Literatura científica selecionada sobre o tema "In-Situ microscopie de fluorescence"
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Artigos de revistas sobre o assunto "In-Situ microscopie de fluorescence"
Pernthaler, Jakob, Annelie Pernthaler e Rudolf Amann. "Automated Enumeration of Groups of Marine Picoplankton after Fluorescence In Situ Hybridization". Applied and Environmental Microbiology 69, n.º 5 (maio de 2003): 2631–37. http://dx.doi.org/10.1128/aem.69.5.2631-2637.2003.
Texto completo da fonteLeger, I., M. Robert-Nicoud e G. Brugal. "Combination of DNA in situ hybridization and immunocytochemical detection of nucleolar proteins: a contribution to the functional mapping of the human genome by fluorescence microscopy." Journal of Histochemistry & Cytochemistry 42, n.º 2 (fevereiro de 1994): 149–54. http://dx.doi.org/10.1177/42.2.8288860.
Texto completo da fonteLu, Fang, Tingting Zhou, Yan Liu, Liying Song, Bin Zhang e Yuyan Li. "Application of Fluorescence In Situ Hybridization Assisted by Fluorescence Microscope in Detection of Her2 Gene in Breast Cancer Patients". Contrast Media & Molecular Imaging 2022 (11 de agosto de 2022): 1–6. http://dx.doi.org/10.1155/2022/3087681.
Texto completo da fonteBuchanan, Bailey C., e Jeong-Yeol Yoon. "Microscopic Imaging Methods for Organ-on-a-Chip Platforms". Micromachines 13, n.º 2 (19 de fevereiro de 2022): 328. http://dx.doi.org/10.3390/mi13020328.
Texto completo da fonteTatarov, Boyan, Detlef Müller, Matthias Tesche e Sung-Kyun Shin. "Lidar Innovations for Technologies and Environmental Sciences (LITES) – An Remote Sensing Infrastructure Facility: Setup and Measurements Examples". EPJ Web of Conferences 237 (2020): 07017. http://dx.doi.org/10.1051/epjconf/202023707017.
Texto completo da fonteLeitch, A. R., W. Mosgoller, T. Schwarzacher, M. D. Bennett e J. S. Heslop-Harrison. "Genomic in situ hybridization to sectioned nuclei shows chromosome domains in grass hybrids". Journal of Cell Science 95, n.º 3 (1 de março de 1990): 335–41. http://dx.doi.org/10.1242/jcs.95.3.335.
Texto completo da fonteDeerinck, Thomas J., Maryann E. Martone, Varda Lev-Ram, David P. L. Green, Roger Y. Tsien, David L. Spector, Sui Huang e Mark H. Ellisman. "3-Dimensional immunolabeling and in situ hybridization detection using fluorescence photooxidation and intermediate-voltage Electron Microscopy". Proceedings, annual meeting, Electron Microscopy Society of America 52 (1994): 164–65. http://dx.doi.org/10.1017/s0424820100168554.
Texto completo da fonteJovin, Thomas M., Michel Robert-Nicoud, Donna J. Arndt-Jovin e Thorsten Schormann. "3-D imaging of cells using a confocal laser scanning microscope and digital image processing". Proceedings, annual meeting, Electron Microscopy Society of America 46 (1988): 96–97. http://dx.doi.org/10.1017/s0424820100102560.
Texto completo da fonteShah, Jyotsna S., Olivia Mark, Eddie Caoili, Akhila Poruri, Richard I. Horowitz, Alan D. Ashbaugh e Ranjan Ramasamy. "A Fluorescence In Situ Hybridization (FISH) Test for Diagnosing Babesiosis". Diagnostics 10, n.º 6 (6 de junho de 2020): 377. http://dx.doi.org/10.3390/diagnostics10060377.
Texto completo da fonteShah, Jyotsna S., e Ranjan Ramasamy. "Fluorescence In Situ Hybridization (FISH) Tests for Identifying Protozoan and Bacterial Pathogens in Infectious Diseases". Diagnostics 12, n.º 5 (21 de maio de 2022): 1286. http://dx.doi.org/10.3390/diagnostics12051286.
