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Journal articles on the topic 'Single cell recordings'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 March 2023

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1

Hardcastle, Valerie Gray, and C. Matthew Stewart. "Neuroscience and the Art of Single Cell Recordings." Biology & Philosophy 18, no. 1 (2003): 195–208. http://dx.doi.org/10.1023/a:1023356317286.

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2

Meyburg, Sven, Günter Wrobel, Regina Stockmann, Jürgen Moers, Sven Ingebrandt, and Andreas Offenhäusser. "Single cell recordings with pairs of complementary transistors." Applied Physics Letters 89, no. 1 (2006): 013901. http://dx.doi.org/10.1063/1.2219339.

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3

Gubian, Michele, Colin J. Davis, James S. Adelman, and Jeffrey S. Bowers. "Comparing single-unit recordings taken from a localist model to single-cell recording data: a good match." Language, Cognition and Neuroscience 32, no. 3 (2016): 380–91. http://dx.doi.org/10.1080/23273798.2016.1259482.

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4

Du, Jiangang, Ingmar H. Riedel-Kruse, Janna C. Nawroth, Michael L. Roukes, Gilles Laurent, and Sotiris C. Masmanidis. "High-Resolution Three-Dimensional Extracellular Recording of Neuronal Activity With Microfabricated Electrode Arrays." Journal of Neurophysiology 101, no. 3 (2009): 1671–78. http://dx.doi.org/10.1152/jn.90992.2008.

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Microelectrode array recordings of neuronal activity present significant opportunities for studying the brain with single-cell and spike-time precision. However, challenges in device manufacturing constrain dense multisite recordings to two spatial dimensions, whereas access to the three-dimensional (3D) structure of many brain regions appears to remain a challenge. To overcome this limitation, we present two novel recording modalities of silicon-based devices aimed at establishing 3D functionality. First, we fabricated a dual-side electrode array by patterning recording sites on both the fron

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5

Krenkel, Martin, Mareike Toepperwien, Frauke Alves, and Tim Salditt. "Three-dimensional single-cell imaging with X-ray waveguides in the holographic regime." Acta Crystallographica Section A Foundations and Advances 73, no. 4 (2017): 282–92. http://dx.doi.org/10.1107/s2053273317007902.

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X-ray tomography at the level of single biological cells is possible in a low-dose regime, based on full-field holographic recordings, with phase contrast originating from free-space wave propagation. Building upon recent progress in cellular imaging based on the illumination by quasi-point sources provided by X-ray waveguides, here this approach is extended in several ways. First, the phase-retrieval algorithms are extended by an optimized deterministic inversion, based on a multi-distance recording. Second, different advanced forms of iterative phase retrieval are used, operational for singl

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Rey, Hernan G., Matias J. Ison, Carlos Pedreira, et al. "Single-cell recordings in the human medial temporal lobe." Journal of Anatomy 227, no. 4 (2014): 394–408. http://dx.doi.org/10.1111/joa.12228.

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7

Li, W. C., S. R. Soffe, and Alan Roberts. "A Direct Comparison of Whole Cell Patch and Sharp Electrodes by Simultaneous Recording From Single Spinal Neurons in Frog Tadpoles." Journal of Neurophysiology 92, no. 1 (2004): 380–86. http://dx.doi.org/10.1152/jn.01238.2003.

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High-impedance, sharp intracellular electrodes were compared with whole cell patch electrodes by recording from single spinal neurons in immobilized frog tadpoles. A range of neuron properties were examined using sharp or patch test electrodes while making simultaneous recordings with a second control patch electrode. Overall, test patch electrodes did not significantly alter the activity recorded by the control electrode, and recordings from the two electrodes were essentially identical. In contrast, sharp electrode recordings differed from initial control patch recordings. In some cases, dif

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8

Vaithianathan, Thirumalini, Kandiah Manivannan, Ralf Kleene, et al. "Single Channel Recordings From Synaptosomal AMPA Receptors." Cell Biochemistry and Biophysics 42, no. 1 (2005): 075–86. http://dx.doi.org/10.1385/cbb:42:1:075.

