Bibliografías temáticas / Amplification du signal (chimie)

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Literatura académica sobre el tema "Amplification du signal (chimie)"

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Publicado: 22 de febrero de 2025

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Artículos de revistas sobre el tema "Amplification du signal (chimie)"

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Scrimin, Paolo y Leonard J. Prins. "Sensing through signal amplification". Chemical Society Reviews 40, n.º 9 (2011): 4488. http://dx.doi.org/10.1039/c1cs15024c.

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Urdea, Mickey S. "Branched DNA Signal Amplification". Nature Biotechnology 12, n.º 9 (septiembre de 1994): 926–28. http://dx.doi.org/10.1038/nbt0994-926.

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Shibata, T. y K. Fujimoto. "Noisy signal amplification in ultrasensitive signal transduction". Proceedings of the National Academy of Sciences 102, n.º 2 (29 de diciembre de 2004): 331–36. http://dx.doi.org/10.1073/pnas.0403350102.

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Nallur, G. "Signal amplification by rolling circle amplification on DNA microarrays". Nucleic Acids Research 29, n.º 23 (1 de diciembre de 2001): 118e—118. http://dx.doi.org/10.1093/nar/29.23.e118.

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Pai, Supriya, Ana Roberts y Andrew D. Ellington. "Aptamer amplification: divide and signal". Expert Opinion on Medical Diagnostics 2, n.º 12 (19 de noviembre de 2008): 1333–46. http://dx.doi.org/10.1517/17530050802562016.

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Bijnen, F. G. C., J. v. Dongen, J. Reuss y F. J. M. Harren. "Thermoacoustic amplification of photoacoustic signal". Review of Scientific Instruments 67, n.º 6 (junio de 1996): 2317–24. http://dx.doi.org/10.1063/1.1146939.

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Zhu, Lei y Eric V. Anslyn. "Signal Amplification by Allosteric Catalysis". Angewandte Chemie International Edition 45, n.º 8 (13 de febrero de 2006): 1190–96. http://dx.doi.org/10.1002/anie.200501476.

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Dailey, James M., Anjali Agarwal, Colin J. McKinstrie y Paul Toliver. "Optical Signal Filtering Using Phase-Sensitive Amplification and De-Amplification". IEEE Photonics Technology Letters 28, n.º 16 (15 de agosto de 2016): 1743–46. http://dx.doi.org/10.1109/lpt.2016.2566925.

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Shibata, T. y K. Fujimoto. "2P167 Noisy signal amplification in ultrasensitive signal transduction network". Seibutsu Butsuri 44, supplement (2004): S151. http://dx.doi.org/10.2142/biophys.44.s151_3.

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Brooks, Adam D., Kimy Yeung, Gregory G. Lewis y Scott T. Phillips. "A strategy for minimizing background signal in autoinductive signal amplification reactions for point-of-need assays". Analytical Methods 7, n.º 17 (2015): 7186–92. http://dx.doi.org/10.1039/c5ay00508f.

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Tesis sobre el tema "Amplification du signal (chimie)"

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Rabin, Charlie. "Nouvelles stratégies d'amplification moléculaire d'un signal basées sur l'activation de dérivés pro-quinoniques : de l'activation d'un catalyseur biomoléculaire au déclenchement d'une réaction auto-catalytique". Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCC079/document.

