Littérature scientifique sur le sujet « Multiplexed fluorescence imaging »
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Articles de revues sur le sujet "Multiplexed fluorescence imaging"
Cappella, Paolo, et Fabio Gasparri. « Highly Multiplexed Phenotypic Imaging for Cell Proliferation Studies ». Journal of Biomolecular Screening 19, no 1 (29 juillet 2013) : 145–57. http://dx.doi.org/10.1177/1087057113495712.
Texte intégralLiu, Hsiou-Yuan, Jingshan Zhong et Laura Waller. « Multiplexed phase-space imaging for 3D fluorescence microscopy ». Optics Express 25, no 13 (21 juin 2017) : 14986. http://dx.doi.org/10.1364/oe.25.014986.
Texte intégralLuo, Teng, Ting Zhou, Yihua Zhao, Liwei Liu et Junle Qu. « Multiplexed fluorescence lifetime imaging by concentration-dependent quenching ». Journal of Materials Chemistry B 6, no 13 (2018) : 1912–19. http://dx.doi.org/10.1039/c8tb00095f.
Texte intégralKo, Jina, Juhyun Oh, Maaz S. Ahmed, Jonathan C. T. Carlson et Ralph Weissleder. « Ultra‐fast Cycling for Multiplexed Cellular Fluorescence Imaging ». Angewandte Chemie 132, no 17 (20 avril 2020) : 6906–13. http://dx.doi.org/10.1002/ange.201915153.
Texte intégralKo, Jina, Juhyun Oh, Maaz S. Ahmed, Jonathan C. T. Carlson et Ralph Weissleder. « Ultra‐fast Cycling for Multiplexed Cellular Fluorescence Imaging ». Angewandte Chemie International Edition 59, no 17 (6 mars 2020) : 6839–46. http://dx.doi.org/10.1002/anie.201915153.
Texte intégralGamber, Kevin, Arne Christians, Spencer Schwarz, Adam Northcutt, Jason Forys, Thomas Campbell et Crystal Winkeler. « Quantitative Immune Profiling of Human Tumor Tissues with Multiplexed ChipCytometry ». Journal of Immunology 206, no 1_Supplement (1 mai 2021) : 68.05. http://dx.doi.org/10.4049/jimmunol.206.supp.68.05.
Texte intégralMizuno, T., E. Hase, T. Minamikawa, Y. Tokizane, R. Oe, H. Koresawa, H. Yamamoto et T. Yasui. « Full-field fluorescence lifetime dual-comb microscopy using spectral mapping and frequency multiplexing of dual-comb optical beats ». Science Advances 7, no 1 (janvier 2021) : eabd2102. http://dx.doi.org/10.1126/sciadv.abd2102.
Texte intégralXu, Jian, Tianyue Zhang, Shenyu Yang, Ziwei Feng, Haoying Li, Dejiao Hu, Fei Qin et al. « Plasmonic Nanoprobes for Multiplexed Fluorescence-Free Super-Resolution Imaging ». Advanced Optical Materials 6, no 20 (5 août 2018) : 1800432. http://dx.doi.org/10.1002/adom.201800432.
Texte intégralLv, Yanlu, Jiulou Zhang, Dong Zhang, Wenjuan Cai, Nanguang Chen et Jianwen Luo. « In vivosimultaneous multispectral fluorescence imaging with spectral multiplexed volume holographic imaging system ». Journal of Biomedical Optics 21, no 6 (3 juin 2016) : 060502. http://dx.doi.org/10.1117/1.jbo.21.6.060502.
Texte intégralKeshri, Puspam, Bin Zhao, Tianfa Xie, Yousef Bagheri, James Chambers, Yubing Sun et Mingxu You. « Quantitative and Multiplexed Fluorescence Lifetime Imaging of Intercellular Tensile Forces ». Angewandte Chemie 133, no 28 (10 juin 2021) : 15676–83. http://dx.doi.org/10.1002/ange.202103986.
Texte intégralThèses sur le sujet "Multiplexed fluorescence imaging"
Chouket, Raja. « New dimensions for multiplexed fluorescence imaging ». Electronic Thesis or Diss., Sorbonne université, 2019. http://www.theses.fr/2019SORUS606.
