Relevant bibliographies by topics / Single channel recording

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

Academic literature on the topic 'Single channel recording'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Single channel recording"

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Berg, H. "Single channel recording." Bioelectrochemistry and Bioenergetics 39, no. 1 (February 1996): 152. http://dx.doi.org/10.1016/s0302-4598(96)90039-2.

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Plested, Andrew J. R. "Single-Channel Recording of Ligand-Gated Ion Channels." Cold Spring Harbor Protocols 2016, no. 8 (August 2016): pdb.top087239. http://dx.doi.org/10.1101/pdb.top087239.

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Mortensen, Martin, and Trevor G. Smart. "Single-channel recording of ligand-gated ion channels." Nature Protocols 2, no. 11 (November 2007): 2826–41. http://dx.doi.org/10.1038/nprot.2007.403.

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Franciolini, F., and A. Petris. "Single channel recording and gating function of ionic channels." Experientia 44, no. 3 (March 1988): 183–88. http://dx.doi.org/10.1007/bf01941702.

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Carter, Alison A., and Robert E. Oswald. "Linear prediction and single-channel recording." Journal of Neuroscience Methods 60, no. 1-2 (August 1995): 69–78. http://dx.doi.org/10.1016/0165-0270(94)00221-2.

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Yang, Youshan, and Fred J. Sigworth. "Single-Channel Properties of IKs Potassium Channels." Journal of General Physiology 112, no. 6 (December 1, 1998): 665–78. http://dx.doi.org/10.1085/jgp.112.6.665.

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Expressed in Xenopus oocytes, KvLQT1 channel subunits yield a small, rapidly activating, voltage- dependent potassium conductance. When coexpressed with the minK gene product, a slowly activating and much larger potassium current results. Using fluctuation analysis and single-channel recordings, we have studied the currents formed by human KvLQT1 subunits alone and in conjunction with human or rat minK subunits. With low external K+, the single-channel conductances of these three channel types are estimated to be 0.7, 4.5, and 6.5 pS, respectively, based on noise analysis at 20 kHz bandwidth of currents at +50 mV. Power spectra computed over the range 0.1 Hz–20 kHz show a weak frequency dependence, consistent with current interruptions occurring on a broad range of time scales. The broad spectrum causes the apparent single-channel current value to depend on the bandwidth of the recording, and is mirrored in very “flickery” single-channel events of the channels from coexpressed KvLQT1 and human minK subunits. The increase in macroscopic current due to the presence of the minK subunit is accounted for by the increased apparent single-channel conductance it confers on the expressed channels. The rat minK subunit also confers the property that the outward single-channel current is increased by external potassium ions.
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Dynes, Joseph L., Anna Amcheslavsky, and Michael D. Cahalan. "Genetically targeted single-channel optical recording reveals multiple Orai1 gating states and oscillations in calcium influx." Proceedings of the National Academy of Sciences 113, no. 2 (December 28, 2015): 440–45. http://dx.doi.org/10.1073/pnas.1523410113.

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Orai1 comprises the pore-forming subunit of the Ca2+ release-activated Ca2+ (CRAC) channel. When bound and activated by stromal interacting molecule 1 (STIM1), an endoplasmic reticulum (ER)-resident calcium sensor, Orai1 channels possess high selectivity for calcium but extremely small conductance that has precluded direct recording of single-channel currents. We have developed an approach to visualize Orai1 activity by fusing Orai1 to fluorescent, genetically encoded calcium indicators (GECIs). The GECI–Orai1 probes reveal local Ca2+ influx at STIM1–Orai1 puncta. By whole cell recording, these fusions are fully functional as CRAC channels. When GECI–Orai1 and the CRAC-activating domain (CAD) of STIM1 were coexpressed at low levels and imaged using a total internal reflectance fluorescence microscope, cells exhibited sporadic fluorescence transients the size of diffraction-limited spots and the brightness of a few activated GECI proteins. Transients typically rose rapidly and fell into two classes according to duration: briefer “flickers” lasting only a few hundred milliseconds, and longer “pulses” lasting one to several seconds. The size, intensity, trace shape, frequency, distribution, physiological characteristics, and association with CAD binding together demonstrate that GECI–Orai1 fluorescence transients correspond to single-channel Orai1 responses. Single Orai1 channels gated by CAD, and small Orai1 puncta gated by STIM1, exhibit repetitive fluctuations in single-channel output. CAD binding supports a role in open state maintenance and reveals a second phase of CAD/STIM1 binding after channel opening. These first recordings of single-channel Orai1 currents reveal unexpected dynamics, and when paired with CAD association, support multiple single-channel states.
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Popović, Nenad B., Nadica Miljković, and Mirjana B. Popović. "Simple gastric motility assessment method with a single-channel electrogastrogram." Biomedical Engineering / Biomedizinische Technik 64, no. 2 (April 24, 2019): 177–85. http://dx.doi.org/10.1515/bmt-2017-0218.

