Canale del potassio (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Canale del potassio" in Italian language version.

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Global rank Italian rank

39nih.gov

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35doi.org

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15oadoi.org

799^th place

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3archive.org

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(EN) Hille, Bertil, Chapter 5: Potassium Channels and Chloride Channels, in Ion channels of excitable membranes, Sunderland, Mass, Sinauer, 2001, pp. 131–168, ISBN 0-87893-321-2.
(EN) Jessell, Thomas M.; Kandel, Eric R.; Schwartz, James H., Chapter 6: Ion Channels, in Principles of Neural Science, 4th, New York, McGraw-Hill, 2000, pp. 105–124, ISBN 0-8385-7701-6.
Rang, HP, Pharmacology, Edinburgh, Churchill Livingstone, 2003, p. 60, ISBN 0-443-07145-4.

doi.org

dx.doi.org

(EN) Littleton JT, Ganetzky B, Ion channels and synaptic organization: analysis of the Drosophila genome, in Neuron, vol. 26, n. 1, 2000, pp. 35–43, DOI:10.1016/S0896-6273(00)81135-6, PMID 10798390.
Kobayashi T, Washiyama K, Ikeda K, Inhibition of G protein-activated inwardly rectifying K+ channels by ifenprodil, in Neuropsychopharmacology, vol. 31, n. 3, Mar 2006, pp. 516–24, DOI:10.1038/sj.npp.1300844, PMID 16123769.
Enyedi P, Czirják G, Molecular background of leak K+ currents: two-pore domain potassium channels, in Physiological Reviews, vol. 90, n. 2, Apr 2010, pp. 559–605, DOI:10.1152/physrev.00029.2009, PMID 20393194.
Lotshaw DP, Biophysical, pharmacological, and functional characteristics of cloned and native mammalian two-pore domain K+ channels, in Cell Biochemistry and Biophysics, vol. 47, n. 2, 2007, pp. 209–56, DOI:10.1007/s12013-007-0007-8, PMID 17652773.
Fink M, Lesage F, Duprat F, Heurteaux C, Reyes R, Fosset M, Lazdunski M, A neuronal two P domain K+ channel stimulated by arachidonic acid and polyunsaturated fatty acids, in The EMBO Journal, vol. 17, n. 12, Jun 1998, pp. 3297–308, DOI:10.1093/emboj/17.12.3297, PMC 1170668, PMID 9628867.
Goldstein SA, Bockenhauer D, O'Kelly I, Zilberberg N, Potassium leak channels and the KCNK family of two-P-domain subunits, in Nature Reviews. Neuroscience, vol. 2, n. 3, Mar 2001, pp. 175–84, DOI:10.1038/35058574, PMID 11256078.
Sano Y, Inamura K, Miyake A, Mochizuki S, Kitada C, Yokoi H, Nozawa K, Okada H, Matsushime H, Furuichi K, A novel two-pore domain K+ channel, TRESK, is localized in the spinal cord, in The Journal of Biological Chemistry, vol. 278, n. 30, Jul 2003, pp. 27406–12, DOI:10.1074/jbc.M206810200, PMID 12754259.
Czirják G, Tóth ZE, Enyedi P, The two-pore domain K+ channel, TRESK, is activated by the cytoplasmic calcium signal through calcineurin, in The Journal of Biological Chemistry, vol. 279, n. 18, Apr 2004, pp. 18550–8, DOI:10.1074/jbc.M312229200, PMID 14981085.
Kindler CH, Yost CS, Gray AT, Local anesthetic inhibition of baseline potassium channels with two pore domains in tandem, in Anesthesiology, vol. 90, n. 4, Apr 1999, pp. 1092–102, DOI:10.1097/00000542-199904000-00024, PMID 10201682.
Meadows HJ, Randall AD, Functional characterisation of human TASK-3, an acid-sensitive two-pore domain potassium channel, in Neuropharmacology, vol. 40, n. 4, Mar 2001, pp. 551–9, DOI:10.1016/S0028-3908(00)00189-1, PMID 11249964.
Kindler CH, Paul M, Zou H, Liu C, Winegar BD, Gray AT, Yost CS, Amide local anesthetics potently inhibit the human tandem pore domain background K+ channel TASK-2 (KCNK5), in The Journal of Pharmacology and Experimental Therapeutics, vol. 306, n. 1, Jul 2003, pp. 84–92, DOI:10.1124/jpet.103.049809, PMID 12660311.
Punke MA, Licher T, Pongs O, Friederich P, Inhibition of human TREK-1 channels by bupivacaine, in Anesthesia and Analgesia, vol. 96, n. 6, Jun 2003, pp. 1665–73, DOI:10.1213/01.ANE.0000062524.90936.1F, PMID 12760993.
Duprat F, Lesage F, Fink M, Reyes R, Heurteaux C, Lazdunski M, TASK, a human background K+ channel to sense external pH variations near physiological pH, in The EMBO Journal, vol. 16, n. 17, Sep 1997, pp. 5464–71, DOI:10.1093/emboj/16.17.5464, PMC 1170177, PMID 9312005.
Reyes R, Duprat F, Lesage F, Fink M, Salinas M, Farman N, Lazdunski M, Cloning and expression of a novel pH-sensitive two pore domain K+ channel from human kidney, in The Journal of Biological Chemistry, vol. 273, n. 47, Nov 1998, pp. 30863–9, DOI:10.1074/jbc.273.47.30863, PMID 9812978.
Meadows HJ, Benham CD, Cairns W, Gloger I, Jennings C, Medhurst AD, Murdock P, Chapman CG, Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel, in Pflügers Archiv, vol. 439, n. 6, Apr 2000, pp. 714–22, DOI:10.1007/s004240050997, PMID 10784345.
Patel AJ, Honoré E, Lesage F, Fink M, Romey G, Lazdunski M, Inhalational anesthetics activate two-pore-domain background K+ channels, in Nature Neuroscience, vol. 2, n. 5, May 1999, pp. 422–6, DOI:10.1038/8084, PMID 10321245.
