Ion Channels/Excitable Membranes

Glutamate Receptor Ion Channels: Structure, Regulation, and Function

Traynelis, S. F., Wollmuth, L. P., McBain, C. J., Menniti, F. S., Vance, K. M., Ogden, K. K., Hansen, K. B., Yuan, H., Myers, S. J., & Dingledine, R. (2010) · Pharmacological Reviews · doi:10.1124/pr.109.002451 · Cited by 3,568

TRP channels as cellular sensors

Clapham, D. E. (2003) · Nature · doi:10.1038/nature02196 · Cited by 2,779

Synaptic Energy Use and Supply

Harris, J. J., Jolivet, R., & Attwell, D. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.019 · Cited by 1,747

The action potential in mammalian central neurons

Bean, B. P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2148 · Cited by 1,785

The mitochondrial calcium uniporter is a highly selective ion channel

Kirichok, Y., Krapivinsky, G., & Clapham, D. E. (2004) · Nature · doi:10.1038/nature02246 · Cited by 1,409

Variability, compensation and homeostasis in neuron and network function

Marder, E., & Goaillard, J.-M. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1949 · Cited by 1,212

Physiology and function of the tight junction

Anderson, J. M., & Van Itallie, C. M. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a002584 · Cited by 1,059

Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men

Rorsman, P., & Ashcroft, F. M. (2018) · Physiological Reviews · doi:10.1152/physrev.00008.2017 · Cited by 793

Overview of the voltage-gated sodium channel family

Yu (2003) · Genome biology · doi:10.1186/gb-2003-4-3-207 · Cited by 694

Neuromodulatory properties of inflammatory cytokines and their impact on neuronal excitability

Vezzani, A., & Viviani, B. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.027 · Cited by 670

Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model mice

Tong, X., Ao, Y., Faas, G. C., Nwaobi, S. E., Xu, J., Haustein, M. D., Anderson, M. A., Mody, I., Olsen, M. L., Sofroniew, M. V., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3691 · Cited by 592

SWELL1, a Plasma Membrane Protein, Is an Essential Component of Volume-Regulated Anion Channel

Qiu, Z., Dubin, A. E., Mathur, J., Tu, B., Reddy, K., Miraglia, L. J., Reinhardt, J., Orth, A. P., & Patapoutian, A. (2014) · Cell · doi:10.1016/j.cell.2014.03.024 · Cited by 571

Principles of Neural Design

Sterling, P., & Laughlin, S. (2015) · doi:10.7551/mitpress/9780262028707.001.0001 · Cited by 482

Linking neural activity and molecular oscillations in the SCN

Colwell, C. S. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3086 · Cited by 474

Crystal structure of an orthologue of the NaChBac voltage-gated sodium channel

Zhang, X., Ren, W., DeCaen, P., Yan, C., Tao, X., Tang, L., Wang, J., Hasegawa, K., Kumasaka, T., He, J., et al. (2012) · Nature · doi:10.1038/nature11054 · Cited by 466

CNG AND HCN CHANNELS: Two Peas, One Pod

Craven, K. B., & Zagotta, W. N. (2006) · Annual Review of Physiology · doi:10.1146/annurev.physiol.68.040104.134728 · Cited by 432

Motor Unit

Heckman, C. J., & Enoka, R. M. (2012) · Comprehensive Physiology · doi:10.1002/cphy.c100087 · Cited by 414

Spine-Neck Geometry Determines NMDA Receptor-Dependent Ca2+ Signaling in Dendrites

Noguchi, J., Matsuzaki, M., Ellis-Davies, G. C. R., & Kasai, H. (2005) · Neuron · doi:10.1016/j.neuron.2005.03.015 · Cited by 419

The Neuronal Channel NALCN Contributes Resting Sodium Permeability and Is Required for Normal Respiratory Rhythm

Lu, B., Su, Y., Das, S., Liu, J., Xia, J., & Ren, D. (2007) · Cell · doi:10.1016/j.cell.2007.02.041 · Cited by 381