Texte intégralOur research group had previously developed the OPIOM protocols for fluorescence imaging. By exploiting their cross sections of fluorescence photoswiching, OPIOM can selectively extract the response of reversibly photoswitchable fluorophores (RSFs) in the presence of spectrally interfering fluorophores. However, OPIOM allowed us to discriminate only 3 spectrally similar reversibly photoswitchable fluorescent proteins (RSFPs). The goal of this PhD was to augment this number. To reach this goal, a new automated instrumental setup called photoswichometer was first developed to express and screen the rich photochemical signature of 22 RSFPs by analyzing their fluorescence response to light jumps with intensities covering 5 orders of magnitude. This signature has been first exploited in a new fluorescence imaging protocol called HIGHLIGHT, which capitalized on OPIOM and further improved its selectivity. In HIGHLIGHT, the RSFs are submitted to harmonic light modulation and their contribution to the overall fluorescence emission signals is selectively retrieved from exploiting their singular non-linear response under optimized conditions. HIGHLIGHT has been implemented to image RSFPs in cells without interference of autofluorescence, to perform multiplexed imaging of 3 RSFPs which could not be discriminated with OPIOM, and used for its intrinsic optical sectioning. The RSF signature has been then used in a second fluorescence imaging protocol called LIGHTNING. In contrast to OPIOM and HIGHLIGHT which exploit the cross sections of fluorescence photoswitching in a steady-state regime of low light intensity, LIGHTNING exploits the transient time fluorescence response of RSFs under multiple illuminations involving various ranges of light intensities for RSF discrimination. Thus, LIGHTNING allowed us to improve the multiplexing degree of dynamic contrast in fluorescence imaging up to 20 RSFP among 22 studied RSFPs
Behrooz, Ali. « Multiplexed fluorescence diffuse optical tomography ». Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/50401.
Texte intégralLuthman, Anna Siri Naemi. « Spectrally resolved detector arrays for multiplexed biomedical fluorescence imaging ». Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/274904.
Texte intégralWarren, Sean. « Development and application of multiplexed fluorescence imaging to chemotaxis signalling pathways ». Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/25117.
Texte intégralWatabe, Tetsuya. « Booster, a Red-Shifted Genetically Encoded Förster Resonance Energy Transfer (FRET) Biosensor Compatible with Cyan Fluorescent Protein/Yellow Fluorescent Protein-Based FRET Biosensors and Blue Light-Responsive Optogenetic Tools ». Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263527.
Texte intégralWu, Juwell Wendy. « Near-infrared emitting quantum dots for cellular and vascular fluorescent labeling in in vivo multiplexed imaging studies ». Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/68460.
Texte intégralCataloged from PDF version of thesis.
Includes bibliographical references (p. 199-217).
In vivo multimodal, multiplexed microscopy allows real-time observation of hematopoietic cells, their stem and progenitor cells and metastatic cancer cells in their native bone marrow (BM) environment. Multiplexing has made possible detailed studies of the BM's microarchitecture, which helps define the niche of these cells; it has nonetheless been limited by the paucity of suitable probes fluorescent in the near-infrared spectrum that is favored by tissue optics. This project attempts to address this problem by developing cellular and vascular fluorescent imaging probes comprised of semiconductor nanocrystals, or quantum dots (QDs), with tunable fluorescence between 65o-8oonm and exhibiting photostability, robust quantum yield and narrow fluorescence profiles that are critical for such applications. The synthesis of alloyed CdTexSe1 x QDs will be detailed in the thesis. Reproducibility and workability in subsequent steps are emphasized in the methods. Special attention is also paid to the difference between working with alloyed versus single semiconductor QDs, especially the need to achieve physical and spectral uniformity when composition and its gradient are also variable. The steps for creating biological probes from these QD fluorophores are also described. They include overcoating, water solubilization and functionalization for cellular uptake and vascular retention. Finally, the thesis returns to its motivation and reports novel methods, developed using NIR QD vascular imaging probes, for visualizing in vivo 3-D imaging data of the murine BM and characterizing the tissue's architecture. Measuring the Euclidean distance between BM osteoblasts and blood vessels is presented to exemplify a potential platform for describing the geographic relationships between cells, molecules and structural components in any tissue.
by Juwell Wendy Wu.
Ph.D.
Fries, Maximilian Werner. « Multiplexed biochemical imaging reveals the extent and complexity of non-genetic heterogeneity in DNA damage-induced caspase dynamics ». Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/273868.
