Relevant bibliographies by topics / Microscope

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Microscope'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Microscope"

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J. H., Youngblom, Wilkinson J., and Youngblom J.J. "Telepresence Confocal Microscopy." Microscopy and Microanalysis 6, S2 (2000): 1164–65. http://dx.doi.org/10.1017/s1431927600038319.

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The advent of the Internet has allowed the development of remote access capabilities to a growing variety of microscopy systems. The Materials MicroCharacterization Collaboratory, for example, has developed an impressive facility that provides remote access to a number of highly sophisticated microscopy and microanalysis instruments. While certain types of microscopes, such as scanning electron microscopes, transmission electron microscopes, scanning probe microscopes, and others have already been established for telepresence microscopy, no one has yet reported on the development of similar ca
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Sutriyono, Widodo, and Retno Suryandari. "Addition of Illuminator Fiber Optic to Produce 3 Dimension Effects in Micrographic Observation Using Upright Microscope." Proceeding International Conference on Science and Engineering 3 (April 30, 2020): 493–96. http://dx.doi.org/10.14421/icse.v3.551.

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Microscope is one of the tools used in practicums with high intensity. The use of a microscope adjusts to the object to be observed in order to obtain optimal micrographic results. Stereo microscopes are used to observe three-dimensional objects. Upright microscopes are used to observe two-dimensional objects. This study aims to combine the two advantages of stereo microscopy that can produce three-dimensional micrography with the advantages of an upright microscope that has a high total magnification. The method used in this study is an experimental method by adding an optical fiber illuminat
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Davidson, Michael W. "50 Most Frequently Asked Questions About Optical Microscopy." Microscopy Today 8, no. 6 (2000): 12–19. http://dx.doi.org/10.1017/s1551929500052780.

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A significant percentage of technical experts who employ optical microscopes have had little or no formal training in optical microscope basics. Some, typically, were required to use microscopes during their technical education but, in general, microscope terminology and technology was a sideline to their major training. As a result, many useful basic microscope technical details were not learned because they were not necessary to accomplish what was needed in order to survive their major class work. At Florida State University, we try to make the [earning of microscope technology an inherent
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Peckham, Michelle. "What is a microscope? How the microscope has evolved over three hundred and fifty years." Journal of Physics: Conference Series 2877, no. 1 (2024): 012091. http://dx.doi.org/10.1088/1742-6596/2877/1/012091.

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Abstract The microscope is named from the Greek mikrós (small) and skopeîn (to see). The first light microscopes were described over three hundred and fifty years ago, building on the development of lenses for the telescope. The publication of Micrographia in 1665 popularised the microscope and yet its technological development only really took off in the 1800s in parallel with many other technological developments of the time. Key to building microscopes reproducibly was the theoretical understanding of how the image is formed in the microscope, developed by Ernst Abbe in the 1880s as part of
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O'Keefe, Michael A., John H. Turner, John A. Musante, et al. "Laboratory Design for High-Performance Electron Microscopy." Microscopy Today 12, no. 3 (2004): 8–17. http://dx.doi.org/10.1017/s1551929500052093.

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Since publication of the classic text on the electron microscope laboratory by Anderson, the proliferation of microscopes with field emission guns, imaging filters and hardware spherical aberration correctors (giving higher spatial and energy resolution) has resulted in the need to construct special laboratories. As resolutions iinprovel transmission electron microscopes (TEMs) and scanning transmission electron microscopes (STEMs) become more sensitive to ambient conditions. State-of-the-art electron microscopes require state-of-the-art environments, and this means careful design and implemen
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Youngblom, J. H., J. Wilkinson, and J. J. Youngblom. "Confocal Laser Scanning Microscopy By Remote Access." Microscopy Today 7, no. 7 (1999): 32–33. http://dx.doi.org/10.1017/s1551929500064798.

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In recent years there have been a growing number of facilities interested in developing remote access capabilities to a variety of microscopy systems. While certain types of microscopes, such as electron microscopes and scanning probe microscopes have been well established for telepresence microscopy, no one has yet reported on the development of similar capabilities for the confocal microscope.At California State University, home to the CSUPERB (California State University Program for Education and Research in Biotechnology) Confocal Microscope Core Facility, we have established a remote acce
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Johnson, W. Travis. "Advantages of Simultaneous Imaging Using an Atomic Force Microscope Integrated with an Inverted Light Microscope." Microscopy Today 19, no. 6 (2011): 22–29. http://dx.doi.org/10.1017/s1551929511001222.