Gray AT, Zhao BB, Kindler CH, Winegar BD, Mazurek MJ, Xu J, Chavez RA, Forsayeth JR, Yost CS, Volatile anesthetics activate the human tandem pore domain baseline K+ channel KCNK5, in Anesthesiology, vol. 92, n. 6, Jun 2000, pp. 1722–30, DOI:10.1097/00000542-200006000-00032, PMID 10839924.
Rogawski MA, Bazil CW, New molecular targets for antiepileptic drugs: alpha(2)delta, SV2A, and K(v)7/KCNQ/M potassium channels, in Current Neurology and Neuroscience Reports, vol. 8, n. 4, Jul 2008, pp. 345–52, DOI:10.1007/s11910-008-0053-7, PMC 2587091, PMID 18590620.
Mikko Hellgren, Lars Sandberg e Olle Edholm, A comparison between two prokaryotic potassium channels (KirBac1.1 and KcsA) in a molecular dynamics (MD) simulation study, in Biophysical Chemistry, vol. 120, n. 1, 1º marzo 2006, pp. 1–9, DOI:10.1016/j.bpc.2005.10.002. URL consultato il 24 maggio 2017.
Youxing Jiang, Alice Lee e Jiayun Chen, Crystal structure and mechanism of a calcium-gated potassium channel, in Nature, vol. 417, n. 6888, 30 maggio 2002, pp. 515–522, DOI:10.1038/417515a. URL consultato il 25 maggio 2017.
Chunguang Kong, Weizhong Zeng e Sheng Ye, Distinct gating mechanisms revealed by the structures of a multi-ligand gated K(+) channel, in eLife, vol. 1, 13 dicembre 2012, pp. e00184, DOI:10.7554/eLife.00184. URL consultato il 25 maggio 2017.
Yu Cao, Xiangshu Jin e Hua Huang, Crystal structure of a potassium ion transporter, TrkH, in Nature, vol. 471, n. 7338, 17 marzo 2011, pp. 336–340, DOI:10.1038/nature09731. URL consultato il 25 maggio 2017.
Peng Yuan, Manuel D. Leonetti e Alexander R. Pico, Structure of the Human BK Channel Ca2+-Activation Apparatus at 3.0 Å Resolution, in Science (New York, N.Y.), vol. 329, n. 5988, 9 luglio 2010, pp. 182–186, DOI:10.1126/science.1190414. URL consultato il 25 maggio 2017.
Yunkun Wu, Yi Yang e Sheng Ye, Structure of the gating ring from the human large-conductance Ca2+-gated K+ channel, in Nature, vol. 466, n. 7304, pp. 393–397, DOI:10.1038/nature09252.
V. B. Luzhkov e J. Åqvist, Ions and blockers in potassium channels: insights from free energy simulations, in Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics, vol. 1747, n. 1, 14 febbraio 2005, pp. 109–120, DOI:10.1016/j.bbapap.2004.10.006. URL consultato il 25 maggio 2017.
David J. Posson, Jason G. McCoy e Crina M. Nimigean, The voltage-dependent gate in MthK potassium channels is located at the selectivity filter, in Nature Structural & Molecular Biology, vol. 20, n. 2, 1º febbraio 2013, pp. 159–166, DOI:10.1038/nsmb.2473. URL consultato il 25 maggio 2017.
Kene N. Piasta, Douglas L. Theobald e Christopher Miller, Potassium-selective block of barium permeation through single KcsA channels, in The Journal of General Physiology, vol. 138, n. 4, 1º ottobre 2011, pp. 421–436, DOI:10.1085/jgp.201110684. URL consultato il 25 maggio 2017.
Steve W. Lockless, Ming Zhou e Roderick MacKinnon, Structural and thermodynamic properties of selective ion binding in a K+ channel, in PLoS biology, vol. 5, n. 5, 1º maggio 2007, pp. e121, DOI:10.1371/journal.pbio.0050121. URL consultato il 25 maggio 2017.
Yee Ling Lam, Weizhong Zeng e David Bryant Sauer, The conserved potassium channel filter can have distinct ion binding profiles: Structural analysis of rubidium, cesium, and barium binding in NaK2K, in The Journal of General Physiology, vol. 144, n. 2, 25 maggio 2017, pp. 181–192, DOI:10.1085/jgp.201411191. URL consultato il 25 maggio 2017.
Rui Guo, Weizhong Zeng e Hengjun Cui, Ionic interactions of Ba2+ blockades in the MthK K+ channel, in The Journal of General Physiology, vol. 144, n. 2, 25 maggio 2017, pp. 193–200, DOI:10.1085/jgp.201411192. URL consultato il 25 maggio 2017.
Susan I. V. Judge e Christopher T. Bever Jr., Potassium channel blockers in multiple sclerosis: Neuronal Kv channels and effects of symptomatic treatment, in Pharmacology & Therapeutics, vol. 111, n. 1, 1º luglio 2006, pp. 224–259, DOI:10.1016/j.pharmthera.2005.10.006. URL consultato il 25 maggio 2017.
G. Krapivinsky, E. A. Gordon e K. Wickman, The G-protein-gated atrial K+ channel IKAch is a heteromultimer of two inwardly rectifying K+-channel proteins, in Nature, vol. 374, 1º marzo 1995, pp. 135–141, DOI:10.1038/374135a0. URL consultato il 25 maggio 2017.
(EN) Shawn Corey, Grigory Krapivinsky e Luba Krapivinsky, Number and Stoichiometry of Subunits in the Native Atrial G-protein-gated K+ Channel, IKACh, in Journal of Biological Chemistry, vol. 273, n. 9, 27 febbraio 1998, pp. 5271–5278, DOI:10.1074/jbc.273.9.5271. URL consultato il 25 maggio 2017.
Kevin Wickman, Grigory Krapivinsky e Shawn Corey, Structure, G Protein Activation, and Functional Relevance of the Cardiac G Protein-Gated K+ Channel, IKACh, in Annals of the New York Academy of Sciences, vol. 868, 1º aprile 1999, pp. 386–398, DOI:10.1111/j.1749-6632.1999.tb11300.x. URL consultato il 25 maggio 2017.