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9

Lu, Huo, Mitra J. Hartmann, and James M. Bower. "Correlations Between Purkinje Cell Single-Unit Activity and Simultaneously Recorded Field Potentials in the Immediately Underlying Granule Cell Layer." Journal of Neurophysiology 94, no. 3 (2005): 1849–60. http://dx.doi.org/10.1152/jn.01275.2004.

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Evidence from both anatomical and physiological studies suggests that the ascending segment of the granule cell axon provides a large, driving input to overlying Purkinje cells. In the current experiments, we used dual recording electrodes to simultaneously record spike activity of Purkinje cells and multiunit field potential activity in the directly underlying granule cell layer. These dual recordings were performed both during periods of spontaneous (“background”) firing and also after peripheral tactile stimulation. The results demonstrate that in the large majority of cases, there is a str

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10

Bruhn, Brandon R., Haiyan Liu, Stefan Schuhladen, Alan J. Hunt, Aghapi Mordovanakis, and Michael Mayer. "Dual-pore glass chips for cell-attached single-channel recordings." Lab Chip 14, no. 14 (2014): 2410–17. http://dx.doi.org/10.1039/c4lc00370e.

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11

Duong Dinh, Thien An, Eberhard Jüngling, Karl-Heinz Strotmann, Martin Westhofen, and Andreas Lückhoff. "Ultrasonic bath depth control and regulation in single cell recordings." Pflügers Archiv - European Journal of Physiology 452, no. 6 (2006): 784–88. http://dx.doi.org/10.1007/s00424-006-0090-5.

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12

Hamilton, K. L., and D. C. Eaton. "Single-channel recordings from amiloride-sensitive epithelial sodium channel." American Journal of Physiology-Cell Physiology 249, no. 3 (1985): C200—C207. http://dx.doi.org/10.1152/ajpcell.1985.249.3.c200.

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We report here the first evidence in intact epithelial cells of unit conductance events from an amiloride-sensitive Na+ channel. The events were observed when patch-clamp recordings were made from the apical surface of cultured epithelial kidney cells (A6). The channel characteristics are as follows. Single-channel conductance ranged between 7 and 10 pS (mean = 8.4 +/- 1.3), the current-voltage (I-V) relationship displayed little if any nonlinearity over a range of +/- 80 mV (with respect to the patch pipette), and the channel Na+/K+ selectivity was approximately 3-4:1. Amiloride, a cationic b

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13

Rae, JL, and J. Fernandez. "Perforated Patch Recordings in Physiology." Physiology 6, no. 6 (1991): 273–77. http://dx.doi.org/10.1152/physiologyonline.1991.6.6.273.

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Perforated patch techniques allow measurement of cell voltages, currents, and capacitance without an electrode penetrating thy cytosol. Since intracellular messengers and regulators are not washed out, physiological processes run down slowly. In perforated outside-out vesicles, single-channel currents can be measured while their regulatory cascades remain intact.

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14

Zechner, Christoph, Michael Unger, Serge Pelet, Matthias Peter, and Heinz Koeppl. "Scalable inference of heterogeneous reaction kinetics from pooled single-cell recordings." Nature Methods 11, no. 2 (2014): 197–202. http://dx.doi.org/10.1038/nmeth.2794.

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15

Bronstein, L., C. Zechner, and H. Koeppl. "Bayesian inference of reaction kinetics from single-cell recordings across a heterogeneous cell population." Methods 85 (September 2015): 22–35. http://dx.doi.org/10.1016/j.ymeth.2015.05.012.

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16

Zheng, Jie. "Patch Fluorometry: Shedding New Light on Ion Channels." Physiology 21, no. 1 (2006): 6–12. http://dx.doi.org/10.1152/physiol.00041.2005.

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Patch fluorometry has emerged as a new approach to the study of the structure-function relationship in membrane-embedded functional ion channels. Simultaneous fluorescent and electrical recordings are achieved from a small number of channels in a cell-free membrane patch, yielding high recording sensitivities. Further improvement of this approach should permit direct observation of the gating motion of a single-channel protein.

