Gotowe bibliografie tematyczne / Microscopy

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Gotowa bibliografia na temat „Microscopy”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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Artykuły w czasopismach na temat "Microscopy"

Schatten, G., J. Pawley, and H. Ris. "Integrated microscopy resource for biomedical research at the university of wisconsin at madison." Proceedings, annual meeting, Electron Microscopy Society of America 45 (August 1987): 594–97. http://dx.doi.org/10.1017/s0424820100127451.

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The High Voltage Electron Microscopy Laboratory [HVEM] at the University of Wisconsin-Madison, a National Institutes of Health Biomedical Research Technology Resource, has recently been renamed the Integrated Microscopy Resource for Biomedical Research [IMR]. This change is designed to highlight both our increasing abilities to provide sophisticated microscopes for biomedical investigators, and the expansion of our mission beyond furnishing access to a million-volt transmission electron microscope. This abstract will describe the current status of the IMR, some preliminary results, our upcomin

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Chen, Xiaodong, Bin Zheng, and Hong Liu. "Optical and Digital Microscopic Imaging Techniques and Applications in Pathology." Analytical Cellular Pathology 34, no. 1-2 (2011): 5–18. http://dx.doi.org/10.1155/2011/150563.

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The conventional optical microscope has been the primary tool in assisting pathological examinations. The modern digital pathology combines the power of microscopy, electronic detection, and computerized analysis. It enables cellular-, molecular-, and genetic-imaging at high efficiency and accuracy to facilitate clinical screening and diagnosis. This paper first reviews the fundamental concepts of microscopic imaging and introduces the technical features and associated clinical applications of optical microscopes, electron microscopes, scanning tunnel microscopes, and fluorescence microscopes.

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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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Youngblom, J. H., J. Wilkinson, and J. J. Youngblom. "Telepresence Confocal Microscopy." Microscopy Today 8, no. 10 (2000): 20–21. http://dx.doi.org/10.1017/s1551929500054146.

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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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Brooks, Donald A. "The College of Microscopy — Meeting Rapidly Growing Microscopy Demands." Microscopy Today 15, no. 4 (2007): 51. http://dx.doi.org/10.1017/s1551929500055735.

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The McCrone Group Inc. recently announced the completion of a 40,000 sq ft addition to house its new College of Microscopy. Since its founding in 1956, The McCrone Group has grown into a multi-faceted organization and now encompasses three main organizations, McCrone Associates - the analytical service and consulting firm; McCrone Microscopes & Accessories - the microscope and instrument sales group; and, the College of Microscopy - the microscopy learning center. The newly completed addition houses the first and only College of Microscopy and offers the largest array of basic and advanced

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Martone, Maryann E. "Bridging the Resolution Gap: Correlated 3D Light and Electron Microscopic Analysis of Large Biological Structures." Microscopy and Microanalysis 5, S2 (1999): 526–27. http://dx.doi.org/10.1017/s1431927600015956.

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One class of biological structures that has always presented special difficulties to scientists interested in quantitative analysis is comprised of extended structures that possess fine structural features. Examples of these structures include neuronal spiny dendrites and organelles such as the Golgi apparatus and endoplasmic reticulum. Such structures may extend 10's or even 100's of microns, a size range best visualized with the light microscope, yet possess fine structural detail on the order of nanometers that require the electron microscope to resolve. Quantitative information, such as su

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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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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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Möller, Lars, Gudrun Holland, and Michael Laue. "Diagnostic Electron Microscopy of Viruses With Low-voltage Electron Microscopes." Journal of Histochemistry & Cytochemistry 68, no. 6 (2020): 389–402. http://dx.doi.org/10.1369/0022155420929438.

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Diagnostic electron microscopy is a useful technique for the identification of viruses associated with human, animal, or plant diseases. The size of virus structures requires a high optical resolution (i.e., about 1 nm), which, for a long time, was only provided by transmission electron microscopes operated at 60 kV and above. During the last decade, low-voltage electron microscopy has been improved and potentially provides an alternative to the use of high-voltage electron microscopy for diagnostic electron microscopy of viruses. Therefore, we have compared the imaging capabilities of three l

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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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Rozprawy doktorskie na temat "Microscopy"

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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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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Wright, Adele Hart. "Design, development, and application of an automated precision scanning microscope stage with a controlled environment." Thesis, Georgia Institute of Technology, 1997. http://hdl.handle.net/1853/16409.

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Yu, Enhua. "Crossed and uncrossed retinal fibres in normal and monocular hamsters : light and electron microscopic studies /." [Hong Kong : University of Hong Kong], 1990. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13014316.

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Toledo, Acosta Bertha Mayela. "Multimodal image registration in 2D and 3D correlative microscopy." Thesis, Rennes 1, 2018. http://www.theses.fr/2018REN1S054/document.

