Relevant bibliographies by topics / Cells Microscopy

Contents

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

Academic literature on the topic 'Cells Microscopy'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Cells Microscopy"

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Kosaka, Yudai, and Tetsuhiko Ohba. "3P174 Study on membrane microfluidity of living cells using Muller Matrix microscopy(12. Cell biology,Poster)." Seibutsu Butsuri 53, supplement1-2 (2013): S240. http://dx.doi.org/10.2142/biophys.53.s240_5.

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Yimei Huang, Yimei Huang, Hongqin Yang Hongqin Yang, Xiuqiu Shen Xiuqiu Shen, Yuhua Wang Yuhua Wang, Liqin Zheng Liqin Zheng, Hui Li Hui Li, and Shusen Xie Shusen Xie. "Visualizing NO in live cells by confocal laser scanning microscopy." Chinese Optics Letters 10, s1 (2012): S11701–311703. http://dx.doi.org/10.3788/col201210.s11701.

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Mao, Hong, Robin Diekmann, Hai Po H. Liang, Victoria C. Cogger, David G. Le Couteur, Glen P. Lockwood, Nicholas J. Hunt, et al. "Cost-efficient nanoscopy reveals nanoscale architecture of liver cells and platelets." Nanophotonics 8, no. 7 (July 9, 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 microscope allows the introduction of highly affordable and low-maintenance SMLM hardware and methods to laboratories that, for example, lack access to core facilities housing high-end commercial microscopes for SMLM and EM. Using our custom-built microscope and freely available software from image acquisition to analysis, we image LSECs and platelets with lateral resolution down to about 50 nm. Furthermore, we use this microscope to examine the effect of drugs and toxins on cellular morphology.
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Horky, D., I. Lauschova, M. Klabusay, M. Doubek, P. Sheer, S. Palsa, and J. Doubek. "Appearance of iron-labeled blood mononuclear cells in electron microscopy." Veterinární Medicína 51, No. 3 (March 19, 2012): 89–92. http://dx.doi.org/10.17221/5525-vetmed.

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Mononuclear cells from rabbit bone marrow were cultured for 14 days in cell-free medium for hematopoietic cells together with iron oxid nanoparticles, and then they were processed by technique for free cells for TEM (transmission electron microscopy). Staining with turnbull blue was used for the detection of iron using a light microscope. It was shown that iron nanoparticles were incorporated into the cytoplasm of mononuclear cells during 14 days cultivation. Here they were localized within different sized vacuoles with distinct membranes.
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McIntosh, J. Richard. "Electron Microscopy of Cells." Journal of Cell Biology 153, no. 6 (June 11, 2001): F25—F32. http://dx.doi.org/10.1083/jcb.153.6.f25.

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Vodyanoy, Vitaly. "High Resolution Light Microscopy of Live Cells." Microscopy Today 13, no. 3 (May 2005): 26–29. http://dx.doi.org/10.1017/s1551929500051609.

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All living creatures, including humans, are made of cells. The majority of life forms exist as single cells that perform all functions to continue independent life. Some cell structures, cell organelles and particularly bacteria and viruses are commonly too small to be fully observed with an optical microscope. Therefore, an electron microscope is required. Since samples examined with an electron microscope are exposed to very high vacuum, it is impossible to view living cells. The sample preparation for electron microscopy requires that living cells be killed, frozen, dehydrated, and impregnated with heavy metals.
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Brama, Elisabeth, Christopher J. Peddie, Gary Wilkes, Yan Gu, Lucy M. Collinson, and Martin L. Jones. "ultraLM and miniLM: Locator tools for smart tracking of fluorescent cells in correlative light and electron microscopy." Wellcome Open Research 1 (December 13, 2016): 26. http://dx.doi.org/10.12688/wellcomeopenres.10299.1.

