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Alon Greenbaum

Researcher at California Institute of Technology

Publications -  71
Citations -  4501

Alon Greenbaum is an academic researcher from California Institute of Technology. The author has contributed to research in topics: Microscopy & Medicine. The author has an hindex of 26, co-authored 58 publications receiving 3453 citations. Previous affiliations of Alon Greenbaum include Tel Aviv University & University of California, Los Angeles.

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Q&A: How can advances in tissue clearing and optogenetics contribute to our understanding of normal and diseased biology?

TL;DR: This Q&A delineates recent advances and practical challenges associated with these two techniques when applied body-wide in tissue clearing and optogenetics.
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High throughput on-chip analysis of high-energy charged particle tracks using lensfree imaging

TL;DR: In this paper, the authors demonstrate a high-throughput charged particle analysis platform based on lensfree on-chip microscopy for rapid ion track analysis using allyl diglycol carbonate, i.e., CR-39 plastic polymer as the sensing medium.
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Quantitative analysis of illumination and detection corrections in adaptive light sheet fluorescence microscopy.

TL;DR: In this paper , the illumination beam angular properties are controlled by two galvanometer scanners, while a deformable mirror is positioned in the detection path to correct for optical aberrations.
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Ontogeny of cellular organization and LGR5 expression in porcine cochlea revealed using tissue clearing and 3D imaging

TL;DR: In this paper , the porcine cochlea was analyzed in 3D using tissue clearing and light-sheet microscopy, and the resulting 3D images can be employed to compare cochelleae across different ages and conditions, investigate the ontogeny of cochlear cytoarchitecture, and produce quantitative expression maps of LGR5, a marker of co-lear progenitors in mice.
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Light-guided sectioning for precise in situ localization and tissue interface analysis for brain-implanted optical fibers and GRIN lenses

TL;DR: Light-guided sectioning (LiGS) as discussed by the authors preserves the tissue with its optical implant in place and allows staining and clearing of a volume up to 500μm in depth, which could help increase reproducibility through identification of fiber-to-target localization and molecular profiling.