Nikhil T. Awatade
Newcastle, NSW, Australia
Last Updated: 09/26/2026
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Found 18 publications
Inflammation-induced loss of CFTR-expressing airway ionocytes in non-eosinophilic asthma.
Journal: Respirology (Carlton, Vic.)
Published: February 13, 2024
Comparison of commercially available differentiation media on cell morphology, function, and anti-viral responses in conditionally reprogrammed human bronchial epithelial cells.
Journal: Scientific reports
Published: May 10, 2023
The Complex Association between COPD and COVID-19.
Journal: Journal of clinical medicine
Published: May 04, 2023
Type 2 Immunity and Its Impact on COVID-19 Infection in the Airways.
Journal: Viruses
Published: December 14, 2022
Molecular Dynamics and Theratyping in Airway and Gut Organoids Reveal R352Q-CFTR Conductance Defect.
Molecular Dynamics and Theratyping in Airway and Gut Organoids Reveal R352Q-CFTR Conductance Defect.
Journal: American journal of respiratory cell and molecular biology
Published: April 26, 2022
Novel Antioxidant Therapy with the Immediate Precursor to Glutathione, γ-Glutamylcysteine (GGC), Ameliorates LPS-Induced Cellular Stress in In Vitro 3D-Differentiated Airway Model from Primary Cystic Fibrosis Human Bronchial Cells.
Journal: Antioxidants (Basel, Switzerland)
Published: October 12, 2020
An open-source high-content analysis workflow for CFTR function measurements using the forskolin-induced swelling assay.
Journal: Bioinformatics (Oxford, England)
Published: June 06, 2020
Significant functional differences in differentiated Conditionally Reprogrammed (CRC)- and Feeder-free Dual SMAD inhibited-expanded human nasal epithelial cells.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: April 23, 2020
Human Primary Epithelial Cell Models: Promising Tools in the Era of Cystic Fibrosis Personalized Medicine.
Journal: Frontiers in pharmacology
Published: September 10, 2018
The effect of premature termination codon mutations on CFTR mRNA abundance in human nasal epithelium and intestinal organoids: a basis for read-through therapies in cystic fibrosis.
Journal: Human mutation
Published: July 02, 2018
Last Updated: 09/26/2026