Calcium-activated potassium channels

Stability constants of metal-ion complexes

Sillén, L. G., Martell, A. E., Bjerrum, J., & Schwarzenbach, G. (1964) · Medical Entomology and Zoology · Cited by 3,983

Biophysical and Molecular Mechanisms of Shaker Potassium Channel Inactivation

Hoshi, T., Zagotta, W. N., & Aldrich, R. W. (1990) · Science · doi:10.1126/science.2122519 · Cited by 1,527

Relaxation of Arterial Smooth Muscle by Calcium Sparks

Nelson, M. T., Cheng, H., Rubart, M., Santana, L. F., Bonev, A. D., Knot, H. J., & Lederer, W. J. (1995) · Science · doi:10.1126/science.270.5236.633 · Cited by 1,399

Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence

Noda, M., Shimizu, S., Tanabe, T., Takai, T., Kayano, T., Ikeda, T., Takahashi, H., Nakayama, H., Kanaoka, Y., Minamino, N., et al. (1984) · Nature · doi:10.1038/312121a0 · Cited by 1,349

Small-Conductance, Calcium-Activated Potassium Channels from Mammalian Brain

Kohler, M.-L., Hirschberg, B., Bond, C. T., Kinzie, J. M., Marrion, N. V., Maylie, J., & Adelman, J. P. (1996) · Science · doi:10.1126/science.273.5282.1709 · Cited by 946

Ca2+-activated K+ currents in neurones: types, physiological roles and modulation

Sah, P. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)80026-9 · Cited by 892

Mutations in the K+ channel signature sequence

Heginbotham, L., Lü, Z., Abramson, T., & MacKinnon, R. (1994) · Biophysical Journal · doi:10.1016/s0006-3495(94)80887-2 · Cited by 853

Varieties of Calcium-Activated Potassium Channels

Latorre, R., Oberhauser, A. F., Labarca, P. P., & Alvarez, O. A. (1989) · Annual Review of Physiology · doi:10.1146/annurev.ph.51.030189.002125 · Cited by 735

The Coupling of Neurotransmitter Receptors to Ion Channels in the Brain

Nicoll, R. A. (1988) · Science · doi:10.1126/science.2456612 · Cited by 729

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Harley, H. G., Brook, J. D., Rundle, S. A., Crow, S., Reardon, W., Buckler, A., Harper, P. S., Housman, D. E., & Shaw, D. J. (1992) · Nature · doi:10.1038/355545a0 · Cited by 725

Functional reduction of SK3-mediated currents precedes AMPA-receptor-mediated excitotoxicity in dopaminergic neurons

Benítez, B. A., Belálcazar, H. M., Anastasía, A., Mamah, D. T., Zorumski, C. F., Mascó, D. H., Herrera, D. G., & de Erausquin, G. A. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.10.024 · Cited by 27

Modulation of BK Channel Gating by the β2 Subunit Involves Both Membrane-Spanning and Cytoplasmic Domains of Slo1

Lee, U. S., Shi, J., & Cui, J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2323-10.2010 · Cited by 27

Mechanisms involved in the swelling of erythrocytes caused by Pacific and Caribbean ciguatoxins

Sauviat, M., Garrec, R. L., Masson, J., Lewis, R. J., Vernoux, J., Molgó, J., Laurent, D., & Benoit, É. (2005) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2005.10.007 · Cited by 27

Molecular Mechanisms for Large Conductance Ca2+-Activated K+ Channel Activation by a Novel Opener, 12,14-Dichlorodehydroabietic Acid

Sakamoto, K., Nonomura, T., Ohya, S., Muraki, K., Ohwada, T., & Imaizumi, Y. (2005) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.105.093856 · Cited by 27

Hypotonicity induced K+ and anion conductive pathways activation in eel intestinal epithelium

Lionetto, M. G., Giordano, M. E., Nuccio, F. D., Nicolardi, G., Hoffmann, E. K., & Schettino, T. (2005) · Journal of Experimental Biology · doi:10.1242/jeb.01440 · Cited by 27