Clues to understanding cold sensation: Thermodynamics and electrophysiological analysis of the cold receptor TRPM8

Brauchi, S., Orio, P., & Latorre, R. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406773101 · Cited by 375

Structural basis for partial agonist action at ionotropic glutamate receptors

Jin, R., Banke, T. G., Mayer, M. L., Traynelis, S. F., & Gouaux, E. (2003) · Nature Neuroscience · doi:10.1038/nn1091 · Cited by 367

Anion transport and supramolecular medicinal chemistry

Gale, P. A., Davis, J. T., & Quesada, R. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00159b · Cited by 359

Closing gaps: linking elements that control stomatal movement

Kollist, H., Nuhkat, M., & Roelfsema, M. R. G. (2014) · New Phytologist · doi:10.1111/nph.12832 · Cited by 357

On the Initiation and Propagation of Dendritic Spikes in CA1 Pyramidal Neurons

Gasparini, S., Migliore, M., & Magee, J. C. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.2520-04.2004 · Cited by 337

HODGKIN–HUXLEY AXON IS MADE OF MEMRISTORS

CHUA, L., SBITNEV, V., & KIM, H. (2012) · International Journal of Bifurcation and Chaos · doi:10.1142/s021812741230011x · Cited by 319

Phosphoinositides regulate ion channels

Hille, B., Dickson, E. J., Kruse, M., Vivas, O., & Suh, B.-C. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2014.09.010 · Cited by 312

Silencing Neurons: Tools, Applications, and Experimental Constraints

Wiegert, J. S., Mahn, M., Prigge, M., Printz, Y., & Yizhar, O. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.050 · Cited by 312

Diffusion of Macromolecules in the Brain: Implications for Drug Delivery

Wolak, D. J., & Thorne, R. G. (2013) · Molecular Pharmaceutics · doi:10.1021/mp300495e · Cited by 299

Phospholipase C in Living Cells

Horowitz, L. F., Hirdes, W., Suh, B.-C., Hilgemann, D. W., Mackie, K., & Hille, B. (2005) · The Journal of General Physiology · doi:10.1085/jgp.200509309 · Cited by 299

A genomic view of the sea urchin nervous system

Burke, R. D., Angerer, L. M., Elphick, M. R., Humphrey, G. W., Yaguchi, S., Kiyama, T., Liang, S., Mu, X., Agca, C., Klein, W. H., et al. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.08.007 · Cited by 293

Chemotaxis of sperm cells

Friedrich, B. M., & Jülicher, F. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703530104 · Cited by 287

Anomalous Diffusion in Purkinje Cell Dendrites Caused by Spines

Santamaria, F., Wils, S., De Schutter, E., & Augustine, G. J. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.025 · Cited by 279

The reticular nucleus revisited: Intrinsic and network properties of a thalamic pacemaker

FUENTEALBA, P., & STERIADE, M. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.01.002 · Cited by 263

CACNA1H mutations in autism spectrum disorders

Splawski, I., Yoo, D. S., Stotz, S. C., Cherry, A., Clapham, D. E., & Keating, M. T. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m603316200 · Cited by 255

Prototypic and arkypallidal neurons in the dopamine-intact external globus pallidus

Abdi, A., Mallet, N., Mohamed, F. Y., Sharott, A., Dodson, P. D., Nakamura, K. C., Suri, S., Avery, S. V., Larvin, J. T., Garas, F. N., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4662-14.2015 · Cited by 247

Interactions Between Membrane Conductances Underlying Thalamocortical Slow-Wave Oscillations

DESTEXHE, A., & SEJNOWSKI, T. J. (2003) · Physiological Reviews · doi:10.1152/physrev.00012.2003 · Cited by 241

Extracellular tau is toxic to neuronal cells

Gómez-Ramos, A., Díaz-Hernández, M., Cuadros, R., Hernández, F., & Avila, J. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.07.078 · Cited by 241

