Multiphoton Microscopy in the Biomedical Sciences XVIII
Proceedings Volume 10498 is from: Logo
27 January - 1 February 2018
San Francisco, California, United States
Front Matter: Volume 10498
Proc. SPIE 10498, Front Matter: Volume 10498, 1049801 (30 March 2018);
Keynote Session
Proc. SPIE 10498, Seeing molecular vibrations: chemical imaging for biomedicine (Conference Presentation), 1049802 ();
Proc. SPIE 10498, Spectroscopic signatures of cells metabolism and extracellular species using phasor-FLIM (Conference Presentation), 1049803 ();
Proc. SPIE 10498, Metabolic imaging of tumor for diagnosis and response for therapy, 1049804 (23 February 2018);
Proc. SPIE 10498, Photoacoustic tomography: ultrasonically beating optical diffusion for deep imaging (Conference Presentation), 1049805 ();
Metabolism/NADH/FAD/Tryptophan I
Proc. SPIE 10498, Ultra-fast HPM detectors improve NAD(P)H FLIM, 1049806 (23 February 2018);
Proc. SPIE 10498, Multiparametric analysis of cisplatin-induced changes in cancer cells using FLIM , 1049807 (23 February 2018);
Proc. SPIE 10498, Phasor fluorescence lifetime microscopy of NADH to analyze metabolic activity of adipocytes (Conference Presentation), 1049808 ();
Proc. SPIE 10498, Single-cell metabolism predicts drug response in patient-derived pancreatic cancer organoids (Conference Presentation), 1049809 ();
Metabolism/NADH/FAD/Tryptophan II
Proc. SPIE 10498, Two-photon luminescence lifetime imaging microscopy (LIM) to follow up cell metabolism and oxygen consumption during theranostic applications, 104980A (23 February 2018);
Proc. SPIE 10498, Metabolic imaging for breast cancer detection and treatment: a role for mitochondrial Complex I function, 104980B (23 February 2018);
Proc. SPIE 10498, Non-invasive metabolic imaging of melanoma progression (Conference Presentation), 104980D ();
Proc. SPIE 10498, Mitochondrial protein knockouts induce changes in the fluorescence lifetimes of NAD(P)H and FAD (Conference Presentation), 104980F ();
Proc. SPIE 10498, Multimodal autofluorescence detection of cancer: from single cells to living organism, 104980G (23 February 2018);
Technology and In Vivo Imaging I
Proc. SPIE 10498, Liquid tunable microscopy under two-photon excitation regime (Conference Presentation), 104980H ();
Proc. SPIE 10498, Module for multiphoton high-resolution hyperspectral imaging and spectroscopy, 104980K (23 February 2018);
Proc. SPIE 10498, A time-gated large-array SPAD camera for picosecond resolution real-time FLIM (Conference Presentation), 104980M ();
Proc. SPIE 10498, Unmixing spectrally overlapping FRET biosensors in vivo using multispectral FLIM (Conference Presentation), 104980O ();
Proc. SPIE 10498, Two-photon FLIM imaging and femtosecond laser nano processing of IPS cells and stem cells (Conference Presentation), 104980P ();
Proc. SPIE 10498, Measuring upconversion nanoparticles photoluminescence lifetime with FastFLIM and phasor plots, 104980Q (23 February 2018);
Proc. SPIE 10498, Near infrared fluorescence lifetime FRET imaging of target engagement at multiscale (Conference Presentation), 104980R ();
Proc. SPIE 10498, Towards monitoring conformational changes of the GPCR neurotensin receptor 1 by single-molecule FRET, 104980T (23 February 2018);
Proc. SPIE 10498, A non-Euclidean phasor approach for distinction of fluorescent compounds using two-photon fluorescence lifetime imaging microscopy in ex vivo human skin (Conference Presentation), 104980U ();
Proc. SPIE 10498, Macroscopic time-resolved imaging of tumor (Conference Presentation), 104980V ();
Proc. SPIE 10498, FastFLIM, the all-in-one engine for measuring photoluminescence lifetime of 100 picoseconds to 100 milliseconds , 104980W (23 February 2018);
Proc. SPIE 10498, In vivo measurement of astrocytic endfoot Ca2+ and parenchymal vessel responses during 4-AP induced epilepsy using two-photon fluorescence lifetime microscopy, 104980X (23 February 2018);