Glial Cell Line-Derived Neurotrophic Factor and Target-Dependent Regulation of Large-Conductance KCaChannels in Developing Chick Lumbar Motoneurons

Martin‐Caraballo, M., & Dryer, S. E. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-23-10201.2002 · Cited by 27

3 The membrane defect in hereditary stomatocytosis

Stewart, G. W. (1993) · Baillière s Clinical Haematology · doi:10.1016/s0950-3536(05)80151-9 · Cited by 27

The Role of DPO-1 and XE991-Sensitive Potassium Channels in Perivascular Adipose Tissue-Mediated Regulation of Vascular Tone

Tsvetkov, D., Tano, J., Kaßmann, M., Wang, N., Schubert, R., & Gollasch, M. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00335 · Cited by 26

Multiple metals in children’s deciduous teeth: results from a community-initiated pilot study

Friedman, A., Bauer, J. A., Austin, C. E., Downs, T. J., Tripodis, Y., Heiger‐Bernays, W., White, R. F., Arora, M., & Henn, B. C. (2021) · Journal of Exposure Science & Environmental Epidemiology · doi:10.1038/s41370-021-00400-x · Cited by 26

Luminal cholinergic signalling in airway lining fluid: a novel mechanism for activating chloride secretion via Ca2+‐dependent Cl‐and K+channels

Hollenhorst, M. I., Lips, K. S., Wolff, M., Wess, J., Gerbig, S., Takáts, Z., Kummer, W., & Fronius, M. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01883.x · Cited by 26

Chronic muscle stimulation improves muscle function and reverts the abnormal surface EMG pattern in Myotonic Dystrophy: a pilot study

Chisari, C., Bertolucci, F., Dalise, S., & Rossi, B. (2013) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/1743-0003-10-94 · Cited by 26

Modulation of Ca2+‐activated K+ currents and Ca2+‐dependent action potentials by exocytosis in goldfish bipolar cell terminals

Palmer, M. J. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.105205 · Cited by 26

Effect of 17β-Estradiol on mRNA Expression of Large- Conductance, Voltage-Dependent, and Calcium-Activated Potassium Channel α and β Subunits in Guinea Pig

Jamali, K. A., Naylor, B. R., Kelly, M. J., & Rønnekleiv, O. K. (2003) · Endocrine · doi:10.1385/endo:20:3:227 · Cited by 26

α‐Catulin CTN‐1 is required for BK channel subcellular localization in C. elegans body‐wall muscle cells

Chen, B., Liu, P., Wang, S. J., Ge, Q., Zhan, H., Mohler, W. A., & Wang, Z. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.194 · Cited by 26

Steady-State and Closed-State Inactivation Properties of Inactivating BK Channels

Ding, J. P., & Lingle, C. J. (2002) · Biophysical Journal · doi:10.1016/s0006-3495(02)75588-4 · Cited by 26

Human Amylin Actions on Rat Cholinergic Basal Forebrain Neurons: Antagonism of Beta-Amyloid Effects

Jhamandas, J. H., Harris, K. H., Cho, C., Fu, W., & MacTavish, D. (2003) · Journal of Neurophysiology · doi:10.1152/jn.01138.2002 · Cited by 26

Decreased potassium channel IK1 and its regulator neurotrophin-3 (NT-3) in inflamed human bowel

Arnold, S. J., Facer, P., Yiangou, Y., Chen, M. X., Plumpton, C., Tate, S., Bountra, C., Chan, C. L. H., Williams, N. S., & Anand, P. (2003) · Neuroreport · doi:10.1097/00001756-200302100-00006 · Cited by 26

Mutational analysis of dendritic Ca2+ kinetics in rodent Purkinje cells: role of parvalbumin and calbindin D28k

Schmidt, H., Stiefel, K. M., Račay, P., Schwaller, B., & Eilers, J. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00013.x · Cited by 27