Texto completo da fonteTeses / dissertações sobre o assunto "In-Situ microscopie de fluorescence"
Roussille, Ludovic. "Suivi quantitatif in situ d'interactions biomoléculaire par microscopie optique SEEC". Thesis, Le Mans, 2012. http://www.theses.fr/2012LEMA1030/document.
Texto completo da fonteThis thesis was supported by National Agency for Research with the project: ANR PNANO-07 SEEC. The Surface Enhanced Ellipsometric Contrast (SEEC) microscopy has invented in 2000 at Le Mans (France). This technique allows the visualization of nanoscopic object between crossed analyzer and polarizer. It’s possible if some special multilayer surfaces are used. There surfaces must have the particularity to not change the polarization of light during the reflection. Until the beginning of the project the SEEC microscopy was useful only for air observations. The goal of the thesis was to adapt this technique to observe on gold surfaces immerged in water and to compare the performance of the SEEC microscopy with Surface Plasmonique Resonance (SPR) in that configuration. The SPR is a biomolecular interaction study reference technique. SEEC microscopy lateral resolution was evaluate by fluorescence microscopy. Next, we realize two model experiments monitor in parallel by SEEC microscopy and by SPR: BSA immobilization and biotinylated IgG fixation by immobilized streptavidine. To compare measurements efficiently we did a huge preparation work (surface functionalizations and microfluidic) to have exactly same conditions in both techniques.Our results show SEEC microscopy cannot replace SPR for biomolecular interaction studies but it can be used as cheap immunological diagnostic technique. This work gives the path to follow on that direction
Man, Hiu Mun. "Characterisation of enzymatic catalysis by microscopy and electrochemistry : application to H2/O2 bio-fuel cells". Electronic Thesis or Diss., Aix-Marseille, 2022. http://theses.univ-amu.fr.lama.univ-amu.fr/221207_MAN_82cby815lbx134rmsegm855nh_TH.pdf.
Texto completo da fonteEnzyme biofuel cells, which use enzymes to convert chemical energy into electricity, hold promise as one of the most promising alternative and clean energy resources. However, the immobilization of such enzymes on an electrode for efficient catalysis still raises many challenges. In order to access spatially resolved information, it is necessary to couple electrochemistry to other surface techniques. In this thesis, confocal laser scanning fluorescence microscopy was coupled with electrochemistry for the characterization of electro-enzymatic catalysis. The main reaction studied was the oxygen reduction reaction catalyzed by bilirubin oxidase from Myrothecium verrucaria. This reaction involves a consumption of protons coupled with electron transfer. Using in situ analysis, the local pH variations that occur near the bioelectrode during the enzymatic catalysis are visualized thanks to a fluorophore whose emission depends on the pH, fluorescein. The activity of the enzyme was first probed by UV-vis spectroscopy and electrochemistry. We then showed that the intensity of the fluorescence recorded is directly proportional to the catalytic current. Profiles of proton depletion at the electrochemical interface in buffered and unbuffered electrolytes were reconstructed to determine the influence of ionic strength on the local environment of enzymes. Finally, the enzymes were labeled with fluorophores, making it possible to reveal the local heterogeneities of their interfacial distribution
Mudry, Emeric. "Resolution improvement in fluorescence and phase optical microscopy". Phd thesis, Université Paul Cézanne - Aix-Marseille III, 2012. http://tel.archives-ouvertes.fr/tel-00822086.
Texto completo da fonteMilhiet, Elodie. "Nanospectroscopie de molécules d’intérêt biologique". Paris 11, 2007. http://www.theses.fr/2007PA112150.
Texto completo da fonteSingle-molecule-like spectroscopy plays a major role in many domains, from fundamental physics to biology. In this framework, my dissertation focuses on instrumental and theoretical developments of two biological-related applications. The first experiment aims at characterizing the dynamics of calcium binding by the fluorescent calcium probe Oregon-green Bapta5N commonly employed in cell signaling analysis. To achieve it, I have developed an experimental set-up of fluorescence correlation spectroscopy that exhibits sensitivity close to that of single-molecule detection. Either monophotonic or biphotonic excitations can be used. I have investigated the several aspects of the photophysics of the probe and evaluated the interest and limitations of such an approach for future in-vivo measurements. The second one is devoted to the development of a semi-quantitative Fluorescent In-Situ Hybridization (FISH) technique for mapping gene expression in the adult drosophila brain. Two difficulties have to be solved. First, we succeeded in obtaining reproducible results with drosophila adult brain. Secondly, while most of the FISH protocols are not quantitative since they need a strong enzymatic, we achieved semi-quantitative detection of RNA probes. I will present results on a new approach for which enzymatic detection is replaced by a sensitive detection and a protocol which reduces autofluorescence contribution. Results will be presented for several genes in adult drosophila brain to validate the methods as well as an interesting application on a mental retardation disease. To conclude, I show that the method exhibits a single RNA sensitivity which opens the way to new applications
Lefrançois, Pauline. "Développement d’un microréacteur biomimétique pour l'analyse in situ d'activités enzymatiques par couplage de l’électrochimie et de la microscopie de fluorescence". Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0759/document.
