Calcium-activated potassium channels

Stability constants of metal-ion complexes

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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

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Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence

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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

Peripheral channelopathies as targets for potassium channel

Dunne, M. J. (2001)

GABA Receptor and KCa Channel-mediated Electrical Suppression in Anoxic Cortical Pyramidal Neurons of the Painted Turtle (Chrysemys picta bellii)

Hogg, D. W. (2015) · TSpace (University of Toronto)

1-Ethyl-Benzimidazolinone

Taglialatela, M., & Luisi, R. (2008) · xPharm: The Comprehensive Pharmacology Reference · doi:10.1016/b978-008055232-3.63555-x

pH sensitive fluorescent sensors

Barman, D. N. (2007) · doi:10.32469/10355/4972

MECHANISMS OF SEIZURE REDUCTION BY LOW FREQUENCY ELECTRICAL STIMULATION

Toprani, S. (2014) · OhioLink ETD Center (Ohio Library and Information Network)

TRPV4 in Ventilator-induced Lung Injury – Mechanisms of Endothelial Mechanotransduction and Barrier Regulation in the Lung

Michalick, L. (2017) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-12514

Characterization of the Ionic Currents In Cultured Small Intensely Fluorescent Cells from Superior Cervical Ganglia of Neonatal Rats

Alexander, S. A. (1999) · MacSphere (McMaster University) · doi:10.71548/5284

Reconstitution in planar lipid bilayers of ion channels synthesized in ovo and in vitro

Lyford, L. K., & Rosenberg, R. L. (2003) · Membrane science and technology/Membrane science and technology series · doi:10.1016/s0927-5193(03)80037-2

Using a computational model to analyze the effects of firing frequency on synchrony of a network of gap junction-coupled hypoglossal motoneurons

Memelli, H., Horn, K. G., Wittie, L. D., & Solomon, I. C. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63488-7.00006-9

An Investigation into the Combined Tocolytic Effect of Magnesium and Other Tocolytics

Osaghae, B. E. (2019) · University of Liverpool · doi:10.17638/03054120

Molecular Properties of Ion Channels

Jan, L. Y., & Jan, Y. N. (2004) · Elsevier eBooks · doi:10.1016/b978-012148660-0/50007-x

Activity-Dependent Calcium Dynamics in Spinal Cord Lamina I Neurons

Harding, E. K. (2018) · TSpace (University of Toronto)

Ebola: Destroys Na+/K+ Ion Exchange to Accelerate Electrolyte Imbalance by Scorpion Venom-like SystemPreprint

Liu, W., & hualan, L. (2021) · doi:10.33774/chemrxiv-2021-1n5l8

Bibliography

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Potassium channels

Mourre, C. (2002) · CRC Press eBooks · doi:10.1201/9780203219096.ch8

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Potassium Channels

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Ion Channel Protein Superfamily

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Neurophysiologische Grundlagen

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Ebola virus destroys electrolyte balance to accelerate fusion by scorpion venom-like and GP120/Rab27a GTPase-like system

Liu, W., & hualan, L. (2022) · Trace Elements and Electrolytes · doi:10.5414/te500042

Participação dos canais para K+ e Ca2+ no controle das propriedades eletrofisiológicas dos motoneurônios parassimpáticos respiratórios do núcleo motor dorsal do vago

de Souza, V. F. (2022) · doi:10.11606/t.17.2022.tde-03012023-124100

Molecular mechanism of HNTX-I activates the intermediate-conductance Ca2+-activated K+ (IK) channels

Wubulikasimu, A., He, Z., Long, Y., Yuan, F., Hou, W., Liao, Q., Chen, H., & Rong, M. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.125197

Characterization of endogenous Kv1.3 channel isoforms in T cells.