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Abstract Surface electrogastrography (EGG) is a non-invasive technique that is used to record myoelectrical activity of the stomach using cutaneous electrodes placed on the abdomen. Gastric motility assessment by EGG is a candidate for standard clinical procedure based on the quantification of parameters characteristic of gastric motility disorders. Despite its noticeable benefits, EGG is not widely implemented in clinical practice. The main reasons are: (1) lack of standardization of electrode placement, (2) time-consuming diagnostic procedures and (3) a complex multi-channel recording setup. We proposed a methodology in which an easy-to-use single-channel EGG, with a less time-consuming protocol (<1 h), would provide sufficient information for gastric motility assessment. Recordings from the three anatomical landmarks in 20 healthy young subjects were compared under two conditions, fasting and postprandial by evaluating the dominant frequency (DF). Our results showed that there is a statistically significant increase of DF after meal ingestion (p<0.05) in each of the three channels. However, when the study group was divided into two subgroups based on body mass index (BMI), the most appropriate recording location was above the body of the stomach (according to statistical significance p=7.82×10−6). We showed that a less time-consuming recording session with light meal intake could be used for the assessment of gastric myoelectrical activity (GMA).
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Schoenfeld, R. L. "From Einthoven's galvanometer to single-channel recording." IEEE Engineering in Medicine and Biology Magazine 21, no. 3 (May 2002): 90–96. http://dx.doi.org/10.1109/memb.2002.1016853.

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Pottosin, Igor I. "Single channel recording in the chloroplast envelope." FEBS Letters 308, no. 1 (August 10, 1992): 87–90. http://dx.doi.org/10.1016/0014-5793(92)81057-s.

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Dissertations / Theses on the topic "Single channel recording"

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Weatherill, Eve Elizabeth. "Combining single-molecule fluorescence and single-channel recording in droplet interface bilayers." Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:99610130-0550-4dd9-b6ee-6ce2297a5bb9.

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Single-channel recordings (SCR) and single-molecule Fluorescence (SMF) are invaluable tools for studying membrane proteins. Combining these two techniques would allow for structural dynamics to be correlated with function at the single-molecule level. However, the different requirements of SCR and SMF measurements present a long-standing challenge. Droplet interface bilayers (DIBs) are a model membrane system in which parallelisation of such measurements is possible using optical single-channel recording to resolve the conductance of multiple proteins simultaneously. In this project, two approaches were evaluated for obtaining simultaneous measurements in DIBs: the first sought to report on structural changes associated with a gating bacterial mechanosensitive channel, MscS; the second sought to resolve kinetics of the spontaneous β-barrel folding mechanism. For both approaches, functional, labelled protiens were produced and characterised using ensemble measurements to confirm that the state-transition of interest was accompanied by a change in fluorescent signal. Characterisation of MscS in DIBs revealed that control of lateral tension (a requirement to stimulate mechanosensitive channel gating) posed a major experimental challenge, rendering further pursuit of this candidate impossible. However in the case of β-barrel folding, the single-molecule fluorescence alone revealed a rare but fast transition from a membrane-associated unfolded to a folded state. While further work is needed to fully exploit simultaneous measurements, significant progress towards this goal is presented in this work, in particular the development of reagents, experimental procedures and analytical tools.
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Spruce, Austen Edwin. "Potassium conductances of skeletal muscle investigated using single channel recording." Thesis, University of Leicester, 1986. http://hdl.handle.net/2381/33614.

