Bibliografías temáticas / Confocal fluorescence microscopy

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Literatura académica sobre el tema "Confocal fluorescence microscopy"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 24 de enero de 2023

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Artículos de revistas sobre el tema "Confocal fluorescence microscopy"

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Zhibin Wang, Zhibin Wang, Guohua Shi Guohua Shi, and Yudong Zhang Yudong Zhang. "Adaptive aberration correction in confocal scanning fluorescence microscopy." Chinese Optics Letters 12, s1 (2014): S11103–311105. http://dx.doi.org/10.3788/col201412.s11103.

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Volkov, I. A., N. V. Frigo, L. F. Znamenskaya, and O. R. Katunina. "Application of Confocal Laser Scanning Microscopy in Biology and Medicine." Vestnik dermatologii i venerologii 90, no. 1 (February 24, 2014): 17–24. http://dx.doi.org/10.25208/0042-4609-2014-90-1-17-24.

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Fluorescence confocal laser scanning microscopy and reflectance confocal laser scanning microscopy are up-to-date highend study methods. Confocal microscopy is used in cell biology and medicine. By using confocal microscopy, it is possible to study bioplasts and localization of protein molecules and other compounds relative to cell or tissue structures, and to monitor dynamic cell processes. Confocal microscopes enable layer-by-layer scanning of test items to create demonstrable 3D models. As compared to usual fluorescent microscopes, confocal microscopes are characterized by a higher contrast
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Wright, S. J., J. S. Walker, H. Schatten, C. Simerly, J. J. McCarthy, and G. Schatten. "Confocal fluorescence microscopy with the tandem scanning light microscope." Journal of Cell Science 94, no. 4 (December 1, 1989): 617–24. http://dx.doi.org/10.1242/jcs.94.4.617.

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Applications of the tandem scanning confocal microscope (TSM) to fluorescence microscopy and its ability to resolve fluorescent biological structures are described. The TSM, in conjunction with a cooled charge-coupled device (cooled CCD) and conventional epifluorescence light source and filter sets, provided high-resolution, confocal data, so that different fluorescent cellular components were distinguished in three dimensions within the same cell. One of the unique features of the TSM is the ability to image fluorochromes excited by ultraviolet light (e.g. Hoechst, DAPI) in addition to fluore
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Welzel, J., Raphaela Kästle, and Elke C. Sattler. "Fluorescence (Multiwave) Confocal Microscopy." Dermatologic Clinics 34, no. 4 (October 2016): 527–33. http://dx.doi.org/10.1016/j.det.2016.06.002.

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Nie, Shuming, Daniel T. Chiu, and Richard N. Zare. "Real-time observation of single molecules by confocal fluorescence microscopy." Proceedings, annual meeting, Electron Microscopy Society of America 53 (August 13, 1995): 60–61. http://dx.doi.org/10.1017/s0424820100136672.

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The ability to detect, identify, and manipulate individual molecules offer exciting possibilities in many fields, including chemical analysis, materials research, and the biological sciences. A particularly powerful approach is to combine the exquisite sensitivity of laser-induced fluorescence and the spatial localization and imaging capabilities of diffraction-limited or near-field optical microscopes. Unlike scanning tunneling microscopy (STM) and atomic force microscopy (AFM), which lack molecular specificity, optical spectroscopy and microscopy techniques can be used for real-time monitori
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Jason Kirk. "Beyond the Hype - Is 2-Photon Microscopy Right for You?" Microscopy Today 11, no. 2 (April 2003): 26–29. http://dx.doi.org/10.1017/s1551929500052469.

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Confocal microscopes have come a long way in the past decade. Not only are they more stable and easier to use than ever before, but their cost has dropped enough that multi-user facilities are finding competition from individual labs using the new breed of "personal" confocals. In fact it has, in some cases, become the de facto standard for fluorescence imaging regardless of whether the user actually has requirements for it or not.But, researchers always have an ear out for something better. Enter 2-photon microscopy (2PLSM). The “bigger & badder” cousin of the confocal microscope has beco
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Cheng, P. C., S. J. Pan, A. Shih, W. S. Liou, M. S. Park, T. Watson, J. Bhawalkar, and P. Prasard. "Two-Photon Laser Scanning Confocal Microscopy." Microscopy and Microanalysis 3, S2 (August 1997): 847–48. http://dx.doi.org/10.1017/s1431927600011120.