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In-resin fluorescence (IRF) protocols preserve fluorescent proteins in resin-embedded cells and tissues for correlative light and electron microscopy, aiding interpretation of macromolecular function within the complex cellular landscape. Dual-contrast IRF samples can be imaged in separate fluorescence and electron microscopes, or in dual-modality integrated microscopes for high resolution correlation of fluorophore to organelle. IRF samples also offer a unique opportunity to automate correlative imaging workflows. Here we present two new locator tools for finding and following fluorescent cells in IRF blocks, enabling future automation of correlative imaging. The ultraLM is a fluorescence microscope that integrates with an ultramicrotome, which enables ‘smart collection’ of ultrathin sections containing fluorescent cells or tissues for subsequent transmission electron microscopy or array tomography. The miniLM is a fluorescence microscope that integrates with serial block face scanning electron microscopes, which enables ‘smart tracking’ of fluorescent structures during automated serial electron image acquisition from large cell and tissue volumes.
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Jester, J. V., H. D. Cavanagh, and M. A. Lemp. "In vivo confocal imaging of the eye using tandem scanning confocal microscopy (TSCM)." Proceedings, annual meeting, Electron Microscopy Society of America 46 (1988): 56–57. http://dx.doi.org/10.1017/s0424820100102365.

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New developments in optical microscopy involving confocal imaging are now becoming available which dramatically increase resolution, contrast and depth of focus by optically sectioning through structures. The transparency of the anterior ocular structures, cornea and lens, make microscopic visualization and optical sectioning of the living intact eye an interesting possibility. Of the confocal microscopes available, the Tandem Scanning Reflected Light Microscope (referred to here as the Tandem Scanning Confocal Microscope), developed by Professors Petran and Hadravsky at Charles University in Pilzen, Czechoslovakia, permits real-time image acquisition and analysis facilitating in vivo studies of ocular structures.Currently, TSCM imaging is most successful for the cornea. The corneal epithelium, stroma, and endothelium have been studied in vivo and photographed in situ. Confocal scanning images of the superficial epithelium, similar to those obtained by scanning electron microscopy, show both light and dark surface epithelial cells.
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Li, Ying, Jianglei Di, Li Ren, and Jianlin Zhao. "Deep-learning-based prediction of living cells mitosis via quantitative phase microscopy." Chinese Optics Letters 19, no. 5 (2021): 051701. http://dx.doi.org/10.3788/col202119.051701.

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Häberle, W. "Force microscopy on living cells." Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures 9, no. 2 (March 1991): 1210. http://dx.doi.org/10.1116/1.585206.

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Dissertations / Theses on the topic "Cells Microscopy"

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Kuhn, Jeffrey Russell. "Modulated polarization microscopy : a new instrument for visualizing cytoskeletal dynamics in living cells /." Digital version accessible at:, 2000. http://wwwlib.umi.com/cr/utexas/main.

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Cacovich, Stefania. "Electron microscopy studies of hybrid perovskite solar cells." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/276753.

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Over the last five years hybrid organic-inorganic metal halide perovskites have attracted strong interest in the solar cell community as a result of their high power conversion efficiency and the solid opportunity to realise a low-cost as well as industry-scalable technology. Nevertheless, several aspects of this novel class of materials still need to be explored and the level of our understanding is rapidly and constantly evolving, from month to month. This dissertation reports investigations of perovskite solar cells with a particular focus on their local chemical composition. The analytical characterisation of such devices is very challenging due to the intrinsic instability of the organic component in the nanostructured compounds building up the cell. STEM-EDX (Scanning Transmission Electron Microscopy - Energy Dispersive X-ray spectroscopy) was employed to resolve at the nanoscale the morphology and the elemental composition of the devices. Firstly, a powerful procedure, involving FIB (Focus Ion Beam) sample preparation, the acquisition of STEM-EDX maps and the application of cutting edge post-processing data techniques based on multivariate analysis was developed and tested. The application of this method has drastically improved the quality of the signal that can be extracted from perovskite thin films before the onset of beam-induced transformations. Morphology, composition and interfaces in devices deposited by using different methodologies and external conditions were then explored in detail by combining multiple complementary advanced characterisation tools. The observed variations in the nanostructure of the cells were related to different photovoltaic performance, providing instructive indications for the synthesis and fabrication routes of the devices. Finally, the main degradation processes that affect perovskite solar cells were probed. STEM-EDX was used in conjunction with the application of in situ heating, leading to the direct observation of elemental species migration within the device, reported here for the first time with nanometric spatial resolution. Further analyses, involving a set of experiments aimed to study the effects of air exposure and light soaking on the cells, were designed and performed, providing evidence of the main pathways leading to the drastic drop in the device performance.
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Wong, Tsz-wai Terence, and 黃子維. "Optical time-stretch microscopy: a new tool for ultrafast and high-throughput cell imaging." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hub.hku.hk/bib/B5066234X.

