Anita Balazs

Berlin, BE, Germany

Last Updated: 09/26/2026

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Found 20 publications

Clade 2.3.4.4b H5N1 influenza A virus exhibits high infectivity in human respiratory tract models.

Clade 2.3.4.4b H5N1 influenza A virus exhibits high infectivity in human respiratory tract models.

Journal: The Journal of infection
Published: February 25, 2026

Reflection confocal microscopy for quantitative assessment of airway surface layer dysregulation and pharmacological rescue in cystic fibrosis under near-physiological conditions.

Reflection confocal microscopy for quantitative assessment of airway surface layer dysregulation and pharmacological rescue in cystic fibrosis under near-physiological conditions.

Journal: Scientific reports
Published: September 17, 2025

Human induced pluripotent stem cells for in vitro modeling of impaired mucociliary clearance in cystic fibrosis lung disease.

Human induced pluripotent stem cells for in vitro modeling of impaired mucociliary clearance in cystic fibrosis lung disease.

Journal: Stem cell research & therapy
Published: July 22, 2025

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.

Journal: JCI insight
Published: June 02, 2025

Don't forget the mucus barrier in pulmonary drug delivery!

Don't forget the mucus barrier in pulmonary drug delivery!

Journal: The Journal of physiology
Published: March 19, 2025

Lung tissue-optimized gene editing in human cystic fibrosis models following topical application of lipid nanoparticles.

Lung tissue-optimized gene editing in human cystic fibrosis models following topical application of lipid nanoparticles.

Journal: Journal of controlled release : official journal of the Controlled Release Society
Published: February 07, 2025

The potentiator ivacaftor is essential for pharmacological restoration of F508del-CFTR function and mucociliary clearance in cystic fibrosis.

The potentiator ivacaftor is essential for pharmacological restoration of F508del-CFTR function and mucociliary clearance in cystic fibrosis.

Journal: JCI insight
Published: October 10, 2024

Store-independent activation of STIM1-ORAI1 by SPCA2 determines the basal CFTR activity in secretory epithelial cells.

Store-independent activation of STIM1-ORAI1 by SPCA2 determines the basal CFTR activity in secretory epithelial cells.

Journal: Current biology : CB
Published: September 16, 2024

SARS-CoV-2 Infection of Human Lung Air-Liquid Interface Cultures Reveals Basal Cells as Relevant Targets.

SARS-CoV-2 Infection of Human Lung Air-Liquid Interface Cultures Reveals Basal Cells as Relevant Targets.

Journal: The Journal of infectious diseases
Published: July 23, 2024

A cell-permeable nanobody to restore F508del cystic fibrosis transmembrane conductance regulator activity.

A cell-permeable nanobody to restore F508del cystic fibrosis transmembrane conductance regulator activity.

Journal: Nature chemical biology
Published: May 17, 2024

Personalized CFTR Modulator Therapy for G85E and N1303K Homozygous Patients with Cystic Fibrosis.

Personalized CFTR Modulator Therapy for G85E and N1303K Homozygous Patients with Cystic Fibrosis.

Journal: International journal of molecular sciences
Published: June 21, 2023

RECAST: Study protocol for an observational study for the understanding of the increased REsilience of Children compared to Adults in SARS-CoV-2 infecTion.

RECAST: Study protocol for an observational study for the understanding of the increased REsilience of Children compared to Adults in SARS-CoV-2 infecTion.

Journal: BMJ open
Published: April 17, 2023
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Last Updated: 09/26/2026