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Two-photon fluorescence microscopy has become an important research tool in both biological and material sciences. The technique uses long wavelength, typically in the near IR, as the excitation light to obtain shorter wavelength fluorescence (e.g. visible light). Because of the low linear absorption coefficient of most biological and polymeric specimens, this technique allows deeper penetration of the excitation beam, achieving optical sectioning to a depth of 250μm or more into the specimen. As a result of the quadratic dependency of the two-photon induced fluorescence to the excitation inte
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Oostveldt, P., and S. Bauwens. "Quantitative fluorescence in confocal microscopy." Journal of Microscopy 158, no. 2 (May 1990): 121–32. http://dx.doi.org/10.1111/j.1365-2818.1990.tb02985.x.

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VISSCHER, K., G. J. BRAKENHOFF, and T. D. VISSER. "Fluorescence saturation in confocal microscopy." Journal of Microscopy 175, no. 2 (August 1994): 162–65. http://dx.doi.org/10.1111/j.1365-2818.1994.tb03479.x.

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Ragazzi, Moira, Simonetta Piana, Caterina Longo, Fabio Castagnetti, Monica Foroni, Guglielmo Ferrari, Giorgio Gardini, and Giovanni Pellacani. "Fluorescence confocal microscopy for pathologists." Modern Pathology 27, no. 3 (September 13, 2013): 460–71. http://dx.doi.org/10.1038/modpathol.2013.158.

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Tesis sobre el tema "Confocal fluorescence microscopy"

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Eigenbrot, Ilya Vladimirovich. "A time-resolved confocal fluorescence microscope." Thesis, Imperial College London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342331.

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Alawadhi, Fahimah. "Statistical image analysis and confocal microscopy." Thesis, University of Bath, 2001. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341639.

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Jiang, Shihong. "Non-scanning fluorescence confocal microscopy using laser speckle illumination." Thesis, University of Nottingham, 2005. http://eprints.nottingham.ac.uk/10139/.

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Confocal scanning microscopy (CSM) is a much used and advantageous form of microscopy. Although CSM is superior to conventional microscopy in many respects, a major disadvantage is the complexity of the scanning process and the sometimes long time to perform the scan. In this thesis a novel non-scanning fluorescence confocal microscopy is investigated. The method uses a random time-varying speckle pattern to illuminate the specimen, recording a large number of independent full-field frames without the need for a scanning system. The recorded frames are then processed in a suitable way to give
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Wang, Xiao. "Confocal angle resolved linear dichroism microscopy for structural fluorescence imaging." Ecole centrale de Marseille, 2013. http://tel.archives-ouvertes.fr/docs/00/87/10/10/PDF/Wang-Thesis.pdf.

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La microscopie de fluorescence a récemment été complétée par une technique appelée dichroïsme linéaire résolu angulairement, basé sur le fait que l'absorption de la lumière est un processus sensible à l'orientation moléculaire. En analysant la réponse d'émission de fluorescence en fonction de l'orientation de la polarisation de la lumière excitatrice, cette technique permet de remonter à l'information d'orientation sur un ensemble de molécules fluorescentes, plus précisément son angle d'orientation moyenne et l'amplitude de ses fluctuations angulaires autour de cette moyenne. Dans cette thèse,
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Gösch, Michael. "Microfluidic analysis and parallel confocal detection of single molecules /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-663-4/.

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Risi, Matthew D. "Advances In Combined Endoscopic Fluorescence Confocal Microscopy And Optical Coherence Tomography." Diss., The University of Arizona, 2014. http://hdl.handle.net/10150/332772.