Texto completo da fonteEnzymatic reactions are involved in many physiological phenomena in living organisms. These reactions are based on protons and electrons transfers and can lead to the production of by-products. Among them, reactive oxygen and nitrogen species (ROS and RNS) are of great interest as they play a double role: on the one hand by allowing the organism to react to a stress by the activation of signaling redox pathways, and on the other hand, ROS and RNS can cause oxidative damages to tissues ensuing dysfunctions in the organism. The high reactivity of such species induce their short lifetimes (ns-min) and leads to uncertainties when it comes to the study of some enzymatic reactions in bulk. This PhD project aims to develop a biomimetic microreactor for the study of enzymatic ac-tivities producing ROS/RNS. Indeed, by confining a reaction within a cell-sized compartment (20-100 μm diameter), the generated species (H2O2, NO•, NO2-) could be analyzed in situ with a quantita-tive and kinetic resolution. Giant unilamellar vesicles are formed in physiological conditions and are used as microreactors for the monitoring of enzymatic activities of glucose oxidase and NO-synthases. Fluorescence microscopy allows individual vesicle observation and the monitoring of reactions trig-gered by microinjection. Then, released species are detected in real-time by electrochemistry in order to decipher the diverse enzymatic pathways of NO-Synthases
Cabriel, Clément. "Three-dimensional and multicolour approaches in super-resolution fluorescence microscopy for biology". Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS220.
Texto completo da fonteCell biology relies on imaging tools to provide structural and dynamic information about samples. Among them, fluorescence microscopy offers a compromise between high specificity and low toxicity. Recently, super-resolution methods overcame the diffraction barrier to unlock new fields of investigation. Single molecule approaches prove especially useful for three-dimensional nanoscale imaging, and allow couplings between different detection modalities. Still, their use is hindered by the complexity of the methods as well as the lack of reproducibility between experiments.We propose new methods to render super-localisation microscopy more easily applicable to relevant studies in cell biology, chemistry and material science. First, we introduce dedicated protocols and samples to eliminate sources of error in calibration and performance measurement acquisitions. We also provide examples of uses of three-dimensional super-localisation for state-of-the-art studies in the frameworks of cell adhesion and bacterial resistance to drugs.Then, we focus on the development of a novel optical method that provides unbiased results in three-dimensional single molecule localisation microscopy. This is achieved through the combination of two complementary axial detection strategies: point spread function shaping on the one hand, and supercritical angle fluorescence detection on the other hand. By cross-correlating and merging the lateral and axial positions provided by the different sources, we achieve quasi-isotropic localisation precisions down to 15 nanometres over a 1-micrometre capture range. We demonstrate the insensibility of the method to imaging non-idealities such as axial drift, chromatic aberration and sample tilt, and we propose applications in neurobiology and bacteria labelling.Finally, we introduce two new post-processing approaches for the demixing of simultaneous multi-species acquisitions. They are based respectively on the measurement of the spot sizes, and on the assessment of the dynamic blinking behaviour of molecules. After demonstrating a proof of principle, we assess the impact of the different parameters likely to influence the results. Eventually, we discuss leads to improve the demixing performances, and we discuss the coupling possibilities with complementary single molecule localisation techniques
Wang, Ruixing. "STED-fluorescence correlation spectroscopy for dynamic observations in cell biology : from theoretical to practical approaches". Thesis, Aix-Marseille, 2018. http://www.theses.fr/2018AIXM0163/document.
