<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(2)</volume><submitter>De la Cadena A</submitter><pubmed_abstract>Nonlinear microscopy encompasses several imaging techniques that leverage laser technology to probe intrinsic molecules of biological specimens. These native molecules produce optical fingerprints that allow nonlinear microscopes to reveal the chemical composition and structure of cells and tissues in a label-free and non-destructive fashion, information that enables a plethora of applications, e.g., real-time digital histopathology or image-guided surgery. Because state-of-the-art lasers exhibit either a limited bandwidth or reduced wavelength tunability, nonlinear microscopes lack the spectral support to probe different biomolecules simultaneously, thus losing analytical potential. Therefore, a conventional nonlinear microscope requires multiple or tunable lasers to individually excite e</pubmed_abstract><journal>Biomedical optics express</journal><pagination>491-505</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10890845</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Simultaneous label-free autofluorescence multi-harmonic microscopy driven by the supercontinuum generated from a bulk nonlinear crystal.</pubmed_title><pmcid>PMC10890845</pmcid><pubmed_authors>De la Cadena A</pubmed_authors><pubmed_authors>Boppart SA</pubmed_authors><pubmed_authors>Park J</pubmed_authors><pubmed_authors>Monroy GL</pubmed_authors><pubmed_authors>Tehrani KF</pubmed_authors><pubmed_authors>Renteria CA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Simultaneous label-free autofluorescence multi-harmonic microscopy driven by the supercontinuum generated from a bulk nonlinear crystal.</name><description>Nonlinear microscopy encompasses several imaging techniques that leverage laser technology to probe intrinsic molecules of biological specimens. These native molecules produce optical fingerprints that allow nonlinear microscopes to reveal the chemical composition and structure of cells and tissues in a label-free and non-destructive fashion, information that enables a plethora of applications, e.g., real-time digital histopathology or image-guided surgery. Because state-of-the-art lasers exhibit either a limited bandwidth or reduced wavelength tunability, nonlinear microscopes lack the spectral support to probe different biomolecules simultaneously, thus losing analytical potential. Therefore, a conventional nonlinear microscope requires multiple or tunable lasers to individually excite e</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-05-18T12:53:22.8Z</modification><creation>2025-05-18T12:53:22.8Z</creation></dates><accession>S-EPMC10890845</accession><cross_references><pubmed>38404303</pubmed><doi>10.1364/BOE.504832</doi></cross_references></HashMap>