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Confocal microendoscopy provides real-time high resolution cellular level images via a minimally invasive procedure. Results from an ongoing clinical study to detect ovarian cancer with a novel confocal fluorescent microendoscope are presented. As an imaging modality, confocal fluorescence microendoscopy typically requires exogenous fluorophores, has a relatively limited penetration depth (100μm), and often employs specialized aperture configurations to achieve real-time imaging in vivo. Two primary research directions designed to overcome these limitations and improve diagnostic capability a
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Slimani, Amel. "Photonic approach for the study of dental hard tissues and carious lesion detection." Thesis, Montpellier, 2017. http://www.theses.fr/2017MONTT125.

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Les propriétés photoniques des tissus durs dentaires nous ont permis d’étudier l’email et la dentine a un niveau moléculaire (in vitro) en utilisant des techniques de microscopie optique non linéaires. La microscopie confocale Raman est technique d’imagine de haute résolution permettant d’analyse d’échantillon sans préparation spécifique ni marquage. Cette méthode nous a permis de reconstituer une cartographie de la réticulation du collagène et de la cristallinité au niveau de la jonction émail-dentine et cela avec une résolution spatiale non atteinte jusque-là. Cette analyse c
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Tsutae, Fernando Massayuki. "Espectroscopia de correlação de fluorescência aplicada em estudos de sistemas moleculares, biológicos e celulares." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-14102016-101124/.

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A espectroscopia de correlação de fluorescência (FCS) é uma das diferentes técnicas de análise por imagens de alta resolução espacial e temporal de biomoléculas em concentrações extremamente baixas. Ela se tornou uma técnica extremamente poderosa e sensível em áreas como bioquímica e biofísica. Como uma técnica bem estabelecida, ela é utilizada para medir concentrações locais de biomoléculas, através da marcação com moléculas fluorescentes. Coeficientes de difusão e constantes cinéticas também podem ser medidos através de FCS assim como detecção de molécula única. Ela também pode dar informaçã
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Kakade, Rohan. "Improved resolution and signal-to-noise ratio performance of a confocal fluorescence microscope." Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/33699/.

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A culmination of theory, techniques and devices stemming from a wide variety of sources and disciplines, optical microscopy presents vast possibilities for visualisation of small structures. One of the most fundamental yet significant optical microscopy techniques is Confocal Fluorescence Microscopy (CFM). CFM is studied here by analysing its performance with respect to the two most important metrics - Signal-to-noise ratio and 3D optical resolution. Several authors have commented on the inherent inefficiency of imaging systems such as CFM to utilise the available light when providing resoluti
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Ferro, Daniela Peixoto 1981. "Aplicação da biofotônica para o estudo de cicatrizes." [s.n.], 2015. http://repositorio.unicamp.br/jspui/handle/REPOSIP/312786.

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Orientador: Konradin Metze<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas<br>Made available in DSpace on 2018-08-26T20:44:11Z (GMT). No. of bitstreams: 1 Ferro_DanielaPeixoto_D.pdf: 2964245 bytes, checksum: 202d309cf65f632d47c7811d4958535d (MD5) Previous issue date: 2015<br>Resumo: A aplicação integrada de técnicas modernas, como a Geração do Segundo Harmônico (SHG) e os tempos de vida da fluorescência (FLIM), com análise de imagens matemáticas nos permitem visualizar detalhes não vistos por microscopia de luz convencional. O objetivo deste estudo foi
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Libros sobre el tema "Confocal fluorescence microscopy"

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Muller, Michiel. Introduction to confocal fluorescence microscopy. 2nd ed. Bellingham, Wash: SPIE Press, 2006.

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Brian, Matsumoto, and American Society for Cell Biology., eds. Cell biological applications of confocal microscopy. 2nd ed. Amsterdam: Academic Press, 2002.

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Periasamy, Ammasi, and Wilson Tony. Confocal, multiphoton, and nonlinear microscopic imaging III: 17-18 June 2007, Munich, Germany. Edited by SPIE (Society), Optical Society of America, European Optical Society, Wissenschaftliche Gesellschaft Lasertechnik, and Deutsche Gesellschaft für Lasermedizin. Bellingham, Wash., USA: SPIE, 2007.