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The exponential expansion in the field of biophotonics over the past half-century has been leading to ubiquitous basic science investigations, ranging from single cell to brain networking analysis. There is also one biophotonics technology used in clinic, which is optical coherence tomography, mostly for high-speed and high-resolution endoscopy. To keep up such momentum, new biophotonics technologies should be aiming at improving either the spatial resolution or temporal resolution of optical imaging. To this end, this thesis will address a new imaging technique which has an ultra-high temporal resolution. The applications and its cost-effective implementations will also be encompassed. In the first part, I will introduce an entirely new optical imaging modality coined as optical time-stretch microscopy. This technology allows ultra-fast real-time imaging capability with an unprecedented line-scan rate (~10 million frames per second). This ultrafast microscope is renowned as the world’s fastest camera. However, this imaging system is previously not specially designed for biophotonics applications. Through the endeavors of our group, we are able to demonstrate this optical time-stretch microscopy for biomedical applications with less biomolecules absorption and higher diffraction limited resolution (<2 μm). This ultrafast imaging technique is particularly useful for high-throughput and high-accuracy cells/drugs screening applications, such as imaging flow cytometry and emulsion encapsulated drugs imaging. In the second part, two cost-effective approaches for implementing optical time-stretch confocal microscopy are discussed in details. We experimentally demonstrate that even if we employ the two cost-effective approaches simultaneously, the images share comparable image quality to that of captured by costly specialty 1μm fiber and high-speed ( >16 GHz bandwidth) digitizer. In other words, the cost is drastically reduced while we can preserve similar image quality. At the end, I will be wrapping up my thesis by concluding all my work done and forecasting the future challenges concerning the development of optical time-stretch microscopy. In particular, three different research directions are discussed.
published_or_final_version
Electrical and Electronic Engineering
Master
Master of Philosophy
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Wätjen, Jörn Timo. "Microscopic Characterisation of Solar Cells : An Electron Microscopy Study of Cu(In,Ga)Se2 and Cu2ZnSn(S,Se)4 Solar Cells." Doctoral thesis, Uppsala universitet, Fasta tillståndets elektronik, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-199432.

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The sun provides us with a surplus of energy convertible to electricity using solar cells. This thesis focuses on solar cells based on chalcopyrite (CIGSe) as well as kesterite (CZTS(e)) absorber layers. These materials yield record efficiencies of 20.4 % and 11.1 %, respectively. Especially for CZTS(e), the absorber layers often do not consist of one single desired phase but can exhibit areas with deviating material properties, referred to as secondary phases. Furthermore, several material layers are required for a working solar cell, each exhibiting interfaces. Even though secondary phases and interfaces represent a very small fraction of the solar cell they can have a profound influence on the over-all electrical solar cell characteristics. As such, it is crucial to understand how secondary phases and interfaces influence the local electrical characteristics. Characterising secondary phases and interfaces is challenging due to their small sample volume and relatively small differences in composition amongst others. This is where electronmicroscopy, especially transmission electron microscopy, offers valuable insight to material properties on the microscopic scale. The main challenge is, however, to link these material properties to the corresponding electrical characteristics of a solar cell. This thesis uses electron beam induced current imaging and introduces a new method for JV characterisation of solar cells on the micron scale. Combining microscopic structural and electrical characterisation techniques allowed identifying and characterising local defects found in the absorber layer of CIGS solar cells after thermal treatment. Furthermore, CZTSe solar cells in this thesis exhibited a low photo-current density which is traced to the formation of a current blocking ZnSe secondary phase at the front contact interface. The electron microscopy work has contributed to an understanding of the chemical stability of CZTS and has shown the need for an optimised back contact interface in order to avoid chemical decomposition reactions and formation of detrimental secondary phases. With this additional knowledge, a comprehensive picture of the material properties from the macroscopic down to the microscopic level can be attained throughout all required material layers.
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Barnes, Clifford Alexander. "Supra-vital atomic force microscopy of living cultured cells." Thesis, University of Ulster, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.494333.