Texte intégralDeiss, Frédérique. « Développement de réseaux multiplexés de biocapteurs électrochimiques ». Thesis, Bordeaux 1, 2009. http://www.theses.fr/2009BOR13883/document.
Texte intégralThis work presents the development of optoelectrochemical micro- and nanosensor arrays for bioanalytical applications. These platforms respond to the growing need in research and diagnostic for tools allowing multiple and simultaneous analysis in small-volume samples. These new high density biochips are made from coherent optical fiber bundles: one face is micro- or nanostructured by chemical etching and then functionnalized with biological probes. The first biochip is a fluorescent DNA nanosensor array where probes have been immobilized by electrodeposition of a polypyrrole thin film. The detection of the hybridization is remotely performed through the imaging fiber. Different probes were succesfully addressed onto the same nanostructured array thanks to electrochemical cantilevers. The second biochip allows multiplexed sandwich immunoassays using electrochimiluminescent imaging resolved at the single bead level. In particular, the development of this new readout mechanism allows extending electrochemiluminescent detection for multiplexed immunoassays. Design and implementations of both platforms take advantages of different physical and chemical techniques, especially electrochemical, to obtain biochips with a great potential through high density and high multiplexing level
Ho, Derek. « CMOS Contact Imagers for Spectrally-multiplexed Fluorescence DNA Biosensing ». Thesis, 2013. http://hdl.handle.net/1807/35849.
Texte intégral« Identifying and Characterizing Type 1 and Type 2 Eosinophil Subtypes ». Doctoral diss., 2020. http://hdl.handle.net/2286/R.I.57159.
Texte intégralDissertation/Thesis
Doctoral Dissertation Biochemistry 2020
Livres sur le sujet "Multiplexed fluorescence imaging"
Luthman, Anna Siri. Spectrally Resolved Detector Arrays for Multiplexed Biomedical Fluorescence Imaging. Cham : Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-98255-7.
Texte intégralLuthman, Anna Siri. Spectrally Resolved Detector Arrays for Multiplexed Biomedical Fluorescence Imaging. Springer, 2018.
Trouver le texte intégralLuthman, Anna Siri. Spectrally Resolved Detector Arrays for Multiplexed Biomedical Fluorescence Imaging. Springer International Publishing AG, 2019.
Trouver le texte intégralChapitres de livres sur le sujet "Multiplexed fluorescence imaging"
Peng, Leilei. « Fourier Multiplexed Fluorescence Lifetime Imaging ». Dans Methods in Molecular Biology, 157–72. New York, NY : Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1593-5_11.
Texte intégralChouket, Raja, Ruikang Zhang, Agnès Pellissier-Tanon, Annie Lemarchand, Agathe Espagne, Thomas Le Saux et Ludovic Jullien. « Out-of-Phase Imaging after Optical Modulation (OPIOM) for Multiplexed Fluorescence Imaging Under Adverse Optical Conditions ». Dans Methods in Molecular Biology, 191–227. New York, NY : Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1593-5_13.
Texte intégralChouket, Raja, Ruikang Zhang, Agnès Pellissier-Tanon, Annie Lemarchand, Agathe Espagne, Thomas Le Saux et Ludovic Jullien. « Correction to : Out-of-Phase Imaging after Optical Modulation (OPIOM) for Multiplexed Fluorescence Imaging Under Adverse Optical Conditions ». Dans Methods in Molecular Biology, C1. New York, NY : Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1593-5_22.
Texte intégralJia, Yunlong, Françoise Bleicher, Jonathan Reboulet et Samir Merabet. « Bimolecular Fluorescence Complementation (BiFC) and Multiplexed Imaging of Protein–Protein Interactions in Human Living Cells ». Dans Methods in Molecular Biology, 173–90. New York, NY : Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1593-5_12.
Texte intégralMoffitt, J. R., et X. Zhuang. « RNA Imaging with Multiplexed Error-Robust Fluorescence In Situ Hybridization (MERFISH) ». Dans Visualizing RNA Dynamics in the Cell, 1–49. Elsevier, 2016. http://dx.doi.org/10.1016/bs.mie.2016.03.020.
Texte intégral« Bio-Mediated Synthesis of Quantum Dots for Fluorescent Biosensing and Bio-Imaging Applications ». Dans Materials Research Foundations, 185–223. Materials Research Forum LLC, 2021. http://dx.doi.org/10.21741/9781644901571-7.
