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Статті в журналах з теми "Polarized light microscope"
McCrone, Walter C. "The Case for Polarized Light Microscopy." Microscopy Today 4, no. 7 (September 1996): 16–19. http://dx.doi.org/10.1017/s1551929500060971.
Повний текст джерелаChatterjee, Sanjib, and Y. Pavan Kumar. "Un-polarized light transmission DIC microscope." Journal of Optics 45, no. 4 (November 4, 2015): 297–301. http://dx.doi.org/10.1007/s12596-015-0293-2.
Повний текст джерелаBernal, J. A., M. Andres, S. López Salguero, V. Jovani, P. Vela-Casasempere, and E. Pascual. "THU0414 ORDINARY LIGHT MICROSCOPY IS ABLE TO IDENTIFY MOST CRYSTAL-CONTAINING SYNOVIAL FLUIDS." Annals of the Rheumatic Diseases 79, Suppl 1 (June 2020): 444.1–445. http://dx.doi.org/10.1136/annrheumdis-2020-eular.6071.
Повний текст джерелаOldenbourg, Rudolf. "New polarized-light microscope for fast and orientation independent measurement of birefringent fine structure." Proceedings, annual meeting, Electron Microscopy Society of America 51 (August 1, 1993): 82–83. http://dx.doi.org/10.1017/s0424820100146254.
Повний текст джерелаHsu, Julia W. P., E. B. McDaniel, and S. C. McClain. "Development of Polarization Modulation Near-Field Scanning Optical Microscope and its Application to Mapping Defect-Induced Birefringence in SrTiO3 Bicrystals." Microscopy and Microanalysis 4, S2 (July 1998): 314–15. http://dx.doi.org/10.1017/s1431927600021693.
Повний текст джерелаOLDENBOURG, R., and G. MEI. "New polarized light microscope with precision universal compensator." Journal of Microscopy 180, no. 2 (November 1995): 140–47. http://dx.doi.org/10.1111/j.1365-2818.1995.tb03669.x.
Повний текст джерелаClarke, Theodore M. "Rediscovery of Darkfieid Dispersion Staining while Building a Universal Student Microscope." Microscopy Today 11, no. 1 (February 2003): 24–28. http://dx.doi.org/10.1017/s1551929500052299.
Повний текст джерелаShribak, M., and R. Oldenbourg. "Scanned aperture polarized light microscope with liquid crystal compensator." Microscopy and Microanalysis 9, S02 (August 2003): 1154–55. http://dx.doi.org/10.1017/s1431927603445777.
Повний текст джерелаZemke, Valentina, Volker Haag, and Gerald Koch. "Wood identification of charcoal with 3D-reflected light microscopy." IAWA Journal 41, no. 4 (September 11, 2020): 478–89. http://dx.doi.org/10.1163/22941932-bja10033.
Повний текст джерелаQiu, Caimin, Jianling Chen, Zexian Hou, Chaoxian Xu, Shusen Xie, and Hongqin Yang. "Effect of light polariztion on pattern illumination super-resolution imaging." Journal of Innovative Optical Health Sciences 09, no. 03 (May 2016): 1641001. http://dx.doi.org/10.1142/s1793545816410017.
Повний текст джерелаДисертації з теми "Polarized light microscope"
Santa, Nestor. "Demonstration of Optical Microscopy and Image Processing to Classify Respirable Coal Mine Dust Particles." Thesis, Virginia Tech, 2021. http://hdl.handle.net/10919/103919.
Повний текст джерелаM.S.