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Kevin, Foskett J., and Grinstein Sergio 1950-, eds. Noninvasive techniques in cell biology. New York: Wiley-Liss, 1990.

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David, Shotton, ed. Electronic light microscopy: The principles and practice of video-enhanced contrast, digital intensified fluorescence, and confocal scanning light microscopy. New York: Wiley-Liss, 1993.

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T, Mason W., ed. Fluorescent and luminescent probes for biological activity: A practical guide to technology for quantitative real-time analysis. London: Academic Press, 1993.

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Conference on Multidimensional Spectroscopy: Acquisition, Interpretation, and Automation (1998 San Jose, Calif.). Proceedings of three-dimensional and multidimensional microscopy: Image acquisition and processing V : 27-29 January 1998, San Jose, California. Edited by Cogswell Carol J, Society of Photo-optical Instrumentation Engineers., and International Biomedical Optics Society. Bellingham, Wash., USA: SPIE, 1998.

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name, No. Three-dimensional and multidimensional microscopy: Image acquisition and processing X : 28-29 January 2003, San Jose, California, USA. Bellingham, WA: SPIE, 2003.

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R, José-Angel Conchello, Carol J. Cogswell, and Wilson Tony. Three-dimensional and multidimensional microscopy: Image acquisition and processing XIII : 24-26 January 2006, San Jose, California, USA. Edited by Society of Photo-optical Instrumentation Engineers. Bellingham, Wash: SPIE, 2006.

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José-Angel, Conchello R., Cogswell Carol J, Wilson Tony, and Society of Photo-optical Instrumentation Engineers., eds. Three-dimensional and multidimensional microscopy: Image acquisition and processing XII : 25-27 January 2005, San Jose, California, USA. Bellingham, Wash., USA: SPIE, 2005.

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Capítulos de libros sobre el tema "Confocal fluorescence microscopy"

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Naredi-Rainer, Nikolaus, Jens Prescher, Achim Hartschuh, and Don C. Lamb. "Confocal Microscopy." In Fluorescence Microscopy, 165–202. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527687732.ch5.

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Naredi-Rainer, Nikolaus, Jens Prescher, Achim Hartschuh, and Don C. Lamb. "Confocal Microscopy." In Fluorescence Microscopy, 175–213. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527671595.ch5.

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Jerome, W. Gray, and Robert L. Price. "Fluorescence Microscopy." In Basic Confocal Microscopy, 37–71. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-97454-5_3.

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Jerome, W. Gray (Jay), and Robert L. Price. "Fluorescence Microscopy." In Basic Confocal Microscopy, 29–59. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-78175-4_3.

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Gerritsen, Hans C. "Confocal Fluorescence Lifetime Imaging." In Fluorescence Microscopy and Fluorescent Probes, 35–46. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1866-6_3.

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Demandolx, Denis, and Jean Davoust. "Subcellular Cytofluorometry in Confocal Microscopy." In Fluorescence Microscopy and Fluorescent Probes, 279–83. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1866-6_43.

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Jerome, W. Gray. "The Theory of Fluorescence." In Basic Confocal Microscopy, 21–36. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-97454-5_2.

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Jerome, W. Gray (Jay). "The Theory of Fluorescence." In Basic Confocal Microscopy, 17–28. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-78175-4_2.

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Hibbs, Alan R. "Fluorescence Immunolabelling." In Confocal Microscopy for Biologists, 259–77. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48565-7_11.

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Gomez-Lazaro, M., A. Freitas, and C. C. Ribeiro. "Confocal Raman microscopy." In Fluorescence Imaging and Biological Quantification, 65–83. Boca Raton : Taylor & Francis, 2017.: CRC Press, 2017. http://dx.doi.org/10.1201/9781315121017-5.

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Actas de conferencias sobre el tema "Confocal fluorescence microscopy"

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Rüttinger, Steffen, Peter Kapusta, Volker Völlkopf, Felix Koberling, Rainer Erdmann, and Rainer Macdonald. "Fluorescence performance standards for confocal microscopy." In BiOS, edited by Ammasi Periasamy, Peter T. C. So, and Karsten König. SPIE, 2010. http://dx.doi.org/10.1117/12.840501.

