P. P. Mondal

This paper introduces oSMLM to decode the orientation of single molecules from PSF shape and direction, achieving 20 nm localization precision and 5-degree orientation precision.

corrSMLM improves single-molecule localization microscopy by detecting fortunate molecules, reducing noise, and enhancing localization precision and signal-to-noise ratio.

This paper uses single-molecule super-resolution microscopy to study NS2B3 protein cluster formation on mitochondria during dengue virus infection, revealing a correlation with mitochondrial fragmentation.

The paper introduces a high-throughput imaging cytometry system (SMMIC) that enables volumetric interrogation of live specimens with high resolution and flow rate.

This paper introduces scanSMLM, a scanning SMLM system for rapid 3D volume imaging, demonstrating its ability to visualize HA clustering in 3D cells and quantify biophysical parameters.

The paper introduces leSMLM, a technique that detects fortunate molecules to improve spatial resolution in SMLM, achieving a PAR-shift of 6 nm and 11 nm with longer exposure times.

The paper develops a light sheet optical tweezer (LOT) to trap and pattern microscopic particles and live cells, showing increased stiffness and single-degree-of-freedom movement.

This study investigates how Amodiaquin dihydrochloride dihydrate affects SARS-CoV-2 S-protein entry into cells, showing prolonged membrane retention and non-endocytic entry.

This paper introduces parallel-iLIFE, a high-throughput volume flow cytometry method that enables real-time analysis of mitochondrial networks in HeLa cells with sub-cellular resolution.

This paper introduces POSSIBLE microscopy to achieve ultra-superresolution imaging by selecting bright molecules with narrow size-distribution, resulting in better-resolved clusters in NIH3T3 cells.