doi.org

Yunkun Wu, Yi Yang e Sheng Ye, Structure of the gating ring from the human large-conductance Ca2+-gated K+ channel, in Nature, vol. 466, n. 7304, pp. 393–397, DOI:10.1038/nature09252.

harvard.edu

adsabs.harvard.edu

G. Krapivinsky, E. A. Gordon e K. Wickman, The G-protein-gated atrial K+ channel IKAch is a heteromultimer of two inwardly rectifying K+-channel proteins, in Nature, vol. 374, 1º marzo 1995, pp. 135–141, DOI:10.1038/374135a0. URL consultato il 25 maggio 2017.
Kevin Wickman, Grigory Krapivinsky e Shawn Corey, Structure, G Protein Activation, and Functional Relevance of the Cardiac G Protein-Gated K+ Channel, IKACh, in Annals of the New York Academy of Sciences, vol. 868, 1º aprile 1999, pp. 386–398, DOI:10.1111/j.1749-6632.1999.tb11300.x. URL consultato il 25 maggio 2017.

jbc.org

(EN) Shawn Corey, Grigory Krapivinsky e Luba Krapivinsky, Number and Stoichiometry of Subunits in the Native Atrial G-protein-gated K+ Channel, IKACh, in Journal of Biological Chemistry, vol. 273, n. 9, 27 febbraio 1998, pp. 5271–5278, DOI:10.1074/jbc.273.9.5271. URL consultato il 25 maggio 2017.