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Cette thèse porte sur la définition d'un schéma de recalage automatique en microscopie corrélative 2D et 3D, en particulier pour des images de microscopie optique et électronique (CLEM). Au cours des dernières années, la CLEM est devenue un outil d'investigation important et puissant dans le domaine de la bio-imagerie. En utilisant la CLEM, des informations complémentaires peuvent être collectées à partir d'un échantillon biologique. La superposition des différentes images microscopiques est généralement réalisée à l'aide de techniques impliquant une assistance manuelle à plusieurs étapes, ce

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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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Rea, Nigel P. "Interference and laser feedback optical microscopy." Thesis, University of Oxford, 1995. http://ora.ox.ac.uk/objects/uuid:989c9fca-947d-490c-9f34-38065a7c57d9.

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This thesis concerns the development of simple, compact scanning optical microscopes which can obtain confocal and interference images. The effects of feeding the reflected signal back into the laser cavity of a confocal microscope are investigated and exploited. Monomode optical fibres are used to perform the spatial filtering required for confocal microscopy and, later, as the source of reference beams for interferometry. The theory describing the basic operation of the microscopes is developed. The optical systems are modelled using scalar diffraction theory and the effects of optical feedb

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Romero, Leiro Freddy José. "Poly-articulated microrobotics for correlative AFM-in-SEM microscopy." Electronic Thesis or Diss., Sorbonne université, 2023. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2023SORUS520.pdf.

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La microscopie corrélative est le résultat de la combinaison de deux ou plusieurs techniques de microscopie pour fournir des informations complémentaires sur un échantillon. En utilisant un microscope électronique à balayage (MEB) et un microscope à force atomique (AFM), la microscopie corrélative AFM-in-SEM permet non seulement la caractérisation 3D d'échantillons observés à l'intérieur d'un MEB, mais aussi la manipulation de micro- et nanostructures avec une très grande précision. Cette technique peut être appliquée à divers échantillons dans les domaines de la biologie, de l'électronique et

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Mattocks, Philip. "Scanning tunnelling microscopy and atomic force microscopy of semiconducting materials." Thesis, University of Manchester, 2012. https://www.research.manchester.ac.uk/portal/en/theses/scanning-tunnelling-microscopy-and-atomic-force-microscopy-of-semiconducting-materials(9bc10301-2c4d-4dfb-a374-f65ee37ae23a).html.

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Michael Faraday first documented semiconducting behaviour in 1833 whenhe observed that the resistance of silver sulphide decreased with temperature,contrary to the behaviour of normal conducting materials. Up untilthe middle of the twentieth century, semiconductors were used as photodetectors,thermisters and rectifiers. In 1947 the invention of the transistor byBardeen and Brattain lead to the integrated circuit and paved the way formodern electronics. The need to produce smaller and faster transistors hasdriven research into new semiconductors. This thesis will first introduce the physics of

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Książki na temat "Microscopy"

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

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Goodhew, Peter J. Electron microscopy and analysis. 2nd ed. Taylor & Francis, 1988.

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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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Slayter, Elizabeth M. Light and electron microscopy. Cambridge University Press, 1992.

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

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Thomas, Mulvey, and Sheppard C. J. R, eds. Advances in optical and electron microscopy. Academic Press, 1994.

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R, Beanland, and Humphreys F. J, eds. Electron microscopy and analysis. 3rd ed. Taylor & Francis, 2001.

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Thomas, Mulvey, and Sheppard C. J. R, eds. Advances in optical and electron microscopy. Academic Press, 1994.

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Pluta, Maksymilian. Advanced light microscopy. PWN, 1988.

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Części książek na temat "Microscopy"

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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Nichols, Gary, Shen Luk, and Clive Roberts. "Microscopy." In Solid State Characterization of Pharmaceuticals. John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9780470656792.ch9.

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Allen, Terence. "Microscopy." In Particle Size Measurement. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0417-0_6.

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Buxbaum, Engelbert. "Microscopy." In Biophysical Chemistry of Proteins. Springer US, 2010. http://dx.doi.org/10.1007/978-1-4419-7251-4_1.

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Sprott, G. Dennis, and Terry J. Beveridge. "Microscopy." In Methanogenesis. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2391-8_3.

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Keiser, Gerd. "Microscopy." In Graduate Texts in Physics. Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-0945-7_8.

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Dehonor, Mariamne, Carlos López-Barrón, and Christopher W. Macosko. "Microscopy." In Handbook of Polymer Synthesis, Characterization, and Processing. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118480793.ch20.

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Gooch, Jan W. "Microscopy." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7487.

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Sims, Tony, and Qiuyu Wang. "Microscopy." In Biomedical Science Practice. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780198831228.003.0007.

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This chapter focuses on microscopy, which is the use of a microscope to examine and analyse objects that would normally be too small to be seen with the naked eye. Microscopes that use a single lens are called simple microscopes; those with more than one are compound microscopes. Microscopes are perhaps the most widely used instruments in biomedical science. They have contributed greatly to the knowledge and understanding of pathological processes, and are used in all branches of biomedical science. Light microscopes are used to look at cells and tissues. The electron microscope, with its vast

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Ruzin, Steven E. "Epifluorescence Microscopy." In Techniques in Light Microscopy. Oxford University PressOxford, 2024. http://dx.doi.org/10.1093/oso/9780198885832.003.0008.

