Chad Michael Hobson

This study shows that Myo1e/f regulate phagocytic podosomes and the phagocytic ring to ensure efficient cup closure in macrophages.

This study uses advanced microscopy to observe fibrin fiber branching during clot formation, revealing that branching occurs through mature fiber binding rather than splitting or protofibril association.

The paper introduces a machine learning-enabled pipeline for volumetric FLIM imaging in living systems, enabling long-term and high-speed data acquisition and analysis.

This paper presents a device for adapting upright light sheet fluorescence microscopy to image samples at air-liquid interface, demonstrating its use on three biological specimens.

OpticalFlow3D measures amorphous motion in 3D fluorescence microscopy images without requiring segmentation or prior motion definitions.

HD2Net improves fluorescence microscopy image quality by simultaneously denoising and correcting aberrations without additional hardware, outperforming existing methods in resolution and contrast.

This paper introduces a deep learning method to correct optical aberrations in fluorescence microscopy, improving image quality and enabling better downstream analysis.