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WS19.1 LCI in young children with CF – N2 or SF6 ?

Journal of cystic fibrosis, 2017-06, Vol.16, p.S32-S32

2017

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218 Lack of T cells reduces structural lung damage in mice with cystic fibrosis-like lung disease

Journal of cystic fibrosis, 2017-06, Vol.16, p.S118-S118

2017

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The CFTR defect and Pseudomonas bronchiectasis: the missing link

Paediatric respiratory reviews, 2010, Vol.11, p.S48-S49

Mall, M.A

2010

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35 Nasal potential difference in βENaC-overexpressing mouse reveals pH-sensitive channel hyperactivity and shift of subunits stoichiometry

Journal of cystic fibrosis, 2017-06, Vol.16, p.S72-S72

2017

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75 Role of the IL1 signaling pathway in the development of type 2 airway inflammation in juvenile Scnn1b-Tg mice

Journal of cystic fibrosis, 2017-06, Vol.16, p.S83-S83

2017

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WS09.3 Abnormal ion transport in non-CF chronic rhinosinusitis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S16-S16

2017

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WS06.2 Altered epithelial Cl− secretion in primary human nasal epithelial cells of patients with chronic rhinosinusitis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S9-S10

2016

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38 Relationship between planar cell polarity protein network signaling and airway remodeling in CF

Journal of cystic fibrosis, 2017-06, Vol.16, p.S73-S73

2017

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WS17.3 SLC26A9 channel functionality is characterised in epithelial cells

Journal of cystic fibrosis, 2014-06, Vol.13, p.S35-S35

2014

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WS02.2 Role of soluble and membrane-associated neutrophil elastase activity in cystic fibrosis sputum

Journal of cystic fibrosis, 2017-06, Vol.16, p.S3-S3

2017

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WS07.4 MBW and MRI as sensitive markers of stable CF lung disease and at exacerbation in children and adolescents

Journal of cystic fibrosis, 2015-06, Vol.14, p.S13-S13

2015

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WS06.5 SLC26A9 chloride channels: Generation and functional characterization of stably-overexpressing FRT epithelial cells

Journal of cystic fibrosis, 2015-06, Vol.14, p.S12-S12

2015

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ePS06.3 Neutrophil elastase activity on the surface of sputum neutrophils is associated with severity of cystic fibrosis lung disease

Journal of cystic fibrosis, 2015-06, Vol.14, p.S53-S53

2015

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Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele

The New England journal of medicine, 2019-11, Vol.381 (19), p.1809-1819

2019

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EPS4.1 Longitudinal automated airway and air-trapping analysis on CT from school age children with mild cystic fibrosis lung disease

Journal of cystic fibrosis, 2017-06, Vol.16, p.S44-S44

2017

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WS13.1 QR-010, an investigational RNA therapeutic, improves CFTR activity in cystic fibrosis subjects homozygous for the F508del mutation

Journal of cystic fibrosis, 2017-06, Vol.16, p.S23-S23

2017

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P061 FTR-Modulator therapy during pregnancy in a mother with F508del carrier status and high-grade suspicion of cystic fibrosis in the foetus

Journal of cystic fibrosis, 2023-06, Vol.22, p.S81-S81

2023

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138 Dysregulation of epithelial miR-148b contributes to goblet cell metaplasia, inflammation and alveolar damage in cystic fibrosis lung disease

Journal of cystic fibrosis, 2015-06, Vol.14, p.S93-S93

2015

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WS23.3 ICM is sensitive to detect potentiation of CFTR-mediated Cl− secretion in patients with cystic fibrosis and the G551D mutation treated with ivacaftor

Journal of cystic fibrosis, 2014-06, Vol.13, p.S43-S43

2014

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WS04.1 Impaired mucus clearance promotes Aspergillus fumigatus-induced type 2 airway inflammation in cystic fibrosis-like lung disease in mice

