<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(3)</volume><submitter>Treacy PJ</submitter><pubmed_abstract>&lt;h4>Background and objective&lt;/h4>Multi-photon microscopy (MPM) is a 3-dimension fluorescence imaging technique that combines the excitation of two low-energy photons, enabling less photo-bleaching and deeper penetration of the imaged tissue. Two signals are detected, autofluorescence (AF), from natural intracellular fluorophores [such as nicotinamide adenine dinucleotide phosphate (NADP) and flavine adenine dinucleotide (FAD) transformation], and second harmonic generation (SHG), a physical property of the laser enhancing non-centrosymmetric structures such as collagen fibers. MPM can give both visual and quantitative information of a fresh tissue (without the need of processing, cutting or staining the tissue), aiding in the progress towards optimizing a real-time imaging device. The obje</pubmed_abstract><journal>Translational andrology and urology</journal><pagination>508-518</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10080359</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Value of multiphoton microscopy in uro-oncology: a narrative review.</pubmed_title><pmcid>PMC10080359</pmcid><pubmed_authors>Tewari AK</pubmed_authors><pubmed_authors>Khosla A</pubmed_authors><pubmed_authors>Tsavaras N</pubmed_authors><pubmed_authors>Durand M</pubmed_authors><pubmed_authors>Falagario UG</pubmed_authors><pubmed_authors>Treacy PJ</pubmed_authors><pubmed_authors>Kyprianou N</pubmed_authors><pubmed_authors>Wiklund P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Value of multiphoton microscopy in uro-oncology: a narrative review.</name><description>&lt;h4>Background and objective&lt;/h4>Multi-photon microscopy (MPM) is a 3-dimension fluorescence imaging technique that combines the excitation of two low-energy photons, enabling less photo-bleaching and deeper penetration of the imaged tissue. Two signals are detected, autofluorescence (AF), from natural intracellular fluorophores [such as nicotinamide adenine dinucleotide phosphate (NADP) and flavine adenine dinucleotide (FAD) transformation], and second harmonic generation (SHG), a physical property of the laser enhancing non-centrosymmetric structures such as collagen fibers. MPM can give both visual and quantitative information of a fresh tissue (without the need of processing, cutting or staining the tissue), aiding in the progress towards optimizing a real-time imaging device. The obje</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-04-19T14:30:21.631Z</modification><creation>2025-04-19T14:30:21.631Z</creation></dates><accession>S-EPMC10080359</accession><cross_references><pubmed>37032746</pubmed><doi>10.21037/tau-21-973</doi></cross_references></HashMap>