Perisomatic GABA Release and Thalamocortical Integration onto Neocortical Excitatory Cells Are Regulated by Neuromodulators

Kruglikov, I., & Rudy, B. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.024 · Cited by 209

Regulation of glucagon release in mouse α‐cells by KATP channels and inactivation of TTX‐sensitive Na+ channels

Göpel, S. O., Kanno, T., Barg, S., Weng, X. ‐., Gromada, J., & Rorsman, P. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00509.x · Cited by 229

Hyperpolarization‐activated cation channels in fast‐spiking interneurons of rat hippocampus

Aponte, Y., Lien, C., Reisinger, E., & Jonas, P. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2005.104042 · Cited by 213

Perineuronal Nets Enhance the Excitability of Fast-Spiking Neurons

Balmer, T. S. (2016) · eneuro · doi:10.1523/eneuro.0112-16.2016 · Cited by 220

Ion-channel noise places limits on the miniaturization of the brain's wiring

Faisal, A. A., White, J. A., & Laughlin, S. B. (2005) · Current Biology · doi:10.1016/j.cub.2005.05.056 · Cited by 216

Ion channels in the RPE

WIMMERS, S., KARL, M., & STRAUSS, O. (2007) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2006.12.002 · Cited by 207

Dendritic Mechanisms Underlying Rapid Synaptic Activation of Fast-Spiking Hippocampal Interneurons

Hu, H., Martina, M., & Jonas, P. (2010) · Science · doi:10.1126/science.1177876 · Cited by 202

How multiple conductances determine electrophysiological properties in a multicompartment model

Taylor, A. L., Goaillard, J.-M., & Marder, E. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4438-08.2009 · Cited by 202

Robustness of burst firing in dissociated purkinje neurons with acute or long-term reductions in sodium conductance

Swensen, A. M., & Bean, B. P. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3929-04.2005 · Cited by 197

Correlations in ion channel expression emerge from homeostatic tuning rules

O'Leary, T., Williams, A. H., Caplan, J. S., & Marder, E. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1309966110 · Cited by 192

Molecular Mechanisms for Bacterial Potassium Homeostasis

Stautz, J., Hellmich, Y., Fuss, M. F., Silberberg, J. M., Devlin, J. R., Stockbridge, R. B., & Hänelt, I. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.166968 · Cited by 189

Regulation of synaptic transmission and plasticity by neuronal nicotinic acetylcholine receptors

McKay, B. E., Placzek, A. N., & Dani, J. A. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.07.001 · Cited by 181

The sodium leak channel, NALCN, in health and disease

Cochet-Bissuel, M., Lory, P., & Monteil, A. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00132 · Cited by 172

The neuronal channelopathies

Kullmann, D. M. (2002) · Brain · doi:10.1093/brain/awf130 · Cited by 168

Molecular Dynamics Studies of Interfacial Water at the Alumina Surface

Argyris, D., Ho, T., Cole, D. R., & Striolo, A. (2011) · The Journal of Physical Chemistry C · doi:10.1021/jp109244c · Cited by 167

Action potentials drive body wall muscle contractions in Caenorhabditis elegans

Gao, S., & Zhen, M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1012346108 · Cited by 149

Ether a go-go Potassium Channels as Human Cervical Cancer Markers

Farias, L. M. B., Ocaña, D. B., Díaz, L., Larrea, F., Avila-Chávez, E., Cadena, A., Hinojosa, L. M., Lara, G., Villanueva, L. A., Vargas, C., et al. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-1204 · Cited by 164

Common Molecular Pathways Mediate Long-Term Potentiation of Synaptic Excitation and Slow Synaptic Inhibition

Huang, C. S., Shi, S.-H., Ule, J., Ruggiu, M., Barker, L. A., Darnell, R. B., Jan, Y. N., & Jan, L. Y. (2005) · Cell · doi:10.1016/j.cell.2005.07.033 · Cited by 157

Adaptive evolution of voltage-gated sodium channels: The first 800 million years

Zakon, H. H. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1201884109 · Cited by 156

