Littérature scientifique sur le sujet « Fluorescent Bioimaging »
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Articles de revues sur le sujet "Fluorescent Bioimaging"
ZHU, MING-QIANG, GUO-FENG ZHANG, CHONG LI, YA-JING LI, MATTHEW P. ALDRED et ALEXANDER D. Q. LI. « PHOTOSWITCHABLE NANOFLUOROPHORES FOR INNOVATIVE BIOIMAGING ». Journal of Innovative Optical Health Sciences 04, no 04 (octobre 2011) : 395–408. http://dx.doi.org/10.1142/s1793545811001423.
Texte intégralGedara, Sriyani Menike Korale, Zi-You Ding, Iresha Lakmali Balasooriya, Yingchao Han et Merita Nirmali Wickramaratne. « Hydrothermal Synthesis and In Vivo Fluorescent Bioimaging Application of Eu3+/Gd3+ Co-Doped Fluoroapatite Nanocrystals ». Journal of Functional Biomaterials 13, no 3 (29 juillet 2022) : 108. http://dx.doi.org/10.3390/jfb13030108.
Texte intégralWang, Xinyue, Dandan Sang, Liangrui Zou, Shunhao Ge, Yu Yao, Jianchao Fan et Qinglin Wang. « Multiple Bioimaging Applications Based on the Excellent Properties of Nanodiamond : A Review ». Molecules 28, no 10 (12 mai 2023) : 4063. http://dx.doi.org/10.3390/molecules28104063.
Texte intégralYang, Yufei, Fucheng Gao, Yandong Wang, Hui Li, Jie Zhang, Zhiwei Sun et Yanyan Jiang. « Fluorescent Organic Small Molecule Probes for Bioimaging and Detection Applications ». Molecules 27, no 23 (1 décembre 2022) : 8421. http://dx.doi.org/10.3390/molecules27238421.
Texte intégralLuo, Xiaofeng, Jiaqi Meng, Baolin Li, Aidong Peng et Zhiyuan Tian. « Development of fluorescent nanoparticles with aggregation-induced delayed fluorescence features, improved brightness and photostability for living cells imaging ». New Journal of Chemistry 43, no 27 (2019) : 10735–43. http://dx.doi.org/10.1039/c9nj01945f.
Texte intégralLin, Zhong, Hong Wang, Maolin Yu, Xiang Guo, Chonghua Zhang, Haitao Deng, Peisheng Zhang et al. « Photoswitchable ultrahigh-brightness red fluorescent polymeric nanoparticles for information encryption, anti-counterfeiting and bioimaging ». Journal of Materials Chemistry C 7, no 37 (2019) : 11515–21. http://dx.doi.org/10.1039/c9tc04054d.
Texte intégralPéresse, Tiphaine, et Arnaud Gautier. « Next-Generation Fluorogen-Based Reporters and Biosensors for Advanced Bioimaging ». International Journal of Molecular Sciences 20, no 24 (5 décembre 2019) : 6142. http://dx.doi.org/10.3390/ijms20246142.
Texte intégralSong, Chenxi, Shubiao Zhang, Quan Zhou, Hua Hai, Defeng Zhao et Yunze Hui. « Upconversion nanoparticles for bioimaging ». Nanotechnology Reviews 6, no 2 (1 avril 2017) : 233–42. http://dx.doi.org/10.1515/ntrev-2016-0043.
Texte intégralTerai, Takuya, et Tetsuo Nagano. « Fluorescent probes for bioimaging applications ». Current Opinion in Chemical Biology 12, no 5 (octobre 2008) : 515–21. http://dx.doi.org/10.1016/j.cbpa.2008.08.007.
Texte intégralPu, Kan-Yi, et Bin Liu. « Fluorescent Conjugated Polyelectrolytes for Bioimaging ». Advanced Functional Materials 21, no 18 (15 août 2011) : 3408–23. http://dx.doi.org/10.1002/adfm.201101153.
Texte intégralThèses sur le sujet "Fluorescent Bioimaging"
Choi, Angela On Ki. « Fluorescent nanocrystals for bioimaging ». Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=114126.
