Steven G. Thomas

This study identifies PBF/PTTG1IP as an endogenous regulator of cell adhesion, polarity, and directional motility by analyzing knockout models and phosphoproteomic data.

This study uses expansion microscopy to quantitatively analyze the structure of platelet aggregates under normal and perturbed conditions.

This study demonstrates isotropic expansion of the nucleus using expansion microscopy to investigate nanoscale DNA damage response structures.

This paper presents an analysis workflow for quantifying platelet spreading and morphology using image segmentation and machine learning, with tools available in KNIME and ilastik.

The paper introduces a topological data analysis method for analyzing single molecule localization microscopy data, improving segmentation and quantifying nano-structure.

This study optimizes CRISPR-Cas9 for single molecule imaging by improving mEos variants and shows endogenous labeling enables accurate quantification of CXCR4.