Rapid three-dimensional isotropic imaging of living cells using Bessel beam plane illumination

By T. Planchon, Liang Gao, D. Milkie, Michael W. Davidson, J. Galbraith, C. Galbraith, Eric Betzig. Nature Methods, 2011

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A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation. (2015, positive): “The stress granules were imaged using a fast DSLM microscope with structured illumination (Planchon et al., 2011).”
Content-aware image restoration: pushing the limits of fluorescence microscopy (2018, background): “Such trade-offs are often depicted by a design-space tetrahedron [11] that has resolution, speed, phototoxicity, and depth at its four vertices (Figure 1a) with the volume being limited by a total photon budget [12].”
Clarifying Tissue Clearing (2015, neutral): “…illumination microscopy (Holekamp et al., 2008), diSPIM (Wu et al., 2013), two-photon lightsheet (Planchon et al., 2011), Bessel beam lightsheet (Planchon et al., 2011), lattice lightsheet (Chen et al., 2014), and SCAPE (Bouchard et al., 2015), are limited to samples only a few hundreds…”
Fast functional imaging of multiple brain regions in intact zebrafish larvae using Selective Plane Illumination Microscopy (2013, methodology): “Beyond the expected gain in optical sectioning efficiency provided by this method (Planchon et al., 2011), the self-healing property of Bessel beams may permit to mitigate the problems of streaking.”
Lattice Light Sheet Microscopy: Imaging Molecules to Embryos at High Spatiotemporal Resolution (2014, positive): “S4) conceptually similar to ourearlierBesselmicroscope (7,8).”