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Généralement, diagnostiquer une pathologie donnée à un stade de développement précoce favorise le pronostic vital du patient atteint. Une telle performance nécessite de détecter des marqueurs présents à des seuils de concentrations bas dans des fluides biologiques souvent complexes. Pour détecter ces concentrations extrêmement faibles en analyte donné, la stratégie employée au cours de ce travail est l’amplification moléculaire du signal. Pour cela, différentes approches sont possibles (i) amplifier le signal issu de l’évènement de reconnaissance cible/sonde, (ii et iii) amplifier le signal par régénération ou réplication de la cible. Les stratégies conçues au cours de ce travail de thèse se focalisent principalement sur la détection de petites molécules, telles que l’eau oxygénée ou encore l’anion fluorure, mais avec à terme l’idée de les étendre à la détection indirecte de biomarqueurs ou protéines d’intérêts. La première partie de cette thèse se focalise sur l’amplification moléculaire d’un signal par une catalyse allostérique en utilisant la réaction de reconstitution d’une apoenzyme donnée avec son cofacteur tandis que la seconde partie de cette thèse repose sur la mise en place de systèmes d’amplification catalytique et auto-catalytique pour la détection d’H2O2, grâce à des dérivés pro-quinoniques porteurs de groupement acide/ester boronique. La distinction entre les systèmes catalytique et auto-catalytique se fait selon qu’H2O2 est régénéré ou amplifié au cours de la réaction
Generally, diagnosing a given pathology at an early stage of development promotes the patient's prognosis. Such a performance requires the detection of specific markers which are present in complex biological fluids at low concentration level. To detect these extremely low analyte concentrations, the strategy employed in this work is the molecular amplification of the signal. To this end, different approaches are possible (i) amplifying the signal resulting from the target / probe recognition event, (ii and iii) amplifying the signal by regeneration or replication of the target. The strategies conceived during this thesis work mainly focus on the detection of small molecules, such as hydrogen peroxide or fluoride anion, but with the idea of extending them to the indirect detection of biomarkers or proteins of interest. The first part of this thesis focuses on the molecular amplification of a signal by allosteric catalysis using the reconstitution reaction of a given apoenzyme with its cofactor. The second part of this thesis is based on the implementation of catalytic and auto-catalytic amplification systems for the detection of H2O2, thanks to pro-quinonic derivatives bearing boronic acid/ester group. The distinction between catalytic and auto-catalytic systems is based on whether H2O2 is regenerated or amplified during the reaction
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Beltrami, Coline. "Développement d'un biocapteur plasmonique pour la détection en faibles concentrations de miARNs dans le cadre du don d'organes". Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPAST196.

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La surveillance des conditions physiologiques de donneurs d'organes en état de mort cérébrale est cruciale pour prévenir la dégradation des tissus. Ce suivi peut être effectué en observant la réponse inflammatoire (tempête cytokinique) à travers des biomarqueurs spécifiques : les miARNs. Ce travail propose d'utiliser l'imagerie par résonance plasmonique de surface (SPRI) pour détecter quantitativement ces miARNs. Cette recherche vise à développer un biocapteur SPRI plus sensible et spécifique pour détecter les miARNs à des concentrations inférieures à la limite de détection de ces systèmes.Tout d'abord, une fonctionnalisation de la surface d'or de la biopuce mieux orientée a été développée afin d'améliorer l'accessibilité des biorécepteurs. Ensuite, des sondes modifiées avec des bases LNA ont été employées pour renforcer l'affinité avec le miARN cible. En parallèle, une stratégie d'amplification par sandwich du signal SPRI a été conçue en utilisant des nanoparticules d'or, et un modèle cinétique a été élaboré pour prédire le facteur d'amplification. Les AuNPs ont été synthétisées en une seule étape à température ambiante et fonctionnalisées pour être spécifiques vis-à-vis du miARN et solubles en solution saline. Ces approches combinées ont conduit à une amplification du signal de plus de deux ordres de grandeur et à une limite de détection de miARNs dans la gamme du picomolaire
Monitoring the physiological conditions of brain-deceased organ donors is crucial to prevent tissue degradation. Tracking this degradation can be done by following the inflammatory response (i.e. cytokine storm) through specific biomarkers like miRNAs. This work proposes using Surface Plasmon Resonance Imaging (SPRI) to quantitatively detect those miRNAs. To achieve detection at concentrations below the usual SPRI limits, this research focuses on developing a more sensitive and specific SPRI biosensor for miRNA detection. Firstly, a new surface functionalization better oriented was developed for the SPRI gold biochip to improve bioreceptor accessibility. LNA-modified probes were then employed to enhance the affinity with the target miRNA. Secondly, a signal amplification strategy was designed using gold nanoparticles (AuNPs) in a sandwich-like assay, and a kinetic model predicting the amplification factor was developed. The AuNPs were synthesized in a one-step process at ambiant temperature and functionalized for miRNA specificity and solubility in saline solution.These combined approaches led to more than two orders of magnitude signal amplification and a detection limit in the picomolar range
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Goggins, Sean. "Enzyme-triggered catalytic signal amplification". Thesis, University of Bath, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681045.