Precise temperature compensation of phase in a rhythmic motor pattern

Tang, L. S., Goeritz, M. L., Caplan, J. S., Taylor, A. L., Fisek, M., & Marder, E. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000469 · Cited by 156

Mechanical signatures of transducer gating in the Drosophila ear

Albert, J. T., Nadrowski, B., & Göpfert, M. C. (2007) · Current Biology · doi:10.1016/j.cub.2007.05.004 · Cited by 151

Modulation of Kv4.2 Channel Expression and Gating by Dipeptidyl Peptidase 10 (DPP10)

Jerng, H. H., Qian, Y., & Pfaffinger, P. J. (2004) · Biophysical Journal · doi:10.1529/biophysj.104.042358 · Cited by 142

Evolution of voltage-gated ion channels at the emergence of Metazoa

Moran, Y., Barzilai, M. G., Liebeskind, B. J., & Zakon, H. H. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.110270 · Cited by 139

Glutamate mediates acute glucose transport inhibition in hippocampal neurons

Porras, O. H., Loaiza, A., & Barros, L. F. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1882-04.2004 · Cited by 139

Serotonin Affects Movement Gain Control in the Spinal Cord

Wei, K., Glaser, J. I., Deng, L., Thompson, C. K., Stevenson, I. H., Wang, Q., Hornby, T. G., Heckman, C. J., & Kording, K. P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1855-14.2014 · Cited by 135

Electrophysiological classes of neocortical neurons.

Contreras, D. (2004) · Neural Networks · doi:10.1016/j.neunet.2004.04.003 · Cited by 124

A family of fluoride-specific ion channels with dual-topology architecture

Stockbridge, R. B., Robertson, J. L., Kolmakova-Partensky, L., & Miller, C. (2013) · eLife · doi:10.7554/elife.01084 · Cited by 120

Is a new paradigm needed to explain how inhaled anesthetics produce immobility?

Eger, E. I., Raines, D. E., Shafer, S. L., Hemmings, H. C., & Sonner, J. M. (2008) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e318182aedb · Cited by 119

Robustness of a rhythmic circuit to short- and long-term temperature changes

Tang, L. S., Taylor, A. L., Rinberg, A., & Marder, E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1443-12.2012 · Cited by 119

Design and implementation of functional nanoelectronic interfaces with biomolecules, cells, and tissue using nanowire device arrays.

Timko, B. P., Cohen-Karni, T., Qing, Q., Tian, B., & Lieber, C. M. (2010) · IEEE Transactions on Nanotechnology · doi:10.1109/tnano.2009.2031807 · Cited by 114

Ih from synapses to networks: HCN channel functions and modulation in neurons

Combe, C. L., & Gasparini, S. (2021) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2021.06.002 · Cited by 101

Nanosecond Electric Pulses: A Novel Stimulus for Triggering Ca2+ Influx into Chromaffin Cells Via Voltage-Gated Ca2+ Channels

Craviso, G. L., Choe, S., Chatterjee, P., Chatterjee, I., & Vernier, P. T. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9573-1 · Cited by 107

Expression of Kv1 Potassium Channels in Mouse Hippocampal Primary Cultures: Development and Activity-Dependent Regulation

Grosse, G., Draguhn, A., Höhne, L., Tapp, R., Veh, R. W., & Ahnert-Hilger, G. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-05-01869.2000 · Cited by 104

Lipid-dependent gating of a voltage-gated potassium channel

Zheng, H., Liu, W., Anderson, L. Y., & Jiang, Q.-X. (2011) · Nature Communications · doi:10.1038/ncomms1254 · Cited by 106

Dopamine D 2 Receptor Modulation of K + Channel Activity Regulates Excitability of Nucleus Accumbens Neurons at Different Membrane Potentials

Perez, M. F., White, F. J., & Hu, X.-T. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00254.2006 · Cited by 102

Ion permeation through a Cl − -selective channel designed from a CLC Cl − /H + exchanger