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Zeskind, Benjamin J. "Quantitative imaging of living cells by deep ultraviolet microscopy." Thesis, Massachusetts Institute of Technology, 2006. http://hdl.handle.net/1721.1/38693.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2006.
Includes bibliographical references (p. 139-145).
Developments in light microscopy over the past three centuries have opened new windows into cell structure and function, yet many questions remain unanswered by current imaging approaches. Deep ultraviolet microscopy received attention in the 1950s as a way to generate image contrast from the strong absorbance of proteins and nucleic acids at wavelengths shorter than 300 nm. However, the lethal effects of these wavelengths limited their usefulness in studies of cell function, separating the contributions of protein and nucleic acid proved difficult, and scattering artifacts were a significant concern. We have used short exposures of deep-ultraviolet light synchronized with an ultraviolet-sensitive camera to observe mitosis and motility in living cells without causing necrosis, and quantified absorbance at 280 nm and 260 nm together with tryptophan native fluorescence in order to calculate maps of nucleic acid mass, protein mass, and quantum yield in unlabeled cells. We have also developed a method using images acquired at 320nm and 340nm, and an equation for Mie scattering, to determine a scattering correction factor for each pixel at 260nm and 280nm. These developments overcome the three main obstacles to previous deep UV microscopy efforts, creating a new approach to imaging unlabeled living cells that acquires quantitative information about protein and nucleic acid as a function of position and time.
by Benjamin J. Zeskind.
Ph.D.
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Joensuu, Jenny. "Online Image Analysis of Jurkat T Cells using in situ Microscopy." Thesis, Linköpings universitet, Institutionen för fysik, kemi och biologi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-153313.

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Cell cultivation in bioreactors would benefit from developed monitoring systems with online real-time imaging to evaluate cell culture conditions and processes. This opportunity can be provided with the newly developed in situ Microscope also called ISM. The ISM probe is mounted into the wall of a bioreactor and consists of a measurement zone with an illuminating light source to obtain real-time images of moving cells in suspension. The instrument is linked to advanced imaging analysis software which can be specifically adapted for the objects in study. The aim of this project is to analyze the T lymphocyte cell line Jurkat T cells using the ISM equipment and identify specific features of the cells that can be obtained. The results show that the equipment and linked software are suitable for monitoring cell density, cell size distribution and cell surface analysis of the Jurkat cells during cultivation. The ISM could also detect induced changes in cell size caused by osmotic shifts and the course of an infection occurring in the cell suspension using a developed software for online real-time monitoring.
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Al-Rekabi, Zeinab. "Investigating Mechanotransduction and Mechanosensitivity in Mammalian Cells." Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/30256.

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Living organisms are made up of a multitude of individual cells that are surrounded by biomolecules and fluids. It is well known that cells are highly regulated by biochemical signals; however it is now becoming clear that cells are also influenced by the mechanical forces and mechanical properties of the local microenvironment. Extracellular forces causing cellular deformation can originate from many sources, such as fluid shear stresses arising from interstitial or blood flow, mechanical stretching during breathing or compression during muscle contraction. Cells are able to sense variations in the mechanical properties (elasticity) of their microenvironment by actively probing their surroundings by utilizing specialized proteins that are involved in sensing and transmitting mechanical information. The actin cytoskeleton and myosin-II motor proteins form a contractile (actomyosin) network inside the cell that is connected to the extracellular microenvironment through focal adhesion and integrin sites. The transmission of internal actomyosin strain to the microenvironment via focal adhesion sites generates mechanical traction forces. Importantly, cells generate traction forces in response to extracellular forces and also to actively probe the elasticity of the microenvironment. Many studies have demonstrated that extracellular forces can lead to rapid cytoskeletal remodeling, focal adhesion regulation, and intracellular signalling which can alter traction force dynamics. As well, cell migration, proliferation and stem cell fate are regulated by the ability of cells to sense the elasticity of their microenvironment through the generation of traction forces. In vitro studies have largely explored the influence of substrate elasticity and extracellular forces in isolation, however, in vivo cells are exposed to both mechanical cues simultaneously and their combined effect remains largely unexplored. Therefore, a series of experiments were performed in which cells were subjected to controlled extracellular forces as on substrates of increasing elasticity. The cellular response was quantified by measuring the resulting traction force magnitude dynamics. Two cell types were shown to increase their traction forces in response to extracellular forces only on substrates of specific elasticities. Therefore, cellular traction forces are regulated by an ability to sense and integrate at least two pieces of mechanical information - elasticity and deformation. Finally, this ability is shown to be dependent on the microtubule network and regulators of myosin-II activity.
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Muys, James Johan. "Cellular Analysis by Atomic Force Microscopy." Thesis, University of Canterbury. Electrical and Computer Engineering, 2006. http://hdl.handle.net/10092/1158.