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Amplification is essential in order to achieve low limits of detection (LOD) within analyte detection assays. Over recent years, chemists have developed a multitude of amplification methodologies for the detection of a variety of analytes with varying signal readouts. Typically, these methodologies are focussed upon one of four main amplification strategies; target, label, signal or receptor amplification. Herein, a thorough review of the current literature has been compiled highlighting both the advantages and disadvantages of each strategy. Despite the increasing number of amplification methodologies being described, there is still significant demand for improving analyte assay efficiency and sensitivity. In particular, rapid and sensitive protein detection that can be performed at the point-of-care (POC) setting is highly desirable for the effective treatment and control of infectious diseases. In collaboration with medical diagnostics company Atlas Genetics Ltd., a new electrochemical substrate for the ratiometric detection of alkaline phosphatase (ALP), a commonly-used enzyme label within enzyme-linked immunosorbent assays (ELISA), was developed capable of delivering an ALP LOD of 0.3 pM within 30 minutes. When applied to the detection of C-reactive protein (CRP), a model biomarker used to diagnose inflammation, the substrate was shown to be significantly more reproducible than a commonly-used commercially-available electrochemical ALP substrate. In order to improve the sensitivity of an ELISA, a novel signal amplification methodology was then developed. Based upon a double-catalyst signal amplification strategy, an organometallic transfer hydrogenation catalyst was utilised in combination with the enzyme label to afford a hybrid synthetic and biological amplification cascade. To achieve selective enzyme-triggered catalyst activation, an enzyme substrate termed a proligand was synthesised. In the presence of the enzyme, self-immolation of the proligand occurs to release a ligand, capable of binding to an iridium pre-catalyst to generate a ligand-accelerated active catalyst. Catalyst activity could be observed through ratiometric electrochemical analysis through the use of an electroactive aldehyde as the catalyst substrate. An ALP LOD of 7.6 pM after 33 minutes was obtained for this amplification methodology but when applied to the detection of CRP however, a significant background reaction, found to be caused by the iridium pre-catalyst, limited sensitivity. The versatility of the signal amplification methodology was nevertheless demonstrated through the enzyme-triggered catalytic reduction of a range of different aldehydes with alternative signal readouts, enabling signal transduction and amplification to be easily achieved within a single procedure.
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White, Stephanie Rushbrook. "In vitro expression as a signal amplification system". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0009/NQ52446.pdf.

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Nassif, Rachel. "Design and optimization of polymer nanostructures for signal amplification". Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=22002.

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Biomolecule detection assay applications range from diagnostics and pathogen detection, to the design of targeted medical care and drug development. A current limitation of this approach lies in the inherently small quantity of the analytes being detected. Therefore, a method to efficiently amplify either the analyte or the detection signal is necessary. We report a signal amplification approach that relies on self-assembled polymeric nanospheres, containing a large number of luminescent transition metal centers in their core and a biological recognition unit on their periphery. Initially, block copolymers containing a hydrophobic ruthenium bipyridine block, a hydrophilic PEG block, and a biotin biological recognition block were synthesized. Self-assembly of these copolymers in water, results in nanospheres that can be tethered to a target analyte using the biotin-streptavidin interaction. The ability to tether such a large number of metallic centers to each analyte provides a simple approach to signal amplification through luminescence.
Les analyses de détection biomoléculaire ont des applications qui s'étendent du diagnostic et de la détection de microbes pathogènes, à la conception de soins médicaux spécifiques et au développement de nouveaux médicaments. Une limitation actuelle de cette approche repose sur le fait que les analytes à détecter sont présentes qu'en faibles quantités. Par conséquent, une méthode efficace d'amplification de l'analyte ou du signal de détection est nécessaire. Nous présentons ici une approche d'amplification du signal qui se fonde sur les nanosphères polymères auto-assemblés, contenant dans leur noyau un grand nombre de centres luminescents basé sur des métaux de transition, et, sur leur périphérie, une unité biologique pour la reconnaissance. Tout d'abord, les copolymères à bloc contenant un bloc hydrophobe de bipyridine de ruthénium, un bloc hydrophile de PEG, et un bloc d'identification biologique de biotine, ont été synthétisés. L'auto-assemblage de ces copolymères dans l'eau donne lieu à la formation des nanosphères qui peuvent être attachés à un analyte cible en utilisant l'interaction entre la biotine et la streptavidin. La capacité d'attacher un si grand nombre de centres métalliques à chaque analyte fournit une méthode simple d'amplification du signal par la luminescence.
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Lai, Ming-fai y 黎明輝. "All-optical signal processing based on optical parametric amplification". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2008. http://hub.hku.hk/bib/B41508877.

