Samuel T. Hess

Biological and chemical applications of fluorescence correlation spectroscopy: a review.

Focal volume optics and experimental artifacts in confocal fluorescence correlation spectroscopy.

Quantitative analysis of the fluorescence properties of intrinsically fluorescent proteins in living cells.

Imaging coexisting fluid domains in biomembrane models coupling curvature and line tension.

Quantitative electron microscopy and fluorescence spectroscopy of the membrane distribution of influenza hemagglutinin.

Ultra-high resolution imaging by fluorescence photoactivation localization microscopy.

Large-scale fluid/fluid phase separation of proteins and lipids in giant plasma membrane vesicles.

Imaging and shape analysis of GUVs as model plasma membranes: effect of trans DOPC on membrane properties.

Shape analysis of giant vesicles with fluid phase coexistence by laser scanning microscopy to determine curvature, bending elasticity, and line tension.

Dynamic clustered distribution of hemagglutinin resolved at 40 nm in living cell membranes discriminates between raft theories.

Three-dimensional sub-100 nm resolution fluorescence microscopy of thick samples.

Nanoscale imaging of molecular positions and anisotropies.

Chapter 12: Nanoscale biological fluorescence imaging: breaking the diffraction barrier.

Red lights, camera, photoactivation!

Imaging biological structures with fluorescence photoactivation localization microscopy.

Ultrahigh resolution imaging of biomolecules by fluorescence photoactivation localization microscopy.

A small peptide modeled after the NRAGE repeat domain inhibits XIAP-TAB1-TAK1 signaling for NF-κB activation and apoptosis in P19 cells.

Elongated membrane zones boost interactions of diffusing proteins.

Superresolution imaging of multiple fluorescent proteins with highly overlapping emission spectra in living cells.

Nanoscale organization of mitochondrial microcompartments revealed by combining tracking and localization microscopy.

Triple-color super-resolution imaging of live cells: resolving submicroscopic receptor organization in the plasma membrane.

Optical nanoscopy: from acquisition to analysis.

Actin mediates the nanoscale membrane organization of the clustered membrane protein influenza hemagglutinin.

Super Resolution Microscopy Reveals that Caveolin-1 Is Required for Spatial Organization of CRFB1 and Subsequent Antiviral Signaling in Zebrafish.