Inhalation of fine particles in underground coal environments can lead to chronic lung diseases, such as coal worker’s pneumoconiosis or progressive massive fibrosis (PMF), which is the most severe form of disease. During the last two decades, the rates of reported cases of PMF in underground coal miners have more than doubled. Many authors have suggested different reasons to explain this trend, including the extraction of thinner coal deposits, mining techniques, changes in mineral content, and the use of high-powered cutting equipment. However, detailed information of specific dust constituents and monitoring the variability of dust concentrations during work shifts are needed to determine possible dust sources and comprehend the more recent changing disease patterns. A dust-monitoring system that provides accurate and timely data on specific respirable coal mine dust (RCMD) constituents would enable the deployment of effective control strategies to mitigate exposure to respirable hazards. Optical microscopy (OM) has been used for a long time to analyze and identify dust particles. More recent advances in portable microscopy have allowed the microscope analysis to be implemented in the field. On the other hand, automated image processing techniques are rapidly progressing and powerful imaging hardware has become a reality in handy small devices. OM and image processing technologies offer a path for near real-time applications that have not been explored for RCMD monitoring yet. In this work, a novel monitoring concept is explored using OM and image processing to classify RCMD particles. Images from dust samples captured with a polarizing microscope were used to build a classification model based on optical properties. The method herein described showed outstanding accuracy for separating coal and mineral fractions. Additionally, the Identification of silica particles in the mineral fraction was investigated and has proved more challenging. A particular finding suggests that particle loading density in the images plays an important role in classification accuracy.
Cao, Shuiyan. "Using plasmonic nanostructures to control electrically excited light emission." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS042/document.
Повний текст джерелаIn this thesis, we use different plasmonic nanostructures to control the emission of electrically-excited light. Our electrical emission is from an “STM-nanosource” which uses the inelastic tunnel current between the tip of a scanning tunneling microscope (STM) and a metallic sample, to locally excite both localized and propagating surface plasmon polaritons. The interaction of our STM-nanosource and a circular plasmonic lens (a series of concentric slits etched in a thick gold film) produces a radially polarized microsource of low angular spread (≈±4°). The influence of the structural parameters on the angular spread of the resulting microsource is also investigated. In addition, a low angular spread (<±7°) for a large wavelength range (650-850 nm) is achieved. Thus this electrically-driven microsource of nearly collimated light has a broad spectral response and is optimal over a wide energy range, especially in comparison with other resonant plasmonic structures such as Yagi-Uda nanoantennas. The interaction of our STM-nanosource and an elliptical plasmonic lens (a single elliptical slit etched in a thick gold film) is also studied. When the STM excitation is located at the focal point position of the elliptical plasmonic lens, a directional light beam of low angular spread is acquired. Moreover, in the experiment we find that by changing the eccentricity of the elliptical plasmonic lens, the emission angle is varied. It is found that the larger the eccentricity of the elliptical lens, the higher the emission angle. This study provides a better understanding of how plasmonic nanostructures shape the emission of light. The interaction of STM-excited SPPs and a planar plasmonic multi-layer stack structure is also investigated. It is demonstrated that using STM excitation we can probe the optical band structure of the Au-SiO₂-Au stack. We find that the thickness of the dielectric plays an important role in changing the coupling between the modes. We also compare the results obtained by both laser and STM excitation of the same stack structure. The results indicate that the STM technique is superior in sensitivity. These findings highlight the potential of the STM as a sensitive optical nanoscopic technique to probe the optical bands of plasmonic nanostructures. Finally, the interaction of an STM-nanosource and an individual triangular plate is also studied. We find that when the STM excitation is centered on the triangular plate, there is no directional light emission. However, when the STM-nanosource is located on the edge of the triangle, directional light emission is obtained. This study provides us a novel avenue to achieve directional light emission. We also study probing the optical LDOS of the triangle with the STM-nanosource. Thus, our results show that the manipulation of light is achieved through SPP-matter interactions. Using plasmonic nanostructures, we control the collimation, polarization, and direction of the light originating from the STM-nanosource
Gomes, Claudia Messias. "Influência da diminuição da temperatura sobre o fuso meiótico de oócitos de camundongas e de mulheres maturados in vitro." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/5/5139/tde-22072011-132252/.
