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Optical control of protein activity by fluorescent protein domains.
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Widely accessible method for superresolution fluorescence imaging of living systems.
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Reversible photoswitching in fluorescent proteins: a mechanistic view.
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A unique series of reversibly switchable fluorescent proteins with beneficial properties for various applications.
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Protein-flexibility mediated coupling between photoswitching kinetics and surrounding viscosity of a photochromic fluorescent protein.
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Low-temperature chromophore isomerization reveals the photoswitching mechanism of the fluorescent protein Padron.
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Diffraction-unlimited all-optical imaging and writing with a photochromic GFP.
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Red fluorescent protein with reversibly photoswitchable absorbance for photochromic FRET.
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