Auswahl der wissenschaftlichen Literatur zum Thema „In-Situ fluorescence microscopy“
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Zeitschriftenartikel zum Thema "In-Situ fluorescence microscopy"
Lu, Fang, Tingting Zhou, Yan Liu, Liying Song, Bin Zhang und 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 (11.08.2022): 1–6. http://dx.doi.org/10.1155/2022/3087681.
Der volle Inhalt der QuelleSERWER, PHILIP, SHIRLEY J. HAYES, KAREN LIEMAN und GARY A. GRIESS. „In situ fluorescence microscopy of bacteriophage aggregates“. Journal of Microscopy 228, Nr. 3 (Dezember 2007): 309–21. http://dx.doi.org/10.1111/j.1365-2818.2007.01855.x.
Der volle Inhalt der QuelleLiv, Nalan, Daan S. B. van Oosten Slingeland, Jean-Pierre Baudoin, Pieter Kruit, David W. Piston und Jacob P. Hoogenboom. „Electron Microscopy of Living Cells During in Situ Fluorescence Microscopy“. ACS Nano 10, Nr. 1 (08.12.2015): 265–73. http://dx.doi.org/10.1021/acsnano.5b03970.
Der volle Inhalt der QuelleBallard, S. G., und D. C. Ward. „Fluorescence in situ hybridization using digital imaging microscopy.“ Journal of Histochemistry & Cytochemistry 41, Nr. 12 (Dezember 1993): 1755–59. http://dx.doi.org/10.1177/41.12.8245423.
Der volle Inhalt der QuelleBouffier, Laurent, und Thomas Doneux. „Coupling electrochemistry with in situ fluorescence (confocal) microscopy“. Current Opinion in Electrochemistry 6, Nr. 1 (Dezember 2017): 31–37. http://dx.doi.org/10.1016/j.coelec.2017.06.015.
Der volle Inhalt der QuelleLeger, I., M. Robert-Nicoud und 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, Nr. 2 (Februar 1994): 149–54. http://dx.doi.org/10.1177/42.2.8288860.
Der volle Inhalt der QuelleReinhardt, Susanne C. M., Luciano A. Masullo, Isabelle Baudrexel, Philipp R. Steen, Rafal Kowalewski, Alexandra S. Eklund, Sebastian Strauss et al. „Ångström-resolution fluorescence microscopy“. Nature 617, Nr. 7962 (24.05.2023): 711–16. http://dx.doi.org/10.1038/s41586-023-05925-9.
Der volle Inhalt der QuelleCollinson, Lucy M. „Smart Microscopy: Automation of CLEM using In situ Fluorescence Detection“. Microscopy and Microanalysis 25, S2 (August 2019): 1018–19. http://dx.doi.org/10.1017/s1431927619005828.
Der volle Inhalt der QuelleArend, J., A. Wetzel und B. Middendorf. „In-situ-investigation of superplasticizer-particle-interaction by fluorescence microscopy“. Materials Today: Proceedings 5, Nr. 7 (2018): 15292–97. http://dx.doi.org/10.1016/j.matpr.2018.05.008.
Der volle Inhalt der QuelleFetni, Raouf, Patrick Scott, Frédérique Tihy, Claude-Lise Richer und Nicole Lemieux. „Increased resolution of in situ hybridization signal by electron microscopy: A comparison with fluorescence microscopy“. Genome 42, Nr. 5 (01.10.1999): 1001–7. http://dx.doi.org/10.1139/g99-071.
Der volle Inhalt der QuelleDissertationen zum Thema "In-Situ fluorescence microscopy"
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.
Der volle Inhalt der QuelleEnzyme 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
Roussille, Ludovic. „Suivi quantitatif in situ d'interactions biomoléculaire par microscopie optique SEEC“. Thesis, Le Mans, 2012. http://www.theses.fr/2012LEMA1030/document.
Der volle Inhalt der QuelleThis 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
Ashok, Mahima. „Analysis of HER2 testing in breast cancer“. Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/29711.
Der volle Inhalt der QuelleCommittee Chair: Griffin, Paul; Committee Member: Butera, Robert; Committee Member: Halpern, Michael; Committee Member: Nichols, Richard; Committee Member: Vidakovic, Brani. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Yara, Ricardo. „Localização in situ e caracterização molecular da bactéria endossimbionte de Pleurotus ostreatus“. Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/11/11137/tde-21082006-150238/.