Inhibition of the human intermediate conductance Ca2+-activated K+ channel, hIK1, by volatile anesthetics

Namba, T., Ishii, T. M., Ikeda, M., Hisano, T., Itoh, T., Hirota, K., Adelman, J. P., & Fukuda, K. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00254-5 · Cited by 26

Glucocorticoids stimulate the activity of large-conductance Ca2+-activated K+ channels in pituitary GH3 and AtT-20 cells via a non-genomic mechanism

Huang, M.-H., So, E. C., Liu, Y., & Wu, S. (2005) · Steroids · doi:10.1016/j.steroids.2005.09.009 · Cited by 25

Novel BK channel openers containing dehydroabietic acid skeleton: Structure–activity relationship for peripheral substituents on ring C

Cui, Y., Yasutomi, E., Otani, Y., Yoshinaga, T., Ido, K., Sawada, K., & Ohwada, T. (2008) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2008.08.078 · Cited by 25

Small conductance Ca2+-activated K+ channels regulate firing properties and excitability in parasympathetic cardiac motoneurons in the nucleus ambiguus

Lin, M., Hatcher, J. T., Chen, Q.-H., Wurster, R. D., & Cheng, Z. J. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00134.2010 · Cited by 25

Synthesis and biological evaluation of N-methyl-laudanosine iodide analogues as potential SK channel blockers

Graulich, A., Mercier, F., Scuvée‐Moreau, J., Seutin, V., & Liégeois, J. (2004) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2004.11.025 · Cited by 25

BK and Kv3.1 Potassium Channels Control Different Aspects of Deep Cerebellar Nuclear Neurons Action Potentials and Spiking Activity

Pedroarena, C. M. (2011) · The Cerebellum · doi:10.1007/s12311-011-0279-9 · Cited by 25

Direct Observation of a Preinactivated, Open State in BK Channels with β2 Subunits

Benzinger, G. R., Xia, X., & Lingle, C. J. (2006) · The Journal of General Physiology · doi:10.1085/jgp.200509425 · Cited by 25

Identification of a pharmacophore of SKCa channel blockers

Dilly, S., Graulich, A., Farce, A., Seutin, V., Liégeois, J., & Chavatte, P. (2005) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756360500210989 · Cited by 25

Impaired function of alpha‐2 adrenoceptors in smooth muscle of mesenteric arteries from spontaneously hypertensive rats

Feres, T., Borges, A. C. R., Silva, E. G., Paiva, A. C. M., & Paiva, T. B. (1998) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0702177 · Cited by 25

In vivo cholinergic modulation of the cellular properties of medial entorhinal cortex neurons

Tsuno, Y., Schultheiss, N. W., & Hasselmo, M. E. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.250431 · Cited by 27

Voltage sensor of ion channels and enzymes

Gonzalez, C. L., Contreras, G. F., Peyser, A., Larsson, H. P., Neely, A., & Latorre, R. (2011) · Biophysical Reviews · doi:10.1007/s12551-011-0061-8 · Cited by 23

Potassium channels in pancreatic duct epithelial cells: their role, function and pathophysiological relevance

Venglovecz, V., Rakonczay, Z., Gray, M. A., & Hegyi, P. J. (2014) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-014-1585-0 · Cited by 24

Modulation of BK Channel by MicroRNA-9 in Neurons After Exposure to HIV and Methamphetamine

Tatro, E. T., Hefler, S., Shumaker-Armstrong, S., Soontornniyomkij, B., Yang, M., Yermanos, A., Wren, N., Moore, D. J., & Achim, C. L. (2013) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-013-9446-8 · Cited by 24

Short-term plasticity and modulation of synaptic transmission at mammalian inhibitory cholinergic olivocochlear synapses

Katz, E., & Elgoyhen, A. B. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00224 · Cited by 24

