Cystic Fibrosis Latest Advances

Molecular Prosthetics and CFTR Modulators Additively Increase Secretory HCO3- Flux in Cystic Fibrosis Airway Epithelia.

Journal: ACS chemical biology

Published: October 20, 2025

Evaluation of Methicillin-Resistant Staphylococcus aureus Eradication in People With Cystic Fibrosis.

Journal: The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG

Published: October 20, 2025

An effective response to respiratory inhibition by a Pseudomonas aeruginosa excreted quinoline promotes Staphylococcus aureus fitness and survival in co-culture.

Journal: Journal of bacteriology

Published: October 20, 2025

Altered proteome of a cystic fibrosis cell line model upon exposure to Pseudomonas aeruginosa biofilms.

Journal: Microbiology resource announcements

Published: October 20, 2025

Pediatric Liver Diseases: Next-Generation Therapies.

Journal: Clinics in liver disease

Published: October 18, 2025

Lack of SLC26A9-mediated chloride secretion causes mucus plugging and severe respiratory distress in neonatal mice.

Journal: JCI insight

Published: October 17, 2025

The PA2803-encoded PcrP exhibits a novel non-catalytic function and contributes to polymyxin B resistance in P. aeruginosa.

Journal: Journal of bacteriology

Published: October 17, 2025

Comment: Doxycycline vs Vancomycin for the Treatment of MRSA-Associated Acute Pulmonary Exacerbations in People With Cystic Fibrosis.

Journal: The Annals of pharmacotherapy

Published: October 16, 2025

Isolated Hypoglyceamia in Children with Cystic Fibrosis: Role of Pancreatic Insufficiency and Glucagon Response.

Journal: Journal of clinical research in pediatric endocrinology

Published: October 15, 2025

miR-17-5p: bridging the gap between disease mechanisms and therapeutic innovations.

Journal: Epigenomics

Published: October 11, 2025

Corrigendum to "Dyspnea-related kinesiophobia as a barrier on cystic fibrosis: The role of children and parents"[Respirat. Med. 248 (2025) 108364].

Journal: Respiratory medicine

Published: October 11, 2025

Long-term culturing of Pseudomonas aeruginosa in static, minimal nutrient medium results in increased pyocyanin production, reduced biofilm production, and loss of motility.

Journal: Applied and environmental microbiology

Published: October 10, 2025

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Molecular Prosthetics and CFTR Modulators Additively Increase Secretory HCO3- Flux in Cystic Fibrosis Airway Epithelia.

Molecular Prosthetics and CFTR Modulators Additively Increase Secretory HCO3- Flux in Cystic Fibrosis Airway Epithelia.

Evaluation of Methicillin-Resistant Staphylococcus aureus Eradication in People With Cystic Fibrosis.

Evaluation of Methicillin-Resistant Staphylococcus aureus Eradication in People With Cystic Fibrosis.

An effective response to respiratory inhibition by a Pseudomonas aeruginosa excreted quinoline promotes Staphylococcus aureus fitness and survival in co-culture.

An effective response to respiratory inhibition by a Pseudomonas aeruginosa excreted quinoline promotes Staphylococcus aureus fitness and survival in co-culture.

Altered proteome of a cystic fibrosis cell line model upon exposure to Pseudomonas aeruginosa biofilms.

Altered proteome of a cystic fibrosis cell line model upon exposure to Pseudomonas aeruginosa biofilms.

Pediatric Liver Diseases: Next-Generation Therapies.

Pediatric Liver Diseases: Next-Generation Therapies.

Lack of SLC26A9-mediated chloride secretion causes mucus plugging and severe respiratory distress in neonatal mice.

Lack of SLC26A9-mediated chloride secretion causes mucus plugging and severe respiratory distress in neonatal mice.

The PA2803-encoded PcrP exhibits a novel non-catalytic function and contributes to polymyxin B resistance in P. aeruginosa.

The PA2803-encoded PcrP exhibits a novel non-catalytic function and contributes to polymyxin B resistance in P. aeruginosa.

Comment: Doxycycline vs Vancomycin for the Treatment of MRSA-Associated Acute Pulmonary Exacerbations in People With Cystic Fibrosis.

Comment: Doxycycline vs Vancomycin for the Treatment of MRSA-Associated Acute Pulmonary Exacerbations in People With Cystic Fibrosis.

Isolated Hypoglyceamia in Children with Cystic Fibrosis: Role of Pancreatic Insufficiency and Glucagon Response.

Isolated Hypoglyceamia in Children with Cystic Fibrosis: Role of Pancreatic Insufficiency and Glucagon Response.

miR-17-5p: bridging the gap between disease mechanisms and therapeutic innovations.

miR-17-5p: bridging the gap between disease mechanisms and therapeutic innovations.

Corrigendum to "Dyspnea-related kinesiophobia as a barrier on cystic fibrosis: The role of children and parents"[Respirat. Med. 248 (2025) 108364].

Corrigendum to "Dyspnea-related kinesiophobia as a barrier on cystic fibrosis: The role of children and parents"[Respirat. Med. 248 (2025) 108364].

Long-term culturing of Pseudomonas aeruginosa in static, minimal nutrient medium results in increased pyocyanin production, reduced biofilm production, and loss of motility.

Long-term culturing of Pseudomonas aeruginosa in static, minimal nutrient medium results in increased pyocyanin production, reduced biofilm production, and loss of motility.