nih.gov

ncbi.nlm.nih.gov

(EN) Littleton JT, Ganetzky B, Ion channels and synaptic organization: analysis of the Drosophila genome, in Neuron, vol. 26, n. 1, 2000, pp. 35–43, DOI:10.1016/S0896-6273(00)81135-6, PMID 10798390.
Kobayashi T, Washiyama K, Ikeda K, Inhibition of G protein-activated inwardly rectifying K+ channels by ifenprodil, in Neuropsychopharmacology, vol. 31, n. 3, Mar 2006, pp. 516–24, DOI:10.1038/sj.npp.1300844, PMID 16123769.
Enyedi P, Czirják G, Molecular background of leak K+ currents: two-pore domain potassium channels, in Physiological Reviews, vol. 90, n. 2, Apr 2010, pp. 559–605, DOI:10.1152/physrev.00029.2009, PMID 20393194.
Lotshaw DP, Biophysical, pharmacological, and functional characteristics of cloned and native mammalian two-pore domain K+ channels, in Cell Biochemistry and Biophysics, vol. 47, n. 2, 2007, pp. 209–56, DOI:10.1007/s12013-007-0007-8, PMID 17652773.
Fink M, Lesage F, Duprat F, Heurteaux C, Reyes R, Fosset M, Lazdunski M, A neuronal two P domain K+ channel stimulated by arachidonic acid and polyunsaturated fatty acids, in The EMBO Journal, vol. 17, n. 12, Jun 1998, pp. 3297–308, DOI:10.1093/emboj/17.12.3297, PMC 1170668, PMID 9628867.
Goldstein SA, Bockenhauer D, O'Kelly I, Zilberberg N, Potassium leak channels and the KCNK family of two-P-domain subunits, in Nature Reviews. Neuroscience, vol. 2, n. 3, Mar 2001, pp. 175–84, DOI:10.1038/35058574, PMID 11256078.
Sano Y, Inamura K, Miyake A, Mochizuki S, Kitada C, Yokoi H, Nozawa K, Okada H, Matsushime H, Furuichi K, A novel two-pore domain K+ channel, TRESK, is localized in the spinal cord, in The Journal of Biological Chemistry, vol. 278, n. 30, Jul 2003, pp. 27406–12, DOI:10.1074/jbc.M206810200, PMID 12754259.
Czirják G, Tóth ZE, Enyedi P, The two-pore domain K+ channel, TRESK, is activated by the cytoplasmic calcium signal through calcineurin, in The Journal of Biological Chemistry, vol. 279, n. 18, Apr 2004, pp. 18550–8, DOI:10.1074/jbc.M312229200, PMID 14981085.
Kindler CH, Yost CS, Gray AT, Local anesthetic inhibition of baseline potassium channels with two pore domains in tandem, in Anesthesiology, vol. 90, n. 4, Apr 1999, pp. 1092–102, DOI:10.1097/00000542-199904000-00024, PMID 10201682.
Meadows HJ, Randall AD, Functional characterisation of human TASK-3, an acid-sensitive two-pore domain potassium channel, in Neuropharmacology, vol. 40, n. 4, Mar 2001, pp. 551–9, DOI:10.1016/S0028-3908(00)00189-1, PMID 11249964.
Kindler CH, Paul M, Zou H, Liu C, Winegar BD, Gray AT, Yost CS, Amide local anesthetics potently inhibit the human tandem pore domain background K+ channel TASK-2 (KCNK5), in The Journal of Pharmacology and Experimental Therapeutics, vol. 306, n. 1, Jul 2003, pp. 84–92, DOI:10.1124/jpet.103.049809, PMID 12660311.
Punke MA, Licher T, Pongs O, Friederich P, Inhibition of human TREK-1 channels by bupivacaine, in Anesthesia and Analgesia, vol. 96, n. 6, Jun 2003, pp. 1665–73, DOI:10.1213/01.ANE.0000062524.90936.1F, PMID 12760993.
Lesage F, Guillemare E, Fink M, Duprat F, Lazdunski M, Romey G, Barhanin J, TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure, in The EMBO Journal, vol. 15, n. 5, Mar 1996, pp. 1004–11, PMC 449995, PMID 8605869.