Hypobaric Hypoxia-Induced Learning and Memory Impairment: Elucidating the Role of Small Conductance Ca2+-Activated K+ Channels

Kushwah, N., Jain, V., Dheer, A., Kumar, R., Prasad, D. N., & Khan, N. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.07.026 · Cited by 24

Voltage-dependent dynamics of the BK channel cytosolic gating ring are coupled to the membrane-embedded voltage sensor

Miranda, P., Holmgren, M., & Giráldez, T. (2018) · eLife · doi:10.7554/elife.40664 · Cited by 24

Synthesis and Radioligand Binding Studies of C-5- and C-8-Substituted 1-(3,4-Dimethoxybenzyl)-2,2-dimethyl-1,2,3,4-tetrahydroisoquinoliniums as SK Channel Blockers Related to N -Methyl-laudanosine and N -Methyl-noscapine

Graulich, A., Scuvée‐Moreau, J., Seutin, V., & Liégeois, J. (2005) · Journal of Medicinal Chemistry · doi:10.1021/jm049025p · Cited by 24

Involvement of actin cytoskeleton in modulation of Ca2+-activated K+ channels from rat hippocampal CA1 pyramidal neurons

Huang, H., Rao, Y., Sun, P., & Gong, L. (2002) · Neuroscience Letters · doi:10.1016/s0304-3940(02)00836-4 · Cited by 23

Signaling path of the action of AVP on distal K+ secretion

Amorim, J. B. O., Musa‐Aziz, R., de Mello-Aires, M., & Malnic, G. (2004) · Kidney International · doi:10.1111/j.1523-1755.2004.00800.x · Cited by 24

Vertebrate rod photoreceptors express both BK and IK calcium‐activated potassium channels, but only BK channels are involved in receptor potential regulation

Pelucchi, B., Grimaldi, A., & Moriondo, A. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21467 · Cited by 24

Electrophysiological properties of BK channels in Xenopus motor nerve terminals

Sun, X., Yazejian, B., & Grinnell, A. D. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2003.060509 · Cited by 24

Metabotropic Modulation of Potassium Channels During Synaptic Plasticity

Fernández‐Fernández, D., & Lamas, J. A. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.02.025 · Cited by 22

Extracellular conserved cysteine forms an intersubunit disulphide bridge in the KCNK5 (TASK-2) K + channel without having an essential effect upon activity

Niemeyer, M. I., Cid, L. P., Valenzuela, X., Paeile, V., & Sepúlveda, F. V. (2003) · Molecular Membrane Biology · doi:10.1080/0968768031000084181 · Cited by 23

β4-Subunit increases Slo responsiveness to physiological Ca2+ concentrations and together with β1 reduces surface expression of Slo in hair cells

Bai, J.-P., Surguchev, A. A., & Navaratnam, D. S. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00449.2010 · Cited by 23

Interactions between β-Catenin and the HSlo Potassium Channel Regulates HSlo Surface Expression

Bian, S., Bai, J.-P., Chapin, H. C., Moëllic, C. L., Dong, H., Caplan, M. J., Sigworth, F. J., & Navaratnam, D. S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028264 · Cited by 23

A Novel ShK-Like Toxic Peptide from the Transcriptome of the Cnidarian Palythoa caribaeorum Displays Neuroprotection and Cardioprotection in Zebrafish

Liao, Q., Gong, G., Siu, S. W. I., Wong, C. T. T., Yu, H., Tse, Y. C., Rádis‐Baptista, G., & Lee, S. M. (2018) · Toxins · doi:10.3390/toxins10060238 · Cited by 23

Sodium–Calcium Exchanger Reverse Mode Sustains Dichotomous Ion Fluxes Required for Procoagulant COAT Platelet Formation

Aliotta, A., Calderara, D. B., Zermatten, M. G., & Alberio, L. (2020) · Thrombosis and Haemostasis · doi:10.1055/s-0040-171670 · Cited by 23

Electrophysiological characterization of ion channels in osteoclasts isolated from human deciduous teeth