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Exocytosis is a fundamental cellular process where membrane-bound secretory granules from within the cell fuse with the plasma membrane to form fusion pore openings through which they expel their contents. This mechanism occurs constitutively in all eukaryotic cells and is responsible for the regulation of numerous bodily functions. Despite intensive study on exocytosis the fusion pore is poorly understood. In this research micro-fabrication techniques were integrated with biology to facilitate the study of fusion pores from cells in the anterior pituitary using the atomic force microscope (AFM). In one method cells were chemically fixed to reveal a diverse range of pore morphologies, which were characterised according to generic descriptions and compared to those in literature. The various pore topographies potentially illustrates different fusion mechanisms or artifacts caused from the impact of chemicals and solvents in distorting dynamic cellular events. Studies were performed to investigate changes in fusion pores in response to stimuli along with techniques designed to image membrane topography with nanometre resolution. To circumvent some deficiencies in traditional chemical fixation methodologies, a Bioimprint replication process was designed to create molecular imprints of cells using imprinting and soft moulding techniques with photo and thermal activated elastomers. Motivation for the transfer of cellular ultrastructure was to enable the non-destructive analysis of cells using the AFM while avoiding the need for chemical fixation. Cell replicas produced accurate images of membrane topology and contained certain fusion pore types similar to those in chemically fixed cells. However, replicas were often dehydrated and overall experiments testing stimuli responses were inconclusive. In a preliminary investigation, a soft replication moulding technique using a PDMS-elastomer was tested on human endometrial cancer cells with the aim of highlighting malignant mutations. Finally, a Biochip comprised of a series of interdigitated microelectrodes was used to position single-cells within an array of cavities using positive and negative dielectrophoresis (DEP). Selective sites either between or on the electrode were exposed as cavities designed to trap and incubate pituitary and cancer cells for analysis by atomic force microscopy (AFMy). Results achieved trapping of pituitary and cancer cells within cavities and demonstrated that positive DEP could be used as a force to effectively position living cells. AFM images of replicas created from cells trapped within cavities illustrated the advantage of integrating the Biochip with Bioimprint for cellular analysis.
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Chhun, Bryant B. "Super-resolution video microscopy of live cells by structured illumination." Diss., Search in ProQuest Dissertations & Theses. UC Only, 2009. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1473623.

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Books on the topic "Cells Microscopy"

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Cells up close. New York, NY: Gareth Stevens Publishing, 2014.

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Hall, Simon Richard. Analytical electron microscopy of cultured mammalian cells. Manchester: Universityof Manchester, 1993.

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Bender, Lionel. Atoms and cells. New York: Gloucester Press, 1990.

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Valtere, Evangelista, and NATO Public Diplomacy Division, eds. From cells to proteins: Imaging nature across dimensions. Dordrecht: Springer, 2005.

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1931-, Kessel Richard G., and Tung Hai-Nan, eds. Freeze fracture images of cells and tissues. New York: Oxford University Press, 1991.

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I︠U︡, Komissarchik I︠A︡, Mironov Vladimir 1954-, and Nikolʹskiĭ N. N, eds. Metody ėlektronnoĭ mikroskopii v biologii i medit︠s︡ine. Sankt-Peterburg: Nauka, 1994.

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Cells illuminated: In vivo optical imaging. Bellingham, Wash., USA: SPIE Press, 2010.

