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Simultaneous, accurate measurement of the 3D position and orientation of single molecules.
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Rational design of true monomeric and bright photoactivatable fluorescent proteins.
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Fluorescence microscopy for simultaneous observation of 3D orientation and movement and its application to quantum rod-tagged myosin V.
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A unique series of reversibly switchable fluorescent proteins with beneficial properties for various applications.
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Optimal 3D single-molecule localization for superresolution microscopy with aberrations and engineered point spread functions.
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Binding-activated localization microscopy of DNA structures.
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Two-color nanoscopy of three-dimensional volumes by 4Pi detection of stochastically switched fluorophores.
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Accuracy of the gaussian point spread function model in 2D localization microscopy.
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Molecular orientation affects localization accuracy in superresolution far-field fluorescence microscopy.
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Optimized localization analysis for single-molecule tracking and super-resolution microscopy.
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