Weidema, A. F., Dixon, S. J., & Sims, S. M. (2000) · Bone · doi:10.1016/s8756-3282(00)00287-8 · Cited by 23

Nociceptin/Orphanin FQ Modulation of Ionic Conductances in Rat Basal Forebrain Neurons

Chin, J. H., Harris, K., MacTavish, D., & Jhamandas, J. H. (2002) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.037945 · Cited by 23

RyR2 Modulates a Ca2+-Activated K+ Current in Mouse Cardiac Myocytes

Mu, Y., Zhao, W., Duan, P., Chen, Y., Zhao, W., Wang, Q., Tu, H., & Zhang, Q. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094905 · Cited by 23

A Limited Access Compartment between the Pore Domain and Cytosolic Domain of the BK Channel

Zhang, Z., Zhou, Y., Ding, J., Xia, X., & Lingle, C. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3812-06.2006 · Cited by 23

NS19504: A Novel BK Channel Activator with Relaxing Effect on Bladder Smooth Muscle Spontaneous Phasic Contractions

Nausch, B., Rode, F., Jørgensen, S., Nardi, A. E., Korsgaard, M. P. G., Hougaard, C. Ø., Bonev, A. D., Brown, W. D., Dyhring, T., Strøbæk, D., et al. (2014) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.113.212662 · Cited by 23

Differential Processing of Excitation by GABAergic Gain Modulation in Canine Caudal Ventral Respiratory Group Neurons

Tonkovic‐Capin, V., Stucke, A. G., Stuth, E. A. E., Tonković-Capin, M., Hopp, F. A., McCrimmon, D. R., & Zuperku, E. J. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00761.2002 · Cited by 23

Functional Interactions in Ca2+ Signaling over Different Time and Distance Scales

Marchant, J. S., & Parker, I. (2000) · The Journal of General Physiology · doi:10.1085/jgp.116.5.691 · Cited by 23

Large Conductance Calcium-Activated Potassium Channels: Their Expression and Modulation of Glutamate Release from Nerve Terminals Isolated from Rat Trigeminal Caudal Nucleus and Cerebral Cortex

Samengo, I. A., Currò, D., Barrese, V., Taglialatela, M., & Martire, M. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1287-1 · Cited by 22

The VRAC blocker DCPIB directly gates the BK channels and increases intracellular Ca 2+ in melanoma and pancreatic duct adenocarcinoma cell lines

Zuccolini, P., Ferrera, L., Remigante, A., Picco, C., Barbieri, R., Bertelli, S., Morán, Ó., Gavazzo, P., & Pusch, M. (2022) · British Journal of Pharmacology · doi:10.1111/bph.15810 · Cited by 22

Regulatory effect of sulphatides on BKCachannels

Chi, S., & Qi, Z. (2006) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706947 · Cited by 22

The Relationship between Duration of Initial Alcohol Exposure and Persistence of Molecular Tolerance Is Markedly Nonlinear

Velázquez‐Marrero, C., Wynne, P. M., Bernardo, A., Palacio, S., Martin, G. E., & Treistman, S. N. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5429-10.2011 · Cited by 21

A Charged Residue in S4 Regulates Coupling among the Activation Gate, Voltage, and Ca2+Sensors in BK Channels

Zhang, G., Yang, H., Liang, H., Yang, J., Shi, J., McFarland, K., Chen, Y., & Cui, J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1174-14.2014 · Cited by 22

Species-specific Differences among KCNMB3 BK β3 Auxiliary Subunits: Some β3 N-terminal Variants May Be Primate-specific Subunits

Zeng, X., Xia, X., & Lingle, C. J. (2008) · The Journal of General Physiology · doi:10.1085/jgp.200809969 · Cited by 22

Positions of β2 and β3 subunits in the large-conductance calcium- and voltage-activated BK potassium channel

