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Artykuły w czasopismach na temat "Microscopy-Based cytometry"
Wessels, J. T., A. C. Busse, J. Mahrt, B. Hoffschulte, G. A. Mueller, A. Tárnok i A. Mittag. "NorthernLights in slide-based cytometry and microscopy". Cytometry Part A 9999A (2010): NA. http://dx.doi.org/10.1002/cyto.a.20863.
Pełny tekst źródłaEcker, Rupert C., i Georg E. Steiner. "Microscopy-based multicolor tissue cytometry at the single-cell level". Cytometry 59A, nr 2 (2004): 182–90. http://dx.doi.org/10.1002/cyto.a.20052.
Pełny tekst źródłaKummrow, A., M. Frankowski, N. Bock, C. Werner, T. Dziekan i J. Neukammer. "Quantitative assessment of cell viability based on flow cytometry and microscopy". Cytometry Part A 83A, nr 2 (18.10.2012): 197–204. http://dx.doi.org/10.1002/cyto.a.22213.
Pełny tekst źródłaMendoza, Maria Gracia Garcia, Alex Sutton, Raymond Kong, Matthew Rodrigues i Haley Pugsley. "A rapid and fully automated in vitro micronucleus assay using imaging flow cytometry and convolutional neural network analysis". Journal of Immunology 208, nr 1_Supplement (1.05.2022): 172.02. http://dx.doi.org/10.4049/jimmunol.208.supp.172.02.
Pełny tekst źródłaSláma, Petr, Zbyšek Sládek i Dušan Ryšánek. "Application of methods for detection of apoptosis and necrosis of bovine blood neutrophil granulocytes in vitro". Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis 54, nr 5 (2006): 107–16. http://dx.doi.org/10.11118/actaun200654050107.
Pełny tekst źródłaAsthana, Vishwaratn, Yuqi Tang, Adam Ferguson, Pallavi Bugga, Anantratn Asthana, Emily R. Evans, Allen L. Chen, Brett S. Stern i Rebekah A. Drezek. "An inexpensive, customizable microscopy system for the automated quantification and characterization of multiple adherent cell types". PeerJ 6 (5.06.2018): e4937. http://dx.doi.org/10.7717/peerj.4937.
Pełny tekst źródłaAdachi, Takahiro, i Takeshi Tsubata. "FRET-based Ca2+ measurement in B lymphocyte by flow cytometry and confocal microscopy". Biochemical and Biophysical Research Communications 367, nr 2 (marzec 2008): 377–82. http://dx.doi.org/10.1016/j.bbrc.2007.12.142.
Pełny tekst źródłaWei, Shu-Gen, Ling-Yun Wan, Ying Wei, Li-Li He, Jin-E. Fu i Li-Mei Pan. "Analysis of ploidy level of Artemisia annua L. based on flow cytometry and confocal laser scanning microscopy". Bangladesh Journal of Botany 50, nr 1 (27.03.2021): 29–35. http://dx.doi.org/10.3329/bjb.v50i1.52668.
Pełny tekst źródłaHeckmann, Mara, Gerald Klanert, Georg Sandner, Peter Lanzerstorfer, Manfred Auer i Julian Weghuber. "Fluorescence microscopy-based quantitation of GLUT4 translocation". Methods and Applications in Fluorescence 10, nr 2 (21.01.2022): 022001. http://dx.doi.org/10.1088/2050-6120/ac4998.
Pełny tekst źródłaLima, Ângela, Christina A. Muzny i Nuno Cerca. "An Indirect Fluorescence Microscopy Method to Assess Vaginal Lactobacillus Concentrations". Microorganisms 12, nr 1 (5.01.2024): 114. http://dx.doi.org/10.3390/microorganisms12010114.
Pełny tekst źródłaRozprawy doktorskie na temat "Microscopy-Based cytometry"
Apichitsopa, Nicha. "Intrinsic cytometry based on computational microscopy". Thesis, Massachusetts Institute of Technology, 2016. http://hdl.handle.net/1721.1/107030.
Pełny tekst źródłaThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Cataloged from student-submitted PDF version of thesis.
Includes bibliographical references (pages 123-131).