Jayaram, H., Accardi, A., Wu, F., Williams, C., & Miller, C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804503105 · Cited by 101

Corelease and Differential Exit via the Fusion Pore of GABA, Serotonin, and ATP from LDCV in Rat Pancreatic β Cells

Braun, M., Wendt, A., Karanauskaite, J., Galvanovskis, J., Clark, A., MacDonald, P. E., & Rorsman, P. (2007) · The Journal of General Physiology · doi:10.1085/jgp.200609658 · Cited by 100

Disrupted ERK Signaling during Cortical Development Leads to Abnormal Progenitor Proliferation, Neuronal and Network Excitability and Behavior, Modeling Human Neuro-Cardio-Facial-Cutaneous and Related Syndromes

Pucilowska, J., Puzerey, P. A., Karlo, J. C., Galan, R. F., & Landreth, G. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1107-12.2012 · Cited by 99

Ca 2+ /cAMP-Sensitive Covariation of I A and I H Voltage Dependences Tunes Rebound Firing in Dopaminergic Neurons

Amendola, J., Woodhouse, A., Martin-Eauclaire, M.-F., & Goaillard, J.-M. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5297-11.2012 · Cited by 99

Molecular Insights from Conformational Ensembles via Machine Learning

Fleetwood, O., Kasimova, M. A., Westerlund, A. M., & Delemotte, L. (2020) · Biophysical Journal · doi:10.1016/j.bpj.2019.12.016 · Cited by 93

Na+ current properties in islet α‐ and β‐cells reflect cell‐specific Scn3a and Scn9a expression

Zhang, Q., Chibalina, M. V., Bengtsson, M., Groschner, L. N., Ramracheya, R., Rorsman, N. J. G., Leiss, V., Nassar, M. A., Welling, A., Gribble, F. M., et al. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.274209 · Cited by 90

Transient sodium current at subthreshold voltages: activation by EPSP waveforms

Carter, B. C., Giessel, A. J., Sabatini, B. L., & Bean, B. P. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.033 · Cited by 86

Tools for Understanding Nanoscale Lipid Regulation of Ion Channels

Robinson, C. V., Rohacs, T., & Hansen, S. B. (2019) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2019.04.001 · Cited by 85

Cell coupling in mouse pancreatic β-cells measured in intact islets of Langerhans

Zhang, Q., Galvanovskis, J., Abdulkader, F., Partridge, C. J., Göpel, S. O., Eliasson, L., & Rorsman, P. (2008) · Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences · doi:10.1098/rsta.2008.0110 · Cited by 80

Membrane Capacitive Memory Alters Spiking in Neurons Described by the Fractional-Order Hodgkin-Huxley Model

Weinberg, S. H. (2015) · PLOS ONE · doi:10.1371/journal.pone.0126629 · Cited by 76

Convergent Evolution of Sodium Ion Selectivity in Metazoan Neuronal Signaling

Gur Barzilai, M., Reitzel, A. M., Kraus, J. E. M., Gordon, D., Technau, U., Gurevitz, M., & Moran, Y. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.06.016 · Cited by 76

Cell Type-Specific Expression of Acid-Sensing Ion Channels in Hippocampal Interneurons

Weng, J.-Y., Lin, Y.-C., & Lien, C.-C. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0582-10.2010 · Cited by 72

Recent advances in gene therapy for neurodevelopmental disorders with epilepsy

Turner, T. J., Zourray, C., Schorge, S., & Lignani, G. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15168 · Cited by 71

Targets of polyamine dysregulation in major depression and suicide: Activity-dependent feedback, excitability, and neurotransmission

Limon, A., Mamdani, F., Hjelm, B. E., Vawter, M. P., & Sequeira, A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.04.010 · Cited by 63

Modulation of a voltage-gated Na + channel by sevoflurane involves multiple sites and distinct mechanisms

Barber, A. F., Carnevale, V., Klein, M. L., Eckenhoff, R. G., & Covarrubias, M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1405768111 · Cited by 60