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Kaastrup, Kaja. "Photopolymerization-based signal amplification : mechanistic characterization and practical implementation". Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/101507.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2015.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 124-135).
Polymerization-based signal amplification is an approach to biosensing that leverages the amplification inherent to radical polymerization to enhance signal associated with molecular recognition. This versatile technique has been implemented with a number of radical polymerization chemistries, including atom-transfer radical polymerization (ATRP), photopolymerization, reversible addition-fragmentation chain transfer polymerization (RAFT), and enzyme-mediated redox polymerization. This thesis focuses on the development of photopolymerization-based signal amplification (PBA) as a platform technology for use at the point-of-care. We sought to build a mechanistic understanding of the system, specifically examining the effects of non-ideal binding reactions and oxygen. One of the greatest barriers to wider implementation of polymerization-based signal amplification is the susceptibility of radical polymerization reactions to oxygen inhibition. Oxygen reacts with initiating and propagating radicals to form peroxy radicals that are unreactive towards propagation, and thus have the effect of terminating the reaction. Chapter 2 describes the development of an air-tolerant monomer solution that allows interfacial photopolymerization reactions to proceed under ambient conditions in as little as 35 seconds where previous implementations of PBA required inert gas purging to remove oxygen and reaction times of 20 minutes or longer. We showed that the inclusion of submicromolar concentrations of eosin, the photoinitiator, in the monomer solution mitigated the effects of oxygen. The ability to perform these reactions under ambient conditions increases their clinical utility by simplifying the procedure and by eliminating purging gases that might be detrimental in some biological applications, specifically those involving cells. Intrigued by eosin's ability to overcome over 1000-fold excess of oxygen, we performed spectroscopic measurements in order to elucidate the mechanisms underlying eosin's resistance towards oxygen inhibition. A dual-monitoring system for measuring eosin consumption and monomer conversion was used to corroborate the hypothesized regeneration of eosin in the presence of oxygen (Chapter 3). This required the development of a method for analyzing absorbance data for polymerizing hydrogels. We further examined the photoactivation kinetics of the eosin/tertiary amine system and the effect of oxygen using absorbance spectroscopy and kinetic modeling (Chapter 4). The spectroscopic investigation revealed that, in addition to the previously postulated reactions in which eosin is regenerated by oxygen, additional reactions between oxygen and eosin in its triplet state and semireduced form occur and must be taken into account. The formation and consumption of the semireduced species informed the construction of a kinetic model, for which the importance of considering the reaction between triplet state eosin and the tertiary amine as two separate steps was clearly demonstrated. Transitioning away from an examination of the amplification chemistry, we next considered the molecular recognition event, exploring the concept of the amplification threshold by investigating the impact of the binding affinity of the molecular recognition event on the limit of detection (Chapter 5). We showed that improvements in binding affinity enhance detection sensitivity. A mass action kinetics based model was used to accurately predict experimental findings and identify the key parameters for predicting the performance of PBA reactions: surface capture probe density, incubation time, concentration and binding affinity of the target molecule. We evaluated the commonly proposed strategy of developing polymeric macrophotoinitiators for improving the sensitivity of photopolymerization-based signal amplification reactions (Chapter 6). Building on earlier work, in which solubility limits were encountered coupling eosin and neutravidin to a poly (acrylic acid-co-acrylamide) backbone, we synthesized a more water-soluble polymeric macrophotoinitiator based on a generation 7 poly (amidoamine) dendrimer scaffold. Although the solubility was improved, a new quenching limitation was identified, demonstrating the complexity of designing polymeric macrophotoinitiators that incorporate eosin as the photoinitiator. In lieu of viable photoinitiator alternatives to eosin, we concluded that future efforts to design polymeric macrophotoinitiators should include features that increase the distance between eosin molecules. We used photopolymerization-based signal amplification to selectively encapsulate a target population of cells in a co-culture (Chapter 7). PBA allows for the selective growth of an immunoprotective hydrogel only at the surfaces of the labeled cells, even in closely contacted cell aggregates. The hydrogel protects the cells against subsequent lysis, allowing for nucleic acid extraction from the unlabeled cells without the need for cell sorting. Finally, we consider the vast, unexplored parameter space for photopolymerization-based signal amplification, surveying alternative photoinitiation chemistries, new approaches to signal interpretation, and future applications.
by Kaja Kaastrup.
Ph. D.
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Lai, Ming-fai. "All-optical signal processing based on optical parametric amplification". Click to view the E-thesis via HKUTO, 2008. http://sunzi.lib.hku.hk/hkuto/record/B41508877.