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This thesis describes studies of unitary currents flowing through two different potassium (K) channels present in sarcolemmal vesicles of the frog, Rana temporaria. The ATP-regulated K-channel is described first and the results are divided into three parts. Firstly, ATP applied to the cytoplasmic face of a membrane patch closes the channels in a dose-dependent fashion. Different nucleotides and other metabolic substances are used in order to find chemicals which can substitute for ATP or which regulate its effect. Secondly, the permeability properties of the channel are described. Ion flux is non-independent. Rubidium (Rb) is permeant, and anomalous mole-fraction behaviour is demonstrated in mixtures of K+and Rb+. The final part investigates the kinetic properties of the channel. Both voltage and ATP affect the rate constants regulating transitions between closed and open states of the channel. In particular, ATP causes the channel to occupy a very long-lived closed state. Block of the channel by tetraethylammonium (TEA) ions applied to either membrane surface is described as well. Block by external TEA+ is very fast and it is suggested that the channel cannot close when blocked. The block by internal TEA+ is slower and some evidence of voltage dependency is seen. The delayed rectifier K-channel is investigated. The first of two parts describes Rb+ permeability of the channel and its effect on open and closed times. The Hodgkin-Huxley model of the channel is questioned by the very different times of occupancy of closed states and differing voltage dependencies of the steps leading to opening of the channel. The second part describes block of the channel by externally applied TEA+ and the blocking reaction is shown to be very fast and voltage dependent.
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Cao, Tuoxin. "Hydrogen Peroxide and Pharmacological Agent Modulation of TRPV2 Channel Gating." VCU Scholars Compass, 2017. http://scholarscompass.vcu.edu/etd/4848.

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Transient receptor potential vanilloid 2 channel (TRPV2) is a Ca2+-permeable ion channel that is highly expressed in leukocytes but is also present in skeletal and cardiac muscle and endocrine cells. The TRPV2 function is implicated in a number of physiological processes, including bacterial phagocytosis, pro-inflammatory cytokine production, cardiac hypertrophy, and cancer development. TRPV2 knockout mice exhibit a high incidence of perinatal mortality, arguing that the channel plays essential roles in physiology. Despite the importance of TRPV2 for normal homeostasis, the mechanisms that control TRPV2 gating in response to pharmacological agonists, heating, membrane stretch, bioactive lipids and reactive oxygen species (ROS) remain poorly understood. Here we demonstrate that TRPV2 is functionally expressed in microglia (i.e., ‘brain macrophages’) and the microglia-like BV-2 cell line, and demonstrate that the gating of an endogenous TRPV2-like conductance is positively modulated by the bacterial toxin lipopolysaccharide (LPS), which is known to cause pro-inflammatory (M1) activation and increase ROS production by NADPH oxidase. To determine how TRPV2 gating is modulated by ROS, we recorded single channel activity in inside-out patches excised from HEK-293 cells expressing GFP-rTRPV2. Unitary currents elicited by the TRPV2 agonist 2-aminophenyl borinate (2-APB) or cannabidiol (CBD) are linear in monovalent recording solutions and give rise to an estimated unitary conductance of ~100pS, which is similar to TRPV1 but significantly smaller than TRPV3. Intriguingly, we find that although TRPV2 is insensitive to ROS (in the form of exogenously applied H2O2) alone, apparent open probability is synergistically enhanced when H2O2 is applied together with CBD. We identify two intracellular Cys residues that are necessary for TRPV2 responses to H2O2 sensitivity and find that these residues are located close to one another, albeit in different subunits, in the TRPV2 structure, suggesting that ROS promote the formation of an inter-subunit disulfide bond that alters sensitivity to pharmacological agonists. We hypothesize that ROS-dependent modulation of TRPV2 activity may be an important contributor to pro-inflammatory activation of microglia underline central nervous system diseases and that TRPV2 antagonism could be a useful therapeutic strategy in the treatment of neuroinflammation.
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Appenrodt, Peter. "Single-channel recordings of potassium channels from guinea-pig inner hair cells." Thesis, University of Sussex, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390054.

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Spreadbury, Ian Clive. "Single channel recordings form the BK channels of outer hair cells of the guinea pig cochlea." Thesis, University of Bristol, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.322611.

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Thei, Federico <1976&gt. "A hybrid technology for parallel recording of single ion channels." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2011. http://amsdottorato.unibo.it/3594/.