Texte intégralL'imagerie par fluorescence reste à introduire dans les cabinets médicaux en raison du manque de fluorophores photo-stables, à haute intensité lumineuse, disponibles sur le marché. Les nanocristaux fluorescents ou boîtes quantiques (BQ), représentent une alternative intéressante par rapport aux teintures organiques car les BQ sont très petits, résistants au photoblanchiment et ont d'excellentes propriétés optiques. L'objectif principal de cette étude est d'utiliser les BQ pour une imagerie en temps réel sur les animaux vivants. L'usage étendu des BQ en biologie est limité en raison de leur biocompatibilité discutable et également en raison du fait que quelques nanocristaux sont composés en partie de métaux lourds. Dans cette étude, les mécanismes cellulaires impliquant la toxicité des BQ de cadmium telluride sont examinés. Après une exposition prolongée aux BQ, des modifications morphologiques et fonctionnelles significatives ont été observées à l'échelle cellulaire et infracellulaire. Nous démontrons que la toxicité induite par les BQ peut entrainer la production d'espèces réactives de l'oxygène, la peroxydation des lipides de la membrane biologique, l'altération du fonctionnement mitochondrial mais aussi des changements du génome et de l'épigénome. Comprendre comment les BQ toxiques endommagent les cellules est un premier pas dans l'établissement de protocoles d'évaluation de la sécurité des nanomatériaux et dans le développement de nouveau nanocristaux non-toxiques. Nous démontrons que la modification de la surface des BQ grâce à des médicaments (ex : N-acetylcysteine) ou des polymères synthétiques peut grandement diminuer leur toxicité, et dans quelques cas, peut aussi rendre les BQ non-toxiques. En utilisant de tel BQ non-toxiques, nous effectuons une démonstration de l'utilisation de la fluorescence infrarouge proche pour effectuer des clichés en temps réel de microlésions cérébrales sur des animaux vivants, à l'aide de méthodes non effractives (ex : voie intra-nasale) pour insérer des nano-sondes ou administrer des nano-thérapies au niveau du cerveau. Des imageries répétées permettent de surveiller la taille des lésions sur les animaux, et prouvent l'efficacité des nano-thérapies dans la prévention de l'expansion de la lésion. Les animaux traités par micelles chargées de nimodipine ou de minocycline ont des lésions moins volumineuses et une meilleure récupération de la fonction motrice. Une évaluation quantitative et un calcul de volume ont été possibles car le signal BQ était séparé de l'autofluorescence tissulaire grâce à de la synchronisation d'image fondé sur la durée de vie fluorescence. L'ensemble des résultats de ces études contribue au développement des BQ et des technologies par fluorescence en imagerie biomédicale, et ceci de deux façons : 1) en présentant des résultats in vitro qui constituent une première étape dans l'évaluation de la sécurité des nanomatériaux. 2) en démontrant des avantages de l'utilisation les BQ infrarouges proches pour l'imagerie non effractives sur les animaux vivants avec des lésions cérébrales et pour la détermination de la réduction des lésions après des nano-thérapies. Ces constatations appuient l'utilisation des BQ fluorescentes créés avec soin et ayant subi des essais précliniques rigoureux pour l'imagerie encéphalique in vivo et s'étendant finalement aux études cliniques.
Si, Yang. « Fluorescent Nanomaterials for Bioimaging and Biosensing : Application on E.coli Bacteria ». Thesis, Cachan, Ecole normale supérieure, 2015. http://www.theses.fr/2015DENS0038/document.
Texte intégralBacteria are the most abundant organisms in the world. Investigations and studies on bacteria can be beneficial to medical research, water resources research and food industry. Fluorescent sensing and labeling are commonly used for bioanalytical purposes. In the quest for very bright and stable labels, novel polymer-based, self-stabilized, fluorescent nanoparticles (FNPs, 60 nm) and fluorescent polymer chains (FPCs, 5 nm) have been developed. In the first part, a methodology to insert these FNPs into E.coli bacteria was developed. To control if the FNPs are indeed internalized, we developed a protocol based upon FNPs luminescence quenching by methylene blue. In the second part, a "sandwich" system is built. By using a streptavidin-biotin link, a bridge between particles (FNP), specific antibodies and bacteria is built. SPR, fluorescent images and SEM images demonstrated the interaction of biotin conjugated FNPs with E.coli bacteria. In the third part, interactions of fluorescent polymer chains with bacteria are investigated. Green fluorescent polymer chains (GFPCs) can easily enter into E.coli bacteria. GFPCs can label the cytoplasm but not the DNA. Red fluorescent polymer chains (RFPCs) can label the membrane of E.coli bacteria easily and efficiently. Both FPCs are highly water-soluble, bright and non-toxic, they are novel fluorescent labels for internal and external biological labeling of bacteria. In the last part, it is demonstrated that pH sensitive FANPs can be used to measure the growth of E.coli. They detect rapidly and accurately bacterial growth by signaling the change of pH resulting from cellular metabolism. Moreover, these particles allow for continuous monitoring a large number of samples for high-throughput screening applications. The studied fluorescent nanomaterials are promising tools for biosensing and bioimaging applications due to their brightness, high photostability and rich functionalisation ability
Kong, Yifei. « Multifunctional fluorescent nanoparticle-bioconjugates : preparation, characterisation and bioimaging applications ». Thesis, University of Leeds, 2015. http://etheses.whiterose.ac.uk/12252/.
