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A revised airway epithelial hierarchy includes CFTR-expressing ionocytes

Nature (London), 2018-08, Vol.560 (7718), p.319

2018

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Method for quantitative study of airway functional microanatomy using micro-optical coherence tomography

PloS one, 2013-01, Vol.8 (1), p.e54473-e54473

2013

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Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout rats

PloS one, 2014-03, Vol.9 (3), p.e91253

2014

Volltextzugriff (PDF)

Ivacaftor Reverses Airway Mucus Abnormalities in a Rat Model Harboring a Humanized G551D-CFTR

American journal of respiratory and critical care medicine, 2020-11, Vol.202 (9), p.1271-1282

2020

Volltextzugriff (PDF)

A novel in vitro model to study prolonged Pseudomonas aeruginosa infection in the cystic fibrosis bronchial epithelium

PloS one, 2023-07, Vol.18 (7), p.e0288002

2023

Volltextzugriff (PDF)

Intranasal micro-optical coherence tomography imaging for cystic fibrosis studies

Science translational medicine, 2019-08, Vol.11 (504)

2019

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A step forward for an intermediate cystic fibrosis population

The European respiratory journal, 2022-08, Vol.60 (2), p.2201040

Birket, Susan E.

2022

Volltextzugriff (PDF)

Flexible, high-resolution micro-optical coherence tomography endobronchial probe toward in vivo imaging of cilia

Optics letters, 2017-02, Vol.42 (4), p.867-870

2017

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A Novel G542X CFTR Rat Model of Cystic Fibrosis Is Sensitive to Nonsense Mediated Decay

Frontiers in physiology, 2020-12, Vol.11, p.611294-611294

2020

Volltextzugriff (PDF)

Particle-Tracking Microrheology Using Micro-Optical Coherence Tomography

Biophysical journal, 2016-09, Vol.111 (5), p.1053-1063

2016

Volltextzugriff (PDF)

Development of a Broadly Protective, Self-Adjuvanting Subunit Vaccine to Prevent Infections by Pseudomonas aeruginosa

Frontiers in immunology, 2020-11, Vol.11, p.583008-583008

2020

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Muc5b Contributes to Mucus Abnormality in Rat Models of Cystic Fibrosis

Frontiers in physiology, 2022-04, Vol.13, p.884166-884166

2022

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ATP12A: Connecting Mucus and Fibrosis in Idiopathic Pulmonary Fibrosis

American journal of respiratory cell and molecular biology, 2023-06, Vol.68 (6), p.603-604

2023

Volltextzugriff (PDF)

Azithromycin Alters Macrophage Phenotype and Pulmonary Compartmentalization during Lung Infection with Pseudomonas

Antimicrobial Agents and Chemotherapy, 2010-06, Vol.54 (6), p.2437-2447

2010

Volltextzugriff (PDF)

An Adeno-Associated Viral Vector Capable of Penetrating the Mucus Barrier to Inhaled Gene Therapy

Molecular therapy. Methods & clinical development, 2018-06, Vol.9, p.296-304

2018

Volltextzugriff (PDF)

Azithromycin Polarizes Macrophages to an M2 Phenotype via Inhibition of the STAT1 and NF-κB Signaling Pathways

The Journal of immunology (1950), 2019-08, Vol.203 (4), p.1021-1030

2019

Volltextzugriff (PDF)

Pneumocystis infection alters the activation state of pulmonary macrophages

Immunobiology (1979), 2017-02, Vol.222 (2), p.188-197

2017

Volltextzugriff (PDF)

Revealing the molecular signaling pathways of mucus stasis in cystic fibrosis

The Journal of clinical investigation, 2019-10, Vol.129 (10), p.4089-4090

2019

Volltextzugriff (PDF)

The Big Impact of Small Airway pH

American journal of respiratory cell and molecular biology, 2021-08, Vol.65 (2), p.123-125

2021

Volltextzugriff (PDF)

Engineered tRNAs suppress nonsense mutations in cells and in vivo

Nature (London), 2023-06, Vol.618 (7966), p.842

2023

Volltextzugriff (PDF)

Excess mucus viscosity and airway dehydration impact COPD airway clearance

The European respiratory journal, 2020-01, Vol.55 (1), p.1900419

2020

Volltextzugriff (PDF)

Ivacaftor partially corrects airway inflammation in a humanized G551D rat

American journal of physiology. Lung cellular and molecular physiology, 2021-06, Vol.320 (6), p.L1093-L1100

2021

Volltextzugriff (PDF)

Acute Infection with a Tobramycin-Induced Small Colony Variant of Staphylococcus aureus Causes Increased Inflammation in the Cystic Fibrosis Rat Lung

Infection and immunity, 2022-11, Vol.90 (11), p.e0023722

2022

Volltextzugriff (PDF)

Inhaled gene therapy of preclinical muco-obstructive lung diseases by nanoparticles capable of breaching the airway mucus barrier

Thorax, 2022-08, Vol.77 (8), p.812

2022

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Understanding and addressing the needs of people with cystic fibrosis in the era of CFTR modulator therapy

The lancet respiratory medicine, 2023-10, Vol.11 (10), p.916-931

2023

Volltextzugriff (PDF)

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A revised airway epithelial hierarchy includes CFTR-expressing ionocytes

Method for quantitative study of airway functional microanatomy using micro-optical coherence tomography

Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout rats

Ivacaftor Reverses Airway Mucus Abnormalities in a Rat Model Harboring a Humanized G551D-CFTR

A novel in vitro model to study prolonged Pseudomonas aeruginosa infection in the cystic fibrosis bronchial epithelium

Intranasal micro-optical coherence tomography imaging for cystic fibrosis studies

A step forward for an intermediate cystic fibrosis population

Flexible, high-resolution micro-optical coherence tomography endobronchial probe toward in vivo imaging of cilia

A Novel G542X CFTR Rat Model of Cystic Fibrosis Is Sensitive to Nonsense Mediated Decay

Particle-Tracking Microrheology Using Micro-Optical Coherence Tomography

Development of a Broadly Protective, Self-Adjuvanting Subunit Vaccine to Prevent Infections by Pseudomonas aeruginosa

Muc5b Contributes to Mucus Abnormality in Rat Models of Cystic Fibrosis

ATP12A: Connecting Mucus and Fibrosis in Idiopathic Pulmonary Fibrosis

Azithromycin Alters Macrophage Phenotype and Pulmonary Compartmentalization during Lung Infection with Pseudomonas

An Adeno-Associated Viral Vector Capable of Penetrating the Mucus Barrier to Inhaled Gene Therapy

Azithromycin Polarizes Macrophages to an M2 Phenotype via Inhibition of the STAT1 and NF-κB Signaling Pathways

Pneumocystis infection alters the activation state of pulmonary macrophages

Revealing the molecular signaling pathways of mucus stasis in cystic fibrosis

The Big Impact of Small Airway pH

Engineered tRNAs suppress nonsense mutations in cells and in vivo

Excess mucus viscosity and airway dehydration impact COPD airway clearance

Ivacaftor partially corrects airway inflammation in a humanized G551D rat

Acute Infection with a Tobramycin-Induced Small Colony Variant of Staphylococcus aureus Causes Increased Inflammation in the Cystic Fibrosis Rat Lung

Inhaled gene therapy of preclinical muco-obstructive lung diseases by nanoparticles capable of breaching the airway mucus barrier

Understanding and addressing the needs of people with cystic fibrosis in the era of CFTR modulator therapy

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