Pérez, J. S. (2023) · UVaDOC UVaDOC University of Valladolid Documentary Repository (University of Valladolid) · doi:10.35376/10324/63662

Danggui Buxue Decoction and its Components Dilate Coronary Artery Through Activating the Kir PathwayPreprint

An, W. Q., Tian, Q., Guo, P., Chen, M., Zhang, T., Yang, P., & Zhang, S. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4939476

BK channels and alcohol tolerance: Insights from studies on Drosophila, nematodes, rodents and cell lines: A systematic review

Ignat, L. A., Tipa, R. O., Cehan, A. R., & Bacârea, V. (2025) · Medicine International · doi:10.3892/mi.2025.232

A NEST-based framework unlocks massively parallel simulation of networks of multi-compartment neurons with customizable subcellular dynamics

Wybo, W. A. M., Ewert, L., Linssen, C., Babu, P. N., Pastorelli, E., Paolucci, P. S., & Morrison, A. (2026) · Communications Biology · doi:10.1101/2025.06.30.662287

Slow intrinsic oscillations in the ventrolateral preoptic nucleus

Perrenoud, Q., Ribot, J., Geoffroy, H., Gallopin, T., Rouach, N., & Rancillac, A. (2026) · iScience · doi:10.1016/j.isci.2026.116477

Cell volume regulation

Baumgarten, C. M., & Feher, J. (2025) · Elsevier eBooks · doi:10.1016/b978-0-12-811114-7.00011-6

The Diverse Roles of K + Channels in Brain Ischemia

Misonou, H., & Trimmer, J. S. (2009) · Humana Press eBooks · doi:10.1007/978-1-60761-280-3_12

Detection of SK2 Channels on Hippocampal Neurons

Maciaszek, J. L. (2012) · OpenCommons - UConn (University of Connecticut)

Maintenance of Neuron Activity by Homeostatic Alterations in Receptors and Ion Channels in a Rett Syndrome Mouse Model

Oginsky, M. F. (2022) · doi:10.57709/6426123

Studies on spreading depolarization in healthy and metabolically compromised brain tissues

Aiba, I. (2012) · UNM’s Digital Repository (University of New Mexico)

Isolation, Synthesis, and Pharmacological Characterization of a Short-Structured Peptide from the Venom of Phidippus Audax that Affects Potassium Currents

Salceda, E., Arenas, I., Olamendi-Portugal, T., Reyes, A., Piña, O., Corzo, G., Soto, E., & Villegas, E. (2026) · International Journal of Peptide Research and Therapeutics · doi:10.1007/s10989-025-10792-1

Serial serum calcium dynamics predict delayed hydrocephalus after spontaneous subarachnoid hemorrhage: development and validation of a clinical nomogram in an observational cohort

Wu, D., Zhai, X., Zhang, X., Xu, H., Hao, L., Wang, C., Wang, S., Wang, Z., Wang, Z., & Wang, Y. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1762189

TMPRSS3 dont les mutations sont responsables des surdités humaines DFNB8/10, joue un rôle crucial dans la survie des cellules sensorielles lors de l'entrée en fonction cochléaire : caractérisation du modèle animal et identification des voies de signalisation impliquées

Fasquelle, L. (2011) · doi:10.70675/be68b6bcz50f8z42b5z9a78z5eebec0861e4

Rôle du canal calcique de type T, Cav3.2 et de ses protéines partenaires dans la tumorogenèse prostatique

Warnier, M. (2013) · doi:10.70675/53c5b77fzdaf1z4e01za903z8f735034bc57

Effets de la modulation des canaux potassium SK et Kv4 sur les déficits moteurs et cognitifs de la maladie de Parkinson

Aidi-Knani, S. (2014) · theses.fr (ABES) · doi:10.70675/9bcb3ccfzbea9z4555z8ab9zebc1216c5e8b

Rôle du canal Nav1.9 dans les mécanismes physiopathologiques de la céphalée migraineuse

Bonnet, C. (2017) · doi:10.70675/244a2cf6zad09z4d71z9371z023d23f3b044

Ca2+ handling in a mice model of CPVT

Wang, Y. (2016) · doi:10.70675/47b5b0ecz0c72z4c19z87e8z1a212cdf1a58

Les cytokines inflammatoires et les canaux ioniques dans la tumorigénèse du cancer colorectal : rôle du TNF et modulation du KCa3.1

