Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pauline, Bardin"'
Publikováno v:
Breathe, Vol 19, Iss 4 (2023)
Externí odkaz:
https://doaj.org/article/e7ba06c153344794a30941027fb934ef
Autor:
Christie Mitri, Zhengzhong Xu, Pauline Bardin, Harriet Corvol, Lhousseine Touqui, Olivier Tabary
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Cystic fibrosis (CF) is the most common genetic disorder among Caucasians, estimated to affect more than 70,000 people in the world. Severe and persistent bronchial inflammation and chronic bacterial infection, along with airway mucus obstruction, ar
Externí odkaz:
https://doaj.org/article/8b5f978c7d3a4c3cb3025ba2c69b94ab
Autor:
Pauline Bardin, Tobias Foussignière, Nathalie Rousselet, Carine Rebeyrol, Joanna C. Porter, Harriet Corvol, Olivier Tabary
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Cystic fibrosis (CF) results from deficient CF transmembrane conductance regulator (CFTR) protein activity leading to defective epithelial ion transport. Pulmonary degradation due to excessive inflammation is the main cause of morbidity and mortality
Externí odkaz:
https://doaj.org/article/2a645916881b4bbc9c54f1e41362ea1b
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and remains the most common life-shortening diseases affecting the exocrine organs. The absence of this channel results in an imbalance
Externí odkaz:
https://doaj.org/article/6a233c8e33a149c79ae8619d09fd836e
Publikováno v:
médecine/sciences
médecine/sciences, EDP Sciences, 2018, 34 (6-7), pp.554-562. ⟨10.1051/medsci/20183406015⟩
médecine/sciences, EDP Sciences, 2018, 34 (6-7), pp.554-562. ⟨10.1051/medsci/20183406015⟩
International audience; La mucoviscidose est la plus fréquente des maladies génétiques dans les populations d’origine caucasienne, caractérisée par des mutations du gène codant le canal chlorure CFTR. Bien que ce gène soit connu depuis 1989,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8a94cba753fdb73d39f041f8428bd89
https://doi.org/10.1051/medsci/20183406015
https://doi.org/10.1051/medsci/20183406015
Autor:
Pauline, Bardin, Emmeline, Marchal-Duval, Florence, Sonneville, Sabine, Blouquit-Laye, Nathalie, Rousselet, Philippe, Le Rouzic, Harriet, Corvol, Olivier, Tabary
Publikováno v:
The Journal of pathology and bacteriology
The Journal of pathology and bacteriology, John Wiley & Sons, 2018, 245 (4), pp.410-420. ⟨10.1002/path.5095⟩
The Journal of pathology and bacteriology, John Wiley & Sons, 2018, 245 (4), pp.410-420. ⟨10.1002/path.5095⟩
International audience; Cystic fibrosis (CF) is the most common lethal genetic disease, caused by CFTR (cystic fibrosis transmembrane conductance regulator) gene mutations. CF is characterized by an ionic imbalance and thickened mucus, which impair m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f906c6f3a0ccd6cf360edc36c538067d
https://www.hal.inserm.fr/inserm-02390385
https://www.hal.inserm.fr/inserm-02390385
Autor:
Nathalie Rousselet, Pauline Bardin, Sabine Blouquit-Laye, Philippe Le Rouzic, Harriet Corvol, Emmeline Marchal-Duval, Olivier Tabary, Florence Sonneville
Publikováno v:
The Journal of pathology and bacteriology
The Journal of pathology and bacteriology, John Wiley & Sons, 2018, 245 (4), pp.410-420. ⟨10.1002/path.5095⟩
The Journal of pathology and bacteriology, John Wiley & Sons, 2018, 245 (4), pp.410-420. ⟨10.1002/path.5095⟩
International audience; Cystic fibrosis (CF) is the most common lethal genetic disease, caused by CFTR (cystic fibrosis transmembrane conductance regulator) gene mutations. CF is characterized by an ionic imbalance and thickened mucus, which impair m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3936fe897630b448a6909972119762a9
https://www.hal.inserm.fr/inserm-02390385
https://www.hal.inserm.fr/inserm-02390385