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Fletcher, A. L. "Cryogenic developments and signal amplification in environmental scanning electron microscopy". Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.599080.

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This thesis describes the development of a cryogenic imaging system for an environmental scanning electron microscope (ESEM). The ESEM is an important new development in electron microscopy since it enables specimens to be viewed in a small pressure of gas - generally this gas is water vapour, although an alternative must be used for cryogenic applications. The presence of the gas also contributes to the imaging mechanism, a process whereby the signal electrons are amplified by the gaseous molecules prior to detection. The purpose of the cryogenic system was to image the complicated, four phase microstructure of ice cream. Although viewed routinely by conventional electron microscopy techniques, the harsh temperature and pressure regimes involved (around -120°C at 10.6 torr) increase the likelihood of introducing artefacts. Therefore, a methodology was developed for imaging ice cream with ESEM in a small pressure of an alternative imaging gas at a much warmer temperature of -80°C. In order to stabilise the ice phase in the samples at a higher temperatures, a system was designed for mixing gases, so that a small amount of water vapour could be mixed into the imaging gas. This system lifted the temperature restrictions of ice cream imaging so it can, in principle, now be imaged at its storage temperature of -20°C. In the search for alternative imaging gases to water vapour, questions were raised about the fundamental way in which the signal electrons interact with the gas. In order to understand the electron amplification properties of the different gases, a Faraday cage was designed and the electron amplification was investigated. We suggest that the ratio of the peak amplification to the plateau amplification gives a semi-quantitative method of determining the imaging quality of the gas. Furthermore, by isolating experimentally the effects of different components of the signal, it was found that the low energy secondary electrons dominate the signal at low pressure, whereas the effect of backscattered electrons becomes more important as the pressure is raised. In addition, the performance of two ESEM detector designs were compared. The new gaseous secondary electron detector (GSED), which was designed to reduce the contribution of some sources of signal, was found to achieve its aim, but some of its overall contrast was sacrificed when compared to the original environmental secondary detector (ESD).
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Oliveira, João Pedro Abreu de. "Parametric analog signal amplification applied to nanoscale cmos wireless digital transceivers". Master's thesis, Faculdade de Ciências e Tecnologia, 2010. http://hdl.handle.net/10362/5439.

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Thesis presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the subject of Electrical and Computer Engineering by the Universidade Nova de Lisboa,Faculdade de Ciências e Tecnologia
Signal amplification is required in almost every analog electronic system. However noise is also present, thus imposing limits to the overall circuit performance, e.g., on the sensitivity of the radio transceiver. This drawback has triggered a major research on the field, which has been producing several solutions to achieve amplification with minimum added noise. During the Fifties, an interesting out of mainstream path was followed which was based on variable reactance instead of resistance based amplifiers. The principle of these parametric circuits permits to achieve low noise amplifiers since the controlled variations of pure reactance elements is intrinsically noiseless. The amplification is based on a mixing effect which enables energy transfer from an AC pump source to other related signal frequencies. While the first implementations of these type of amplifiers were already available at that time, the discrete-time version only became visible more recently. This discrete-time version is a promising technique since it is well adapted to the mainstream nanoscale CMOS technology. The technique itself is based on the principle of changing the surface potential of the MOS device while maintaining the transistor gate in a floating state. In order words, the voltage amplification is achieved by changing the capacitance value while maintaining the total charge unchanged during an amplification phase. Since a parametric amplifier is not intrinsically dependent on the transconductance of the MOS transistor, it does not directly suffer from the intrinsic transconductance MOS gain issues verified in nanoscale MOS technologies. As a consequence, open-loop and opamp free structures can further emerge with this additional contribution. This thesis is dedicated to the analysis of parametric amplification with special emphasis on the MOS discrete-time implementation. The use of the latter is supported on the presentation of several circuits where the MOS Parametric Amplifier cell is well suited: small gain amplifier, comparator, discrete-time mixer and filter, and ADC. Relatively to the latter, a high speed time-interleaved pipeline ADC prototype is implemented in a,standard 130 nm CMOS digital technology from United Microelectronics Corporation (UMC). The ADC is fully based on parametric MOS amplification which means that one could achieve a compact and MOS-only implementation. Furthermore, any high speed opamp has not been used in the signal path, being all the amplification steps implemented with open-loop parametric MOS amplifiers. To the author’s knowledge, this is first reported pipeline ADC that extensively used the parametric amplification concept.
Fundação para a Ciência e Tecnologia through the projects SPEED, LEADER and IMPACT
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Libros sobre el tema "Amplification du signal (chimie)"