With the goal of understanding cells, we propose to study the intrinsic properties of individual cells by combining visual observation from large field-of-view computational microscopy with separation of cells via an integrated label-free microfluidic platform. This intrinsic cytometry will benefit from the parallel and gentle separation of label-free cells via a microfluidic platform and parallel tracking of multiple cells via a large field-of view microscopy in contrast to the gold standard, flow cytometry, which is able to rapidly and singly identify multiple cell properties via scattering of external fluorescent cell markers. In this thesis, a prototype of this integrated platform was designed and fabricated. The prototype consisted of a large field-of-view digital in-line holographic microscopy system and a microfluidic deterministic lateral displacement array which separated particles based on size. Each system was first characterized separately and later integrated such that individual cells inside the deterministic lateral displacement array could be recorded and tracked with the large field-of-view digital in-line holographic microscopy system, showing the promise of our proposed intrinsic cytometry. In future studies, if a microfluidic platform can be designed to investigate multiple intrinsic properties of individual cells on the same platform, the intrinsic cytometer will enable a large pool of quantitative measurement data of cell intrinsic properties that can potentially be used for cell characterization and diagnostics.
by Nicha Apichitsopa.
S.M.
Schumacher, William Charles. "Development of Novel Fluorescence-Based Methods for Detection of Bacillus Anthracis Spores". The Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=osu1222046829.
Pełny tekst źródłaWu, Jianglai. "A light sheet based fluorescence imaging flow cytometer for phytoplankton analysis". HKBU Institutional Repository, 2014. https://repository.hkbu.edu.hk/etd_oa/36.
Pełny tekst źródłaTroisi, Lucie. "Development of a new class of synthetic gene circuits based on protein-protein interactions". Electronic Thesis or Diss., Sorbonne université, 2023. http://www.theses.fr/2023SORUS728.
Pełny tekst źródłaSynthetic biology, by its engineering approach, promise to revolutionize the way scientists manipulate and analyze living systems. In this project, we propose to develop a new class of synthetic gene circuits whose fine tuning rely on the affinity competition between active and inactive forms of a transcription factor. Modelling, together with an in silico evolutionary approach, will be used to determine molecular parameters and network topologies required for a given functionality. Circuits will be assembled accordingly and their expression in mammalian cells measured to confirm the expected response or correct our model. Using this methodology, we plan to build multi-inputs circuits with tunable response function, as well as new bistable and oscillatory circuits. The new investigated class of circuits will also be extended to multi-cellular networks exhibiting symmetry breaking or oscillating patterns. This fundamental project bridging modelling and experimental validation will promote the development of advanced targeting circuits with promising applications in diagnosis, gene therapy and complex tissue engineering
Wu, Cheng-Ham, i 吳政翰. "Label-free Imaging Cytometry of Leukocytes Based on Third Harmonic Generation Microscopy". Thesis, 2017. http://ndltd.ncl.edu.tw/handle/85016410448762663461.
Pełny tekst źródła國立臺灣大學
醫學工程學研究所
105
Blood tests, which analyze the composition of species in blood, are usually the first stage of clinical examination in the hospital. This includes biochemical and complete blood count analysis. The indices of the latter provide information about the health status of a person. The blood cells include erythrocytes (red blood cells, RBCs), leukocytes (white blood cells, WBCs), and thrombocytes (platelets). For a healthy person, the quantities and percentage of these cells will remain in a steady state; thus, studying the variation of cells gives doctors an aspect of diagnosis. However, these processes require blood to be drawn for further analysis (e.g. flow cytometry, histology), which not only takes time and causes pain through an invasive method, but the in vitro samples are affected by the environment. Therefore, an instrument with real-time and non-invasive analysis is highly desired for blood-cell counting. In current studies, nonlinear optical microscopy, such as harmonic generation microscopy (HGM) and two-photon microscopy (2PFM), has been widely used in biological and material studies due to its sub-micron three-dimensional (3D) spatial resolution. Obeying the energy conservation of harmonic generation, there is no energy deposition in tissue, making it more suitable for long-term observation. Additionally, the greatest advantage of HGM is that it needs no extra labeling for samples, making it more suitable for studying living biology, especially in clinics. In this thesis, we developed a real-time and label-free in vivo third-harmonic generation (THG) flow cytometer, and we further distinguished and differentiated different types of WBCs (neutrophils, monocytes, and lymphocytes). The laser source in this study was a homemade femtosecond Cr: forsterite (Cr: F) with a Kerr-lens mode-locking technique. As the wavelength falls within the second optical penetration window, this laser penetrates deeper without out-of- and on-focus photodamage. With the help of high-speed imaging acquisition software and a set of 16-kHz resonant galvanometer mirrors, the rolling cells within vessels could be revealed individually with 30 frames per second (fps) and 512 x 512 pixels in the image output. The results showed that neutrophil shows a stronger THG signal than monocyte and lymphocyte, with a dark multi-lobed nucleus within the cell. In contrast, monocyte and lymphocyte have identical THG intensity, but less than neutrophil, with a single nucleus roughly equal to the cell’s size. Taking the size of each cell into account, WBCs could be differentiated into three groups by a k-means clustering algorithm in a THG intensity-size plot. The cell count and percentage of each type of leukocyte agreed with the regular complete blood count readout, showing that the in vivo THG imaging flow cytometer will be applicable to clinical diagnosis in the future.