Duprat F, Lesage F, Fink M, Reyes R, Heurteaux C, Lazdunski M, TASK, a human background K+ channel to sense external pH variations near physiological pH, in The EMBO Journal, vol. 16, n. 17, Sep 1997, pp. 5464–71, DOI:10.1093/emboj/16.17.5464, PMC 1170177, PMID 9312005.
Reyes R, Duprat F, Lesage F, Fink M, Salinas M, Farman N, Lazdunski M, Cloning and expression of a novel pH-sensitive two pore domain K+ channel from human kidney, in The Journal of Biological Chemistry, vol. 273, n. 47, Nov 1998, pp. 30863–9, DOI:10.1074/jbc.273.47.30863, PMID 9812978.
Meadows HJ, Benham CD, Cairns W, Gloger I, Jennings C, Medhurst AD, Murdock P, Chapman CG, Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel, in Pflügers Archiv, vol. 439, n. 6, Apr 2000, pp. 714–22, DOI:10.1007/s004240050997, PMID 10784345.
Patel AJ, Honoré E, Lesage F, Fink M, Romey G, Lazdunski M, Inhalational anesthetics activate two-pore-domain background K+ channels, in Nature Neuroscience, vol. 2, n. 5, May 1999, pp. 422–6, DOI:10.1038/8084, PMID 10321245.
Gray AT, Zhao BB, Kindler CH, Winegar BD, Mazurek MJ, Xu J, Chavez RA, Forsayeth JR, Yost CS, Volatile anesthetics activate the human tandem pore domain baseline K+ channel KCNK5, in Anesthesiology, vol. 92, n. 6, Jun 2000, pp. 1722–30, DOI:10.1097/00000542-200006000-00032, PMID 10839924.
Rogawski MA, Bazil CW, New molecular targets for antiepileptic drugs: alpha(2)delta, SV2A, and K(v)7/KCNQ/M potassium channels, in Current Neurology and Neuroscience Reports, vol. 8, n. 4, Jul 2008, pp. 345–52, DOI:10.1007/s11910-008-0053-7, PMC 2587091, PMID 18590620.
D. A. Doyle, J. Morais Cabral e R. A. Pfuetzner, The structure of the potassium channel: molecular basis of K+ conduction and selectivity, in Science (New York, N.Y.), vol. 280, n. 5360, 3 aprile 1998, pp. 69–77. URL consultato il 24 maggio 2017.
R. MacKinnon, S. L. Cohen e A. Kuo, Structural conservation in prokaryotic and eukaryotic potassium channels, in Science (New York, N.Y.), vol. 280, n. 5360, 3 aprile 1998, pp. 106–109. URL consultato il 24 maggio 2017.
C. Armstrong, The vision of the pore, in Science (New York, N.Y.), vol. 280, n. 5360, 3 aprile 1998, pp. 56–57. URL consultato il 24 maggio 2017.
Mikko Hellgren, Lars Sandberg e Olle Edholm, A comparison between two prokaryotic potassium channels (KirBac1.1 and KcsA) in a molecular dynamics (MD) simulation study, in Biophysical Chemistry, vol. 120, n. 1, 1º marzo 2006, pp. 1–9, DOI:10.1016/j.bpc.2005.10.002. URL consultato il 24 maggio 2017.
Youxing Jiang, Alice Lee e Jiayun Chen, Crystal structure and mechanism of a calcium-gated potassium channel, in Nature, vol. 417, n. 6888, 30 maggio 2002, pp. 515–522, DOI:10.1038/417515a. URL consultato il 25 maggio 2017.
Chunguang Kong, Weizhong Zeng e Sheng Ye, Distinct gating mechanisms revealed by the structures of a multi-ligand gated K(+) channel, in eLife, vol. 1, 13 dicembre 2012, pp. e00184, DOI:10.7554/eLife.00184. URL consultato il 25 maggio 2017.
Yu Cao, Xiangshu Jin e Hua Huang, Crystal structure of a potassium ion transporter, TrkH, in Nature, vol. 471, n. 7338, 17 marzo 2011, pp. 336–340, DOI:10.1038/nature09731. URL consultato il 25 maggio 2017.
