Frauke Stanke
Carl Neuberg Str. 1
Hannover, NI 30625, Germany
Hannover, NI 30625, Germany
Last Updated: 09/26/2026
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Found 32 publications
Apical and basolateral alpha-1 antitrypsin delivery modulate CFTR and STAT3 in human airway epithelia grown at air-liquid interface.
Journal: Respiratory medicine and research
Published: August 25, 2025
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
NLRP3 regulates epithelial barrier integrity and protects from airway hyperresponsiveness in experimental allergic asthma.
Journal: Frontiers in immunology
Published: June 27, 2025
Genotype and transcript processing of the tumour necrosis factor receptor TNFRSF1A in epithelial cells: implications for survival in cystic fibrosis.
Journal: EBioMedicine
Published: October 10, 2024
Analysis of CFTR mRNA and Protein in Peripheral Blood Mononuclear Cells via Quantitative Real-Time PCR and Western Blot.
Journal: International journal of molecular sciences
Published: December 21, 2023
A Fast Scoring of Human Primary Respiratory Epithelia Grown at Air-Liquid Interface (ALI) to Assess Epithelial Morphology in Research and Personalized Medicine Settings.
Journal: Journal of personalized medicine
Published: November 27, 2023
Editorial: Acute phase proteins as biomarkers and therapeutics in acute and chronic inflammatory conditions.
Journal: Frontiers in pharmacology
Published: January 16, 2023
Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy.
Journal: Frontiers in pharmacology
Published: December 02, 2022
Complementary Dual Approach for In Silico Target Identification of Potential Pharmaceutical Compounds in Cystic Fibrosis.
Journal: International journal of molecular sciences
Published: September 05, 2022
Integrating Text Mining into the Curation of Disease Maps.
Journal: Biomolecules
Published: August 19, 2022
Generation of two TMEM16A knockout iPSC clones each from a healthy human iPSC line, from a Cystic Fibrosis patient specific line with p.Phe508del mutation and from the gene corrected iPSC line.
Journal: Stem cell research
Published: July 08, 2022
Analysis of CF patient survival confirms STAT3 as a CF-modifying gene with changing impact over time.
Journal: Human molecular genetics
Published: April 29, 2022
Last Updated: 09/26/2026