Second/Third Harmonic Generation
Proc. SPIE 10498, Second harmonic generation microscopy of the living human cornea, 1049810 (23 February 2018);
Technology and In Vivo Imaging II
Proc. SPIE 10498, Rapid in vivo vertical tissue sectioning by multiphoton tomography, 1049814 (23 February 2018);
Proc. SPIE 10498, In vivo three-photon imaging of deep cerebellum, 1049816 (23 February 2018);
Coherent Raman I
Proc. SPIE 10498, Bioimaging with a home-built multimodal nonlinear microscope based on a compact fiber-format laser system (Conference Presentation), 104981B ();
Proc. SPIE 10498, From spectroscopy to chemical imaging: machine learning for hyperspectral coherent Raman imagery (Conference Presentation), 104981E ();
Proc. SPIE 10498, Metrology in nonlinear microscopy using harmonic generation nanoprobes (Conference Presentation), 104981F ();
Coherent Raman II
Proc. SPIE 10498, Spectroscopic mapping with coherent IR and Raman microscopy (Conference Presentation), 104981G ();
Proc. SPIE 10498, Integrated SRS and fluorescence imaging for study of thermogenesis and lipid metabolism in vivo, 104981I (23 February 2018);
Proc. SPIE 10498, Hyperspectral imaging with laser-scanning sum-frequency generation microscopy (Conference Presentation), 104981L ();
Coherent Raman III
Proc. SPIE 10498, High-speed multicolor SRS imaging (Conference Presentation), 104981M ();
Proc. SPIE 10498, Dual-phase stimulated Raman scattering microscopy for simultaneous two-color imaging (Conference Presentation), 104981N ();
Proc. SPIE 10498, CARS molecular fingerprinting using a sub-nanosecond supercontinuum light source, 104981P (23 February 2018);
Proc. SPIE 10498, In vivo study of lipid synthesis and lipolysis dynamics by stimulated Raman scattering microscopy, 104981Q (23 February 2018);
Proc. SPIE 10498, Resonantly enhanced coherent anti-Stokes Raman scattering, 104981R (11 April 2018);
Technology and In Vivo Imaging III
Proc. SPIE 10498, In vivo, two-color multiphoton microscopy using a femtosecond diamond Raman laser , 104981V (23 February 2018);
Proc. SPIE 10498, Adaptive optics plug-and-play setup for high-resolution microscopes with multi-actuator adaptive lens, 104981X (23 February 2018);
Proc. SPIE 10498, 3D brain oxygenation measurements in awake hypertensive mice using two photon phosphorescence lifetime imaging, 104981Y (23 February 2018);
Poster Session
Proc. SPIE 10498, Simple fibre based dispersion management for two-photon excited fluorescence imaging through an endoscope, 1049820 (23 February 2018);
Proc. SPIE 10498, Rapid and lossless bandwidth-switching of a fiber-based optical parametric oscillator for multimodal nonlinear microscopy, 1049822 (23 February 2018);
Proc. SPIE 10498, Electronically tunable femtosecond all-fiber optical parametric oscillator for multi-photon microscopy , 1049823 (23 February 2018);
Proc. SPIE 10498, Optimizing Ti:Sapphire laser for quantitative biomedical imaging , 1049824 (23 February 2018);
Proc. SPIE 10498, Spatially confined photoinactivation of bacteria: towards novel tools for detailed mechanistic studies, 1049825 (23 February 2018);
Proc. SPIE 10498, In vivo multiphoton and fluorescence lifetime imaging microscopy of the healthy and cholestatic liver, 1049827 (23 February 2018);
Proc. SPIE 10498, Two-photon activation of endogenous store-operated calcium channels without optogenetics , 1049828 (23 February 2018);
Proc. SPIE 10498, Comparison of excitation wavelengths for in vivo deep imaging of mouse brain , 104982A (23 February 2018);
Proc. SPIE 10498, Stimulated emission and spontaneous loss pump-probe microscopy for background removal, 104982C (23 February 2018);
Proc. SPIE 10498, Rapid volumetric multiphoton imaging with the combination of an ultrasound lens and a resonant mirror, 104982D (23 February 2018);