Wu, R. S., Liu, G., Zakharov, S. I., Chudasama, N. L., Motoike, H. K., Karlin, A., & Marx, S. O. (2012) · The Journal of General Physiology · doi:10.1085/jgp.201210891 · Cited by 22

Low-Dimensional Models of “Neuro-Glio-Vascular Unit” for Describing Neural Dynamics under Normal and Energy-Starved Conditions

Chhabria, K., & Chakravarthy, V. S. (2016) · Frontiers in Neurology · doi:10.3389/fneur.2016.00024 · Cited by 24

Ca2+ Influx and Opening of Ca2+-Activated K+ Channels in Muscle Fibers from Control and mdx Mice

Mallouk, N., & Allard, B. (2002) · Biophysical Journal · doi:10.1016/s0006-3495(02)75642-7 · Cited by 22

Inhibitory pathways in the circular muscle of rat jejunum

Vanneste, G., Robberecht, P., & Lefebvre, R. A. (2004) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0705918 · Cited by 22

Purinergic activation of BK channels in clonal kidney cells (Vero cells)

Hafting, T., & Sand, O. (2000) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2000.00766.x · Cited by 22

Peripheral channelopathies as targets for potassium channel openers

Lawson, K., & Dunne, M. J. (2001) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.10.7.1345 · Cited by 22

Ca2+ regulation of a large conductance K+ channel in cultured rat cerebellar Purkinje neurons

Jacquin, T. D., & Gruol, D. L. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00478.x · Cited by 22

Alcohol withdrawal is associated with a downregulation of large-conductance Ca2+-activated K+ channels in rat inferior colliculus neurons

N’Gouemo, P., & Morad, M. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3346-8 · Cited by 21

The Anti-Botulism Triterpenoid Toosendanin Elicits Calcium Increase and Exocytosis in Rat Sensory Neurons

Fang, X. F., & Cui, Z. J. (2011) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-011-9716-z · Cited by 21

Activation of recombinant human SK4 channels by metal cations

Cao, Y., & Houamed, K. M. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)00194-5 · Cited by 21

Electrophysiological Characterization of Benzofuroindole-Induced Potentiation of Large-Conductance Ca2+-Activated K+ Channels

Ha, T. S., Lim, H., Lee, G. E., Kim, Y., & Park, C. (2005) · Molecular Pharmacology · doi:10.1124/mol.105.016170 · Cited by 21

SERCA activity is required for timely progression through G1/S

Simon, V. R., & Moran, M. F. (2001) · Cell Proliferation · doi:10.1046/j.1365-2184.2001.00192.x · Cited by 21

Are ion channels potential therapeutic targets for Parkinson’s disease?

Daniel, N. H., Aravind, A., & Thakur, P. S. (2021) · NeuroToxicology · doi:10.1016/j.neuro.2021.10.008 · Cited by 20

Multiple Firing Patterns in Deep Dorsal Horn Neurons of the Spinal Cord: Computational Analysis of Mechanisms and Functional Implications

Franc, Y. L., & Masson, G. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00919.2009 · Cited by 19

Dynamic dendritic compartmentalization underlies stimulus-specific adaptation in an insect neuron

Prešern, J., Triblehorn, J. D., & Schul, J. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00945.2014 · Cited by 21

Mg2+ binding to open and closed states can activate BK channels provided that the voltage sensors are elevated

Chen, R., Geng, Y., & Magleby, K. L. (2011) · The Journal of General Physiology · doi:10.1085/jgp.201110707 · Cited by 20

Molecular modeling and docking simulations of scorpion toxins and related analogs on human SKCa2 and SKCa3 channels

Andreotti, N., di Luccio, E., Sampiéri, F., WAARD, M. M. D., & Sabatier, J. (2005) · Peptides · doi:10.1016/j.peptides.2005.01.022 · Cited by 20

Deciphering the Role of Ca2+ Signalling in Cancer Metastasis: From the Bench to the Bedside