Der volle Inhalt der QuelleThe fungus Pleurotus ostreatus, which belongs to white rot basidiomycete group, is a widely cultivated mushroom; this species has high productivity and rusticity, besides its use in biobleaching and bioremediation processes. This biotechnological potential justifies microbial interaction studies between this fungi and others microorganisms. In P. ostreatus mycelia, it has been observed pleomorphic bacteria growing on agar media. This research describes several assays to confirm bacterial presence in this sample. Therefore, the full-cycle rRNA analysis (described for unculturable or fastidious microorganism), ultrastructure and basic microbiology approaches were employed. Basic microbiology approaches indicated slow growing bacteria, which grown faster near to fungi colonies in solid media amended with Tween 80 or Tween 20 (co-culture system). Ultrastructure studies confirm the presence of intracellular and extracellular pleomorphic bacteria. The full-cycle rRNA analysis started with 16S rDNA amplification and sequencing. This approach demonstrated a relation between these bacteria with Burkholderia cepacia complex. By bioinformatics analysis was determinate which DNA probes can be use to identified this bacterial group. The last step for full-cycle rRNA analysis was applying fluorescent in situ hybridization (FISH). This technique confirmed the relationship between 16S rDNA bacterial sequence and bacterial forms. This is the first time that a pleomorphic bacteria from B. cepacia complex is found associated with P. ostreatus.
Emad, Ahmed Anwar Hasanin. „Development and assessment of strategies for non-invasive prenatal diagnosis using fetal cells in maternal blood“. Thèse, Université de Sherbrooke, 2014. http://hdl.handle.net/11143/5855.
Der volle Inhalt der QuelleGalanti, Agostino. „Multi-photochromic architectures : from structure to function“. Thesis, Strasbourg, 2018. http://www.theses.fr/2018STRAF046/document.
Der volle Inhalt der QuelleThe 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
Mongelard, Fabien. „Apport des approches in situ pour l'analyse du phénomène d'inactivation du chromosome X chez les mammifères“. Université Joseph Fourier (Grenoble ; 1971-2015), 1998. http://www.theses.fr/1998GRE10261.
Der volle Inhalt der QuelleChen, X. „TAGGING BIOCONTROL STREPTOMYCES TO STUDY LETTUCE COLONIZATION“. Doctoral thesis, Università degli Studi di Milano, 2015. http://hdl.handle.net/2434/345187.
Der volle Inhalt der QuellePERRIN, CHRISTELE. „Methodologie pour l'analyse quantitative en imagerie microscopique conventionnelle et a fluorescence. Application a l'etude de la proliferation et de l'expression du recepteur a l'egf dans des cellules tumorales mammaires“. Université Joseph Fourier (Grenoble), 1996. http://www.theses.fr/1996GRE10198.
Der volle Inhalt der QuelleKOMATSU, LUIZ G. H. „Estudo comparativo de nanocompósitos de polipropileno modificado sob condições de envelhecimento ambiental e acelerado“. reponame:Repositório Institucional do IPEN, 2016. http://repositorio.ipen.br:8080/xmlui/handle/123456789/26380.
Der volle Inhalt der QuelleMade available in DSpace on 2016-06-22T12:34:18Z (GMT). No. of bitstreams: 0
Dissertação (Mestrado em Tecnologia Nuclear)
IPEN/D
Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
Bücher zum Thema "In-Situ fluorescence microscopy"
Fluorescence in situ hybridization (FISH): Protocols and applications. New York, NY: Humana Press, 2010.
Den vollen Inhalt der Quelle findenLiehr, Thomas. Fluorescence In Situ Hybridization (FISH) — Application Guide. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009.
Den vollen Inhalt der Quelle finden1923-, Sharma Arun Kumar, und Sharma Archana 1932-, Hrsg. Chromosome painting: Principles, strategies, and scope. Dordrecht: Kluwer Academic Publishers, 2001.
Den vollen Inhalt der Quelle findenFried, 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.
Den vollen Inhalt der Quelle findenA, Sharif N., Hrsg. Molecular imaging in neuroscience: A practical approach. Oxford [England]: IRL Press at Oxford University Press, 1993.
Den vollen Inhalt der Quelle findenLiehr, Thomas. Fluorescence in Situ Hybridization: Application Guide. Springer, 2016.
Den vollen Inhalt der Quelle findenLiehr, Thomas. Fluorescence In Situ Hybridization - Application Guide. Springer, 2010.
Den vollen Inhalt der Quelle findenLiehr, Thomas. Fluorescence in Situ Hybridization: Application Guide. Springer Berlin / Heidelberg, 2018.