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Hybrid technologies, thanks to the convergence of integrated microelectronic devices and new class of microfluidic structures could open new perspectives to the way how nanoscale events are discovered, monitored and controlled. The key point of this thesis is to evaluate the impact of such an approach into applications of ion-channel High Throughput Screening (HTS)platforms. This approach offers promising opportunities for the development of new classes of sensitive, reliable and cheap sensors. There are numerous advantages of embedding microelectronic readout structures strictly coupled to sensing elements. On the one hand the signal-to-noise-ratio is increased as a result of scaling. On the other, the readout miniaturization allows organization of sensors into arrays, increasing the capability of the platform in terms of number of acquired data, as required in the HTS approach, to improve sensing accuracy and reliabiity. However, accurate interface design is required to establish efficient communication between ionic-based and electronic-based signals. The work made in this thesis will show a first example of a complete parallel readout system with single ion channel resolution, using a compact and scalable hybrid architecture suitable to be interfaced to large array of sensors, ensuring simultaneous signal recording and smart control of the signal-to-noise ratio and bandwidth trade off. More specifically, an array of microfluidic polymer structures, hosting artificial lipid bilayers blocks where single ion channel pores are embededed, is coupled with an array of ultra-low noise current amplifiers for signal amplification and data processing. As demonstrating working example, the platform was used to acquire ultra small currents derived by single non-covalent molecular binding between alpha-hemolysin pores and beta-cyclodextrin molecules in artificial lipid membranes.
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Every, Mark Robert. "Separation of musical sources and structure from single-channel polyphonic recordings." Thesis, University of York, 2006. http://etheses.whiterose.ac.uk/9883/.

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Jiminez, Gonzalez Aida. "Antenatal foetal monitoring through abdominal phonogram recordings : a single-channel independent component analysis approach." Thesis, University of Southampton, 2010. https://eprints.soton.ac.uk/190815/.

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El, halabi Ramzi. "Blind source separation of single-sensor recordings : Application to ground reaction force signals." Thesis, Lyon, 2018. http://www.theses.fr/2018LYSES031/document.