Texto completo da fonteSuper-resolution techniques offer new insight into the description of the dynamic molecular organization at the plasma membrane. Among these techniques, the stimulated emission depletion (STED) microscopy breaks the optical diffraction limit and reaches the resolution of tens of nanometer. It is a versatile setup that can be combined with other techniques such as fluorescence correlation spectroscopy (FCS), providing both high spatial and temporal resolutions to explore dynamic processes occurring in live cells. This PhD project aims at implementing a STED microscope, and then at combining this STED module with FCS technique for biological applications. Detailed theoretical studies on STED and the combined STED-FCS technique in spatio-temporal aspects were performed. An analytical solution for FCS autocorrelation function was derived in the condition of incomplete STED depletion and a new FCS fitting model was proposed to overcome this problem. The spot variation FCS (svFCS) method has demonstrated its capability to identify the presence of nanodomains constraining the lateral diffusion of molecules at the plasma membrane. The STED-FCS can extend the svFCS approach to the nanoscale evaluating the long-lasting existence of such nanodomains. Within this frame, preliminary Monte Carlo simulations were conducted mimicking molecules diffusing in the presence of dynamic self-assembling/disassembling nanodomains
Galanti, Agostino. "Multi-photochromic architectures : from structure to function". Thesis, Strasbourg, 2018. http://www.theses.fr/2018STRAF046/document.
Texto completo da fonteThe aim of this thesis has been to develop systems capable of responding to external stimuli, based on photochromic units. The goal of such a quest is to increase the complexity of devices and synthetic molecular machines. With the goal of developing more complex artificial devices and machines, we have realised systems containing multiple molecular switches. For the realisation of this thesis, new multi-photochromic systems, or photochromes/nanomaterials hybrids containing azobenzene, diarylethene or spiropyran moieties have been realised and studied. Firstly, we focused on multi-azobenzene systems capable of undergoing large geometric rearrangements during photoisomerisation, as they may be used in the future as constituent elements of host-guest or metal-organic frameworks controllable by luminous stimuli. In a second example, dithienylethene-type photochromic switches have been used to trigger the emission of a porphyrin. This dyad exhibited a reversible modulation of its emission, displaying a particularly highly contrasted response. As a final example, a spiropyran derivative has been combined with anisotropic gold nanoparticles. By inducing the isomerisation of the molecular switch in the AuNR colloidal liquid dispersions, we visualised a large variation of the colloid extinction spectrum, dependent on the LSPR mode wavelength and the spectral overlap with the photoswitch
Zheng, Zheng. "Development of Far-Red / Near-Infrared Luminescent Chromophores and Nanoparticles for in vivo Biphotonic Applications". Thesis, Lyon, 2016. http://www.theses.fr/2016LYSEN024/document.
Texto completo da fonteThe development of fluorophores with efficient two-photon absorption (TPA) and emission properties in the far red/NIR is important, especially for in depth in-vivo optical imaging as this wavelength range corresponds to the optical transparency window of tissues. This thesis investigates the potential of new red emitting fluorophores containing a fluorene ring for in-vivo two-photon microscopy focusing on vascular imaging on one hand and on oxygen pressure measurement on the other hand.A new series of asymmetrical fluorene-based chromophores were designed and synthesized. Their structure-property relationships were systematically investigated. It was found that most of chromophores exhibit aggregation-induced emission behaviors in the NIR region. In addition, a micelle/silica coprotection strategy was proposed to prepare nanoparticles with a less polar interior, which can be used to conserve optical properties of dipole chromophores in aqueous solution. The two-photon excited fluorescence (TPEF) measurements indicate that they all display obvious TPA activities in organic solvent and aqueous suspension. Both the NIR-emissive aggregates and nanoparticles have been successfully used for TPEF imaging of blood vessels inside mouse ear skin. The silica nanoparticles show outstanding staining of the vascular system making them perfect blood pool markers.On a second part, four new fluorene-based two-photon absorbing chromophores have been synthesized and their one- and two-photon photophysical properties were investigated. The optimum chromophore was successfully attached covalently to an oxygen responsive phosphorescent Pd-porphyrin complex by click chemistry. Two new compounds contain four or eight TPA chromophores donor connected to the phosphorescent core. The result demonstrate that the incorporation of a suitable TPA chromophore can effectively enhance the TPA of the system, allowing efficient sensitivity towards oxygen
Gasecka, Alicja. "Polarimetric multiphoton fluorescence microscopy in molecular and biological media". Aix-Marseille 3, 2010. http://www.theses.fr/2010AIX30068.