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Abstract This chapter on fluorescence microscopy provides the theoretical background for all microscope techniques that use fluorescence for imaging samples. It covers the theory of fluorescence and its implementation in microscopy. Here interference filters and dichroic mirrors are described in the context of the ubiquitous epifluorescence microscope, and all fluorescence microscopes and techniques that follow The concepts of photobleaching, the Stokes shift, and fluorescence quantum yield are also discussed. Included is a description of the optical components required for epifluorescence inc

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Streszczenia konferencji na temat "Microscopy"

Bartels, Randy. "NLO Microscopy." In Nonlinear Photonics. Optica Publishing Group, 2024. https://doi.org/10.1364/np.2024.nptu2e.1.

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We demonstrate computational adaptive optical correction for second harmonic generation (SHG) and third harmonic generation (THG) holographic imaging. Results for transmission and epi SHG and transmission THG imaging will be discussed. Full-text article not available; see video presentation

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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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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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Goodman, Douglas S. "Fiber-optic illuminators for microscopy." In OSA Annual Meeting. Optica Publishing Group, 1987. http://dx.doi.org/10.1364/oam.1987.wg6.

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Many illumination problems in microscopy can be solved easily and economically with fiber optics. Modes of illumination not provided by the designers of a microscope can be added. A modular illumination system involving a number of microscopes and sources can be assembled. Various types of illumination can be used simultaneously, e.g., bright field and dark field, transmitted and reflected. Realignment on changing lamps is simplified, since it is merely necessary to align the lamp relative to the fiber input end. Older microscopes with small lamps can be upgraded by using a fiber bundle termin

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Rastogi, Vivek, Shilpi Agarwal, Satish Dubey, Gufran Khan, and Chandra Shakher. "Microscopic urinalysis by digital holographic microscopy." In Holography, Diffractive Optics, and Applications IX, edited by Changhe Zhou, Yunlong Sheng, and Liangcai Cao. SPIE, 2019. http://dx.doi.org/10.1117/12.2537315.

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Dixon, A. E. "Confocal microscopy." In OSA Annual Meeting. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/oam.1993.tue.1.

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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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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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Spector, S. J., C. J. Jacobsen, and D. M. Tennant. "Fabrication of Fresnel zone plates for x-ray microscopy: diffractive optics for soft x-rays." In Diffractive Optics and Micro-Optics. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/domo.1996.dwd.6.

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Fresnel zone plates are diffractive optical elements which are currently being used for high resolution x-ray microscopy. Several groups fabricate zone plates for use in specific microscopes [1] and we present here a summary on the fabrication of zone plates for use in the Scanning Transmission X-ray Microscope at the National Synchrotron Light Source. X-ray microscopy has demonstrated imaging with resolution five times superior to that which can routinely be achieved by visible light microscopy. In addition, x-rays with wavelengths between the carbon (4.2 nm) and oxygen (2.3 nm) K absorption

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Trovatello, C., A. Genco, C. Cruciano, et al. "Hyperspectral microscopy of two-dimensional semiconductors." In Latin America Optics and Photonics Conference. Optica Publishing Group, 2022. http://dx.doi.org/10.1364/laop.2022.th1d.7.

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We present wide-field hyperspectral microscopy images of photoluminescence from two-dimensional semiconductors. The microscope exploits Fourier-transform spectroscopy and uses a common-path birefringent interferometer. Our hyperspectral microscope is a fast tool to characterize 2D materials.

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Raporty organizacyjne na temat "Microscopy"

Snyder, Shelly R., and Henry S. White. Scanning Tunneling Microscopy, Atomic Force Microscopy, and Related Techniques. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada246852.

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Dow, John D. Scanning Tunneling Microscopy. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada249262.

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Legg, Keith O., and Douglas N. Rose. Ion Acoustic Microscopy. Defense Technical Information Center, 1985. http://dx.doi.org/10.21236/ada169492.

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Quate, C. F. Cryogenic Acoustic Microscopy. Defense Technical Information Center, 1986. http://dx.doi.org/10.21236/ada173188.

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Hammel, P. Microscopic subsurface characterization of layered magnetic materials using magnetic resonance force microscopy. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1580650.

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Bentley, J. (Future of electron microscopy). Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/5651701.

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Botkin, D. A. Ultrafast scanning tunneling microscopy. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/270266.

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Witham, Philip. Pinhole Neutral Atom Microscopy. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.1407.

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Weber, Peter M. Time-Resolved Scanning Electron Microscopy. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada455461.

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Hawley, M. E., D. W. Reagor, and Quan Xi Jia. Scanning probe microscopy competency development. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/562576.

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