Alharbi, A., Zhang, Y., & Parrington, J. (2021) · Cancers · doi:10.3390/cancers13020179 · Cited by 20

Presynaptic large-conductance calcium-activated potassium channels control synaptic transmission in the superficial dorsal horn of the mouse

Furukawa, N., Takasusuki, T., Fukushima, T., & Hori, Y. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.08.022 · Cited by 20

Differential Modulation of Respiratory Neuronal Discharge Patterns by GABAA Receptor and Apamin-Sensitive K+ Channel Antagonism

Tonkovic‐Capin, V., Stucke, A. G., Stuth, E. A. E., Tonković-Capin, M., Krolo, M., Hopp, F. A., McCrimmon, D. R., & Zuperku, E. J. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.5.2363 · Cited by 20

Effects of haloperidol on K(+) currents in acutely isolated rat retinal ganglion cells.

Akamine, T., Nishimura, Y., Ito, K., Uji, Y., & Yamamoto, T. (2002) · PubMed · Cited by 20

Calcium Activates SK Channels in the Intact Human Lens

Rhodes, J. D., Collison, D. J., & Duncan, G. (2003) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.03-0013 · Cited by 20

Syntaxin-1A Binds to and Modulates the Slo Calcium-Activated Potassium Channel via an Interaction That Excludes Syntaxin Binding to Calcium Channels

Cibulsky, S. M., Hong, F., & Levitan, I. B. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00789.2004 · Cited by 20

Small conductance calcium-activated K+ channels, SkCa, but not voltage-gated K+ (Kv) channels, are implicated in the antinociception induced by CGS21680, a A2A adenosine receptor agonist

Regaya, I., Pham, T., Andreotti, N., Sauze, N., Carrega, L., Martin‐Eauclaire, M., Jouirou, B., Peragut, J. C., Vacher, H., Rochat, H., et al. (2004) · Life Sciences · doi:10.1016/j.lfs.2004.06.023 · Cited by 20

A Simple Mathematical Model of Second-Messenger Mediated Slow Excitatory Postsynaptic Potentials

Bertrand, P. P., Thomas, E. A., Kunze, W. A. A., & Bornstein, J. C. (2000) · Journal of Computational Neuroscience · doi:10.1023/a:1008969115017 · Cited by 20

Bibliometric analysis of potassium channel research

Shi, J., Shi, S., Shi, S., Jia, Q., Yuan, G., Chu, Y., Wang, H., Hu, Y., & Cui, H. (2019) · Channels · doi:10.1080/19336950.2019.1705055 · Cited by 20

Endothelial KCa channels: Novel targets to reduce atherosclerosis-driven vascular dysfunction

Vera, O. D., Wulff, H., & Braun, A. P. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1151244 · Cited by 20

The Ca2+-activated, large conductance K+-channel (BKCa) is a player in the LH/hCG signaling cascade in testicular Leydig cells

Matzkin, M. E., Lauf, S., Spinnler, K., Rossi, S. P., Köhn, F. M., Kunz, L., Calandra, R. S., Frungieri, M. B., & Mayerhofer, A. (2012) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2012.12.015 · Cited by 19

Computational modeling of spike generation in serotonergic neurons of the dorsal raphe nucleus

Tuckwell, H. C., & Penington, N. J. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.04.001 · Cited by 19

Regulation of Bestrophins by Ca2+: A Theoretical and Experimental Study

Kranjc, A., Grillo, F. W., Rievaj, J., Boccaccio, A., Pietrucci, F., Menini, A., Carloni, P., & Anselmi, C. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004672 · Cited by 19

The synthesis and BK channel-opening activity of N-acylaminoalkyloxime derivatives of dehydroabietic acid

Cui, Y., Liu, X., Zhang, W., Lin, H., Ohwada, T., Ido, K., & Sawada, K. (2015) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2015.12.038 · Cited by 19

Targeting Ion Channels: An Important Therapeutic Implication in Gastrointestinal Dysmotility in Patients With Spinal Cord Injury

Radulovic, M., Anand, P., Korsten, M. A., & Gong, B. (2015) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm15061 · Cited by 19

Altered auditory and vestibular functioning in individuals with low bone mineral density: a systematic review

Singh, N. K., Jha, R. H., Gargeshwari, A., & Kumar, P. (2017) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/s00405-017-4768-4 · Cited by 19

Investigating Potassium Channels in Budding Yeast: A Genetic Sandbox.