Texte intégralTrofymchuk, Kateryna. « Controlled switching of fluorescent organic nanoparticles through energy transfer for bioimaging applications ». Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAJ121/document.
Texte intégralPerformance of biosensing and bioimaging techniques can be improved by fluorescent nanoparticles (NPs) capable of efficient Förster resonance energy transfer (FRET). The aim of my PhD project is to develop bright and photostable dye-loaded polymer NPs capable to undergo efficient FRET beyond the Förster radius. We showed that bulky groups are essential for minimizing self-quenching and bleaching of encapsulated dyes. Moreover, polymer matrix plays a crucial role in controlling the inter-fluorophore communication by excitation energy transfer. Then, by exploiting communication of dyes, we designed NPs exhibiting efficient photoswitching as well as giant light-harvesting. Finally, very small NPs with efficient FRET to their surface were developed and applied for ultra-sensitive molecule detection of proteins. The obtained results provide new insights in the development of bright nanoparticles with efficient energy transfer as well as nano-probes for single-molecule detection
Mastrodonato, Cristiano Matteo. « Elaboration of fluorescent molecular probes and molecular-based nanoparticles for bioimaging purposes ». Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0652/document.
Texte intégralFluorescence-based techniques are popular tools for the study and understanding of biological processes. This has prompted continuous research aimed at the development of a wide range of fluorescent probes specifically designed for specific applications. Among them, fluorescent pH probes are of much interest as pH variations or gradients are involved in many biological events and anomalous alterations are often related to the onset of dysfunctions and diseases. In this framework we have developed a series of promising two-photon pH fluorescent molecular probes. These quadrupolar bolaamphiphilic probes are of great interest, as they combine a steep pH dependence of their optical properties close to neutral pH, ratiometric behavior and large response to two-photon (2P) excitation in the NIR region. As such they offer much promise for ratiometric detection of the pH in biological environments and in situ monitoring of acidification. In parallel, we have been interest in the design of ultrabright nanoparticles for bioimaging purpose (in particular highly sensitive optical imaging). We chose to focus on Fluorescent Organic Nanoparticles made of organic molecules with low molecular weight (FONs) as they offer a flexible route and promising alternatives to toxic quantum dots. In this case the design of the dye used as building blocks of the FONs is of crucial importance and strongly influence the chemical and physical properties of the nanoparticles generated, such as their one and two-photon brightness and both their structural and colloidal stability. In that context a library of novel dipolar chromophores have been synthesized and used to prepare FONs using the nanoprecipitation method. Their properties were thoroughly investigated in order to determine the relationship between the molecular design of the isolated dye and the overall properties of the nanoparticles made of these dyes. As a result, Hyperbright FONs emitting in the green to NIR region and combining giant brightness and remarkable stability have been achieved. They offer major promise for bioimaging based on both excitation and detection in the NIR region
Ardizzone, Antonio. « New fluorescent nanovesicles, by self-assembly of organic fluorophores, sterols and surfactants, as probes for bioimaging ». Doctoral thesis, Universitat Autònoma de Barcelona, 2017. http://hdl.handle.net/10803/403924.