Texto completo da fonteLight-matter interaction in molecular and bio-molecular media can lead to complex processes where optical fields polarizations couple to an assembly of molecular transition dipoles. The manipulation of the optical fields polarization in fluorescence microscopy can in particular give access to fine changes occurring in molecular arrangements. In this PhD thesis we report a method based on a tuneable excitation polarization state complemented by a polarized read-out, applied to polarization-resolved multiphoton fluorescence microscopy. Two-photon fluorescence polarimetry allows to retrieve a quantitative information on the static molecular distribution shape and orientation in different environments such as model lipid membranes, cell membranes, and molecular inclusion compounds that can be strongly heterogeneous. Three-photon fluorescence polarimetry has been furthermore applied in bio-molecular media in order to provide a diagnostics for crystallinity in protein crystals with high sensitivity to their structure and symmetry. The experimental implementation of polarimetric multi-photon microscopy requires to quantify possible polarization distortions originating from the experimental set-up or sample itself, which are thoroughly analyzed
Livros sobre o assunto "In-Situ microscopie de fluorescence"
Liehr, Thomas. Fluorescence In Situ Hybridization (FISH) — Application Guide. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009.
Encontre o texto completo da fonteFluorescence in situ hybridization (FISH): Protocols and applications. New York, NY: Humana Press, 2010.
Encontre o texto completo da fonteAmmasi, Periasamy, e Clegg Robert M, eds. FLIM microscopy in biology and medicine. Boca Raton: Taylor & Francis, 2009.
Encontre o texto completo da fonte1923-, Sharma Arun Kumar, e Sharma Archana 1932-, eds. Chromosome painting: Principles, strategies, and scope. Dordrecht: Kluwer Academic Publishers, 2001.
Encontre o texto completo da fonteFried, Alexander. Studies of phase transitions in supported lipid bilayers by simultaneous in situ fluorescence spectroscopy and atomic force microscopy. Ottawa: National Library of Canada, 2002.
Encontre o texto completo da fonteA, Sharif N., ed. Molecular imaging in neuroscience: A practical approach. Oxford [England]: IRL Press at Oxford University Press, 1993.
Encontre o texto completo da fonteBridger, Joanna M., e Emanuela V. Volpi, eds. Fluorescence in situ Hybridization (FISH). Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-789-1.
Texto completo da fonteLiehr, Thomas, ed. Fluorescence In Situ Hybridization (FISH). Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-52959-1.
Texto completo da fonteHaimovich, Gal, ed. Fluorescence In Situ Hybridization (FISH). New York, NY: Springer US, 2024. http://dx.doi.org/10.1007/978-1-0716-3766-1.
Texto completo da fonteMorel, Gérard. Hybridation in situ en microscopie électronique. Paris: Technique & Documentation, 2001.
Encontre o texto completo da fonteCapítulos de livros sobre o assunto "In-Situ microscopie de fluorescence"
Michalová, Kyra, Zuzana Zemanová, Jana Březinová e Věra Michalová. "Fluorescence in Situ Hybridization (FISH) in Cytogenetics of Leukemia". In Fluorescence Microscopy and Fluorescent Probes, 185–89. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1866-6_27.
Texto completo da fonteRinke, Bernd, Joachim Bradl, Bernhard Schneider, Markus Durm, Michael Hausmann, Horst Ludwig e Christoph Cremer. "“In Situ” Estimates of the Spatial Resolution for “Practical” Fluorescence Microscopy of Cell Nuclei". In Fluorescence Microscopy and Fluorescent Probes, 169–73. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1866-6_24.
Texto completo da fonteIourov, Ivan Y. "Microscopy and Imaging Systems". In Fluorescence In Situ Hybridization (FISH) — Application Guide, 75–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-70581-9_7.
Texto completo da fonteInácio, João, e Maria da Luz Martins. "Microscopic Detection of Yeasts Using Fluorescence In Situ Hybridization". In Methods in Molecular Biology, 71–82. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-257-5_5.