Peng Yuan, Manuel D. Leonetti e Alexander R. Pico, Structure of the Human BK Channel Ca2+-Activation Apparatus at 3.0 Å Resolution, in Science (New York, N.Y.), vol. 329, n. 5988, 9 luglio 2010, pp. 182–186, DOI:10.1126/science.1190414. URL consultato il 25 maggio 2017.
Y. Jiang, A. Pico e M. Cadene, Structure of the RCK domain from the E. coli K+ channel and demonstration of its presence in the human BK channel, in Neuron, vol. 29, n. 3, 1º marzo 2001, pp. 593–601. URL consultato il 25 maggio 2017.
Christoph Antz e Bernd Fakler, Fast Inactivation of Voltage-Gated K(+) Channels: From Cartoon to Structure, in News in Physiological Sciences: An International Journal of Physiology Produced Jointly by the International Union of Physiological Sciences and the American Physiological Society, vol. 13, 1º agosto 1998, pp. 177–182. URL consultato il 25 maggio 2017.
Victor B. Luzhkov, Fredrik Osterberg e Johan Aqvist, Structure-activity relationship for extracellular block of K+ channels by tetraalkylammonium ions, in FEBS letters, vol. 554, n. 1-2, 6 novembre 2003, pp. 159–164. URL consultato il 25 maggio 2017.
David J. Posson, Jason G. McCoy e Crina M. Nimigean, The voltage-dependent gate in MthK potassium channels is located at the selectivity filter, in Nature Structural & Molecular Biology, vol. 20, n. 2, 1º febbraio 2013, pp. 159–166, DOI:10.1038/nsmb.2473. URL consultato il 25 maggio 2017.
K. L. Choi, C. Mossman e J. Aubé, The internal quaternary ammonium receptor site of Shaker potassium channels, in Neuron, vol. 10, n. 3, 1º marzo 1993, pp. 533–541. URL consultato il 25 maggio 2017.
Kene N. Piasta, Douglas L. Theobald e Christopher Miller, Potassium-selective block of barium permeation through single KcsA channels, in The Journal of General Physiology, vol. 138, n. 4, 1º ottobre 2011, pp. 421–436, DOI:10.1085/jgp.201110684. URL consultato il 25 maggio 2017.
J. Neyton e C. Miller, Potassium blocks barium permeation through a calcium-activated potassium channel, in The Journal of General Physiology, vol. 92, n. 5, 1º novembre 1988, pp. 549–567. URL consultato il 25 maggio 2017.
Steve W. Lockless, Ming Zhou e Roderick MacKinnon, Structural and thermodynamic properties of selective ion binding in a K+ channel, in PLoS biology, vol. 5, n. 5, 1º maggio 2007, pp. e121, DOI:10.1371/journal.pbio.0050121. URL consultato il 25 maggio 2017.
Y. Jiang e R. MacKinnon, The barium site in a potassium channel by x-ray crystallography, in The Journal of General Physiology, vol. 115, n. 3, 1º marzo 2000, pp. 269–272. URL consultato il 25 maggio 2017.
Yee Ling Lam, Weizhong Zeng e David Bryant Sauer, The conserved potassium channel filter can have distinct ion binding profiles: Structural analysis of rubidium, cesium, and barium binding in NaK2K, in The Journal of General Physiology, vol. 144, n. 2, 25 maggio 2017, pp. 181–192, DOI:10.1085/jgp.201411191. URL consultato il 25 maggio 2017.
Rui Guo, Weizhong Zeng e Hengjun Cui, Ionic interactions of Ba2+ blockades in the MthK K+ channel, in The Journal of General Physiology, vol. 144, n. 2, 25 maggio 2017, pp. 193–200, DOI:10.1085/jgp.201411192. URL consultato il 25 maggio 2017.
M. T. Kunkel e E. G. Peralta, Identification of domains conferring G protein regulation on inward rectifier potassium channels, in Cell, vol. 83, n. 3, 3 novembre 1995, pp. 443–449. URL consultato il 25 maggio 2017.