Повний текст джерелаIntroduction: The meiotic spindle of most mammals is sensitive to cooling and depolymerizes even after a slight reduction in temperature. This is well described and studied on matured oocytes at metaphase II (MII). However, little is known about the influence of low temperatures under meiotic spindle of imature oocytes. In this way, we sougth to evaluate: 1) the influence of low temperatures on mice oocyte meiotic spindle matured in vitro e 2) the oocyte meiotic spindle from human oocytes matured in vitro and cryopreserved by slow-rate freezing or vitrification at GV stage. Methods: Two experiments were done: the first one on mice and the second one on women.At experiment 1, immature mice oocytes at metaphase I (MI), telophase I (TI) and MII were cultured at 37º C (control), room temperature (22oC) and 4º C for 0, 10, 30 and 60 minutes and then spindle analysis was made with polarized light microscopy (PLM) (LC-Polscope-Oosight image software) or immunocytochemistry (ICC). At experiment 2, GV oocytes retrieved from women submitted to ovulation induction and in vitro fertilization were randomly divided in three groups: fresh oocytes (A), cryopreserved by slow-freezing (B) and cryopreserved by vitrification (C). Fresh, thawed and warmed oocytes were matured in vitro to metaphase II oocytes (MII). A meiotic spindle analysis was done by polarized light microscopy (ICSI Guard Octax). Results: Experiment 1: At time 0 min and 37º C, all oocytes had polymerized spindles both at PLM or ICC. At 4º C, the number of MI oocytes with detectable spindles at PLM was smaller than those analysed by ICC, and it decreased with time, which had also occured with TI oocytes at a smaller proportion. However, at 4º C, TI meiotic spindle recognition with polarized light microscopy and ICC was comparable. When MII oocytes were cultured at 4º C, the spindle visualization decreased proportionally in correlation with culture time at PLM, and the same happened with ICC in a less pronounced manner. At room temperature there was a little descrease regarding visualization of meiotic spindle, both at PLM and ICC, altought it was not significant for TI oocytes. Experiment 2: Oocyte survival immediately after thawing/warming were 44.6% for group B and 79% for group C. After 24 hours of culture, oocyte survival was 29.2% and 69%, respectively. The median time for maturation was 26 hours for groups A and C, and 27 hours for group B. The percentage of MII after maturation in vitro were smaller in group B and similar between groups A and C. The same oocured for spindle visualization which were lower in group B and similar between groups A and C. Conclusions: There was a difference on the percentages of meiotic spindle depolymerization in response to cooling in mice oocytes at different stages of meiotic division. Spindle depolymerization was lower in TI. Also, meiotic spindle depolimerization was proportional to culture time, except for TI oocytes at room temperature.Vitrified GV oocytes had a better survival when warmed, compared to slow-rate frozen oocytes. Vitrified GV oocytes had similar maturation in vitro rates and polymerized spindles detection when compared to fresh oocytes
MacDonald, Donia J. "Wall characteristics of saccular aneurysms from polarized light microscopy." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0006/MQ42172.pdf.
Повний текст джерелаМоскаленко, Роман Андрійович, Роман Андреевич Москаленко, Roman Andriiovych Moskalenko, I. Iashchіchyn, M. Fallah, and Artem Mykhailovych Piddubnyi. "Verification of corpora amylacea amyloid nature via polarized light microscopy." Thesis, Sumy State University, 2015. http://essuir.sumdu.edu.ua/handle/123456789/41281.
Повний текст джерелаBaba, Justin Shekwoga. "The use of polarized light for biomedical applications." Texas A&M University, 2003. http://hdl.handle.net/1969.1/1206.
Повний текст джерелаBurgio, Lucia. "Analysis of pigments on art objects by Raman microscopy and other techniques." Thesis, University College London (University of London), 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369123.
Повний текст джерелаLi, Yanfang. "A study on the use of polarized light in application to noninvasive tissue diagnoistics /." See Full Text at OhioLINK ETD Center (Requires Adobe Acrobat Reader for viewing), 2005. http://www.ohiolink.edu/etd/view.cgi?toledo1134596719.
Повний текст джерелаTypescript. "A dissertation [submitted] as partial fulfillment of the requirements of the Doctor of Philosophy degree in Engineering." Bibliography: leaves 106-120.
Lima, Júlia Magalhães da Costa. "Análise da profundidade de desgaste e da perda mineral no esmalte subjacente à microabrasão após técnica microabrasiva." Universidade Federal da Paraíba, 2009. http://tede.biblioteca.ufpb.br:8080/handle/tede/6669.