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Atomic Force Microscopy (AFM) permits measurements on biological samples below the limits of light microscopy resolution under physiological environments and other controlled conditions. Consequently, AFM has become an increasingly valuable technique in cell biology. One of the most exciting advances in AFM instrumentation has been its integration with the light microscope. This permits investigators to take advantage of the power and utility of light microscopy and scanning probe microscopy simultaneously. In combining a light microscope with an AFM, scanner components must be specifically de
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Graef, M. De, N. T. Nuhfer, and N. J. Cleary. "Implementation Of A Digital Microscopy Teaching Environment." Microscopy and Microanalysis 5, S2 (1999): 4–5. http://dx.doi.org/10.1017/s1431927600013349.

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The steady evolution of computer controlled electron microscopes is dramatically changing the way we teach microscopy. For today’s microscopy student, an electron microscope may be just another program on the desktop of whatever computer platform he or she uses. This is reflected in the use of the term Desktop Microscopy. The SEM in particular has become a mouse and keyboard controlled machine, and running the microscope is not very different from using a drawing program or a word processor. Transmission electron microscopes are headed in the same direction.While one can debate whether or not
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Mao, Hong, Robin Diekmann, Hai Po H. Liang, et al. "Cost-efficient nanoscopy reveals nanoscale architecture of liver cells and platelets." Nanophotonics 8, no. 7 (2019): 1299–313. http://dx.doi.org/10.1515/nanoph-2019-0066.

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AbstractSingle-molecule localization microscopy (SMLM) provides a powerful toolkit to specifically resolve intracellular structures on the nanometer scale, even approaching resolution classically reserved for electron microscopy (EM). Although instruments for SMLM are technically simple to implement, researchers tend to stick to commercial microscopes for SMLM implementations. Here we report the construction and use of a “custom-built” multi-color channel SMLM system to study liver sinusoidal endothelial cells (LSECs) and platelets, which costs significantly less than a commercial system. This
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Kersker, M., C. Nielsen, H. Otsuji, T. Miyokawa, and S. Nakagawa. "The JSM-890 ultra high resolution Scanning Electron Microscope." Proceedings, annual meeting, Electron Microscopy Society of America 47 (August 6, 1989): 88–89. http://dx.doi.org/10.1017/s0424820100152410.

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Historically, ultra high spatial resolution electron microscopy has belonged to the transmission electron microscope. Today, however, ultra high resolution scanning electron microscopes are beginning to challenge the transmission microscope for the highest resolution.To accomplish high resolution surface imaging, not only is high resolution required. It is also necessary that the integrity of the specimen be preserved, i.e., that morphological changes to the specimen during observation are prevented. The two major artifacts introduced during observation are contamination and beam damage, both
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Dissertations / Theses on the topic "Microscope"

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Payton, Oliver David. "High-speed atomic force microscopy under the microscope." Thesis, University of Bristol, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574416.

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SINCE its invention in 1986, the atomic force microscope (AFM) has revolutionised the field of nanotechnology and nanoscience. It is a tool that has enabled research into areas of medicine, advanced materials, biology, chemistry and physics. However due to its low frame rate it is a tool that has been limited to imaging small areas using a time lapse technique. It has only been in recent years that the frame rate of the device has been increased in a tool known as high-speed AFM (HSAFM). This increased frame rate allows, for the first time, biological processes to be viewed in real time or mac
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Franklin, Thomas. "Scanning ionoluminescence microscopy with a helium ion microscope." Thesis, University of Southampton, 2012. https://eprints.soton.ac.uk/352281/.

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The ORIONR PLUS scanning helium ion microscope (HIM) images at sub nanometer resolution. Images of the secondary electron emission have superior resolution and depth of field compared to a scanning electron microscope (SEM). Ionoluminescent imaging is not an area that has been extensively explored by typical ion beam systems as they have large spot sizes in the region of microns, leading to poor spatial resolution. This thesis confirms that the ORIONR PLUS can form images from the ionoluminescent signal, resolutions of 20nm can be obtained for images of bright nanoparticles. Ionoluminescence s
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Baida, Fadi Issam. "Microscopie hybride : association d'un microscope optique en champ proche et d'un microscope à forces atomiques : principe et réalisation." Besançon, 1995. http://www.theses.fr/1995BESA2017.

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Ce travail de recherche se situe dans la dynamique des microscopies dites en "champ proche" ou à sondes locales. La résolution de ces microscopies dépend des effets physiques liés à la géométrie de la sonde et au type d'interaction de cette dernière avec l'échantillon à analyser. Dans ce contexte, nous avons développé, réalisé et exploité un instrument combinant deux détections : l'une optique et l'autre à forces atomiques. La première permet de déterminer la distribution du champ lumineux au voisinage immédiat de l'objet tandis que la détection de force fournit la topographie du même site de
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Szelc, Jedrzej. "THz imaging and microscopy : a multiplexed near-field TeraHertz microscope." Thesis, University of Southampton, 2011. https://eprints.soton.ac.uk/209643/.