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Les signaux multicanaux sont des signaux captés à travers plusieurs canaux ou capteurs, portant chacun un mélange de sources, une partie desquelles est connue alors que le reste des sources reste inconnu. Les méthodes à l’aide desquelles l’isolement ou la séparation des sources est accomplie sont connues par les méthodes de séparation de sources en général, et si le degré d’inconnu est large, par la séparation aveugle des sources (SAS). Cependant, la SAS appliquée aux signaux multicanaux est en fait plus facile de point de vue mathématique que l’application de la SAS sur des signaux monocanaux, ou un seul capteur existe et tous les signaux arrivent au même point pour enfin produire un mélange de sources inconnues. Tel est le domaine de cette thèse. Nous avons développé une nouvelle technique de SAS : une combinaison de plusieurs méthodes de séparation et d’optimisation, basée sur la factorisation non-négative des matrices (NMF). Cette méthode peut être utilisée dans de nombreux domaines comme l’analyse des sons et de la parole, les variations de la bourse, et les séismographes. Néanmoins, ici, les signaux de force de réaction de terre verticaux (VGRF) monocanaux d’un groupe d’athlètes coureurs d’ultra-marathon sont analysés et séparés pour l’extraction du peak passif du peak actif d’une nouvelle manière adaptée à la nature de ces signaux. Les signaux VGRF sont des signaux cyclo-stationnaires caractérisés par des double-peaks, chacun étant très rapide et parcimonieux, indiquant les phases de course de l’athlète. L’analyse des peaks est extrêmement importante pour déterminer et prédire la condition du coureur : problème physiologique, problème anatomique, fatigue etc. De plus, un grand nombre de chercheurs ont prouvé que l’impact du pied postérieur avec la terre d’une manière brutale, l’analyse de ce phénomène peut nous ramener à une prédiction de blessure interne. Ils essayent même d’adopter une technique de course - Non-Heel-strike Running (NHS) - par laquelle ils obligent les coureurs à courir sur le pied-antérieur seulement. Afin d'étudier ce phénomène, la séparation du peak d’impact du VGRF permet d'isoler la source portant les informations patho-physiologiques et le degré de fatigue. Nous avons introduit de nouvelles méthodes de prétraitement et de traitement des signaux VGRF pour remplacer le filtrage de bruit traditionnel utilisé partout, et qui peut parfois détruire les peaks d’impact qui sont nos sources à séparer, base sur le concept de soustraction spectrale pour le filtrage, utilisée avec les signaux de parole, après l’application d’un algorithme d’échantillonnage intelligent et adaptatif qui décompose les signaux en pas isolés. Une analyse des signaux VGRF en fonction du temps a été faite pour la détection et la quantification de la fatigue des coureurs durant les 24 heures de course. Cette analyse a été accomplie au domaine fréquentiel/spectral où nous avons détecté un décalage clair du contenu fréquentiel avec la progression de la course indiquant la progression de la fatigue. Nous avons défini les signaux cyclosparse au domaine temporel, puis traduit cette définition à son équivalent au domaine temps-fréquence utilisant la transformée Fourier a court-temps (STFT). Cette représentation a été décomposée à travers une nouvelle méthode que l’on a appelé Cyclosparse Non-negative Matrix Factorisation (Cyclosparse-NMF), basée sur l’optimisation de la minimisation de la divergence Kullback-Leibler (KL) avec pénalisation liée à la périodicité et la parcimonie des sources, ayant comme but final d’extraire les sources cyclosparse du mélange monocanal appliquée aux signaux VGRF monocanaux. La méthode a été testée sur des signaux analytiques afin de prouver l’efficacité de l’algorithme. Les résultats se sont avéré satisfaisants, et le peak impact a été séparé du mélange VGRF monocanal
The purpose of the presented work is to develop a customized Single-channel Blind Source Separation technique that aims to separate cyclostationary and transient pulse-like patterns/sources from a linear instantaneous mixture of unknown sources. For that endeavor, synthetic signals of the mentioned characteristic were created to confirm the separation success, in addition to real life signals acquired throughout an experiment in which experienced athletes were asked to participate in a 24-hour ultra-marathon in a lab environment on an instrumented treadmill through which their VGRF, which carries a cyclosparse Impact Peak, is continuously recorded with very short discontinuities during which blood is drawn for in-run testing, short enough not to provide rest to the athletes. The synthetic and VGRF signals were then pre-processed, processed for Impact Pattern extraction via a customized Single-channel Blind Source Separation technique that we termed Cyclo-sparse Non-negative Matrix Factorization and analyzed for fatigue assessment. As a result, the Impact Patterns for all of the participating athletes were extracted at 10 different time intervals indicating the progression of the ultra-marathon for 24 hours, and further analysis and comparison of the resulting signals proved major significance in the field of fatigue assessment; the Impact Pattern power monotonically increased for 90% of the subjects by an average of 24.4 15% with the progression of the ultra-marathon during the 24-hour period. Upon computation of the Impact Pattern separation algorithm, fatigue progression showed to be manifested by an increase in reliance on heel-strike impact to push to the bodyweight as a compensation for the decrease in muscle power during propulsion at toe-off. This study among other presented work in the field of VGRF processing forms methods that could be implemented in wearable devices to assess and track runners’ gait as a part of sports performance analysis, rehabilitation phase tracking and classification of healthy vs. unhealthy gait
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Kreir, Mohamed [Verfasser]. "Lipid membranes on microstructured glass : Electrophysiological single channels recordings of reconstituted proteins / Mohamed Kreir. Nanion Technologies GmbH." Bremen : IRC-Library, Information Resource Center der Jacobs University Bremen, 2010. http://d-nb.info/1034989294/34.

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Books on the topic "Single channel recording"

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Sakmann, Bert, and Erwin Neher, eds. Single-Channel Recording. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-7858-1.

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Sakmann, Bert, and Erwin Neher, eds. Single-Channel Recording. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9.

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Sakmann, Bert. Single-Channel Recording. Boston, MA: Springer Science+Business Media, LLC, 2009.

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Single-Channel Recording. 2nd ed. Springer, 2007.

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1942-, Sakmann Bert, and Neher Erwin 1944-, eds. Single-channel recording. 2nd ed. New York: Plenum Press, 1995.

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Coleman, William L., and R. Michael Burger. Extracellular Single-Unit Recording and Neuropharmacological Methods. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199939800.003.0003.

