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Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis

Science (American Association for the Advancement of Science), 2014-08, Vol.345 (6198), p.818-822

2014

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Small Colonies, Bigger Problems? New Evidence That Staphylococcus aureus Small Colony Variants Can Worsen Lung Inflammation in Cystic Fibrosis Rats

Infection and immunity, 2022-11, Vol.90 (11), p.e0041322-e0041322

2022

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Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs

Proceedings of the National Academy of Sciences - PNAS, 2014-02, Vol.111 (6), p.2355-2360

2014

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High Prevalence of Staphylococcus aureus Enterotoxin Gene Cluster Superantigens in Cystic Fibrosis Clinical Isolates

Genes, 2019-12, Vol.10 (12), p.1036

2019

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Parallel evolution of linezolid-resistant Staphylococcus aureus in patients with cystic fibrosis

Microbiology spectrum, 2023-10, Vol.11 (5), p.e0208423-e0208423

2023

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Patient and Caregiver Perceptions of Airway Clearance Methods Used for Cystic Fibrosis

Canadian respiratory journal, 2023, Vol.2023, p.1422319-9

2023

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Pancreatic enzymes digest obstructive meconium from cystic fibrosis pig intestines

Frontiers in pediatrics, 2024-04, Vol.12, p.1387171-1387171

2024

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A birth cohort approach to understanding cystic fibrosis lung infections

Journal of cystic fibrosis, 2024-01, Vol.23 (1), p.8-11

2024

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Sustained Coinfections with Staphylococcus aureus and Pseudomonas aeruginosa in Cystic Fibrosis

American journal of respiratory and critical care medicine, 2021-02, Vol.203 (3), p.328-338

2021

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Surfactant deficiency syndrome in an infant with a C‐terminal frame shift in ABCA3: A case report

Pediatric pulmonology, 2018-05, Vol.53 (5), p.E12-E14

2018

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Pseudomonas eradication and clinical effectivness of Ivacaftor in four Hispanic patients with S549N

Pediatric pulmonology, 2017-07, Vol.52 (7), p.E37-E39

2017

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Elastic mucus strands impair mucociliary clearance in cystic fibrosis pigs

Proceedings of the National Academy of Sciences - PNAS, 2022-03, Vol.119 (13), p.e2121731119-e2121731119

2022

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Pathogen acquisition in patients with cystic fibrosis receiving ivacaftor or lumacaftor/ivacaftor

Pediatric pulmonology, 2019-08, Vol.54 (8), p.1200-1208

2019

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Differential Gene Expression in Human Conducting Airway Surface Epithelia and Submucosal Glands

American journal of respiratory cell and molecular biology, 2009-02, Vol.40 (2), p.189-199

2009

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Mucociliary Transport in Healthy and Cystic Fibrosis Pig Airways

Annals of the American Thoracic Society, 2018-11, Vol.15 (Suppl 3), p.S171-S176

2018

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MRSA strains with distinct accessory genes predominate at different ages in cystic fibrosis

Pediatric pulmonology, 2021-09, Vol.56 (9), p.2868-2878

2021

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Staphylococcus aureus detection from CF respiratory samples is improved using alternative media

Journal of cystic fibrosis, 2022-09, Vol.21 (5), p.888-889

2022

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Tracheomalacia is associated with lower FEV1 and Pseudomonas acquisition in children with CF

Pediatric pulmonology, 2014-10, Vol.49 (10), p.960-970

2014

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Enhancement of respiratory mucosal antiviral defenses by the oxidation of iodide

American journal of respiratory cell and molecular biology, 2011-10, Vol.45 (4), p.874-881

2011

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Sonographic evidence of abnormal tracheal cartilage ring structure in cystic fibrosis

The Laryngoscope, 2015-10, Vol.125 (10), p.2398-2404

2015

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Nitric oxide as a cellular antioxidant: A little goes a long way

Free radical biology & medicine, 2006-02, Vol.40 (3), p.501-506

2006

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Mucus strands from submucosal glands initiate mucociliary transport of large particles

JCI insight, 2019-01, Vol.4 (1)

2019

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Innate Immune Functions of the Airway Epithelium

Contributions to microbiology, 2008, Vol.15, p.147-163

2008

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Acute administration of ivacaftor to people with cystic fibrosis and a G551D-CFTR mutation reveals smooth muscle abnormalities

JCI insight, 2016-04, Vol.1 (4), p.e86183-e86183

2016

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Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis

Small Colonies, Bigger Problems? New Evidence That Staphylococcus aureus Small Colony Variants Can Worsen Lung Inflammation in Cystic Fibrosis Rats

Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs

High Prevalence of Staphylococcus aureus Enterotoxin Gene Cluster Superantigens in Cystic Fibrosis Clinical Isolates

Parallel evolution of linezolid-resistant Staphylococcus aureus in patients with cystic fibrosis

Patient and Caregiver Perceptions of Airway Clearance Methods Used for Cystic Fibrosis

Pancreatic enzymes digest obstructive meconium from cystic fibrosis pig intestines

A birth cohort approach to understanding cystic fibrosis lung infections

Sustained Coinfections with Staphylococcus aureus and Pseudomonas aeruginosa in Cystic Fibrosis

Surfactant deficiency syndrome in an infant with a C‐terminal frame shift in ABCA3: A case report

Pseudomonas eradication and clinical effectivness of Ivacaftor in four Hispanic patients with S549N

Elastic mucus strands impair mucociliary clearance in cystic fibrosis pigs

Pathogen acquisition in patients with cystic fibrosis receiving ivacaftor or lumacaftor/ivacaftor

Differential Gene Expression in Human Conducting Airway Surface Epithelia and Submucosal Glands

Mucociliary Transport in Healthy and Cystic Fibrosis Pig Airways

MRSA strains with distinct accessory genes predominate at different ages in cystic fibrosis

Staphylococcus aureus detection from CF respiratory samples is improved using alternative media

Lack of airway submucosal glands impairs respiratory host defenses

Tracheomalacia is associated with lower FEV1 and Pseudomonas acquisition in children with CF

Enhancement of respiratory mucosal antiviral defenses by the oxidation of iodide

Sonographic evidence of abnormal tracheal cartilage ring structure in cystic fibrosis

Nitric oxide as a cellular antioxidant: A little goes a long way

Mucus strands from submucosal glands initiate mucociliary transport of large particles

Innate Immune Functions of the Airway Epithelium

Acute administration of ivacaftor to people with cystic fibrosis and a G551D-CFTR mutation reveals smooth muscle abnormalities

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