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Bethge, Philipp. "Development of a two-photon excitation STED microscope and its application to neuroscience." Thesis, Bordeaux, 2014. http://www.theses.fr/2014BORD0018/document.

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L’avènement de la microscopie STED (Stimulated Emission Depletion) a bouleversé le domaine desneurosciences du au fait que beaucoup de structures neuronale, tels que les épines dendritiques, lesaxones ou les processus astrocytaires, ne peuvent pas être correctement résolu en microscopiephotonique classique. La microscopie 2-photon est une technique d’imagerie photonique très largement utilisée dans le domaine des neurosciences car elle permet d’imager les événements dynamique en profondeur dans le tissu cérébral, offrant un excellent sectionnement optique et une meilleure profondeur de pénétra
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Battistella, Eliana. "Towards an improved photonic force microscope: a novel technique for biological microscopy." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2017. http://amslaurea.unibo.it/14864/.

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Una delle tecniche più note nello studio topografico di campioni biologici è l’AFM. Ci sono però limitazioni dovute alla presenza del cantilever, il quale pone un limite nella forza minima applicabile su un campione per ottenere un’immagine topografica. Questa forza (ordine dei 10 pN) può essere sufficiente a danneggiare il campione e a deformare i dettagli topografici che si vorrebbero evidenziare. Per superare questo problema si può usare un Photonic Force Microscope, dove il cantilever è sostituito da Optical Tweezers. Questa tecnica permette di effettuare scansioni di campioni biologici ap
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Setiawan, Widagdo. "Fermi Gas Microscope." Thesis, Harvard University, 2012. http://dissertations.umi.com/gsas.harvard:10225.

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Recent advances in using microscopes in ultracold atom experiment have allowed experimenters for the first time to directly observe and manipulate individual atoms in individual lattice sites. This technique enhances our capability to simulate strongly correlated systems such as Mott insulator and high temperature superconductivity. Currently, all ultracold atom experiments with high resolution imaging capability use bosonic atoms. In this thesis, I present our progress towards creating the fermionic version of the microscope experiment which is more suitable for simulating real condensed matt
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Le, Falher Eric. "Le microscope conoscopique." Paris, ENST, 1992. http://www.theses.fr/1993ENST0017.

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Le but de cette these etait la comprehension, l'etude et le developpement d'un microscope conoscopique. Au cours de ce travail nous avons developpe une approche de l'holographie conoscopique fondee sur l'optique physique (methode des ondes). Nous avons developpe le calcul de la fonction de transfert optique tridimensionnelle d'un systeme conoscopique. Nous avons etendu le concept de fonction de transfert tridimensionnelle optique au cas d'un systeme opto-informatique. Cette fonction de transfert tridimensionnelle optique servira d'outil general de modelisation des systemes conoscopiques. Dans
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Le, Falher Eric. "Le microscope conoscopique /." Paris : École nationale supérieure des télécommunications, 1993. http://catalogue.bnf.fr/ark:/12148/cb356172863.

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Siebers, Ellen Mary. "Telescope or microscope." Thesis, University of Iowa, 2012. https://ir.uiowa.edu/etd/2987.

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Books on the topic "Microscope"

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Thomas, Mulvey, and Sheppard C. J. R, eds. Advances inoptical and electron microscopy. Academic, 1990.

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Bradbury, Savile. An introduction to the optical microscope. Bios, 1994.

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Bradbury, Savile. An introduction to the optical microscope. Oxford University Press, 1988.

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Burgess, Jeremy. The magnified world. Rourke Enterprises, 1988.

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Nachtigall, Werner. Exploring with the microscope. Sterling Pub., 1995.

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Doane, Frances W. Canadian contributions to microscopy: An historical account of the development of the first electron microscope in North America and the first 20 years of the Microscopical Society of Canada/Société de microscopie du Canada. Microscopical Society of Canada, 1993.

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W, Doane F., Simon G. T, and Watson J. H. L, eds. Canadian contributions to microscopy: An historical account of the development of the first electron microscope in North America and the first 20 years of the Microscopical Society of Canada / Société de Microscopie du Canada. Microscopial Society of Canada, 1993.

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Reimer, Ludwig. Scanning electron microscopy: Physics of image formation and microanalysis. 2nd ed. Springer, 1998.

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Swain, Kelley. Darwin's microscope. Flambard Press, 2009.

