Fluorescence Lifetime Imaging of Endogenous Fluorophores in Histopathology Sections Reveals Differences Between Normal and Tumor Epithelium in Carcinoma In Situ of the Breast

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Role of Angiogenesis in Human Tumor Dormancy: Animal Models of the Angiogenic Switch

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Warburg, me and Hexokinase 2: Multiple discoveries of key molecular events underlying one of cancers’ most common phenotypes, the “Warburg Effect”, i.e., elevated glycolysis in the presence of oxygen

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Metabolic Mapping of MCF10A Human Breast Cells via Multiphoton Fluorescence Lifetime Imaging of the Coenzyme NADH

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Multiphoton Microscopy of Endogenous Fluorescence Differentiates Normal, Precancerous, and Cancerous Squamous Epithelial Tissues

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Fluorescence lifetime imaging distinguishes basal cell carcinoma from surrounding uninvolved skin

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Time-domain fluorescence lifetime imaging for intracellular pH sensing in living tissues

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Characterization of redox state of two human prostate carcinoma cell lines with different degrees of aggressiveness

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Advanced but Not Localized Prostate Cancer is Associated With Increased Oxidative Stress

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Nonlinear optical imaging and spectral-lifetime computational analysis of endogenous and exogenous fluorophores in breast cancer

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Characterization of vulnerable plaques by multiphoton microscopy

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Innovating lifetime microscopy: a compact and simple tool for life sciences, screening, and diagnostics

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Ultraviolet-induced autofluorescence characterization of normal and tumoral esophageal epithelium cells with quantitation of NAD(P)H

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Analysis of histology specimens using lifetime multiphoton microscopy

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In vitro model for endogenous optical signatures of collagen

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Functional optical detection based on pH dependent fluorescence lifetime

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Applications of Combined Spectral Lifetime Microscopy for Biology

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Fluorescence microscopy of rat embryo sections stained with haematoxylin–eosin and Masson's trichrome method

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Selective fluorescence of eosinophilic structures in grasshopper and mammalian testis stained with haematoxylin-eosin

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Temperature-induced changes in the coenzyme environment of D-amino acid oxidase revealed by the multiple decays of FAD fluorescence

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