Texte intégralActes de conférences sur le sujet "Multiplexed fluorescence imaging"
Le, Vu Nam, Huai Dong Yang, Xin Rong Zhang, Guo Fan Jin et Si Chun Zhang. « Frequency division multiplexed multi-color fluorescence microscope system ». Dans Space Optics and Earth Imaging and Space Navigation, sous la direction de Carl Nardell, Suijian Xue et Huaidong Yang. SPIE, 2017. http://dx.doi.org/10.1117/12.2307240.
Texte intégralJo, YoungJu, Hyungjoo Cho, Wei Sun Park, Geon Kim, DongHun Ryu, Young Seo Kim, Moosung Lee et al. « Label-free multiplexed microtomography of endogenous subcellular dynamics using generalizable deep learning ». Dans CLEO : Applications and Technology. Washington, D.C. : Optica Publishing Group, 2022. http://dx.doi.org/10.1364/cleo_at.2022.ath2i.6.
Texte intégralCheng, Shiyi, Sipei Fu, Yumi Mun Kim, Ji Yi et Lei Tian. « Multiplexed virtual fluorescence labeling from multi-contrast microscopy by deep learning ». Dans High-Speed Biomedical Imaging and Spectroscopy VI, sous la direction de Keisuke Goda et Kevin K. Tsia. SPIE, 2021. http://dx.doi.org/10.1117/12.2578439.
Texte intégralRudkouskaya, A., S. Chen, N. Sinsuebphon, J. E. Mazurkiewicz, M. Ochoa, X. Intes et M. Barroso. « Multiplexed Fluorescence Lifetime in vivo FRET Imaging using a Dark Quencher ». Dans Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C. : OSA, 2019. http://dx.doi.org/10.1364/omp.2019.ow5d.4.
Texte intégralChen, Kun, Rui Yan, Limin Xiang et Ke Xu. « Excitation spectral microscopy for highly multiplexed fluorescence imaging and quantitative biosensing ». Dans High-Speed Biomedical Imaging and Spectroscopy VII, sous la direction de Keisuke Goda et Kevin K. Tsia. SPIE, 2022. http://dx.doi.org/10.1117/12.2612265.
Texte intégralLv, Yanlu, Chuangjian Cai, Jing Bai et Jianwen Luo. « Compact multispectral fluorescence imaging system with spectral multiplexed volume holographic grating ». Dans SPIE BioPhotonics Australasia, sous la direction de Mark R. Hutchinson et Ewa M. Goldys. SPIE, 2016. http://dx.doi.org/10.1117/12.2239925.
Texte intégralPera, Vivian, Dana H. Brooks et Mark Niedre. « A sparse nonnegative demixing algorithm with intrinsic regularization for multiplexed fluorescence tomography ». Dans 2015 IEEE 12th International Symposium on Biomedical Imaging (ISBI 2015). IEEE, 2015. http://dx.doi.org/10.1109/isbi.2015.7164050.
Texte intégralChan, Antony C. S., Edmund Y. Lam et Kevin K. Tsia. « Signal reduction in fluorescence imaging using radio frequency-multiplexed excitation by compressed sensing ». Dans SPIE/COS Photonics Asia, sous la direction de Bahram Jalali, Ming Li, Keisuke Goda et Mohammad H. Asghari. SPIE, 2014. http://dx.doi.org/10.1117/12.2072016.
Texte intégralJiang, Yang, David Cooper, Matthew D. Carson et Eric J. Seibel. « Custom bile duct phantom for first-in-human multiplexed NIR fluorescence peptide imaging ». Dans Design and Quality for Biomedical Technologies XII, sous la direction de Rongguang Liang, T. Joshua Pfefer et Jeeseong Hwang. SPIE, 2019. http://dx.doi.org/10.1117/12.2509893.
Texte intégralZhang, Ruikang, Raja Chouket, Jérome Quérard, Marie-Aude Plamont, Zsolt Kelemen, Agathe Espagne, Alison G. Tebo et al. « Out-of-Phase Imaging after Optical Modulation for Micro-and Macro-scale Multiplexed Fluorescence Imaging Against Autofluorescence and Ambient Light ». Dans Novel Techniques in Microscopy. Washington, D.C. : OSA, 2019. http://dx.doi.org/10.1364/ntm.2019.ns2b.4.
Texte intégral