Texte intégralFinding new fluorescent organic nanoparticles (FONs) with the potential to overcome the limits of common fluorescent probes as molecular fluorophores, fluorescent proteins and inorganic nanoparticles is a subject of strong interest for materials scientists developing new probes for fluorescence microscopy and theranostics. In the recent years, innovative non-liposomal nanovesicles, based on the self-assembly of quaternary ammonium surfactants and sterols, named Quatsomes (QSs), have been developed as promising candidates for applications as multifunctional drug carriers. Within this scenario, the main objective of this Thesis (conducted in the framework of the Marie Skłodowska-Curie ITN “Nano2Fun”) is to explore the possibility of using Quatsomes as a vehicle for nanostructuring in aqueous media several dye molecules, irrespective of their physicochemical and optical properties, in order to obtain new fluorescent organic nanoparticles (FONs) with superior colloidal stability and enhanced fluorescent features, especially with high brightness, in relation to single molecule flurofores and other type of FONS. The self-assembly of molecular organic fluorophores, sterols and quaternary ammonium surfactants into fluorescent Quatsomes was achieved by the DELOS-SUSP method, a compressed CO2 –based process which guarantees a highly homogeneous membrane composition and supramolecular arrangement, which have impact on the optical properties of the obtained FONs. Different strategies have been explored to nanostructurate in aqueous media, by mean of QSs, molecular dyes with different physicochemical properties, including those water- and non-water soluble, analyzing the impact of their nanostructuration on the optical properties of the obtained FONs. Thus, anionic water-soluble dyes, such as fluorescein, were nanostructured over QSs surface, taking advantage of anionic/cationic interaction among dye and vesicles surface. On the other hand, lipophilic and non-water soluble dyes modified with long alkyl chains can be stably incorporated into QSs membrane, as shown in the case of several dyes families, including cyanine, diketopyroolopyrrole (DPPs) and fluorene derivatives. The fluorescent QSs showed superior colloidal and optical stability (up to several months), a high degree of structural homogeneity and high fluorescence performances, overcoming those of other nanostructures of the same dyes. Furthermore, aiming to obtain multicolor nanoparticles, Quatsomes allowed the simultaneous loading within their membrane of different dyes, which showed a highly efficient fluorescence resonance energy transfer (FRET) mechanism, an interesting tool for monitoring the carrier integrity during the drug delivery and for multiplexed imaging applications. Finally, fluorescent Quatsomes were tested as nanoprobes for in vitro cells imaging. It has been demonstrated that fluorene-based Quatsomes (named LysoQS) constitute a strongly specific lysosomal probe ideal for long-term imaging. Furthermore, cyanines-loaded Quatsomes were used as probes for super-resolution microscopy technique (STORM) which allowed visualizing and resolving single Quatsomes structures upon internalization in cells. The results of this Thesis showed that fluorescent Quatsomes, thanks to the advantages offered in comparison with other commonly employed fluorescent labels, constitute a promising fluorescent nanoprobes with possible future applications in bioimaging, theranostics and, generally, nanomedicine.
Nilsson, Ruben. « Optical properties of fluorescent quantum dots for super-resolution bioimaging ». Thesis, KTH, Tillämpad fysik, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-169624.
Texte intégralLesani, Pooria. « Novel Carbon Dot-Based Fluorescent Nanomaterials for Biosensing and Bioimaging ». Thesis, The University of Sydney, 2022. https://hdl.handle.net/2123/27346.
Texte intégralKilic, Nüzhet Inci. « Graphene Quantum Dots as Fluorescent and Passivation Agents for Multimodal Bioimaging ». Thesis, KTH, Tillämpad fysik, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-298302.
Texte intégralSedan deras upptäckt har nolldimensionella kvantprickar av grafen (kol) uppmärksammats inom biorelaterade applikationer, särskilt för deras optiska egenskaper, kemiska stabilitet och enkelt modifierbara yta. Denna avhandling fokuserar på en grön syntesmetod av kvävedopade grafen-kvantprickar för bimodal bioavbildning med röntgenfluorescens och optisk fluorescens. Både konventionella och mikrovågs-assisterade solvotermiska syntesmetoder användes för att undersöka metodernas effekt på de syntetiserade kvantprickarna. Den mikrovågs-assisterade metoden möjliggjorde syntes av uniforma kvantprickar med exciteringsoberoende egenskaper på grund av mycket kontrollerbara reaktionsförhållanden. Det demonstrerades att den molekylära strukturen hos prekursorerna påverkade de optiska fluorescensegenskaperna hos grafen-kvantprickarna. Genom att välja specifika prekursorer erhölls kvantprickar som emitterar i både blått och rött ljus, motsvarande emissionsmaxima vid 438 respektive 605 nm under excitering vid 390 respektive 585 nm. Amin-funktionaliserade Rh-nanopartiklar valdes som en aktiv kärna för röntgenfluorescens, syntetiserad genom en mikrovågs-assisterad hydrotermisk metod med en specialdesignad sockerligand som reduktionsmedel. Dessa nanopartiklar konjugerades med blåemitterande kvantprickar genom EDC-NHS-behandling. De hybrida nanopartiklarna uppvisade grön emission (520 nm) under 490 nm excitation och ledde till en minskad cytotoxicitet uppmätt genom cellanalys i realtid (RTCA) jämfört med endast Rh-nanopartiklar, vilket framhävde passiveringsrollen som kvantprickarna spelar. Hybridkomplexet utgjorde ett multimodalt kontrastmedel för bioavbildning, vilket demonstrerades med konfokalmikroskopi (in vitro) och fantomexperiment med röntgenfluorescens.