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Doglia, Silvia M., L. Bianchi, Roberto Colombo, N. Allam, Hamid Morjani, Michel Manfait, and A. M. Villa. "Confocal fluorescence microscopy of living cells." In Laser Spectroscopy of Biomolecules: 4th International Conference on Laser Applications in Life Sciences, edited by Jouko E. Korppi-Tommola. SPIE, 1993. http://dx.doi.org/10.1117/12.146189.

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Stelzer, Ernst H. K., and Robert Bacallao. "Confocal Fluorescence Microscopy Of Epithelial Cells." In 1988 International Congress on Optical Science and Engineering. SPIE, 1989. http://dx.doi.org/10.1117/12.950336.

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Wang, Yu, Konstantin Maslov, Chulhong Kim, Song Hu, and Lihong V. Wang. "Integrated photoacoustic and fluorescence confocal microscopy." In SPIE BiOS, edited by Alexander A. Oraevsky and Lihong V. Wang. SPIE, 2011. http://dx.doi.org/10.1117/12.874888.

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Luo, Yuan, Chou-Min Chia, Hung-Chun Wang, and Yu-hsin Chia. "Multi-focal holographic slit confocal fluorescence microscopy." In Biomedical Imaging and Sensing Conference, edited by Osamu Matoba, Yasuhiro Awatsuji, Toyohiko Yatagai, and Yoshihisa Aizu. SPIE, 2018. http://dx.doi.org/10.1117/12.2316615.

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Bertero, M., P. Boccacci, and E. R. Pike. "Inverse Problems In Fluorescence Confocal Scanning Microscopy." In 1988 International Congress on Optical Science and Engineering. SPIE, 1989. http://dx.doi.org/10.1117/12.950302.

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Rafeq, S., A. Ernst, A. Majid, G. Michaud, C. Reddy, and F. Herth. "Bronchoscopic Imaging Using Fibered Confocal Fluorescence Microscopy." In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a5772.

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Loterie, Damien, Demetri Psaltis, and Christophe Moser. "Confocal microscopy via multimode fibers: fluorescence bandwidth." In SPIE BiOS, edited by Thomas G. Bifano, Joel Kubby, and Sylvain Gigan. SPIE, 2016. http://dx.doi.org/10.1117/12.2208017.

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Rodrigues, Isabel, Joao Xavier, and Joao Sanches. "Fluorescence Confocal Microscopy Imaging denoising with photobleaching." In 2008 30th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2008. http://dx.doi.org/10.1109/iembs.2008.4649633.

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Fersch, Daniel, Pavel Malý, Jessica Rühe, Victor Lisinetskii, Matthias Hensen, Frank Würthner, and Tobias Brixner. "Single-Molecule Ultrafast Fluorescence-Detected Pump–Probe Microscopy." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/up.2022.m4a.3.

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Informes sobre el tema "Confocal fluorescence microscopy"

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Hoffmeyer, Michaela. In Vivo Fluorescence Confocal Microscopy to Investigate the Role of RhoC in Inflammatory Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, April 2005. http://dx.doi.org/10.21236/ada435616.

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Wickramaratne, Chathuri, Emily Sappington, and Hanadi Rifai. Confocal Laser Fluorescence Microscopy to Measure Oil Concentration in Produced Water: Analyzing Accuracy as a Function of Optical Settings. Journal of Young Investigators, June 2018. http://dx.doi.org/10.22186/jyi.34.6.39-47.

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Morales García, María Dolores. Uso de la fluorescencia y la microscopía confocal en la investigación científica. Sociedad Española de Bioquímica y Biología Molecular (SEBBM), July 2012. http://dx.doi.org/10.18567/sebbmdiv_rpc.2012.07.1.

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Darrow, C., T. Huser, C. Campos, M. Yan, S. Lane, and R. Balhorn. Single Fluorescent Molecule Confocal Microscopy: A New Tool for Molecular Biology Research and Biosensor Development. Office of Scientific and Technical Information (OSTI), March 2000. http://dx.doi.org/10.2172/792442.

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