David A. Stoltz

Intensive Care Medicine

200 Hawkins Dr
Iowa City, IA 52242

Last Updated: 09/26/2026

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Found 95 publications

Considerations for early life genetic therapies in cystic fibrosis.

Considerations for early life genetic therapies in cystic fibrosis.

Journal: American journal of physiology. Lung cellular and molecular physiology

Published: April 29, 2026

Stabilizing and strengthening the US physician-scientist faculty workforce in academic medicine: a proposed institutional framework.

Stabilizing and strengthening the US physician-scientist faculty workforce in academic medicine: a proposed institutional framework.

Journal: JCI insight

Published: April 28, 2026

Age-Specific Risk and Severity of CRS among Cystic Fibrosis Carriers: A Population-Based Cohort Study.

Age-Specific Risk and Severity of CRS among Cystic Fibrosis Carriers: A Population-Based Cohort Study.

Journal: The Annals of otology, rhinology, and laryngology

Published: December 29, 2025

The Increased Risk for Postinfluenza Pneumonia Among Cystic Fibrosis Carriers-A Population-Based Study.

The Increased Risk for Postinfluenza Pneumonia Among Cystic Fibrosis Carriers-A Population-Based Study.

Journal: Open forum infectious diseases

Published: October 07, 2025

Pseudomonas infections persisting after CFTR modulators are widespread throughout the lungs and drive lung inflammation.

Pseudomonas infections persisting after CFTR modulators are widespread throughout the lungs and drive lung inflammation.

Journal: Cell host & microbe

Published: January 28, 2025

Gallbladder mucoceles in dogs: a novel form of acquired CFTR dysfunction causing localized cystic fibrosis-like disease.

Gallbladder mucoceles in dogs: a novel form of acquired CFTR dysfunction causing localized cystic fibrosis-like disease.

Journal: American journal of physiology. Gastrointestinal and liver physiology

Published: October 29, 2024

The pH-sensitive translocation of V-ATPase in the small airway of cystic fibrosis pigs.

The pH-sensitive translocation of V-ATPase in the small airway of cystic fibrosis pigs.

Journal: American journal of physiology. Lung cellular and molecular physiology

Published: September 10, 2024

Development and Initial Characterization of Pigs with DNAI1 Mutations and Primary Ciliary Dyskinesia.

Development and Initial Characterization of Pigs with DNAI1 Mutations and Primary Ciliary Dyskinesia.

Journal: bioRxiv : the preprint server for biology

Published: September 04, 2024

INSIGHTS INTO THE ORIGINS OF CYSTIC FIBROSIS LUNG DISEASE.

INSIGHTS INTO THE ORIGINS OF CYSTIC FIBROSIS LUNG DISEASE.

Journal: Transactions of the American Clinical and Climatological Association

Published: August 13, 2024

Mucociliary clearance is impaired in small airways of cystic fibrosis pigs.

Mucociliary clearance is impaired in small airways of cystic fibrosis pigs.

Journal: American journal of physiology. Lung cellular and molecular physiology

Published: August 06, 2024

Mucociliary Clearance is Impaired in Small Airways of Cystic Fibrosis Pigs.

Mucociliary Clearance is Impaired in Small Airways of Cystic Fibrosis Pigs.

Journal: bioRxiv : the preprint server for biology

Published: June 03, 2024

IL-13 induces loss of CFTR in ionocytes and reduces airway epithelial fluid absorption.

IL-13 induces loss of CFTR in ionocytes and reduces airway epithelial fluid absorption.

Journal: The Journal of clinical investigation

Published: April 22, 2024

Showing 1-12 of 95

Last Updated: 09/26/2026