Повний текст джерелаCoordenação de Aperfeiçoamento de Pessoal de Nível Superior
The main effect of the microabrasion in the enamel is significant erosion. However, there is a gap in the literature about validated and reproducible assessment of the depth of erosion in the enamel surface which is originally curve. AIMS: Evaluate depth of erosion and mineral loss of enamel produced by microabrasion technique in original coronary surface of human teeth. METHODS AND MATERIALS: 40 extracted human molars were randomly spited in four groups, with 10 specimens each, in accordance with the microabrasive treatment: AC- 18% hydrochloric acid and pumice, AF 37% phosphoric acid and pumice, OP Opalustre and WRM Whiteness RM. Each specimens had buccal surface´s laterals isolated so that the central area received the microabrasion treatment. After this procedure, transverse slices not demineralized were prepared and submitted to microradiography and analysis in Polarized Light Microscope. One own terminology had created for the morphology of the interface enamel normal-microabrasioned. This served as base to introduction of a profilometry technique with analysis of digital images, in order to get the depth of erosion on microabrasion´s area. The Intraclass Correlation Test was applied to test technique´s reproducibility. The mineral loss and the depth which it happened had analyzed by transverses plotted at equidistant points of the limit enamel normal-microabrasioned. The dates were analyzed with ANOVA test (p < 0.05). RESULTS: The profilometry technique achieved a good reproducibility (Intraclass Correlation Test of 0,9998) and was validated internally. The AC group was the most aggressive, with a greater depth of erosion (110,51 ± 41,21 μm), and a greater mineral loss (13 ± 3 peso %), with significant difference between WRM group (p < 0,05; 9,41± 4,4 peso %) and OP group (p < 0,05; 9,0 ± 3,8 peso %). The OP group, on the other hand, was the less aggressive, with the lowest values in all parameters analyzed, presenting depth of erosion less than AC group (p < 0,0001), WRM group (p < 0,001; 86,24 ± 27,99 μm) and AF group (p < 0,05; 74,46 ± 42,06 μm). The others two groups achieved intermediate results for depth of erosion and mineral loss. The depth of mineral loss was greater than on AF group (31,38 ± 20,30 μm), however, there wasn´t statistical difference between the groups. CONCLUSIONS: Based on own terminology for the interface enamel normalmicroabrasioned and on the implementation of new technique of profilometry, the agents tested showed a significant difference in the depth of erosion, which was consistent with the mineral loss. However, there wasn´t difference in the depth of mineral loss. Furthermore the new technique of profilometry is proposed to fill a gap in the literature, allowing the determination of physical depth of erosion in areas naturally curves of hard biological tissues.
O principal efeito da microabrasão no esmalte dental é uma erosão significativa. Porém, existe uma lacuna na literatura no que concerne à avaliação validada e reprodutível da profundidade de desgaste na superfície dental natural. OBJETIVOS: Avaliar a profundidade de desgaste e a perda mineral do esmalte dentário resultante da técnica de microabrasão na superfície coronária original de dentes humanos. MATERIAIS E MÉTODOS: 40 terceiros molares humanos extraídos foram divididos aleatoriamente em 4 grupos, de 10 espécimes cada, de acordo com o material microabrasivo utilizado: AC - ácido clorídrico a 18% e pedra-pomes, AF - ácido fosfórico a 37% e pedra-pomes, OP - Opalustre® e WRM - Whiteness RM®. Cada elemento teve as laterais da face vestibular protegidas para que apenas a área central fosse exposta aos agentes microabrasivos. Após o procedimento de microabrasão, cortes transversais não desmineralizados foram preparados e submetidos à radiomicrografia e análise em Microscopia de Luz Polarizada. Uma terminologia própria foi formulada para a morfologia da interface esmalte normalmicroabrasionado. Esta serviu de base à introdução de uma Técnica de Perfilometria com Análise de Imagens Digitais, com o intuito de obter a profundidade de desgaste ao longo da área microabrasionada. O teste de correlação intraclasse foi aplicado para testar a reprodutibilidade da técnica. A quantidade da perda mineral e a profundidade em que esta ocorreu foram analisadas em transversais traçadas em pontos eqüidistantes do limite