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Oliveira, João P. y João Goes. Parametric Analog Signal Amplification Applied to Nanoscale CMOS Technologies. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-1671-5.

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Oliveira, João P. Parametric Analog Signal Amplification Applied to Nanoscale CMOS Technologies. Boston, MA: Springer US, 2012.

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1954-, Sibley David Robert y Housley Miles D, eds. Regulation of cellular signal transduction pathways by densensitization [i.e. desensitization] and amplification. Chichester: J. Wiley, 1994.

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Polya, Gideon Maxwell. Biochemical targets of plant bioactive compounds: A pharmacological reference guide to sites of action and biological effects. London: Taylor & Francis, 2003.

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C, Schultz Jack, Raskin Ilya y Pennsylvania State University. Intercollege Graduate Program in Plant Physiology., eds. Plant signals in interactions with other organisms. Rockville, Md: American Society of Plant Physiologists, 1993.

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Goes, João y João P. Oliveira. Parametric Analog Signal Amplification Applied to Nanoscale CMOS Technologies. Springer, 2012.

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Goes, João y João P. Oliveira. Parametric Analog Signal Amplification Applied to Nanoscale CMOS Technologies. Springer, 2014.

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Parametric Analog Signal Amplification Applied To Nanoscale Cmos Technologies. Springer, 2012.

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Nanomaterials for Water Management: Signal Amplification for Biosensing from Nanostructures. Taylor & Francis Group, 2015.

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Marks, Robert S. y Ibrahim Abdulhalim. Nanomaterials for Water Management: Signal Amplification for Biosensing from Nanostructures. Pan Stanford Publishing, 2015.

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Capítulos de libros sobre el tema "Amplification du signal (chimie)"

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Schmeckebier, Holger. "Signal Amplification". En Quantum-Dot-Based Semiconductor Optical Amplifiers for O-Band Optical Communication, 101–23. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-44275-4_6.

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Weik, Martin H. "signal amplification". En Computer Science and Communications Dictionary, 1577. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/1-4020-0613-6_17336.

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Li, Weitao, Fule Li y Zhihua Wang. "Amplification". En Analog Circuits and Signal Processing, 75–92. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-62012-1_4.

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Schutzbank, Ted E. "Signal Amplification Technologies". En Advanced Techniques in Diagnostic Microbiology, 327–44. Boston, MA: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-3970-7_18.

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Weik, Martin H. "optical signal amplification". En Computer Science and Communications Dictionary, 1186. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/1-4020-0613-6_13143.

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Wang, Yun Wayne. "Signal Amplification Methods". En Clinical Virology Manual, 167–72. Washington, DC, USA: ASM Press, 2016. http://dx.doi.org/10.1128/9781555819156.ch14.

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Philippe, Bart y Patrick Reynaert. "Power Amplification". En Analog Circuits and Signal Processing, 69–95. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-11224-9_4.

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Ju, Huangxian, Xueji Zhang y Joseph Wang. "Signal Amplification for Nanobiosensing". En NanoBiosensing, 39–84. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-9622-0_2.

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Ferreira, Mário F. S. "Optical Pulse Amplification". En Optical Signal Processing in Highly Nonlinear Fibers, 73–90. First edition. | Boca Raton, FL : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9780429262111-6.

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Carr, Ronald I., F. Kwan Wong y Damaso Sadi. "Signal Amplification Systems: Substrate Cascade". En Nonradioactive Labeling and Detection of Biomolecules, 240–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-662-00144-8_17.

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Actas de conferencias sobre el tema "Amplification du signal (chimie)"

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Hagag, Mohamed F., Thomas R. Jones, Karim Seddik y Dimitrios Peroulis. "Signal Amplification in Time-Modulated RF Components with Infinite Superluminality". En 2024 IEEE INC-USNC-URSI Radio Science Meeting (Joint with AP-S Symposium), 367. IEEE, 2024. http://dx.doi.org/10.23919/inc-usnc-ursi61303.2024.10632268.