Regmi, Raju. "Light Sheet Based Microfluidic Flow Cytometry Techniques for High throughput Interrogation and High-resolution Imaging". Thesis, 2014. https://etd.iisc.ac.in/handle/2005/3108.
Pełny tekst źródłaRegmi, Raju. "Light Sheet Based Microfluidic Flow Cytometry Techniques for High throughput Interrogation and High-resolution Imaging". Thesis, 2014. http://hdl.handle.net/2005/3108.
Pełny tekst źródłaHyll, Kari. "Image-based quantitative infrared analysis and microparticle characterisation for pulp and paper applications". Doctoral thesis, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-180722.
Pełny tekst źródłaMätningar av processvariationer och partiklars form och storlek utförs i stor skala inom massa- och pappersindustrin. Två mättekniker med stor potential, infraröd termografi och mikropartikel-karaktärisering, används mest kvalitativt idag. Kvantitativ termografi kräver att provets emittans är känd. Emittansen är en materialegenskap som inte har mätts för många förhållanden som är relevanta inom papperstillverkning. Kvantitativ karaktärisering av partiklar kräver att ett tillräckligt stort antal partiklar analyseras, något som kan göras med flödesmikroskop. Flödesmikroskop för mäldanalys har haft otillräcklig upplösning för att karaktärisera mikrometerstora partiklar, t.ex. fines och fyllmedel. Det har heller inte funnits någon metod som kan särskilja mellan fines och fyllmedel i en blandning. Högupplösta mätinstrument för bildbaserad mikropartikelkaraktärisering utvärderades och jämfördes med en laserdiffraktometer, en mätmetod baserad på ljusspridning genom diffraktion. Laserdiffraktometerns mätresultat påverkades starkt av det brytningsindex som antogs för provet, och hur brytningsindexet ändrades med fukthalt. En högupplöst bildbaserad flödescytometer och en högupplöst fibermätare konstaterades komplettera varandra vid mätningar av mäldens finmaterial. De var även pålitligare än laserdiffraktometern vid mätningar av organiskt finmaterial. En metod för att skilja mellan organiskt och oorganiskt finmaterial i en mäld baserat på deras autofluorescens och ljusspridning presenterades och utvärderades kvalitativt. En metod för att mäta den vinkelberoende och våglängdsintegrerade emittansen hos fiberbaserade material utvecklades och dess mätnoggrannhet utvärderades. Mätningar på ett stort antal prover visade att emittansen varierade betydligt med våglängd, mäldtyp, observationsvinkel, och fukthalt. Genom att använda den uppmätta emittansen kunde den termiska energin som frigjordes av ett säckpappersprov vid brottögonblicket beräknas. Denna energi korrelerade väl med den elastiska energi som lagrades i provet medan det töjdes, fram till tidpunkten för brottet. Sammanfattningsvis har resultaten av detta arbete möjliggjort kvantitativ användning av mikropartikel-karaktärisering och infraröd termografi i massa- och papperstillämpningar.
QC 20160122
Książki na temat "Microscopy-Based cytometry"
Zrazhevskiy, P., i X. Gao. Bioconjugated quantum dots for tumor molecular imaging and profiling. Redaktorzy A. V. Narlikar i Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533060.013.17.
Pełny tekst źródłaCzęści książek na temat "Microscopy-Based cytometry"
van Schaik, Tom, Stefano G. Manzo i Bas van Steensel. "Genome-Wide Mapping and Visualization of Protein–DNA Interactions by pA-DamID". W Methods in Molecular Biology, 215–29. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2140-0_12.
Pełny tekst źródłaZhu, Hongying, i Aydogan Ozcan. "Opto-Fluidics Based Microscopy and Flow Cytometry on a Cell Phone for Blood Analysis". W Methods in Molecular Biology, 171–90. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-2172-0_12.
Pełny tekst źródłaDe Vos, W. H., B. Dieriks, G. Joss i P. Van Oostveldt. "High content image-based cytometry as a tool for nuclear fingerprinting". W EMC 2008 14th European Microscopy Congress 1–5 September 2008, Aachen, Germany, 783–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-85156-1_392.