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17

Anastassiou, Costas A., Rodrigo Perin, György Buzsáki, Henry Markram, and Christof Koch. "Cell type- and activity-dependent extracellular correlates of intracellular spiking." Journal of Neurophysiology 114, no. 1 (2015): 608–23. http://dx.doi.org/10.1152/jn.00628.2014.

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Despite decades of extracellular action potential (EAP) recordings monitoring brain activity, the biophysical origin and inherent variability of these signals remain enigmatic. We performed whole cell patch recordings of excitatory and inhibitory neurons in rat somatosensory cortex slice while positioning a silicon probe in their vicinity to concurrently record intra- and extracellular voltages for spike frequencies under 20 Hz. We characterize biophysical events and properties (intracellular spiking, extracellular resistivity, temporal jitter, etc.) related to EAP recordings at the single-neu

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18

Sturgess, N. C., M. L. J. Ashford, C. A. Carrington, and C. N. Hales. "Single channel recordings of potassium currents in an insulin-secreting cell line." Journal of Endocrinology 109, no. 2 (1986): 201–7. http://dx.doi.org/10.1677/joe.0.1090201.

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ABSTRACT Using the patch-clamp technique we observed three distinct classes of K+ channels which were spontaneously active in excised 'inside-out' membrane patches from an insulin-secreting rat pancreatic islet cell line (CRI-G1). Two of these occurred infrequently, one with a conductance of approximately 7 pS, and the other a conductance of 220 pS. The activation of the 220 pS K+ channel was dependent upon the membrane voltage and was sensitive to the concentration of calcium ions at the cytoplasmic surface of the membrane. The third, and by far the most common class of K+ channel, was charac

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19

Jackson, Andrew, and Eberhard E. Fetz. "Compact Movable Microwire Array for Long-Term Chronic Unit Recording in Cerebral Cortex of Primates." Journal of Neurophysiology 98, no. 5 (2007): 3109–18. http://dx.doi.org/10.1152/jn.00569.2007.

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We describe a small, chronically implantable microwire array for obtaining long-term unit recordings from the cortex of unrestrained nonhuman primates. After implantation, the depth of microwires can be individually adjusted to maintain large-amplitude action potential recordings from single neurons over many months. We present data recorded from the primary motor cortex of two monkeys by autonomous on-board electronic circuitry. Waveforms of individual neurons remained stable for recording periods of several weeks during unrestrained behavior. Signal-to-noise ratios, waveform stability, and r

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20

Eliasof, Scott, and Craig E. Jahr. "Rapid AMPA receptor desensitization in catfish cone horizontal cells." Visual Neuroscience 14, no. 1 (1997): 13–18. http://dx.doi.org/10.1017/s0952523800008713.

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AbstractAMPA and NMDA type glutamate receptors were studied in isolated catfish cone horizontal cells using the whole-cell and outside-out patch-recording techniques. In whole-cell recordings, cyclothiazide (CTZ) enhanced the peak current in response to glutamate (in the presence of NMDA receptor antagonists). In patch recordings, currents evoked by rapid and maintained applications of glutamate desensitized with a time constant of one millisecond. CTZ blocked this rapid desensitization. Recovery from desensitization of the AMPA receptors was rapid, having a time constant of 8.65 ms. In contra

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21

Gommerat, I., G. Jacquet, H. Chagneux, and M. Gola. "Single-channel and whole-cell recordings from on-neurone glial cells in Helix pomatia ganglia." Journal of Neuroscience Methods 50, no. 2 (1993): 243–51. http://dx.doi.org/10.1016/0165-0270(93)90013-h.

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22

Devor, D. C., J. N. Forrest, W. K. Suggs, and R. A. Frizzell. "cAMP-activated Cl- channels in primary cultures of spiny dogfish (Squalus acanthias) rectal gland." American Journal of Physiology-Cell Physiology 268, no. 1 (1995): C70—C79. http://dx.doi.org/10.1152/ajpcell.1995.268.1.c70.