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WenZe, Du, Li XueFeng y Hui Rui. "Signal Format Conversion Based on CNT/PI Waveguide Phase Sensitive Amplification". En 2024 6th International Conference on Natural Language Processing (ICNLP), 763–69. IEEE, 2024. http://dx.doi.org/10.1109/icnlp60986.2024.10692574.

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Sarma, Krishna y Mohd Mansoor Khan. "E-Band Signal Amplification in "Waterless" Thulium-Doped Fibers: Numerical Analysis". En 2024 IEEE 10th International Conference on Photonics (ICP), 18–19. IEEE, 2024. https://doi.org/10.1109/icp60542.2024.10877029.

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Jiang, Sikang, Hongyu Chen, Zhipeng Jia, Zhichao Wang y Ruijie Cai. "A review of ADDoS attack mechanisms, amplification vulnerability discovery, and mitigation". En Fifth International Conference on Signal Processing and Computer Science (SPCS 2024), editado por Haiquan Zhao y Lei Chen, 86. SPIE, 2025. https://doi.org/10.1117/12.3054167.

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SHIKANO, YUTAKA. "ON SIGNAL AMPLIFICATION FROM WEAK-VALUE AMPLIFICATION". En Summer Workshop on Physics, Mathematics, and All That Quantum Jazz. WORLD SCIENTIFIC, 2014. http://dx.doi.org/10.1142/9789814602372_0006.

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Munster, Petr, Josef Vojtech, Petr Sysel, Radim Sifta, Vit Novotny, Tomas Horvath, Stanislav Sima y Miloslav Filka. "Φ-OTDR signal amplification". En SPIE Optics + Optoelectronics, editado por Francesco Baldini, Jiri Homola y Robert A. Lieberman. SPIE, 2015. http://dx.doi.org/10.1117/12.2179026.

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Bel'dyugin, I. M., V. F. Efimkov, I. G. Zubarev y S. I. Mikhailov. "Small signal SBS: amplification". En International Conference on Lasers, Applications, and Technologies '07, editado por Valentin A. Orlovich, Vladislav Panchenko y Ivan A. Scherbakov. SPIE, 2007. http://dx.doi.org/10.1117/12.752884.

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Adler, Karl E., Mary C. Tyler, Alvydas Mikulskis, Mike O'Malley, Jeff J. Broadbent, Eva E. Golenko, Andy L. Johnson, Steve Lott, Anis H. Khimani y Mark N. Bobrow. "Signal amplification on microarrays: techniques and advances in tyramide signal amplification (TSA)". En BiOS 2001 The International Symposium on Biomedical Optics, editado por Michael L. Bittner, Yidong Chen, Andreas N. Dorsel y Edward R. Dougherty. SPIE, 2001. http://dx.doi.org/10.1117/12.427977.

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Shikano, Yutaka. "On signal amplification via weak measurement". En INTERNATIONAL CONFERENCE ON QUANTITATIVE SCIENCES AND ITS APPLICATIONS (ICOQSIA 2014): Proceedings of the 3rd International Conference on Quantitative Sciences and Its Applications. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4903102.

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Shore, K. A. "Small Signal Amplification In Semiconductor Lasers". En Hague International Symposium, editado por M. J. Adams. SPIE, 1987. http://dx.doi.org/10.1117/12.941206.

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Informes sobre el tema "Amplification du signal (chimie)"

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Cromwell, R. Signal Processing Studies Program Optical Signal Amplification. Volume 2. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 1987. http://dx.doi.org/10.21236/ada188054.

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Roehrig, H. y M. Browne. Signal Processing Studies Program Optical Signal Amplification. Volume 1. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 1987. http://dx.doi.org/10.21236/ada188055.

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More, T. Directionality and signal amplification in cryogenic dark matter detection. Office of Scientific and Technical Information (OSTI), mayo de 1996. http://dx.doi.org/10.2172/387535.

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Smith, David A., Alan Willner y Kathryn Li. Optically-Amplified Scalable WDM Networks Using Acousto-Optic Filters for Amplification Gain Equalization and Signal Routing. Fort Belvoir, VA: Defense Technical Information Center, octubre de 1997. http://dx.doi.org/10.21236/ada334120.

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