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Selsam, Millicent Ellis. Greg's Microscope. Harper & Row, 1990.

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Book chapters on the topic "Microscope"

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Maddalena, Laura, Paolo Pozzi, Nicolò G. Ceffa, Bas van der Hoeven, and Elizabeth C. Carroll. "Optogenetics and Light-Sheet Microscopy." In Neuromethods. Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-2764-8_8.

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AbstractLight-sheet microscopy is a powerful method for imaging small translucent samples in vivo, owing to its unique combination of fast imaging speeds, large field of view, and low phototoxicity. This chapter briefly reviews state-of-the-art technology for variations of light-sheet microscopy. We review recent examples of optogenetics in combination with light-sheet microscopy and discuss some current bottlenecks and horizons of light sheet in all-optical physiology. We describe how 3-dimensional optogenetics can be added to an home-built light-sheet microscope, including technical notes ab
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Weik, Martin H. "microscope." In Computer Science and Communications Dictionary. Springer US, 2000. http://dx.doi.org/10.1007/1-4020-0613-6_11513.

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Breinig, Marianne. "Heisenberg Microscope." In Compendium of Quantum Physics. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-70626-7_84.

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Mitsuhashi, Jun. "Microscope Photography." In Invertebrate Tissue Culture Methods. Springer Japan, 2002. http://dx.doi.org/10.1007/978-4-431-67875-5_37.

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Gross, Herbert, Fritz Blechinger, and Bertram Achtner. "Microscope Optics." In Handbook of Optical Systems. Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527699247.ch7.

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Gooch, Jan W. "Polarizing Microscope." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8919.

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Jain, Aakanchha, Richa Jain, and Sourabh Jain. "Compound Microscope." In Basic Techniques in Biochemistry, Microbiology and Molecular Biology. Springer US, 2020. http://dx.doi.org/10.1007/978-1-4939-9861-6_8.

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Wu, Xiaohua. "Fluorescence Microscope." In Encyclopedia of Systems Biology. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_1021.

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Elkins, Kelly M. "The microscope." In Introduction to Forensic Chemistry. CRC Press, 2018. http://dx.doi.org/10.4324/9780429454530-3.

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Weik, Martin H. "simple microscope." In Computer Science and Communications Dictionary. Springer US, 2000. http://dx.doi.org/10.1007/1-4020-0613-6_17459.

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Conference papers on the topic "Microscope"

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Milner, R., and M. W. Phaneuf. "Comparative Carburization of Heat Resistant Alloys." In CORROSION 1998. NACE International, 1998. https://doi.org/10.5006/c1998-98431.

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Abstract Two high strength, centrifugally cast heat resistant materials were examined under near identical pack carburizing conditions. The first material represented an alloy class which is becoming the most popular for replacement coils in ethylene pyrolysis furnaces due to its large improvement in carburization resistance over HP based alloys. The second material represented the next generation of alloys to be used for this purpose. Additionally, several investigative techniques were employed to illustrate some of the strengths and weaknesses of each technique. A recent advance in microscop
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Bueno, Gloria, Jesus Ruiz-Santaquiteria, Noelia Vallez, Jesus Salido, Gabriel Cristóbal, and Oscar Deniz. "Telemicroscopy system applied to digital microscopy with a low-cost automated microscope." In Applications of Digital Image Processing XLVII, edited by Andrew G. Tescher and Touradj Ebrahimi. SPIE, 2024. http://dx.doi.org/10.1117/12.3028227.

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Webb, Robert H. "Microlaser microscope." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.mpp4.

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A scanned laser microscope with no moving parts is described. The source for this device is an array of 250 000 microlasers on a single substrate, each laser being typically 2 mm in diameter. The entire array is imaged on the microscope's object plane, but only one laser emits light at a given instant. Thus, as the array is electronically scanned, the illumination spot moves over the object. In the simplest configuration, a beam splitter returns light from the object to a detector, and the resulting voltage stream is synchronously displayed on a television monitor. The microscope can thus be p
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Masters, Barry R., and Andreas A. Thaer. "Confocal Microscopy of the Human In Vivo Cornea." In Ophthalmic and Visual Optics. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/ovo.1993.osab.2.

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The in-vivo observation of the living cornea by the technique of confocal microscopy provides en face images of high contrast and resolution1-4 . In contrast to Nipkow disk pinhole confocal microscopes,1-4 slit based confocal systems collect more light form the eye.5-6 The development of the wide-field specular microscope by Koester was limited by the low numerical aperture of the applanating cone objective7,8. Recent developments of a high numerical aperture for the wide-field specular microscope has resulted in a confocal microscope for the eye.9,10 We describe a new flying slit confocal mic
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Incardona, Nicolo, Angel Tolosa, Gabriele Scrofani, Manuel Martinez-Corral, and Genaro Saavedra. "The Lightfield Eyepiece: an Add-on for 3D Microscopy." In 3D Image Acquisition and Display: Technology, Perception and Applications. Optica Publishing Group, 2022. http://dx.doi.org/10.1364/3d.2022.3tu5a.6.

