Pharmacology of Potassium Channels
暂无分享,去创建一个
G. Kaczorowski | H. Knaus | R. Koch | M. L. García | M. Hanner | W. Schmalhofer | R. Slaughter | Maria L. Garcia
[1] M. Sanguinetti,et al. Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel , 1996, Nature.
[2] N. Marrion,et al. Small-Conductance, Calcium-Activated Potassium Channels from Mammalian Brain , 1996, Science.
[3] O. McManus,et al. High-conductance calcium-activated potassium channels; Structure, pharmacology, and function , 1996, Journal of bioenergetics and biomembranes.
[4] M. Sanguinetti,et al. Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[5] M. Sanguinetti,et al. Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides. , 1996, Circulation research.
[6] I. Khaytin,et al. Identification of three separate binding sites on SHK toxin, a potent inhibitor of voltage-dependent potassium channels in human T-lymphocytes and rat brain. , 1996, Biochemical and biophysical research communications.
[7] F. Ashcroft,et al. Promiscuous coupling between the sulphonylurea receptor and inwardly rectifying potassium channels , 1996, Nature.
[8] V. Uebele,et al. Functional Differences in Kv1.5 Currents Expressed in Mammalian Cell Lines Are Due to the Presence of Endogenous Kvβ2.1 Subunits (*) , 1996, The Journal of Biological Chemistry.
[9] O. Pongs,et al. Distribution of high-conductance Ca(2+)-activated K+ channels in rat brain: targeting to axons and nerve terminals , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[10] D. Owen,et al. The modulation of the rate of inactivation of the mKv1.1 K+ channel by the β subunit, Kvβ1 and lack of effect of a Kvβ1 N‐terminal peptide , 1996 .
[11] R. Johns,et al. Synthesis and biological characterisation of a series of iberiotoxin analogues. , 2009, International journal of peptide and protein research.
[12] I. Khaytin,et al. Chemical synthesis and characterization of ShK toxin: a potent potassium channel inhibitor from a sea anemone. , 2009, International journal of peptide and protein research.
[13] P. Smith,et al. Cloning and functional expression of the cDNA encoding a novel ATP‐sensitive potassium channel subunit expressed in pancreatic β‐cells, brain, heart and skeletal muscle , 1995 .
[14] C. Roumestand,et al. Determination of the three-dimensional solution structure of noxiustoxin: analysis of structural differences with related short-chain scorpion toxins. , 1995, Biochemistry.
[15] O. McManus,et al. Functional reconstitution of the large-conductance, calcium-activated potassium channel purified from bovine aortic smooth muscle. , 1995, Biochemistry.
[16] A. Brown,et al. Cloned human inward rectifier K+ channel as a target for class III methanesulfonanilides. , 1995, Circulation research.
[17] V. Uebele,et al. A Novel K+ Channel β-Subunit (hKvβ1.3) Is Produced via Alternative mRNA Splicing (*) , 1995, The Journal of Biological Chemistry.
[18] J. Inazawa,et al. Reconstitution of IKATP: An Inward Rectifier Subunit Plus the Sulfonylurea Receptor , 1995, Science.
[19] F. van de Ven,et al. Determination of the three-dimensional solution structure of scyllatoxin by 1H nuclear magnetic resonance. , 1995, Journal of molecular biology.
[20] James E. Hall,et al. Topology of the pore-region of a K+ channel revealed by the NMR-derived structures of scorpion toxins , 1995, Neuron.
[21] M. Lazdunski,et al. Kalicludines and Kaliseptine , 1995, The Journal of Biological Chemistry.
[22] J. Tytgat,et al. The α-Dendrotoxin Footprint on a Mammalian Potassium Channel (*) , 1995, The Journal of Biological Chemistry.
[23] G. Kaczorowski,et al. [125I]margatoxin, an extraordinarily high affinity ligand for voltage-gated potassium channels in mammalian brain. , 1995, Biochemistry.
[24] R. MacKinnon,et al. An inhibitor of the Kv2.1 potassium channel isolated from the venom of a Chilean tarantula , 1995, Neuron.
[25] K. Ishii,et al. The voltage‐dependent K+ channel (Kv1.5) cloned from rabbit heart and facilitation of inactivation of the delayed rectifier current by the rat β subunit , 1995, FEBS letters.
[26] D. Choquet,et al. Chemical synthesis, structural and functional characterisation of noxiustoxin, a powerful blocker of lymphocyte voltage-dependent K+ channels. , 1995, Biochemical and biophysical research communications.
[27] S. Damjanovich,et al. Beta-scorpion toxin 2 from Centruroides noxius blocks voltage-gated K+ channels in human lymphocytes. , 1995, Biochemical and biophysical research communications.
[28] B. Rudy,et al. Alternative splicing of the human Shaker K+ channel β1 gene and functional expression of the β2 gene product , 1995 .
[29] R. MacKinnon,et al. Solution structure of the potassium channel inhibitor agitoxin 2: Caliper for probing channel geometry , 1995, Protein science : a publication of the Protein Society.
[30] H. Shear,et al. Characterization of a voltage-gated K+ channel beta subunit expressed in human heart. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[31] R. J. Hill,et al. WIN 17317-3: novel nonpeptide antagonist of voltage-activated K+ channels in human T lymphocytes. , 1995, Molecular pharmacology.
[32] A. Treasurywala,et al. Novel inhibitors of potassium ion channels on human T lymphocytes. , 1995, Journal of medicinal chemistry.
[33] C. Wernstedt,et al. Characterization of a potassium channel toxin from the Caribbean Sea anemone Stichodactyla helianthus. , 1995, Toxicon : official journal of the International Society on Toxinology.