Den vollen Inhalt der Quelle finden(Editor), Arun Kumar Sharma, und Archana Sharma (Editor), Hrsg. Chromosome Painting: Principles, Strategies and Scope. Springer, 2001.
Den vollen Inhalt der Quelle findenSharma, Arun Kumar, und Archana Sharma. Chromosome Painting: Principles, Strategies and Scope. Springer London, Limited, 2012.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "In-Situ fluorescence microscopy"
Michalová, Kyra, Zuzana Zemanová, Jana Březinová und 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.
Der volle Inhalt der QuelleRinke, Bernd, Joachim Bradl, Bernhard Schneider, Markus Durm, Michael Hausmann, Horst Ludwig und 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.
Der volle Inhalt der QuelleIourov, 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.
Der volle Inhalt der QuelleMarkaki, Yolanda, Daniel Smeets, Marion Cremer und 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.
Der volle Inhalt der QuelleEdwards, 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.
Der volle Inhalt der QuelleSmolka, John A., und 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.
Der volle Inhalt der QuelleCasanova-Moreno, Jannu, Zhinan Landis Yu, Jonathan Massey-Allard, Brian Ditchburn, Jeff F. Young und 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.
Der volle Inhalt der QuelleGrohme, Markus A., Olga Frank und Jochen C. Rink. „Preparing Planarian Cells for High-Content Fluorescence Microscopy Using RNA in Situ Hybridization and Immunocytochemistry“. In Methods in Molecular Biology, 121–55. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3275-8_8.
Der volle Inhalt der QuelleSchmidt, Hannes, und Thilo Eickhorst. „Gold-FISH: In Situ Hybridization of Microbial Cells for Combined Fluorescence and Scanning Electron Microscopy“. In Springer Protocols Handbooks, 545–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-52959-1_53.
Der volle Inhalt der QuelleKarygianni, Lamprini, Elmar Hellwig und Ali Al-Ahmad. „Multiplex Fluorescence In Situ Hybridization (M-FISH) and Confocal Laser Scanning Microscopy (CLSM) to Analyze Multispecies Oral Biofilms“. In Methods in Molecular Biology, 65–72. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0467-9_5.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "In-Situ fluorescence microscopy"
Samuel, B. A., und 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.
Der volle Inhalt der QuelleSon, Jeonghwan, Biagio Mandracchia und 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.
Der volle Inhalt der QuelleKubarev, 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.
Der volle Inhalt der QuelleBai, Yeran, Zhongyue Guo, Fátima Pereira, Michael Wagner und 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, herausgegeben von Garth J. Simpson, Ji-Xin Cheng und Wei Min. SPIE, 2022. http://dx.doi.org/10.1117/12.2611781.
Der volle Inhalt der QuelleQu, Min, und 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.
Der volle Inhalt der QuelleKlimas, Aleksandra, Brendan R. Gallagher, Emma DiBernardo, Zhangyu Cheng und 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, herausgegeben von Thomas G. Brown, Tony Wilson und Laura Waller. SPIE, 2023. http://dx.doi.org/10.1117/12.2647983.
Der volle Inhalt der QuelleBottiroli, Giovanni F., Piera Balzarini, Anna C. Croce, Donata Locatelli, Simona Vaccino und Carlo Pelliciari. „Fluorescence resonance energy transfer (FRET) microscopy: a tool for in situ study of cellular structures“. In International Symposium on Biomedical Optics Europe '94, herausgegeben von Hans-Jochen Foth, Aaron Lewis, Halina Podbielska, Michel Robert-Nicoud, Herbert Schneckenburger und Anthony J. Wilson. SPIE, 1995. http://dx.doi.org/10.1117/12.200887.
Der volle Inhalt der QuelleUpadhyay, Jagannath, Daniel S. Park, Karsten E. Thompson und Dimitris E. Nikitopoulos. „3D Measurements of Nano-Particle Transport in Complex 2.5D Micro-Models“. In ASME 2015 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/imece2015-50635.
Der volle Inhalt der QuelleKung, C.-Y., M. D. Barnes, N. Lermer, W. B. Whitten und 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.
Der volle Inhalt der QuelleMcMahon, Nathan, Allison Solanki, Jocelyn Jones, Sunjong Kwon, Young-Hwan Chang, Koei Chin, Michel Nederlof, Joe Gray und Summer L. Gibbs. „Fluorescent Imaging for In Situ Measurement of Drug Target Engagement and Cell Signaling Pathways“. In Microscopy Histopathology and Analytics. Washington, D.C.: OSA, 2020. http://dx.doi.org/10.1364/microscopy.2020.mw4a.5.
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