esmalte normal-microabrasionado. Os dados obtidos foram analisados com o teste ANOVA (p < 0,05). RESULTADOS: A Técnica de Perfilometria obteve uma boa reprodutibilidade (coeficiente de correlação intraclasse de 0,9998) e foi validada internamente. O grupo AC foi o mais agressivo, apresentando a maior profundidade de desgaste (110,51 ± 41,21 μm), e a maior perda mineral (13 ± 3 peso %), com diferenças significantes em relação aos grupos WRM (p < 0,05; 9,41± 4,4 peso %) e OP (p < 0,05; 9,0 ± 3,8 peso %). O grupo OP, por outro lado, foi o menos agressivo com os menores valores para todos os parâmetros analisados, apresentando uma profundidade de desgaste menor em relação aos grupos AC (p < 0,0001), WRM (p < 0,001; 86,24 ± 27,99 μm) e AF (p < 0,05; 74,46 ± 42,06 μm). Os outros dois grupos apresentaram resultados intermediários para profundidade de desgaste e quantidade de perda mineral. Não houve diferença quanto à profundidade de perda mineral CONCLUSÃO: Com base em uma terminologia própria para a interface esmalte normal-microabrasionado e na aplicação de uma nova Técnica de Perfilometria, os agentes testados mostraram uma significativa diferença quanto à profundidade de desgaste, que foi condizente com a perda mineral. A nova Técnica de Perfilometria propõe o preenchimento de uma lacuna na literatura, permitindo a determinação física de profundidade de desgaste em superfícies naturalmente curvas de tecidos biológicos duros.
Lucisano, Marília Pacifico. "Efeito do uso sistêmico de alendronato sódico no tecido ósseo e nas estruturas dentárias mineralizadas: estudo químico, mecânico e morfológico, em modelo murino." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/58/58135/tde-04022011-114321/.
Повний текст джерелаBisphosphonates represent a class of drugs that act on bone metabolism and are widely used in the prevention and treatment of osteopenic and osteoporotic states. The objectives of this study were to evaluate, in vivo, the effect of the systemic use of sodium alendronate on: the mineral bone density of rats, by radiographic optical densitometry and dual-energy x-ray absorptiometry (DXA); the mineralized dental structures of murine incisors, by analysis of infrared (IR) spectrometry, fluorescence spectroscopy, cross-sectional microhardness (CSMH), scanning electron microscopy (SEM) and polarized light microscopy (PLM). Forty-five Wistar rats aged 36-42 days and weighing 200-230 g were assigned to two groups: experimental (n= 25) and control (n= 20). The experimental group received two weekly doses of 1 mg/kg of chemically pure sodium alendronate diluted in distilled water, via gavage, while the animals of the control group received only distilled water. After 60 days, the animals were killed by anesthetic overdose, and the maxillary incisors were extracted and the tibias were removed. The mineral bone density of the tibias was analyzed radiographically and by DXA. The maxillary incisors were subjected to the following evaluations: chemical analysis by IR spectrometry and fluorescence spectroscopy, enamel and dentin CSMH, SEM and PLM. The results were subjected to statistical analysis by the Kruskal-Wallis non-parametric test, using the SAS (Statistical Analysis System) software for Windows version 9.1.3. The significance level was set at 5%. The experimental group presented higher mineral bone density (p<0.05) than the control group, by radiographic optical densitometry and DXA. The chemical analysis by IR spectrometry and fluorescence spectroscopy revealed the presence of alendronate in the mineralized dental structure of the specimens of the experimental group, with a percentage of incorporation of 0.0018% per tooth. The results of enamel and dentin CSMH did not show statistically significant difference between the experimental and control groups (p>0.05). There were no significant morphological differences among the specimens of the groups by SEM and PLM. Based on the obtained results, it may be concluded that the treatment with sodium alendronate caused an increase in the mineral bone density of the proximal tibial metaphysis, and that alendronate was incorporated in the mineralized dental structures without causing significant effects in the enamel and dentin microhardness and morphology of rat incisors.
Книги з теми "Polarized light microscope"
Viney, Christopher. Transmitted polarised light microscopy (The microscope series). McCrone Research Institute, 1990.