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Small biogenic changes in voltage such as action potentials in neurons can be monitored using extracellular single unit recording techniques. This technique allows for investigation of neuronal electrical activity in a manner that is not disruptive to the cell membrane, and individual neurons can be recorded from for extended periods of time. This chapter discusses the basic requirements for an extracellular recording setup, including different types of electrodes, apparatus for controlling electrode position and placement, recording equipment, signal output, data analysis, and the histological confirmation of recording sites usually required for in vivo recordings. A more advanced extracellular recording technique using piggy-back style multibarrel electrodes that allows for localized pharmacological manipulation of neuronal properties is described in detail. Strategies for successful signal isolation, troubleshooting advice such as noise reduction, and suggestions for general laboratory equipment are also discussed.
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Stålberg, Erik. Electromyography. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0007.

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Electromyography (EMG) has been used since the 1940s in the diagnosis of neuromuscular disorders. It has particularly developed with the advent of computers and recording equipment with integrated software. This has made methods of analysis fast, robust, and precise, helping to deal with increasing numbers of patients. Indications have changed dynamically over the years, with the development of new EMG methods themselves and complementary methods used in this field for diagnosis such as histochemistry, genetics, and imaging techniques. This chapter focuses mainly on the routine methods based on recordings with concentric or monopolar needle electrodes, but will also briefly review some of the other EMG methods. There is an increasing understanding of the relationship between the generators (muscle fibres) and the recorded signal that helps interpretation of the recordings. The parameters used for quantitation of the EMG signal are discussed. The findings in pathological conditions are discussed and some practical hints on EMG studies given.
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Maslon, Laurence. A Few of My Favorite Things. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199832538.003.0010.

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The technology to reproduce a film’s soundtrack for home consumption didn’t arrive fully until the early 1950s; it was no surprise that the Capitol soundtrack recording to the 1955 film of Oklahoma! was the biggest seller of its day. Film soundtracks gave home listeners a second chance to hear their favorite scores and often, as in the case of West Side Story, the film soundtrack provided a new opportunity to discover the music (that soundtrack stayed longer at No. 1 than any album in history to this day). The performer who sold more soundtrack albums than anyone else in the 1960s was Julie Andrews, whose simultaneous recordings of the films Mary Poppins and The Sound of Music made her the most ubiquitous singer in pop culture.
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Cook, Nicholas. Seeing Sound, Hearing the Body. Edited by Yael Kaduri. Oxford University Press, 2016. http://dx.doi.org/10.1093/oxfordhb/9780199841547.013.7.

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This chapter argues that visual and embodied dimensions of performance are integral to the experience of live music. The author describes this as the “old multimedia,” since the principles of intermedial alignment and meaning production in performance are in essence the same as in the “new multimedia” that forms the dominant mode of music consumption in the twenty-first century. The chapter largely consists of an extended case study based on two filmed performances by Glenn Gould of the first movement of Anton Webern’sPiano Variations, Op. 27. It addresses the role in Gould’s interpretations of hand lifts, body sway, and other physical gestures; the way in which his interpretation changed over time, as evidenced not only by these filmed performances but also by his audio recordings; the differences between interpretations designed for film and for sound recording; and what all this implies about the relationship between composer and performer.
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Vassanelli, Stefano. Implantable neural interfaces. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199674923.003.0050.

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Establishing direct communication with the brain through physical interfaces is a fundamental strategy to investigate brain function. Starting with the patch-clamp technique in the seventies, neuroscience has moved from detailed characterization of ionic channels to the analysis of single neurons and, more recently, microcircuits in brain neuronal networks. Development of new biohybrid probes with electrodes for recording and stimulating neurons in the living animal is a natural consequence of this trend. The recent introduction of optogenetic stimulation and advanced high-resolution large-scale electrical recording approaches demonstrates this need. Brain implants for real-time neurophysiology are also opening new avenues for neuroprosthetics to restore brain function after injury or in neurological disorders. This chapter provides an overview on existing and emergent neurophysiology technologies with particular focus on those intended to interface neuronal microcircuits in vivo. Chemical, electrical, and optogenetic-based interfaces are presented, with an analysis of advantages and disadvantages of the different technical approaches.
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Book chapters on the topic "Single channel recording"

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Wyllie, David J. A. "Single-Channel Recording." In Neuromethods, 69–119. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-492-6_3.

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Benndorf, Klaus. "Low-Noise Recording." In Single-Channel Recording, 129–45. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_5.

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Penner, Reinhold. "A Practical Guide to Patch Clamping." In Single-Channel Recording, 3–30. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_1.

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Jonas, Peter. "Fast Application of Agonists to Isolated Membrane Patches." In Single-Channel Recording, 231–43. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_10.