Pełny tekst źródłaNazeer, Nazim, Pooja Ratre, Kaniz Zehra Zaidi, Vikas Gurjar, Rakhi Dewangan, Arpit Bhargava i Pradyumna Kumar Mishra. "Exploring Semiconductor Quantum Dots for Nanophotonic Applications". W Reshaping Healthcare with Cutting-Edge Biomedical Advancements, 235–88. IGI Global, 2024. http://dx.doi.org/10.4018/979-8-3693-4439-2.ch011.
Pełny tekst źródłaX. Chen, Cindy, Hillel B. Price i Adam Wax. "Holography Cytometry: Imaging of Cells in Flow". W Holography - Recent Advances and Applications [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.106581.
Pełny tekst źródłaMuhammad, Ismail, Micah Pukuma Sale i Tanko Mahmoud Mohammed. "Advanced Techniques and Unusual Samples for Malaria Diagnosis". W Infectious Diseases. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.113756.
Pełny tekst źródłaSchwietzer, Ysabel Alessa, Katharina Helene Susek, Ziqing Chen, Evren Alici i Arnika Kathleen Wagner. "A tractable microscopy- and flow cytometry-based method to measure natural killer cell-mediated killing and infiltration of tumor spheroids". W Methods in Cell Biology. Elsevier, 2022. http://dx.doi.org/10.1016/bs.mcb.2022.07.011.
Pełny tekst źródłaGakamsky, Dmitry M., i Israel Pecht. "Evaluating receptor stoichiometry by fluorescence resonance energy transfer". W Receptors: Structure and function, 113–36. Oxford University PressOxford, 2001. http://dx.doi.org/10.1093/oso/9780199638819.003.0005.
Pełny tekst źródłaStreszczenia konferencji na temat "Microscopy-Based cytometry"
Shaked, Natan T. "Quantitative imaging flow cytometry based on digital holographic microscopy". W Optical Methods for Inspection, Characterization, and Imaging of Biomaterials VI, redaktorzy Pietro Ferraro, Simonetta Grilli i Demetri Psaltis. SPIE, 2023. http://dx.doi.org/10.1117/12.2674432.
Pełny tekst źródłaPan, Feng, Wen Xiao, Lu Xin, Hao Wang, Ran Peng i Xi Xiao. "High-throughput and high-precision flow cytometry based on digital holographic microscopy". W Optical Methods for Inspection, Characterization, and Imaging of Biomaterials VI, redaktorzy Pietro Ferraro, Simonetta Grilli i Demetri Psaltis. SPIE, 2023. http://dx.doi.org/10.1117/12.2674497.
Pełny tekst źródłaKong, Lingjie, Jianyong Tang i Meng Cui. "In vivoimaging flow cytometry based on laser scanning two-photon microscopy at kHz cross-sectional frame rate". W SPIE BiOS, redaktorzy Ammasi Periasamy, Peter T. C. So i Karsten König. SPIE, 2016. http://dx.doi.org/10.1117/12.2211418.
Pełny tekst źródłaPicazo-Bueno, Jose Angel, Álvaro Barroso, Steffi Ketelhut, Vicente Micó, Jürgen Schenekenburger i Björn Kemper. "Multimodal imaging flow cytometry based on single capture bright field and digital holographic microscopy for the analysis of living cells". W Optical Methods for Inspection, Characterization, and Imaging of Biomaterials VI, redaktorzy Pietro Ferraro, Simonetta Grilli i Demetri Psaltis. SPIE, 2023. http://dx.doi.org/10.1117/12.2673841.
Pełny tekst źródłaDmitrieva, Valentina Viktorovna, i Evgeny Valeryevich Polyakov. "THE MEDICAL INFORMATION SYSTEM CONCEPT FOR ACUTE LYMPHOBLASTIC LEUKEMIA DIAGNOSING". W NEW TECHNOLOGIES IN MEDICINE, BIOLOGY, PHARMACOLOGY AND ECOLOGY. Institute of information technology, 2021. http://dx.doi.org/10.47501/978-5-6044060-1-4.06.
Pełny tekst źródłaXue, Liang, Nan Sun, Keding Yan, Fei Liu i Shouyu Wang. "High-speed quantitative interferometric microscopy based phase imaging cytometer". W SPIE/COS Photonics Asia, redaktorzy Qingming Luo, Xingde Li, Ying Gu i Yuguo Tang. SPIE, 2014. http://dx.doi.org/10.1117/12.2070398.
Pełny tekst źródłaDarabi, Jeff, i Joseph Schober. "A Microfluidic Platform for On-Chip Analysis of Circulating Tumor Cells". W ASME 2021 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/fedsm2021-65766.
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