Fluorescence techniques dominate the field of live-cell microscopy, but bleaching and
motion blur from too long integration times limit dynamic investigations of small objects. High …

Small structures, as inside living cells, move on millisecond timescales, which is usually far
beyond the imaging rate of superresolution fluorescence microscopes. In contrast, label-free …

Cells change their shape within seconds, cellular protrusions even on subsecond
timescales enabling various responses to stimuli of approaching bacteria, viruses or …

Living cells are highly dynamic systems with cellular structures being often below the optical
resolution limit. Super-resolution microscopes, usually based on fluorescence cell labelling …

Mechanical manipulation of single cytoskeleton filaments and their monitoring over long
times is difficult because of fluorescence bleaching or phototoxic protein degradation. The …

Live-cell imaging technology using fluorescent proteins (green fluorescent protein and its
homologues) has revolutionized the study of cellular dynamics,. But tools that can …

In eukaryotic cells, organelles and the cytoskeleton undergo highly dynamic yet organized
interactions capable of orchestrating complex cellular functions. Visualizing these …

Live cell microscopy using fluorescent proteins and small fluorescent probes is a well-
established and essential tool for cell biology; however, there is a considerable need for …

We demonstrate broadband Fourier‐transform coherent anti‐Stokes Raman scattering (FT‐
CARS) spectral microscopy with a pixel dwell time of 42 μs, which is~ 50 times shorter than …

Cell biology came about with the ability to first visualize cells. As microscopy techniques
advanced, the early microscopists became the first cell biologists to observe the inner …