Texto completo da fonteFigueiredo, Joana, Ana Sofia Ribeiro, Tânia Mestre, Sofia Esménio, Martina Fonseca, Joana Paredes, Raquel Seruca e João M. Sanches. "Capturing quantitative features of protein expression from in situ fluorescence microscopic images of cancer cell populations". In Fluorescence Imaging and Biological Quantification, 279–97. Boca Raton : Taylor & Francis, 2017.: CRC Press, 2017. http://dx.doi.org/10.1201/9781315121017-15.
Texto completo da fonteEdwards, Matthew S. "Using in situ substratum sterilization and fluorescence microscopy in studies of microscopic stages of marine macroalgae". In Sixteenth International Seaweed Symposium, 253–59. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4449-0_29.
Texto completo da fonteMarkaki, Yolanda, Daniel Smeets, Marion Cremer e Lothar Schermelleh. "Fluorescence In Situ Hybridization Applications for Super-Resolution 3D Structured Illumination Microscopy". In Nanoimaging, 43–64. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-137-0_4.
Texto completo da fonteSmolka, John A., e Samantha C. Lewis. "In Situ Analysis of Mitochondrial DNA Synthesis Using Metabolic Labeling Coupled to Fluorescence Microscopy". In Methods in Molecular Biology, 99–106. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-2922-2_8.
Texto completo da fonteLoseva, Elizaveta, Jaap van Krugten, Aniruddha Mitra e Erwin J. G. Peterman. "Single-Molecule Fluorescence Microscopy in Sensory Cilia of Living Caenorhabditis elegans". In Single Molecule Analysis, 133–50. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3377-9_7.
Texto completo da fonteCasanova-Moreno, Jannu, Zhinan Landis Yu, Jonathan Massey-Allard, Brian Ditchburn, Jeff F. Young e Dan Bizzotto. "In Situ Spectroelectrochemical Fluorescence Microscopy for Visualizing Interfacial Structure and Dynamics in Self-assembled Monolayers". In Luminescence in Electrochemistry, 21–77. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-49137-0_2.
Texto completo da fonteTrabalhos de conferências sobre o assunto "In-Situ microscopie de fluorescence"
Samuel, B. A., e M. A. Haque. "In-Situ Nanoscale Single Fiber Fragmentation Using Fluorescence Microscopy". In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-43367.
Texto completo da fonteSon, Jeonghwan, Biagio Mandracchia e Shu Jia. "Miniaturized optical fluorescence microscopy system for parallel in situ imaging". In Frontiers in Optics. Washington, D.C.: OSA, 2020. http://dx.doi.org/10.1364/fio.2020.fw5e.2.
Texto completo da fonteKung, C.-Y., M. D. Barnes, N. Lermer, W. B. Whitten e J. M. Ramsey. "Confinement, Detection, and Manipulation of Individual Molecules in Attoliter Volumes". In Laser Applications to Chemical and Environmental Analysis. Washington, D.C.: Optica Publishing Group, 1998. http://dx.doi.org/10.1364/lacea.1998.lma.4.
Texto completo da fonteDursun, Gizem, e Ufuk Ozkaya. "Microscopic Fluorescence In Situ Hybridization (FISH) Image Synthesis with Generative Adversarial Networks". In 2021 29th Signal Processing and Communications Applications Conference (SIU). IEEE, 2021. http://dx.doi.org/10.1109/siu53274.2021.9477999.
Texto completo da fonteQu, Min, e Yanming Zhang. "The study on improving fluorescence microscopy image effects of genomic in situ hybridization". In 2010 3rd International Conference on Biomedical Engineering and Informatics (BMEI). IEEE, 2010. http://dx.doi.org/10.1109/bmei.2010.5640551.
Texto completo da fonteBai, Yeran, Zhongyue Guo, Fátima Pereira, Michael Wagner e Ji-Xin Cheng. "Microbial identification and metabolic analysis by mid-infrared photothermal imaging fluorescence in-situ hybridization". In Advanced Chemical Microscopy for Life Science and Translational Medicine 2022, editado por Garth J. Simpson, Ji-Xin Cheng e Wei Min. SPIE, 2022. http://dx.doi.org/10.1117/12.2611781.
Texto completo da fonteKlimas, Aleksandra, Brendan R. Gallagher, Emma DiBernardo, Zhangyu Cheng e Yongxin Zhao. "MAGNIFY: molecule anchorable gel-enabled nanoscale in-situ fluorescence microscopy for nanoscale imaging of biomolecules". In Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XXX, editado por Thomas G. Brown, Tony Wilson e Laura Waller. SPIE, 2023. http://dx.doi.org/10.1117/12.2647983.