Banerjee, Anusuya. « Novel, Targettable Bioimaging Probes Using Conjugates of Quantum Dots and DNA ». Thesis, Paris 6, 2016. http://www.theses.fr/2016PA066376/document.
Texte intégralQuantum dots (QD) are new generation of versatile probes for biology, particularly for bioimaging. For specific applications, QDs are conjugated to biomolecules such as nucleic acid or proteins and subsequently targeted to unique intra-cellular pathways. Building upon the state-of-the-art ligands for water-dispersible QDs developed by the lab, a novel and highly generalizable method to conjugate DNA to QD is developed in this thesis. This method employs thiols present on polymers on QDs for conjugation to maleimide-functionalized DNA. Extensive characterization of parameters affecting this reaction is carried out and the strategy is extended to other nanoparticles and biomolecules. Following this, a novel method to conjugate proteins to QD via DNA hybridization is discussed. Using a model protein Transferrin (Tf), the unique properties of thus generated QD-DNA-Tf conjugates are studied in-vitro and in-cellulo. These conjugates are subsequently used for tracking endosomal dynamics for up-to 20 minutes, exploiting the fullest potential of QDs for live imaging. In the last part, additional studies on factors affecting the ‘biological performance’ of QDs are carried out. Using a range of highly adaptable polymeric ligands developed by the group, interactions of surface-modified QDs with the biological interface are probed. Systematic biochemical and cellular experiments demonstrate that QDs coated with zwitterionic polymers have superior antifouling properties compared to poly(ethylene glycol)-based polymers and stability in diverse biological contexts
Livres sur le sujet "Fluorescent Bioimaging"
R, Viviani V., et Ohmiya Y, dir. Luciferases and fluorescent proteins : Principles and advances in biotechnology and bioimaging, 2007. Trivandrum : Transworld Research Network, 2007.
Trouver le texte intégralChapitres de livres sur le sujet "Fluorescent Bioimaging"
Xu, Jie, et Li Shang. « Fluorescent Metal Nanoclusters for Bioimaging ». Dans Fluorescent Materials for Cell Imaging, 97–128. Singapore : Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5062-1_5.
Texte intégralKailasa, Suresh Kumar, Vaibhavkumar N. Mehta, Nazim Hasan et Hui-Fen Wu. « Fluorescent Carbon Dots for Bioimaging ». Dans Advanced Bioelectronic Materials, 215–28. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118998861.ch6.
Texte intégralRawat, Dipti, et Ragini Raj Singh. « Fluorescent Magnetic Quantum Dots in Bioimaging ». Dans Magnetic Quantum Dots for Bioimaging, 133–52. New York : CRC Press, 2023. http://dx.doi.org/10.1201/9781003319870-6.
Texte intégralDi Martino, Miriam, Francesco Marrafino, Rosita Diana, Pio Iannelli et Simona Concilio. « Fluorescent Probes for Applications in Bioimaging ». Dans Advances in Bionanomaterials II, 243–58. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-47705-9_21.
Texte intégralLi, Youbin, Songjun Zeng et Jianhua Hao. « Lanthanide-Based Upconversion Nanoparticles for Bioimaging Applications ». Dans Fluorescent Materials for Cell Imaging, 129–53. Singapore : Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5062-1_6.
Texte intégralMohan, Nitin, et Huan-Cheng Chang. « Fluorescent Nanodiamonds and Their Prospects in Bioimaging ». Dans Optical Engineering of Diamond, 445–71. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648603.ch13.
Texte intégralSukumar, Uday Kumar, Arutselvan Natarajan, Tarik F. Massoud et Ramasamy Paulmurugan. « Applications of Fluorescent Protein-Based Sensors in Bioimaging ». Dans Topics in Medicinal Chemistry, 149–83. Cham : Springer International Publishing, 2019. http://dx.doi.org/10.1007/7355_2019_90.
Texte intégralXu, Hui, Lihua Wang et Chunhai Fan. « Bioanalysis and Bioimaging with Fluorescent Conjugated Polymers and Conjugated Polymer Nanoparticles ». Dans ACS Symposium Series, 81–117. Washington, DC : American Chemical Society, 2012. http://dx.doi.org/10.1021/bk-2012-1112.ch004.