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Bubel, Andreas. Microstructure and function of cells: Electron micrographs of cell ultrastructure. Chichester, West Sussex, England: E. Horwood, 1989.

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O'Hagan, B. M. G. The effects of atomic force microscopy upon the viability of epithelial cells?. [S.l: The Author], 1996.

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1937-, Lehmann H. Peter, and Kao Yuan S. 1935-, eds. Practical microscopic hematology: A manual for the clinical laboratory and clinical practice. 4th ed. Philadelphia: Lea & Febiger, 1994.

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Book chapters on the topic "Cells Microscopy"

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Borchert, Holger. "Electron Microscopy." In Solar Cells Based on Colloidal Nanocrystals, 63–77. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04388-3_4.

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Hibbs, Alan R. "Imaging Live Cells." In Confocal Microscopy for Biologists, 279–323. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48565-7_12.

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Osafune, Tetsuaki, and Steven D. Schwartzbach. "Serial Section Immunoelectron Microscopy of Algal Cells." In Immunoelectron Microscopy, 259–74. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-783-9_21.

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Perro, Mario, Jacky G. Goetz, and Antonio Peixoto. "Intravital Microscopy." In Imaging from Cells to Animals In Vivo, 17–34. First edition. | Boca Raton : CRC Press, 2020. | Series: Series in cellular and clinical imaging: CRC Press, 2020. http://dx.doi.org/10.1201/9781315174662-3.

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Gray, Colin, and Daniel Zicha. "Microscopy of Living Cells." In Animal Cell Culture, 61–90. Chichester, UK: John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9780470669815.ch3.

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Kolios, Michael C., Eric M. Strohm, and Gregory J. Czarnota. "Acoustic Microscopy of Cells." In Quantitative Ultrasound in Soft Tissues, 315–41. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6952-6_13.

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Choi, Heejun. "FLIM Imaging for Metabolic Studies in Live Cells." In Confocal Microscopy, 339–46. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1402-0_18.

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Häberle, W., D. P. E. Smith, J. K. H. Hörber, and C. P. Czerny. "Scanning Force Microscopy on Living Virus-Infected Cells." In Atomic Force Microscopy/Scanning Tunneling Microscopy, 7–17. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4757-9322-2_2.

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Castejón, Orlando J. "Stellate Cells." In Scanning Electron Microscopy of Cerebellar Cortex, 81–85. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0159-6_11.

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Castejón, Orlando J. "Granule Cells." In Scanning Electron Microscopy of Cerebellar Cortex, 29–37. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0159-6_3.

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Conference papers on the topic "Cells Microscopy"

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Senju, Yosuke. "Three-dimensional ultrastructural analysis of cell-cell junctions in epithelial cells by using super-resolution fluorescence and electron microscopy." In European Microscopy Congress 2020. Royal Microscopical Society, 2021. http://dx.doi.org/10.22443/rms.emc2020.1457.

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Cox, Guy C., Teresa Dibbayawan, and Jose Feijo. "Multiphoton microscopy of cell division in plant cells." In BiOS 2001 The International Symposium on Biomedical Optics, edited by Ammasi Periasamy and Peter T. C. So. SPIE, 2001. http://dx.doi.org/10.1117/12.424548.

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Di Caprio, Giuseppe, Diane Schaak, and Ethan Schonbrun. "Hyperspectral Microscopy of Flowing Cells." In Imaging Systems and Applications. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/isa.2013.im4e.3.

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Fast, Alexander. "Wide-field Surface-Enhanced CARS Microscopy of Cells." In Novel Techniques in Microscopy. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/ntm.2017.nm4c.3.

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Ghosh, Shirsendu. "Microvilli: The ERM Dependent Activation Hubs of T-Cells." In European Microscopy Congress 2020. Royal Microscopical Society, 2021. http://dx.doi.org/10.22443/rms.emc2020.482.

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Weber, Igor. "Oscillatory dynamics of small GTPase Rac1 in motile cells." In European Microscopy Congress 2020. Royal Microscopical Society, 2021. http://dx.doi.org/10.22443/rms.emc2020.1187.

