Md. Sanowar Hossan

The paper identifies PRMT5 as a cancer target, uses multi-omics and machine learning to screen compounds, and identifies a potential inhibitor with high docking scores.

This study identifies phytochemical SIRT1 activators and inhibitors through protein expression, purification, and computational modeling, revealing Catechin and Ginsenosides as promising therapeutic candidates.

This paper identifies natural inhibitors of a membrane protein involved in biofilm formation in Vibrio cholerae through structural modeling, functional analysis, and virtual screening.