps in Knowledge

I. Sermet-Gaudelus, G. Planelles, E. Dreano, 2021, International journal of molecular sciences.

Involvement of CFTR in the pathogenesis of pulmonary arterial hypertension

M. Humbert, C. Péchoux, P. Burgel, 2021, European Respiratory Journal.

Topography of Background EEG Rhythms in Normal Subjects and in Patients with Cerebrovascular Disorders

D. Samson-Dollfus, Y. Vaschalde, E. Dreano, 1989 .

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

B. Kerem, P. Reix, P. Burgel, 2023, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.