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Zeidan, Adel, Daniella Yeheskely-Hayon, Limor Minai, and Dvir Yelin. "Reflectance confocal microscopy of red blood cells: simulation and experiment (Conference Presentation)." In Endoscopic Microscopy XI, edited by Guillermo J. Tearney and Thomas D. Wang. SPIE, 2016. http://dx.doi.org/10.1117/12.2209027.

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Bao, Hongchun, Jingliang Li, and Min Gu. "Detecting Cancer Cells Labeled With Gold Nanorods Using Nonlinear Endomicroscopy." In Novel Techniques in Microscopy. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/ntm.2009.nwd3.

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Popescu, Gabriel. "Random and deterministic transport in live cells quantified by SLIM." In Novel Techniques in Microscopy. Washington, D.C.: OSA, 2011. http://dx.doi.org/10.1364/ntm.2011.ntub1.

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Shaked, Natan T., and Darina Roitshtain. "Flipping Interferometry and Quantitative Spatial Phase Signatures of Cancer Cells." In Novel Techniques in Microscopy. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/ntm.2017.nm2c.3.

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Reports on the topic "Cells Microscopy"

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Lee Sohn, Lydia. Using 3D Super-Resolution Microscopy to Probe Breast Cancer Stem Cells and Their Microenvironment. Fort Belvoir, VA: Defense Technical Information Center, May 2014. http://dx.doi.org/10.21236/ada609488.

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Jalali, Bahram, and Dino Di Carlo. Massively Parallel Rogue Cell Detection Using Serial Time-Encoded Amplified Microscopy of Inertially Ordered Cells in High Throughput Flow. Fort Belvoir, VA: Defense Technical Information Center, August 2011. http://dx.doi.org/10.21236/ada566873.

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Jalali, Bahram, and Dino Di Carlo. Massively Parrell Rogue Cell Detection Using Serial Time-Encoded Amplified Microscopy of Inertially Ordered Cells in High Throughput Flow. Fort Belvoir, VA: Defense Technical Information Center, August 2012. http://dx.doi.org/10.21236/ada576649.

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Sohn, Lydia. Using 3-D Super-Resolution Microscopy to Probe Breast Cancer Stem Cells and Their Microenvironment. Fort Belvoir, VA: Defense Technical Information Center, March 2012. http://dx.doi.org/10.21236/ada560892.

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Sohn, Lydia L. Using 3-D Super-Resolution Microscopy to Probe Breast Cancer Stem Cells and Their Microenvironment. Fort Belvoir, VA: Defense Technical Information Center, March 2013. http://dx.doi.org/10.21236/ada581514.

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MacDonald, Ian C. Lymphatic Metastasis of Breast Cancer Cells: Development of In Vivo Video Microscopy to Study Mechanisms of Lymphatic Spread. Fort Belvoir, VA: Defense Technical Information Center, June 2002. http://dx.doi.org/10.21236/ada407505.

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Stead, A. D., T. W. Ford, A. M. Page, J. T. Brown, and W. Meyer-Ilse. X-ray dense cellular inclusions in the cells of the green alga Chlamydomonas reinhardtii as seen by soft-x-ray microscopy. Office of Scientific and Technical Information (OSTI), April 1997. http://dx.doi.org/10.2172/603459.

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Tong, Wei. Direct methods for dynamic monitoring of secretions from single cells by capillary electrophoresis and microscopy with laser-induced native fluorescence detection. Office of Scientific and Technical Information (OSTI), October 1997. http://dx.doi.org/10.2172/587956.

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Miao, J. Taking X-Ray Diffraction to the Limit: Macromolecular Structures from Femtosecond X-Ray Pulses and Diffraction Microscopy of Cells with Synchrotron Radiation. Office of Scientific and Technical Information (OSTI), June 2004. http://dx.doi.org/10.2172/826961.

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McElfresh, M., J. Belak, R. Rudd, and R. Balhorn. LDRD Final Report 01-ERI-001 Probing the Properties of Cells and Cell Surfaces with the Atomic Force Microscope. Office of Scientific and Technical Information (OSTI), February 2004. http://dx.doi.org/10.2172/15013864.

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You might also be interested in the extended bibliographies on the topic 'Cells Microscopy' for particular source types:
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