Ibrahim, S. (2019) · theses.fr (ABES) · doi:10.70675/c5448d83z840cz458dz90d0za870d8188f29

L'interaction entre le canal calcique Orai3 et la protéine réticulaire STIM2 contribue à la prolifération et la survie des cellules cancéreuses prostatiques

Kouba, S. (2020) · theses.fr (ABES) · doi:10.70675/5b5af316z8676z4980zaa53zd235bf449fcb

Changes in Calcium Cycling and Its Mechanisms in Sinoatrial-node underlying the TAC-induced Heart Failure in Mouse

Xue, J. (2020) · doi:10.70675/84e3c762zd128z4412zae45z780280ad878f

Etude des réseaux moteurs du tronc cérébral impliqués dans l’activité rythmique des muscles des voies aériennes supérieures

Bergé-Laval, V. (2022) · doi:10.70675/113288c1zcad7z4c97z8e66zfa827c1455b2

Génomique de la résistance aux insecticides chez la punaise de lit Cimex lectularius

Haberkorn, C. (2023) · theses.fr (ABES) · doi:10.70675/e800fb57z2c19z40abz8285zc538251d131b

Cortical excitability : Prefrontal conditional bistability for parametric working memory in physiological and Alzheimer's Disease conditions & Somatosensory epileptic network activity following neurodevelopmental interneuron mutations

Leroux, M. (2023) · theses.fr (ABES) · doi:10.70675/d51b586bz96daz4ecbzbac2zc54c3576aef2

Synaptic mechanisms underlying the function of neocortical layer 1 interneurons in the primary visual cortez

Martinez, M. (2025) · theses.fr (ABES) · doi:10.70675/d05e33fcz2cd4z45d4zbe74z5e57fadd4292

Drug repurposing DMSO from an old solvent to a new candidate for the treatment of colitis and sepsis in male mice

Pang, S., Rong, S., Zhang, Y., Tong, S., Gong, Y., Zhao, W., & Dong, H. (2026) · Cell Calcium · doi:10.1016/j.ceca.2026.103155

Advances in epigenetic regulation of potassium channels in chronic pain

Fan, Z., Cao, J., Ren, W., Zhou, J., Zhao, H., Liu, F., & Fang, J. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12055-8

Age-related differences in how tDCS priming modulates cortical inhibition during fatigue recovery

Moore, E. K., Otieno, L. A., Semmler, J. G., Smith, A. E., & Sidhu, S. K. (2026) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2026.06.001

Potassium channels in cancer: from hallmarks to therapeutic targeting

Zhang, Y.-L., Shi, R.-J., & Liang, X.-H. (2026) · Journal of physiology and biochemistry · doi:10.1007/s13105-026-01228-5

BindingDB Entry 50020562: Synthesis and pharmacological testing of polyaminoquinolines as blockers of the apamin-sensitive Ca2+-activated K+ channel (SK(Ca)).

BindingDB (2009) · UC San Diego · doi:10.7270/q2416wsj

BindingDB Entry 50041602: Novel 1,4-benzothiazine derivatives as large conductance Ca2+-activated potassium channel openers.

BindingDB (2013) · UC San Diego · doi:10.7270/q2r49s16

BindingDB Entry 50003719: 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.

BindingDB (2020) · UC San Diego · doi:10.7270/q2th8qfs

BindingDB Entry 50036931: Recent developments in the biology and medicinal chemistry of potassium channel modulators: update from a decade of progress.

BindingDB (2012) · UC San Diego · doi:10.7270/q218376d

BindingDB Entry 50003792: Synthesis and radioligand binding studies of methoxylated 1,2,3,4-tetrahydroisoquinolinium derivatives as ligands of the apamin-sensitive Ca2+-activated K+ channels.

BindingDB (2020) · UC San Diego · doi:10.7270/q2s75k20

Control of Spiking Activity by Persistent Sodium and Hyperpolarization-activated Currents

Ghabel, H. (2022) · Digital Archive @ GSU · doi:10.57709/7030083

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