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Whole cell and single-channel patch-clamp techniques were used to identify and characterize the Cl- currents responsible for adenosine 3',5'-cyclic monophosphate (cAMP)-mediated Cl- secretion in the rectal gland of the spiny dogfish (Squalus acanthias). During whole cell recordings, in cultured rectal gland cells forskolin (10 microM) and 8-(4-chlorophenylthio)adenosine 3',5'-cyclic monophosphate (400 microM) stimulated a 28-fold increase in Cl- conductance (n = 10). This cAMP-activated conductance pathway had a linear current-voltage (I-V) relationship that was time and voltage independent. S

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23

Fox, J. A., B. A. Pfeffer, and G. L. Fain. "Single-channel recordings from cultured human retinal pigment epithelial cells." Journal of General Physiology 91, no. 2 (1988): 193–222. http://dx.doi.org/10.1085/jgp.91.2.193.

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We have applied patch-clamp techniques to on-cell and excised-membrane patches from human retinal pigment epithelial cells in tissue culture. Single-channel currents from at least four ion channel types were observed: three or more potassium-selective channels with single-channel slope conductances near 100, 45, and 25 pS as measured in on-cell patches with physiological saline in the pipette, and a relatively nonselective channel with subconductance states, which has a main-state conductance of approximately 300 pS at physiological ion concentrations. The permeability ratios, PK/PNa, measured

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24

Edelmann, Elke, and Volkmar Leßmann. "Analyzing synaptic plasticity at the single cell level with STDP." Neuroforum 24, no. 3 (2018): A143—A150. http://dx.doi.org/10.1515/nf-2017-a064.

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Abstract Using patch clamp recordings in acutely isolated brain slices allows to investigate molecular processes that are involved in long-term potentiation (LTP) and long-term depression (LTD) at the level of a single postsynaptic neuron. Via the pipette solution in the recording pipette, it is possible to apply inhibitors of signaling cascades selectively into the postsynaptic neuron to unravel the molecular mechanisms of synaptic plasticity. In recent years, LTP research has been increasingly focused on induction protocols for LTP and LTD that rely on a minimal number of repeated synaptic s

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25

Ding, S., and F. Sachs. "Ion Permeation and Block of P2X 2 Purinoceptors: Single Channel Recordings." Journal of Membrane Biology 172, no. 3 (1999): 215–23. http://dx.doi.org/10.1007/s002329900598.

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26

Schaper, Frédéric L. W. V. J., Yan Zhao, Marcus L. F. Janssen, et al. "Single-Cell Recordings to Target the Anterior Nucleus of the Thalamus in Deep Brain Stimulation for Patients with Refractory Epilepsy." International Journal of Neural Systems 29, no. 04 (2019): 1850012. http://dx.doi.org/10.1142/s0129065718500120.

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Deep brain stimulation (DBS) of the anterior nucleus of the thalamus (ANT) is a promising treatment for patients with refractory epilepsy. However, therapy response varies and precise positioning of the DBS lead is potentially essential for maximizing therapeutic efficacy. We investigate if single-cell recordings acquired by microelectrode recordings can aid targeting of the ANT during surgery and hypothesize that the neuronal firing properties of the target region relate to clinical outcome. We prospectively included 10 refractory epilepsy patients and performed microelectrode recordings unde

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27

Sanchez-Aguilera, Alberto, Diek W. Wheeler, Teresa Jurado-Parras, et al. "An update to Hippocampome.org by integrating single-cell phenotypes with circuit function in vivo." PLOS Biology 19, no. 5 (2021): e3001213. http://dx.doi.org/10.1371/journal.pbio.3001213.

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Understanding brain operation demands linking basic behavioral traits to cell-type specific dynamics of different brain-wide subcircuits. This requires a system to classify the basic operational modes of neurons and circuits. Single-cell phenotyping of firing behavior during ongoing oscillations in vivo has provided a large body of evidence on entorhinal–hippocampal function, but data are dispersed and diverse. Here, we mined literature to search for information regarding the phase-timing dynamics of over 100 hippocampal/entorhinal neuron types defined in Hippocampome.org. We identified missin

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Fuzik, János, Amit Zeisel, Zoltán Máté, et al. "Integration of electrophysiological recordings with single-cell RNA-seq data identifies neuronal subtypes." Nature Biotechnology 34, no. 2 (2015): 175–83. http://dx.doi.org/10.1038/nbt.3443.