Знайти повний текст джерелаLaughlin, Gary J. Polarized Light Microscopy. University of Cambridge ESOL Examinations, 2017.
Знайти повний текст джерелаCrippin, James B., and Michael Victor Martinez. Drugs and Explosives Analysis with Polarized Light Microscopy. Taylor & Francis Group, 2009.
Знайти повний текст джерелаCrippin, James B., and Michael Victor Martinez. Drugs and Explosives Analysis with Polarized Light Microscopy. Taylor & Francis Group, 2011.
Знайти повний текст джерелаWoodward, Charles. Familiar Introducton to the Study of Polarized Light: With a Description of, and Instructions for Using, the Table and Hydro-Oxygen Polariscope and Microscope. Creative Media Partners, LLC, 2018.
Знайти повний текст джерелаWoodward, Charles. Familiar Introducton to the Study of Polarized Light; with a Description of, and Instructions for Using, the Table and Hydro-Oxygen Polariscope and Microscope. Creative Media Partners, LLC, 2018.
Знайти повний текст джерелаQualitative Polarized Light Microscopy (Microscopy Handbooks 09). BIOS, 1992.
Знайти повний текст джерелаDelly, John Gustav. Essentials of Polarized Light Microscopy and Ancillary Techniques. The McCrone Group, Inc., 2019.
Знайти повний текст джерелаEssentials of Polarized Light Microscopy and Ancillary Techniques. The McCrone Group, Inc., 2017.
Знайти повний текст джерелаHirohata, A., and J. Y. Kim. Optically Induced and Detected Spin Current. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780198787075.003.0006.
Повний текст джерелаЧастини книг з теми "Polarized light microscope"
Khajuria, Himanshu, Sapna Gupta, and Biswa Prakash Nayak. "Introduction to Polarized Light Microscope." In Forensic Microscopy, 182–90. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.4324/9781003120995-13.
Повний текст джерелаCarlton, Robert Allen. "Polarized Light Microscopy." In Pharmaceutical Microscopy, 7–64. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-8831-7_2.
Повний текст джерелаSaville, B. P. "Polarized Light: Qualitative Microscopy." In Applied Polymer Light Microscopy, 111–49. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-011-7474-9_4.
Повний текст джерелаRochow, Theodore George, and Paul Arthur Tucker. "Microscopy with Polarized Light." In Introduction to Microscopy by Means of Light, Electrons, X Rays, or Acoustics, 89–111. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1513-9_5.
Повний текст джерелаChen, Jenq-Shyong, and Yung-Kuo Huang. "Full-Field Mapping of the Strss-Induced Birefringence on the Internal Interfaces Using A Polarized Low Coherence Light Interference Microscope." In Experimental Analysis of Nano and Engineering Materials and Structures, 917–18. Dordrecht: Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-6239-1_456.
Повний текст джерелаSaville, B. P. "Polarized Light: Theory and Measurements." In Applied Polymer Light Microscopy, 73–109. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-011-7474-9_3.
Повний текст джерелаOliviero, Francesca, and Leonardo Punzi. "Basics of Polarized Light Microscopy." In Synovial Fluid Analysis and The Evaluation of Patients With Arthritis, 79–90. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-99612-3_9.
Повний текст джерелаMa, Hui, Honghui He, and Jessica C. Ramella-Roman. "Mueller Matrix Microscopy." In Polarized Light in Biomedical Imaging and Sensing, 281–320. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04741-1_11.
Повний текст джерелаMeglinski, Igor, Liliya Trifonyuk, Victor Bachinsky, Oleh Vanchulyak, Boris Bodnar, Maxim Sidor, Olexander Dubolazov, et al. "Polarization Correlometry of Microscopic Images of Polycrystalline Networks Biological Layers." In Shedding the Polarized Light on Biological Tissues, 61–73. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-10-4047-4_4.
Повний текст джерелаInnus, Andris, Alain Jomphe, and Hans Darmstadt. "A Method for the Rapid Characterization of Petroleum Coke Microstructure Using Polarized Light Microscopy." In Light Metals 2013, 1069–73. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-65136-1_180.