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Chow, Robert H., and Ludolf Von Rüden. "Electrochemical Detection of Secretion from Single Cells." In Single-Channel Recording, 245–75. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_11.

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Hedrich, Rainer. "Technical Approaches to Studying Specific Properties of Ion Channels in Plants." In Single-Channel Recording, 277–305. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_12.

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Hilgemann, Donald W. "The Giant Membrane Patch." In Single-Channel Recording, 307–27. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_13.

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McBride, Don W., and Owen P. Hamill. "A Fast Pressure-Clamp Technique for Studying Mechanogated Channels." In Single-Channel Recording, 329–40. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_14.

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Stühmer, Walter, and Anant B. Parekh. "Electrophysiological Recordings from Xenopus Oocytes." In Single-Channel Recording, 341–56. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_15.

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Monyer, Hannah, and Peter Jonas. "Polymerase Chain Reaction Analysis of Ion Channel Expression in Single Neurons of Brain Slices." In Single-Channel Recording, 357–73. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4419-1229-9_16.

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Conference papers on the topic "Single channel recording"

1

Rossi, M., M. Bennati, F. Lodesani, S. Branchetti, and M. Tartagni. "A Compact System for Single Ion Channel Recording." In 2007 IEEE Sensors. IEEE, 2007. http://dx.doi.org/10.1109/icsens.2007.4388607.

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Jalilifard, Amir, Ednaldo Brigante Pizzolato, and Md Kafiul Islam. "Emotion classification using single-channel scalp-EEG recording." In 2016 38th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2016. http://dx.doi.org/10.1109/embc.2016.7590833.

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Almustapha, Mohammed D., Muhammad B. Abdulrazaq, Mohammed Z. Ahmed, Ambroze A. Marcel, and Davey Paul. "Decoding and detection for magnetic recording channel using single parity coding." In 2016 Asia-Pacific Magnetic Recording Conference (APMRC). IEEE, 2016. http://dx.doi.org/10.1109/apmrc.2016.7524256.

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Li, Haitao, Sina Parsnejad, and Andrew J. Mason. "Single ion channel CMOS electrochemical instrument for high throughput recording arrays." In 2015 IEEE 58th International Midwest Symposium on Circuits and Systems (MWSCAS). IEEE, 2015. http://dx.doi.org/10.1109/mwscas.2015.7282111.

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Calderon-Piedras, Juan S., Alvaro D. Orjuela-Canon, and David A. Sanabria-Quiroga. "Blind source separation from single channel audio recording using ICA algorithms." In 2014 XIX Symposium on Image, Signal Processing and Artificial Vision (STSIVA). IEEE, 2014. http://dx.doi.org/10.1109/stsiva.2014.7010168.

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Xue-Cheng Jin and Zeng-Fu Wang. "Speech Separation from Background of Music Based on Single-channel Recording." In 18th International Conference on Pattern Recognition (ICPR'06). IEEE, 2006. http://dx.doi.org/10.1109/icpr.2006.1075.

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Zhong, Wei, Zhongping Cao, Xuemei Guo, and Guoli Wang. "A Novel Framework for Maternal ECG Removal from Single-Channel Abdominal Recording." In 2019 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2019. http://dx.doi.org/10.1109/bibm47256.2019.8983397.

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Li, Guojun, Xiaoping Zeng, Xiaona Zhou, Guojun Li, and Qilie Liu. "Robust adaptive fetal heart rate estimation for single-channel abdominal ECG recording." In 2012 5th International Conference on Biomedical Engineering and Informatics (BMEI). IEEE, 2012. http://dx.doi.org/10.1109/bmei.2012.6513193.

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Zhao, Kunyuan, and Dan Xu. "Food Image-Induced Discrete Emotion Recognition Using a Single-Channel Scalp-EEG Recording." In 2019 12th International Congress on Image and Signal Processing, BioMedical Engineering and Informatics (CISP-BMEI). IEEE, 2019. http://dx.doi.org/10.1109/cisp-bmei48845.2019.8966064.

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Jalilifard, Amir, and Ednaldo Brigante Pizzolato. "An efficient K-NN approach for automatic drowsiness detection using single-channel EEG recording." In 2016 38th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2016. http://dx.doi.org/10.1109/embc.2016.7590827.

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