Three homologous subunits form a high affinity peptide-gated ion channel in Hydra

Dürrnagel, S., Kuhn, A., Tsiairis, C. D., Williamson, M., Kalbacher, H., Grimmelikhuijzen, C. J. P., Holstein, T. W., & Gründer, S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.059998 · Cited by 58

Determinants of the Anesthetic Sensitivity of Two-pore Domain Acid-sensitive Potassium Channels

Andres-Enguix, I., Caley, A., Yustos, R., Schumacher, M. A., Spanu, P. D., Dickinson, R., Maze, M., & Franks, N. P. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m610692200 · Cited by 52

Synaptically activated burst-generating conductances may underlie a group-pacemaker mechanism for respiratory rhythm generation in mammals

Del Negro, C. A., Hayes, J. A., Pace, R. W., Brush, B. R., Teruyama, R., & Feldman, J. L. (2010) · Progress in Brain Research · doi:10.1016/b978-0-444-53613-6.00008-3 · Cited by 47

Isoflurane inhibits NaChBac, a prokaryotic voltage-gated sodium channel

Ouyang, W., Jih, T.-Y., Zhang, T.-T., Correa, A. M., & Hemmings, H. C. (2007) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.122929 · Cited by 45

Mutations Linked to Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Affect Allosteric Ca2+ Activation of the α4β2 Nicotinic Acetylcholine Receptor

Rodrigues-Pinguet, N. O., Pinguet, T. J., Figl, A., Lester, H. A., & Cohen, B. N. (2005) · Molecular Pharmacology · doi:10.1124/mol.105.011155 · Cited by 42

Adrenaline-induced hyperpolarization of mouse pancreatic islet cells is mediated by G protein-gated inwardly rectifying potassium (GIRK) channels

Iwanir, S., & Reuveny, E. (2008) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-008-0479-4 · Cited by 41

Conditioning by subthreshold synaptic input changes the intrinsic firing pattern of CA3 hippocampal neurons

Soldado-Magraner, S., Brandalise, F., Honnuraiah, S., Pfeiffer, M., Moulinier, M., Gerber, U., & Douglas, R. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00506.2019 · Cited by 25

A topologically diverse family of fluoride channels

Macdonald, C. B., & Stockbridge, R. B. (2017) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2017.04.003 · Cited by 21

Exocytosis from pancreatic β-cells: mathematical modelling of the exit of low-molecular-weight granule content

Galvanovskis, J., Braun, M., & Rorsman, P. (2011) · Interface Focus · doi:10.1098/rsfs.2010.0006 · Cited by 17

Hydroxynorketamine Blocks N-Methyl-d-Aspartate Receptor Currents by Binding to Closed Receptors

Abbott, J. A., & Popescu, G. K. (2020) · Molecular Pharmacology · doi:10.1124/mol.120.119784 · Cited by 17

Functional characterization of phospholipase C-γ2 mutant protein causing both somatic ibrutinib resistance and a germline monogenic autoinflammatory disorder

Walliser, C., Wist, M., Hermkes, E., Zhou, Y., Schade, A., Haas, J., Deinzer, J., Désiré, L., Li, S. S. C., Stilgenbauer, S., et al. (2018) · Oncotarget · doi:10.18632/oncotarget.26173 · Cited by 17

Modeling sources of interlaboratory variability in electrophysiological properties of mammalian neurons

Tebaykin, D., Tripathy, S. J., Binnion, N., Li, B., Gerkin, R. C., & Pavlidis, P. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00604.2017 · Cited by 15

FireMaster® 550 (FM 550) exposure during the perinatal period impacts partner preference behavior and nucleus accumbens core medium spiny neuron electrophysiology in adult male and female prairie voles, Microtus ochrogaster

Krentzel, A. A., Kimble, L. C., Dorris, D. M., Horman, B. M., Meitzen, J., & Patisaul, H. B. (2021) · Hormones and Behavior · doi:10.1016/j.yhbeh.2021.105019 · Cited by 14