Повний текст джерелаТези доповідей конференцій з теми "Polarized light microscope"
Dai, Xiang, Pavan Chandra Konda, Shiqi Xu, and Roarke Horstmeyer. "Polarization and phase imaging using an LED array microscope." In Polarized light and Optical Angular Momentum for biomedical diagnostics, edited by Jessica C. Ramella-Roman, Hui Ma, I. Alex Vitkin, Daniel S. Elson, and Tatiana Novikova. SPIE, 2021. http://dx.doi.org/10.1117/12.2577344.
Повний текст джерелаHuibin, Yang, Jiawei Song, Nan Zeng, and Hui Ma. "A Stokes imaging microscope system with a large field of view." In Polarized Light and Optical Angular Momentum for Biomedical Diagnostics 2023, edited by Jessica C. Ramella-Roman, Hui Ma, I. Alex Vitkin, Daniel S. Elson, and Tatiana Novikova. SPIE, 2023. http://dx.doi.org/10.1117/12.2648887.
Повний текст джерелаHuang, Tongyu, Qianhao Zhao, and Hui Ma. "Calibration method for multiwavelength Mueller matrix microscope based on dual DoFP polarimeters." In Polarized Light and Optical Angular Momentum for Biomedical Diagnostics 2022, edited by Jessica C. Ramella-Roman, Hui Ma, I. Alex Vitkin, Daniel S. Elson, and Tatiana Novikova. SPIE, 2022. http://dx.doi.org/10.1117/12.2608229.
Повний текст джерелаZhou, Ximing, James D. Dormer, and Baowei Fei. "Development of a polarized hyperspectral microscope for cardiac fiber orientation imaging." In Diagnostic and Therapeutic Applications of Light in Cardiology 2020, edited by Kenton W. Gregory and Laura Marcu. SPIE, 2020. http://dx.doi.org/10.1117/12.2549720.
Повний текст джерелаGonzalez, Mariacarla, Camilo Roa, Arturo Jimenez, Rachelle Gomez-Guevara, V. N. Du Le, Tatiana Novikova, and Jessica C. Ramella-Roman. "Machine learning powered Mueller matrix microscope for collagen and elastin visualization in the mouse cervix." In Polarized Light and Optical Angular Momentum for Biomedical Diagnostics 2022, edited by Jessica C. Ramella-Roman, Hui Ma, I. Alex Vitkin, Daniel S. Elson, and Tatiana Novikova. SPIE, 2022. http://dx.doi.org/10.1117/12.2609978.
Повний текст джерелаVanderlinde, William E., and David A. Stoney. "Forensic Microscopy in the Failure Analysis Laboratory." In ISTFA 2000. ASM International, 2000. http://dx.doi.org/10.31399/asm.cp.istfa2000p0097.
Повний текст джерелаShribak, Michael I., and Rudolf Oldenbourg. "Scanning aperture polarized light microscope: observation of small calcite crystals using oblique illumination." In International Symposium on Biomedical Optics, edited by Jose-Angel Conchello, Carol J. Cogswell, and Tony Wilson. SPIE, 2002. http://dx.doi.org/10.1117/12.467840.
Повний текст джерелаShribak, Michael I., and Rudolf Oldenbourg. "3D imaging properties of a polarized light microscope revealed by birefringence measurements of small calcite crystals." In BiOS 2001 The International Symposium on Biomedical Optics, edited by Jose-Angel Conchello, Carol J. Cogswell, and Tony Wilson. SPIE, 2001. http://dx.doi.org/10.1117/12.424522.
Повний текст джерелаArmitage, Mark. "Polarized Light and electron microscope study of soft dinosaur bone tissue elements from Nanotyrannus lancensis collected at Hell Creek, Montana, USA." In European Microscopy Congress 2020. Royal Microscopical Society, 2021. http://dx.doi.org/10.22443/rms.emc2020.8.
Повний текст джерелаOkamoto, Hiromi, Shun Hashiyada, Yoshio Nishiyama, and Tetsuya Narushima. "Imaging Chiral Plasmons." In JSAP-OSA Joint Symposia. Washington, D.C.: Optica Publishing Group, 2017. http://dx.doi.org/10.1364/jsap.2017.5a_a410_1.
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