David Baddeley

The paper develops a combined microscope platform that integrates quantitative phase contrast and super-resolution fluorescence imaging for high-sensitivity visualization of sub-cellular structures and molecules in their cellular context.

The paper develops a stable, high refractive index buffer for dSTORM super-resolution imaging, improving stability, switching speed, contrast, and refractive index matching.

The paper identifies dynamic nano-scale holes in ER sheets that act as reservoirs for curvature-stabilizing proteins, enabling ER tubule extension and retraction.