Texto completo da fonteKubarev, Alexey. "Development of the in-situ fluorescence microscopy approach to reveal the mechanism of interfacial polymerization of polyamide membranes". In European Microscopy Congress 2020. Royal Microscopical Society, 2021. http://dx.doi.org/10.22443/rms.emc2020.606.
Texto completo da fonteSerabyn, Gene, Kurt Liewer, Chris Lindensmith, Kent Wallace e Jay Nadeau. "Development of a light-field fluorescence microscope for in situ life searches in the solar system". In 2019 IEEE Aerospace Conference. IEEE, 2019. http://dx.doi.org/10.1109/aero.2019.8741627.
Texto completo da fonteKabakci, Kaan A., Abdulkerim Capar, B. Ugur Toreyin, Mertkan Akkoc, Ozan Borazan, Ilknur Turkmen e Lutfiye Durak Ata. "A multi-level thresholding based segmentation method for microscopic fluorescence in situ hybridization (FISH) images". In 2016 24th Signal Processing and Communication Application Conference (SIU). IEEE, 2016. http://dx.doi.org/10.1109/siu.2016.7495873.
Texto completo da fonteRelatórios de organizações sobre o assunto "In-Situ microscopie de fluorescence"
Korenberg, J. R. Human cDNA mapping using fluorescence in situ hybridization. Office of Scientific and Technical Information (OSTI), março de 1993. http://dx.doi.org/10.2172/6659571.
Texto completo da fonteFalkner, Kelly K. Development of a Fluorescence-Based in-situ Barium Sensor. Fort Belvoir, VA: Defense Technical Information Center, outubro de 1999. http://dx.doi.org/10.21236/ada375880.
Texto completo da fonteLucas, J. N., e T. Straume. Chromosome translocations measured by fluorescence in-situ hybridization: A promising biomarker. Office of Scientific and Technical Information (OSTI), outubro de 1995. http://dx.doi.org/10.2172/132690.
Texto completo da fonteKnowles, David S., Stephen H. Lieberman, Michele Davey e Blair Wingfield. Laser Induced Fluorescence Spectroscopy for in-situ Detection of Petroleum Contamination. Fort Belvoir, VA: Defense Technical Information Center, janeiro de 1996. http://dx.doi.org/10.21236/ada348854.
Texto completo da fonteBur, A. J., F. W. Wang, A. Lee, R. E. Lowry, S. C. Roth e T. K. Trout. In SITU fluorescence monitoring of the viscosities of particle-filled polymers in flow. Gaithersburg, MD: National Bureau of Standards, 1988. http://dx.doi.org/10.6028/nist.ir.88-3892.
Texto completo da fonteBur, Anthony J., Francis W. Wang e Ronald E. Dehl. In situ fluorescence monitoring of the viscosities of particle-filled polymers in flow. Gaithersburg, MD: National Bureau of Standards, 1988. http://dx.doi.org/10.6028/nbs.ir.88-3694.
Texto completo da fonteMazel, Charles. In Situ Spectral Properties (Reflectance and Fluorescence) of Benthic Substrates and Organisms. Fort Belvoir, VA: Defense Technical Information Center, setembro de 1997. http://dx.doi.org/10.21236/ada628810.
Texto completo da fonteSharpe, Taylor. Assessing a Fluorescence Spectroscopy Method for In-Situ Microbial Drinking Water Quality. Portland State University Library, janeiro de 2000. http://dx.doi.org/10.15760/etd.5732.
Texto completo da fonteDean, Jay B. Hyperbaric Imaging Equipment: Fluorescence Microscopy for In Vitro Studies of Oxygen Toxicity. Fort Belvoir, VA: Defense Technical Information Center, agosto de 2004. http://dx.doi.org/10.21236/ada425309.
Texto completo da fonteMazel, Charles. A Multispectral Fluorescence and Reflectance Probe for In Situ Characterization of Benthic Environments. Fort Belvoir, VA: Defense Technical Information Center, setembro de 1999. http://dx.doi.org/10.21236/ada630464.
Texto completo da fonte