Lanxin Li
Hengyang, 421001, China
Last Updated: 09/26/2026
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Found 9 publications
Cytotoxicity and inhibitory potential of CUDC-101 in non-small cell lung cancer cells with rare EGFR L861Q mutation.
Journal: Current research in toxicology
Published: June 08, 2024
Almonertinib and alflutinib show novel inhibition on rare EGFR S768I mutant cells.
Journal: Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
Published: February 01, 2024
BDTX-189, a novel tyrosine kinase inhibitor, inhibits cell activity via ERK and AKT pathways in the EGFR C797S triple mutant cells.
Journal: Chemico-biological interactions
Published: January 28, 2024
Correction to: Sensitivity analysis of EGFR L861Q mutation to six tyrosine kinase inhibitors.
Journal: Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
Published: November 20, 2023
CUDC‑101 is a potential target inhibitor for the EGFR‑overexpression bladder cancer cells.
Journal: International journal of oncology
Published: May 19, 2023
Six first-line tyrosine kinase inhibitors reveal novel inhibition potential for the EGFR S768I mutation.
Journal: Toxicology and applied pharmacology
Published: July 29, 2022
Sensitivity analysis of EGFR L861Q mutation to six tyrosine kinase inhibitors.
Journal: Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
Published: February 05, 2022
Showing 1-9 of 9
Last Updated: 09/26/2026