nobelprize.org

The Nobel Prize in Chemistry 2003, su nobelprize.org. URL consultato il 24 maggio 2017.

oadoi.org

(EN) Littleton JT, Ganetzky B, Ion channels and synaptic organization: analysis of the Drosophila genome, in Neuron, vol. 26, n. 1, 2000, pp. 35–43, DOI:10.1016/S0896-6273(00)81135-6, PMID 10798390.
Kobayashi T, Washiyama K, Ikeda K, Inhibition of G protein-activated inwardly rectifying K+ channels by ifenprodil, in Neuropsychopharmacology, vol. 31, n. 3, Mar 2006, pp. 516–24, DOI:10.1038/sj.npp.1300844, PMID 16123769.
Enyedi P, Czirják G, Molecular background of leak K+ currents: two-pore domain potassium channels, in Physiological Reviews, vol. 90, n. 2, Apr 2010, pp. 559–605, DOI:10.1152/physrev.00029.2009, PMID 20393194.
Lotshaw DP, Biophysical, pharmacological, and functional characteristics of cloned and native mammalian two-pore domain K+ channels, in Cell Biochemistry and Biophysics, vol. 47, n. 2, 2007, pp. 209–56, DOI:10.1007/s12013-007-0007-8, PMID 17652773.
Goldstein SA, Bockenhauer D, O'Kelly I, Zilberberg N, Potassium leak channels and the KCNK family of two-P-domain subunits, in Nature Reviews. Neuroscience, vol. 2, n. 3, Mar 2001, pp. 175–84, DOI:10.1038/35058574, PMID 11256078.
Sano Y, Inamura K, Miyake A, Mochizuki S, Kitada C, Yokoi H, Nozawa K, Okada H, Matsushime H, Furuichi K, A novel two-pore domain K+ channel, TRESK, is localized in the spinal cord, in The Journal of Biological Chemistry, vol. 278, n. 30, Jul 2003, pp. 27406–12, DOI:10.1074/jbc.M206810200, PMID 12754259.
Czirják G, Tóth ZE, Enyedi P, The two-pore domain K+ channel, TRESK, is activated by the cytoplasmic calcium signal through calcineurin, in The Journal of Biological Chemistry, vol. 279, n. 18, Apr 2004, pp. 18550–8, DOI:10.1074/jbc.M312229200, PMID 14981085.
Kindler CH, Yost CS, Gray AT, Local anesthetic inhibition of baseline potassium channels with two pore domains in tandem, in Anesthesiology, vol. 90, n. 4, Apr 1999, pp. 1092–102, DOI:10.1097/00000542-199904000-00024, PMID 10201682.
Meadows HJ, Randall AD, Functional characterisation of human TASK-3, an acid-sensitive two-pore domain potassium channel, in Neuropharmacology, vol. 40, n. 4, Mar 2001, pp. 551–9, DOI:10.1016/S0028-3908(00)00189-1, PMID 11249964.
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