M. A. Abou Alaiwa

发表

The vagal ganglia transcriptome identifies candidate therapeutics for airway hyperreactivity

Nicholas L. Bormann, D. Meyerholz, M. Welsh, 2018, American journal of physiology. Lung cellular and molecular physiology.

Early Airway Structural Changes in Cystic Fibrosis Pigs as a Determinant of Particle Distribution and Deposition

E. Hoffman, K. Reynolds, Ching-Long Lin, 2013, Annals of Biomedical Engineering.

Elastic mucus strands impair mucociliary clearance in cystic fibrosis pigs

E. Hoffman, M. Welsh, D. Stoltz, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Mucus strands from submucosal glands initiate mucociliary transport of large particles.

E. Hoffman, M. Welsh, D. Stoltz, 2019, JCI insight.

Gel-forming mucins form distinct morphologic structures in airways

D. Meyerholz, M. Welsh, L. Powers, 2017, Proceedings of the National Academy of Sciences.

Lack of airway submucosal glands impairs respiratory host defenses

E. Hoffman, D. Meyerholz, M. Welsh, 2020, eLife.

Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis.

M. Welsh, D. Stoltz, J. Zabner, 2018, JCI insight.

Repurposing tromethamine as inhaled therapy to treat CF airway disease.

M. Welsh, D. Stoltz, J. Zabner, 2016, JCI insight.

Motile cilia of human airway epithelia contain hedgehog signaling components that mediate noncanonical hedgehog signaling

M. Welsh, S. Keshavjee, Alok S Shah, 2018, Proceedings of the National Academy of Sciences.

Solitary Cholinergic Stimulation Induces Airway Hyperreactivity and Transcription of Distinct Pro-inflammatory Pathways

D. Meyerholz, K. Atanasova, Leah R Reznikov, 2018, Lung.

Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.

M. Welsh, D. Stoltz, J. Zabner, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility.

D. Meyerholz, R. Krishnan, M. Thompson, 2016, American journal of respiratory and critical care medicine.

Tromethamine improves mucociliary clearance in cystic fibrosis pigs

D. Stoltz, J. Zabner, N. Gansemer, 2022, Physiological reports.

Postnatal airway growth in cystic fibrosis piglets.

E. Hoffman, D. Meyerholz, M. Welsh, 2017, Journal of applied physiology.

Monocyte derived macrophages from CF pigs exhibit increased inflammatory responses at birth

R. Gray, D. Stoltz, P. McCray, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Air trapping and airflow obstruction in newborn cystic fibrosis piglets.

E. Hoffman, J. Reinhardt, D. Meyerholz, 2013, American journal of respiratory and critical care medicine.

Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.

E. Hoffman, D. Meyerholz, M. Welsh, 2013, The Journal of clinical investigation.

Antibacterial properties of the CFTR potentiator ivacaftor.

M. Welsh, D. Stoltz, D. Diekema, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Mounier–Kuhn syndrome: a case of tracheal smooth muscle remodeling

D. Meyerholz, M. Eberlein, D. Stoltz, 2016, Clinical case reports.

Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor

D. Stoltz, D. Hornick, J. Zabner, 2015, International forum of allergy & rhinology.

pH modulates the activity and synergism of the airway surface liquid antimicrobials β-defensin-3 and LL-37

M. Welsh, D. Stoltz, J. Zabner, 2014, Proceedings of the National Academy of Sciences.

Airway surface liquid has innate antiviral activity that is reduced in cystic fibrosis.

P. McCray, S. Varga, J. Bartlett, 2020, American journal of respiratory cell and molecular biology.

Reduced Airway Surface pH Impairs Bacterial Killing in the Porcine Cystic Fibrosis Lung

M. Welsh, T. Moninger, C. Wohlford-Lenane, 2012, Nature.

Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.

D. Meyerholz, M. Welsh, A. Comellas, 2016, American journal of physiology. Lung cellular and molecular physiology.

Lentiviral-mediated phenotypic correction of cystic fibrosis pigs.

D. Meyerholz, M. Welsh, L. Powers, 2016, JCI insight.

Acid-Sensing Ion Channel 1a Contributes to Airway Hyperreactivity in Mice

D. Meyerholz, M. Welsh, L. Powers, 2016, PloS one.

Early Lung Disease Exhibits Bacterial-Dependent and -Independent Abnormalities in Cystic Fibrosis Pigs.

E. Hoffman, P. T. Ten Eyck, D. Meyerholz, 2021, American Journal of Respiratory and Critical Care Medicine.

Mucociliary Transport in Healthy and Cystic Fibrosis Pig Airways

D. Stoltz, L. Ostedgaard, A. Fischer, 2018, Annals of the American Thoracic Society.

Effects of Coal Fly Ash Particulate Matter on the Antimicrobial Activity of Airway Surface Liquid

A. Comellas, J. Zabner, V. Grassian, 2017, Environmental health perspectives.

Polarized AAVR expression determines infectivity by AAV gene therapy vectors

J. Zabner, A. Pezzulo, M. A. Abou Alaiwa, 2019, Gene Therapy.

CFTR gene transfer with AAV improves early cystic fibrosis pig phenotypes.

D. Schaffer, M. Welsh, L. Powers, 2016, JCI insight.

Early Airway Structural Changes in Cystic Fibrosis Pigs as a Determinant of Particle Distribution and Deposition

E. Hoffman, K. Reynolds, Ching-Long Lin, 2014, Annals of Biomedical Engineering.

The rapid reduction of infection-related visits and antibiotic use among people with cystic fibrosis after starting Elexacaftor-Tezacaftor-Ivacaftor.

J. Cavanaugh, P. Polgreen, D. Stoltz, 2022, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.