Texte intégralWang, Dan, et Jun Qian. « AIE Luminogens for Three-Photon Fluorescence Bioimaging ». Dans Principles and Applications of Aggregation-Induced Emission, 425–55. Cham : Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-99037-8_18.
Texte intégralWang, Lei, et Guo-Bin Qi. « Supramolecular Self-assembled Nanomaterials for Fluorescence Bioimaging ». Dans In Vivo Self-Assembly Nanotechnology for Biomedical Applications, 1–29. Singapore : Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6913-0_1.
Texte intégralActes de conférences sur le sujet "Fluorescent Bioimaging"
Reineck, Philipp, Amanda Abraham, Nicholas Nunn, Marco Torelli, Alexander Zaitsev, Adam Dalis, Neeraj Prabhakar, Olga Shenderova et Brant C. Gibson. « Multicolor fluorescent nanodiamonds for bioimaging ». Dans Biophotonics Australasia 2019, sous la direction de Ewa M. Goldys et Brant C. Gibson. SPIE, 2019. http://dx.doi.org/10.1117/12.2539890.
Texte intégralZhang, Yong, et WenKai Li. « Upconverting Fluorescent Nanoparticles for Bioimaging and Therapy ». Dans Asia Communications and Photonics Conference. Washington, D.C. : OSA, 2012. http://dx.doi.org/10.1364/acp.2012.as3e.1.
Texte intégralZhang, Yong, et WenKai Li. « Upconverting Fluorescent Nanoparticles for Bioimaging and Therapy ». Dans Asia Communications and Photonics Conference. Washington, D.C. : OSA, 2012. http://dx.doi.org/10.1364/acpc.2012.as3e.1.
Texte intégralChatterjee, Dev K., et Yong Zhang. « Use of upconverting fluorescent nanoparticles for bioimaging ». Dans SPIE OPTO, sous la direction de Zameer U. Hasan, Philip R. Hemmer, Hwang Lee et Charles M. Santori. SPIE, 2012. http://dx.doi.org/10.1117/12.905939.
Texte intégralBaglietto, Silvia, Ibolya E. Kepiro, Gerrit Hilgen, Evelyne Sernagor, Vittorio Murino et Diego Sona. « Segmentation of Retinal Ganglion Cells From Fluorescent Microscopy Imaging ». Dans 4th International Conference on Bioimaging. SCITEPRESS - Science and Technology Publications, 2017. http://dx.doi.org/10.5220/0006110300170023.
Texte intégralAmeli, Corrado, Sonja Fixemer, David Bouvier et Alexander Skupin. « PRAQA : Protein Relative Abundance Quantification Algorithm for 3D Fluorescent Images ». Dans 8th International Conference on Bioimaging. SCITEPRESS - Science and Technology Publications, 2021. http://dx.doi.org/10.5220/0010187400002865.
Texte intégralAmeli, Corrado, Sonja Fixemer, David Bouvier et Alexander Skupin. « PRAQA : Protein Relative Abundance Quantification Algorithm for 3D Fluorescent Images ». Dans 8th International Conference on Bioimaging. SCITEPRESS - Science and Technology Publications, 2021. http://dx.doi.org/10.5220/0010187400210030.
Texte intégralNandy, Papiya, Debbethi Bera, Kunal Pal, Parimal Karmakar et Sukhen Das. « Highly Fluorescent Carbon Nanoparticle : An Emerging Bioimaging Intervention ». Dans MOL2NET 2020, International Conference on Multidisciplinary Sciences, 6th edition. Basel, Switzerland : MDPI, 2020. http://dx.doi.org/10.3390/mol2net-06-06786.
Texte intégralSharko, Olga, Maksim Tatulchenkov, Maksim Kvach, Sergey Pletnev et Vadim Shmanai. « Nanoparticles-based fluorescent conjugates for MRI contrast agents and bioimaging ». Dans 2015 5th International Workshop on Magnetic Particle Imaging (IWMPI). IEEE, 2015. http://dx.doi.org/10.1109/iwmpi.2015.7107068.
Texte intégralSokolov, I. L., A. V. Vasilyeva, A. V. Lunin, A. V. Yaremenko et V. R. Cherkasov. « Fluorescent Superparamagnetic and Paramagnetic Agents for Bioimaging, Sensing and Cell Targeting ». Dans 2018 International Conference Laser Optics (ICLO). IEEE, 2018. http://dx.doi.org/10.1109/lo.2018.8435453.
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