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29

Kitamura, Kazuo, Benjamin Judkewitz, Masanobu Kano, Winfried Denk, and Michael Häusser. "Targeted patch-clamp recordings and single-cell electroporation of unlabeled neurons in vivo." Nature Methods 5, no. 1 (2007): 61–67. http://dx.doi.org/10.1038/nmeth1150.

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30

Criado, J. M., A. de la Fuente, M. Heredia, A. S. Riolobos, and J. Yajeya. "Single-cell recordings: A method for investigating the brain’s activation pattern during exercise." Methods 45, no. 4 (2008): 262–70. http://dx.doi.org/10.1016/j.ymeth.2008.05.007.

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31

Chung, Shin-Ho, and Graham Pulford. "Fluctuation analysis of patch-clamp or whole-cell recordings containing many single channels." Journal of Neuroscience Methods 50, no. 3 (1993): 369–84. http://dx.doi.org/10.1016/0165-0270(93)90043-q.

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32

Zhao, Y., S. Inayat, D. A. Dikin, J. H. Singer, R. S. Ruoff, and J. B. Troy. "Patch clamp technique: Review of the current state of the art and potential contributions from nanoengineering." Proceedings of the Institution of Mechanical Engineers, Part N: Journal of Nanoengineering and Nanosystems 222, no. 1 (2008): 1–11. http://dx.doi.org/10.1243/17403499jnn149.

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The patch clamp technique permits high-resolution recording of the ionic currents flowing through a cell's plasma membrane. In different configurations, this technique has allowed experimenters to record and manipulate the currents that flow either through single ion channels or those that flow across the whole plasma membrane. Unfortunately, the conventional patch clamp method is laborious, requiring the careful fabrication of electrodes, skillful manipulation of the patch pipette towards a cell, and the clever design of electronics and apparatus to allow low-noise recordings. Advances in mic

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33

Kimitsuki, T., T. Mitsuiye, and A. Noma. "Negative shift of cardiac Na+ channel kinetics in cell-attached patch recordings." American Journal of Physiology-Heart and Circulatory Physiology 258, no. 1 (1990): H247—H254. http://dx.doi.org/10.1152/ajpheart.1990.258.1.h247.

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Na+ channel kinetics were studied by recording single-channel currents in the cell-attached patch configuration of the patch-clamp technique in single ventricular cells isolated from guinea pig hearts. The inactivation time course of ensemble currents was accelerated, and the peak amplitude increased temporarily and then decreased within a few minutes after the gigaohm seal formation. After reaching a new steady state, the inactivation-voltage relation was found to have shifted to more negative potentials. The potential of half-maximal inactivation was more negative by 20–31 mV from the restin

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Cerea, Andrea, Valeria Caprettini, Giulia Bruno, et al. "Selective intracellular delivery and intracellular recordings combined in MEA biosensors." Lab on a Chip 18, no. 22 (2018): 3492–500. http://dx.doi.org/10.1039/c8lc00435h.

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35

Akbarali, H. I. "K+ currents in rabbit esophageal muscularis mucosae." American Journal of Physiology-Gastrointestinal and Liver Physiology 264, no. 5 (1993): G1001—G1007. http://dx.doi.org/10.1152/ajpgi.1993.264.5.g1001.

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Single cells were obtained from esophageal muscularis mucosae of the rabbit using enzymatic dispersion. Their electrophysiological properties were studied with both conventional whole cell and nystatin-perforated patch techniques. The latter technique was used to prevent "washout" of intracellular constituents and to maintain endogenous buffering of Ca2+. The average resting potential of these cells was -54 +/- 3.2 mV in the conventional recording and -51 +/- 4.4 mV in perforated patch recordings. In the current-clamp mode, regenerative responses were consistently observed in perforated patch

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36

Kang, J., and J. Caprio. "In vivo responses of single olfactory receptor neurons in the channel catfish, Ictalurus punctatus." Journal of Neurophysiology 73, no. 1 (1995): 172–77. http://dx.doi.org/10.1152/jn.1995.73.1.172.