Mackie, T. D., & Brodsky, J. L. (2018) · PubMed Central · doi:10.1534/genetics.118.301026 · Cited by 19

Effects of Multiple Metal Binding Sites on Calcium and Magnesium-dependent Activation of BK Channels

Hu, L., Yang, H., Shi, J., & Cui, J. (2005) · The Journal of General Physiology · doi:10.1085/jgp.200509317 · Cited by 19

Role of BK Potassium Channels Shaping Action Potentials and the Associated [Ca2+]i Oscillations in GH3 Rat Anterior Pituitary Cells

Miranda, P., de la Peña, P., Gómez‐Varela, D., & Barros, F. (2003) · Neuroendocrinology · doi:10.1159/000069509 · Cited by 19

Paraoxon suppresses Ca2+ spike and afterhyperpolarization in snail neurons: Relevance to the hyperexcitability induction

Vatanparast, J., Janahmadi, M., Asgari, A. R., Sepehri, H., & Haeri-Rohani, A. (2006) · Brain Research · doi:10.1016/j.brainres.2006.02.016 · Cited by 19

Ca2+ activation of hSlo K+ channel is suppressed by N‐terminal GFP tag

Meyer, E., & Fromherz, P. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00548.x · Cited by 19

External Copper Inhibits the Activity of the Large-Conductance Calcium- and Voltage-sensitive Potassium Channel from Skeletal Muscle

Vergara, C., Morera, F. J., & Wolff, D. (2003) · The Journal of Membrane Biology · doi:10.1007/s00232-002-1064-y · Cited by 19

ATP inhibition of a mouse brain large‐conductance K+ (mslo) channel variant by a mechanism independent of protein phosphorylation

Clark, A. G., Hall, S., & Shipston, M. J. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.045aa.x · Cited by 19

Identification and Functional Characterization of Ankyrin-Repeat Family Protein ANKRA as a Protein Interacting with BKCaChannel

Lim, H., & Park, C. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-06-0537 · Cited by 19

Cysteine String Protein Limits Expression of the Large Conductance, Calcium-Activated K+ (BK) Channel

Ahrendt, E., Kyle, B. D., Braun, A. P., & Braun, J. E. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086586 · Cited by 18

Autoradiographic localization of apamin-sensitive Ca2+-dependent K+ channels in rat brain

Mourre, C., Schmid‐Antomarchi, H., Hugues, M., & Lazdunski, M. (1984) · European Journal of Pharmacology · doi:10.1016/0014-2999(84)90329-7 · Cited by 20

Ca2+-activated K+ channels

Ashcroft, F. M. (2000) · Elsevier eBooks · doi:10.1016/b978-012065310-2/50008-4 · Cited by 22

Chapter 8 Calcium-Activated Potassium Channels in Muscle and Brain

Wallner, M., Meera, P., & Toro, L. (1999) · Current topics in membranes · doi:10.1016/s0070-2161(08)60924-7 · Cited by 19

Calcium-Activated K+ Channels (KCa) and Therapeutic Implications

Dudem, S., Sergeant, G. P., Thornbury, K. D., & Hollywood, M. A. (2021) · Handbook of experimental pharmacology · doi:10.1007/164_2021_459 · Cited by 19

Matching molecules to function: neuronal Ca2+-activated K+ channels and afterhyperpolarizations

Stocker, M. (2004) · Toxicon · doi:10.1016/s0041-0101(04)00136-9 · Cited by 4