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Fourier lightfield microscopy is an emerging technique for real-time acquisition of three-dimensional microscopic samples. Here, we present the lightfield eyepiece, an add-on device capable of converting any conventional microscope to a Fourier lightfield microscope.
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Lima, Rui, Takuji Ishikawa, Motohiro Takeda, et al. "Measurement of Erythrocyte Motions in Microchannels by Using a Confocal Micro-PTV System." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-175969.

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Detailed knowledge on the motion of individual red blood cells (RBCs) flowing in microchannels is essential to provide a better understanding on the blood rheological properties and disorders in microvessels. Several studies on both individual and concentrated RBCs have already been performed in the past [1, 2]. However, all studies used conventional microscopes and also ghost cells to obtain visible trace RBCs through the microchannel. Recently, considerable progress in the development of confocal microscopy and consequent advantages of this microscope over the conventional microscopes have l
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Conchello, Jose A., J. Peter Zelten, Frank C. Miele, Bruce H. Davis, and Eric W. Hansen. "Enhanced 3-D reconstruction from confocal microscope images." In OSA Annual Meeting. Optica Publishing Group, 1988. http://dx.doi.org/10.1364/oam.1988.thff1.

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Confocal scanning microscopes are known to possess superior optical sectioning capabilities compared to conventional microscopes. Out-of-focus contributions in a through-focus series of images are significantly reduced by the confocal geometry but not completely removed. This paper reports our initial investigations Into a posterioriimage processing (i.e., deconvolution) for further improvement of depth resolution in confocal microscopy. This project is part of a larger effort In laser scanning fluorescence microscopy for biological and biophysical analyses in living cells. The instrument is b
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Wegscheider, S., A. Georgi, V. Sandoghdar, G. Krausch, and J. Mlynek. "Scanning near-field optical lithography." In The European Conference on Lasers and Electro-Optics. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/cleo_europe.1996.cfa4.

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The resolution of various scanning probe microscopy methods can be applied to the fabrication of nanostructures. Various methods of local material modification based on different microscopic mechanisms have been proposed, examples of which are : material transfer between a scanning tunneling microscope (STM) tip and a substrate, local oxidation of silicon using atomic force microscope (AFM). Scanning near-field optical microscopy (SNOM) is also an attractive candidate for nanofabrication. Here the optical spot size in the near-field is given by the resolution of the SNOM which in turn is deter
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Chen, Wenbin, Yian Yian, Qiju Zhang, et al. "Computed tomographic microscope: theory of microscopic CT." In Optoelectronic Science and Engineering '94: International Conference, edited by Wang Da-Heng, Anna Consortini, and James B. Breckinridge. SPIE, 1994. http://dx.doi.org/10.1117/12.182059.

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Chmelik, Radim. "Advances in digital holographic microscopy: coherence-controlled microscope." In SPIE Optics + Optoelectronics, edited by Miroslav Hrabovský, Miroslav Miler, and John T. Sheridan. SPIE, 2011. http://dx.doi.org/10.1117/12.888733.

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Reports on the topic "Microscope"

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Zhang, X. C. Terahertz Microscope. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada533321.

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Catalyurek, Umit, Michael D. Beynon, Chialin Chang, Tahsin Kurc, Alan Sussman, and Joel Saltz. The Virtual Microscope. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada440466.

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Crewe, A. V., and O. H. Kapp. Electron microscope studies. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6000131.

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Crewe, A. V., and O. H. Kapp. Electron microscope studies. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7015892.

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Day, R. D., and P. E. Russell. Atomic Force Microscope. Office of Scientific and Technical Information (OSTI), 1988. http://dx.doi.org/10.2172/476627.

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Melloch, Michael R. Scanning Probe Microscope. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada388569.

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George, J. S., D. M. Rector, D. M. Ranken, B. Peterson, and J. Kesteron. Virtual pinhole confocal microscope. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/353183.

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Taylor, A. J., G. P. Donati, G. Rodriguez, T. R. Gosnell, S. A. Trugman, and D. I. Some. Femtosecond scanning tunneling microscope. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/672306.

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9

O'Keefe, Michael A. One-Angstrom microscope update. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/809890.

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Kenik, E. (Intermediate voltage electron microscope). Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/5356814.

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