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1. We report for the first time in any teleost, a quantitative in vivo study of recordings from single olfactory receptor neurons (ORNs) in the channel catfish, Ictalurus punctatus, with odorant stimuli. 2. Responses of 69 spontaneously active single ORNs were recorded simultaneously with the electroolfactogram (EOG). Recording times ranged from 10 to 72 min per receptor cell with an average of 24 +/- 15 (SD) min/cell. The averaged spontaneous frequency ranged from < 1 to 12 action potentials/s with a mean frequency of 4.7 +/- 2.5 action potentials/s. 3. Catfish ORNs responded to the odoran

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37

Lipton, Stuart A. "GABA-activated single channel currents in outside-out membrane patches from rat retinal ganglion cells." Visual Neuroscience 3, no. 3 (1989): 275–79. http://dx.doi.org/10.1017/s0952523800010026.

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Abstractγ-aminobutyric acid (GABA) evokes large whole-cell currents in solitary mammalian retinal ganglion cells studied by the patch-clamp method. This evidence suggests that GABA acts directly on the retinal ganglion cells as an inhibitory transmitter as it does elsewhere in the mammalian central nervous system. Here, single-channel recordings of the currents underlying the GABA-induced responses were studied in outside-out patches of cell membrane. In some other preparations, single GABAA channels recorded in the excised patch configuration have been shown to have altered properties in comp

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38

Matsui, Ko, Nobutake Hosoi, and Masao Tachibana. "Simultaneous recordings revealed the characteristics of synaptic transmission from a single bipolar cell to a ganglion cell." Neuroscience Research 31 (January 1998): S113. http://dx.doi.org/10.1016/s0168-0102(98)81971-8.

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39

Meyer, Glenn E. "Single cells in the visual system and images past." Behavioral and Brain Sciences 25, no. 2 (2002): 200–201. http://dx.doi.org/10.1017/s0140525x02400040.

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Various techniques have attempted to localize imagery. However, early findings using single cell recordings of human receptive fields during imagery tasks have had little impact. Reports by Marg and his coworkers (1968) found no evidence for imagery in human Area 17, 18, and 19. Single cells from humans suggest later imagery-related activity in hippocampus, amygdala, entorhinal cortex, and parahippocampal gyrus.

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Desai, Niraj S., Jennifer J. Siegel, William Taylor, Raymond A. Chitwood, and Daniel Johnston. "MATLAB-based automated patch-clamp system for awake behaving mice." Journal of Neurophysiology 114, no. 2 (2015): 1331–45. http://dx.doi.org/10.1152/jn.00025.2015.

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Automation has been an important part of biomedical research for decades, and the use of automated and robotic systems is now standard for such tasks as DNA sequencing, microfluidics, and high-throughput screening. Recently, Kodandaramaiah and colleagues ( Nat Methods 9: 585–587, 2012) demonstrated, using anesthetized animals, the feasibility of automating blind patch-clamp recordings in vivo. Blind patch is a good target for automation because it is a complex yet highly stereotyped process that revolves around analysis of a single signal (electrode impedance) and movement along a single axis.

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Meyer, K., and C. Korbmacher. "Cell swelling activates ATP-dependent voltage-gated chloride channels in M-1 mouse cortical collecting duct cells." Journal of General Physiology 108, no. 3 (1996): 177–93. http://dx.doi.org/10.1085/jgp.108.3.177.

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In the present study we used whole-cell patch clamp recordings to investigate swelling-activated Cl-currents (ICl-swell) in M-1 mouse cortical collecting duct (CCD) cells. Hypotonic cell swelling reversibly increased the whole-cell Cl- conductance by about 30-fold. The I-V relationship was outwardly-rectifying and ICl-swell displayed a characteristic voltage-dependence with relatively fast inactivation upon large depolarizing and slow activation upon hyperpolarizing voltage steps. Reversal potential measurements revealed a selectivity sequence SCN- &gt; I- &gt; Br- &gt; Cl- &gt

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42

Yarotskyy, Viktor, John Malysz, and Georgi V. Petkov. "Properties of single-channel and whole cell Cl− currents in guinea pig detrusor smooth muscle cells." American Journal of Physiology-Cell Physiology 316, no. 5 (2019): C698—C710. http://dx.doi.org/10.1152/ajpcell.00327.2018.

