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Creators/Authors contains: "Ling, Zhi"

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  1. Free, publicly-accessible full text available June 1, 2026
  2. This study introduces a rapid, volumetric live-cell imaging technique for visualizing autofluorescent sub-cellular structures and their dynamics by employing high-resolution Fourier light-field microscopy. We demonstrated this method by capturing lysosomal autofluorescence in fibroblasts and HeLa cells. Additionally, we conducted multicolor imaging to simultaneously observe lysosomal autofluorescence and fluorescently-labeled organelles such as lysosomes and mitochondria. We further analyzed the data to quantify the interactions between lysosomes and mitochondria. This research lays the foundation for future exploration of native cellular states and functions in three-dimensional environments, effectively reducing photodamage and eliminating the necessity for exogenous labels. 
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  3. We propose a denoising-sparse decomposition method for Fourier light-field microscopy to separate signals with different periodicity in complex biological samples. This process allows for enhanced volumetric reconstruction and accurate image analysis. 
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  4. null (Ed.)