Hongyu Li
University Walk
Bristol, ENG, United Kingdom
Bristol, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 20 publications
Clinical, functional and therapeutic evaluation of CFTR variant I507del.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: October 10, 2025
Native CFTR codon bias controls translation rate to balance off-pathway aggregation and channel function by conformational imprinting.
Journal: Scientific reports
Published: August 20, 2025
Two rare variants that affect the same amino acid in CFTR have distinct responses to ivacaftor.
Journal: The Journal of physiology
Published: September 25, 2023
Correlating genotype with phenotype using CFTR-mediated whole-cell Cl- currents in human nasal epithelial cells.
Journal: The Journal of physiology
Published: July 08, 2021
Anion carriers as potential treatments for cystic fibrosis: transport in cystic fibrosis cells, and additivity to channel-targeting drugs.
Journal: Chemical science
Published: August 23, 2019
Anion transport by ortho-phenylene bis-ureas across cell and vesicle membranes.
Journal: Organic & biomolecular chemistry
Published: January 30, 2018
Therapeutic approaches to CFTR dysfunction: From discovery to drug development.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: July 14, 2017
Bypassing CFTR dysfunction in cystic fibrosis with alternative pathways for anion transport.
Journal: Current opinion in pharmacology
Published: June 14, 2017
Two Small Molecules Restore Stability to a Subpopulation of the Cystic Fibrosis Transmembrane Conductance Regulator with the Predominant Disease-causing Mutation.
Journal: The Journal of biological chemistry
Published: August 02, 2016
Last Updated: 09/26/2026