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Multiple types of Cl− channels regulate smooth muscle excitability and contractility in vascular, gastrointestinal, and airway smooth muscle cells. However, little is known about Cl− channels in detrusor smooth muscle (DSM) cells. Here, we used inside-out single channel and whole cell patch-clamp recordings for detailed biophysical and pharmacological characterizations of Cl− channels in freshly isolated guinea pig DSM cells. The recorded single Cl− channels displayed unique gating with multiple subconductive states, a fully opened single-channel conductance of 164 pS, and a reversal potential

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43

Roelfsema, M. Rob G., Ralf Steinmeyer, Marten Staal, and Rainer Hedrich. "Single guard cell recordings in intact plants: light-induced hyperpolarization of the plasma membrane." Plant Journal 26, no. 1 (2001): 1–13. http://dx.doi.org/10.1046/j.1365-313x.2001.01000.x.

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44

Bogner, Franz, and Michael Boppré. "Single cell recordings reveal hydroxydanaidal as the volatile compound attracting insects to pyrrolizidine alkaloids." Entomologia Experimentalis et Applicata 50, no. 2 (1989): 171–84. http://dx.doi.org/10.1111/j.1570-7458.1989.tb02386.x.

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45

OTTER, C. J. DEN, and W. M. VAN DER GOES VAN NATERS. "Single cell recordings from tsetse (Glossina m.morsitans) antennae reveal olfactory, mechano - and cold receptors." Physiological Entomology 17, no. 1 (1992): 33–42. http://dx.doi.org/10.1111/j.1365-3032.1992.tb00987.x.

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46

Frings, S., R. D. Purves, and A. D. C. Macknight. "Single-channel recordings from the apical membrane of the toad urinary bladder epithelial cell." Journal of Membrane Biology 106, no. 2 (1988): 157–72. http://dx.doi.org/10.1007/bf01871398.

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47

Schenda, J., and L. Vollrath*. "Single-cell recordings from chick pineal glands in vitro reveal ultradian and circadian oscillations." Cellular and Molecular Life Sciences 57, no. 12 (2000): 1785–92. http://dx.doi.org/10.1007/pl00000658.

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48

Kafka, Wolf A. "Similarity of reaction spectra and odor discrimination: single receptor cell recordings inAntheraea polyphemus (Saturniidae)." Journal of Comparative Physiology A 161, no. 6 (1987): 867–80. http://dx.doi.org/10.1007/bf00610228.

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White, Kevin A., Geoffrey Mulberry, and Brian N. Kim. "1024-Ch Electrochemical Recordings of Single-cell Neurotransmitter Secretion from Human Neuroblastoma Cells using Monolithic CMOS Bioelectronics." Biophysical Journal 118, no. 3 (2020): 316a—317a. http://dx.doi.org/10.1016/j.bpj.2019.11.1781.

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Hoshi, T., and R. W. Aldrich. "Voltage-dependent K+ currents and underlying single K+ channels in pheochromocytoma cells." Journal of General Physiology 91, no. 1 (1988): 73–106. http://dx.doi.org/10.1085/jgp.91.1.73.

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Abstract:

Properties of the whole-cell K+ currents and voltage-dependent activation and inactivation properties of single K+ channels in clonal pheochromocytoma (PC-12) cells were studied using the patch-clamp recording technique. Depolarizing pulses elicited slowly inactivating whole-cell K+ currents, which were blocked by external application of tetraethylammonium+, 4-aminopyridine, and quinidine. The amplitudes and time courses of these K+ currents were largely independent of the prepulse voltage. Although pharmacological agents and manipulation of the voltage-clamp pulse protocol failed to reveal an

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