Journal of cystic fibrosis, 2016-06, Vol.15, p.S6-S6

2016

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145 A novel tool to study neutrophil elastase activity on neutrophils from cystic fibrosis airway secretions

Journal of cystic fibrosis, 2012-06, Vol.11, p.S93-S93

2012

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Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes

The New England journal of medicine, 2021-08, Vol.385 (9), p.815-825

2021

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WS10.2 Hypoxic epithelial necrosis triggers neutrophilic inflammation via IL-1 receptor signaling in cystic fibrosis-like lung disease

Journal of cystic fibrosis, 2015-06, Vol.14, p.S20-S20

2015

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WS15.6 Upregulation of MicroRNA-148b in cystic fibrosis like lung disease of ßENaC-overexpressing mice

Journal of cystic fibrosis, 2012-06, Vol.11, p.S34-S34

2012

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P020 Therapy with elexacaftor/tezacaftor/ivacaftor in a patient with compound heterozygous CFTR mutation and the complex CFTR-allele Phe508del; Leu467Phe

Journal of cystic fibrosis, 2023-06, Vol.22, p.S69-S70

2023

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WS19.1 LCI in young children with CF – N2 or SF6 ?

218 Lack of T cells reduces structural lung damage in mice with cystic fibrosis-like lung disease

The CFTR defect and Pseudomonas bronchiectasis: the missing link

35 Nasal potential difference in βENaC-overexpressing mouse reveals pH-sensitive channel hyperactivity and shift of subunits stoichiometry

75 Role of the IL1 signaling pathway in the development of type 2 airway inflammation in juvenile Scnn1b-Tg mice

WS09.3 Abnormal ion transport in non-CF chronic rhinosinusitis

WS06.2 Altered epithelial Cl− secretion in primary human nasal epithelial cells of patients with chronic rhinosinusitis

38 Relationship between planar cell polarity protein network signaling and airway remodeling in CF

WS17.3 SLC26A9 channel functionality is characterised in epithelial cells

WS02.2 Role of soluble and membrane-associated neutrophil elastase activity in cystic fibrosis sputum

WS07.4 MBW and MRI as sensitive markers of stable CF lung disease and at exacerbation in children and adolescents

WS06.5 SLC26A9 chloride channels: Generation and functional characterization of stably-overexpressing FRT epithelial cells

ePS06.3 Neutrophil elastase activity on the surface of sputum neutrophils is associated with severity of cystic fibrosis lung disease

Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele

EPS4.1 Longitudinal automated airway and air-trapping analysis on CT from school age children with mild cystic fibrosis lung disease

WS13.1 QR-010, an investigational RNA therapeutic, improves CFTR activity in cystic fibrosis subjects homozygous for the F508del mutation

P061 FTR-Modulator therapy during pregnancy in a mother with F508del carrier status and high-grade suspicion of cystic fibrosis in the foetus

138 Dysregulation of epithelial miR-148b contributes to goblet cell metaplasia, inflammation and alveolar damage in cystic fibrosis lung disease

WS23.3 ICM is sensitive to detect potentiation of CFTR-mediated Cl− secretion in patients with cystic fibrosis and the G551D mutation treated with ivacaftor

WS04.1 Impaired mucus clearance promotes Aspergillus fumigatus-induced type 2 airway inflammation in cystic fibrosis-like lung disease in mice

145 A novel tool to study neutrophil elastase activity on neutrophils from cystic fibrosis airway secretions

Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes

WS10.2 Hypoxic epithelial necrosis triggers neutrophilic inflammation via IL-1 receptor signaling in cystic fibrosis-like lung disease

WS15.6 Upregulation of MicroRNA-148b in cystic fibrosis like lung disease of ßENaC-overexpressing mice

P020 Therapy with elexacaftor/tezacaftor/ivacaftor in a patient with compound heterozygous CFTR mutation and the complex CFTR-allele Phe508del; Leu467Phe

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