[34] J. Clement,et al. Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion. , 1995, Science.
[35] R. MacKinnon,et al. Revealing the architecture of a K+ channel pore through mutant cycles with a peptide inhibitor. , 1995, Science.
[36] O. Pongs. Regulation of the activity of voltage-gated potassium channels by β subunits , 1995 .
[37] M. A. Olson,et al. Cloning and expression of mamba toxins. , 1995, Toxicon.
[38] H. Strauss,et al. A Novel β Subunit Increases Rate of Inactivation of Specific Voltage-gated Potassium Channel α Subunits (*) , 1995, The Journal of Biological Chemistry.
[39] B. Wible,et al. Molecular cloning and functional expression of a novel potassium channel β‐subunit from human atrium , 1995 .
[40] E. Green,et al. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome , 1995, Cell.
[41] L. Pallanck,et al. Functional role of the β subunit of high conductance calcium-activated potassium channels , 1995, Neuron.
[42] Leonard Rj,et al. Stable expression of human Kv1.3 potassium channels resets the resting membrane potential of cultured mammalian cells. , 1995 .
[43] T. Jones,et al. High Conductance Calcium-Activated Potassium Channels , 1995 .
[44] R. North,et al. Ligand- and voltage-gated ion channels , 1995 .
[45] R. Latorre,et al. Characterization of and modulation by a beta-subunit of a human maxi KCa channel cloned from myometrium. , 1995, Receptors & channels.
[46] Y. Jan,et al. Maggot's hair and bug's eye: Role of cell interactions and intrinsic factors in cell fate specification , 1995, Neuron.
[47] H. Rochat,et al. Leiurotoxin I, a scorpion toxin specific for Ca(2+)-activated K+ channels. Structure-activity analysis using synthetic analogs. , 2009, International journal of peptide and protein research.
[48] H. Rochat,et al. The kaliotoxin family enlarged. Purification, characterization, and precursor nucleotide sequence of KTX2 from Androctonus australis venom. , 1994, The Journal of biological chemistry.
[49] B. A. Johnson,et al. Determination of the three-dimensional structure of margatoxin by 1H, 13C, 15N triple-resonance nuclear magnetic resonance spectroscopy. , 1994, Biochemistry.
[50] A. Ménez,et al. On the site by which α‐dendrotoxin binds to voltage‐dependent potassium channels: Site‐directed mutagenesis reveals that the lysine triplet 28–30 is not essential for binding , 1994, FEBS letters.
[51] J. Tseng-Crank,et al. Cloning, expression, and distribution of functionally distinct Ca2+-activated K+ channel isoforms from human brain , 1994, Neuron.
[52] E. Giralt,et al. Kaliotoxin (1-37) shows structural differences with related potassium channel blockers. , 1994, Biochemistry.
[53] B. Martin,et al. Novel K(+)-channel-blocking toxins from the venom of the scorpion Centruroides limpidus limpidus Karsch. , 1994, The Biochemical journal.
[54] Thomas M. Argentieri,et al. Potassium channel blockers as antiarrhythmic drugs , 1994 .
[55] V. Gribkoff,et al. Cloning and expression of a human large-conductance calcium-activated potassium channel. , 1994, Brain research. Molecular brain research.
[56] R. MacKinnon,et al. Transfer of the scorpion toxin receptor to an insensitive potassium channel , 1994, Neuron.
[57] C. Miller,et al. Electrostatic distance geometry in a K+ channel vestibule. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[58] G. Kaczorowski,et al. Covalent attachment of charybdotoxin to the beta-subunit of the high conductance Ca(2+)-activated K+ channel. Identification of the site of incorporation and implications for channel topology. , 1994, The Journal of biological chemistry.
[59] L. Salkoff,et al. Calcium sensitivity of BK-type KCa channels determined by a separable domain , 1994, Neuron.
[60] T. Sun,et al. High-level expression and functional reconstitution of Shaker K+ channels. , 1994, Biochemistry.
[61] L. Pallanck,et al. Cloning and characterization of human and mouse homologs of the Drosophila calcium-activated potassium channel gene, slowpoke. , 1994, Human molecular genetics.
[62] P. Zografos,et al. Characterization of ATP-sensitive potassium channel-blocking activity of ZENECA ZM181,037, a eukalemic diuretic. , 1994, Pharmacology.
[63] M. Garcia-Calvo,et al. Primary sequence and immunological characterization of beta-subunit of high conductance Ca(2+)-activated K+ channel from smooth muscle. , 1994, The Journal of biological chemistry.
[64] R. MacKinnon,et al. Purification and characterization of three inhibitors of voltage-dependent K+ channels from Leiurus quinquestriatus var. hebraeus venom. , 1994, Biochemistry.
[65] G A Gutman,et al. Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines. , 1994, Molecular pharmacology.
[66] Christopher Miller,et al. The charybdotoxin receptor of a Shaker K+ channel: Peptide and channel residues mediating molecular recognition , 1994, Neuron.
[67] O. Pongs,et al. Inactivation properties of voltage-gated K+ channels altered by presence of β-subunit , 1994, Nature.
[68] O. McManus,et al. Tremorgenic indole alkaloids potently inhibit smooth muscle high-conductance calcium-activated potassium channels. , 1994, Biochemistry.
[69] Engineering a uniquely reactive thiol into a cysteine-rich peptide. , 1994, Protein engineering.
[70] O. Pongs,et al. Primary structure of a beta subunit of alpha-dendrotoxin-sensitive K+ channels from bovine brain. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[71] O. Pongs,et al. Antibodies specific for distinct Kv subunits unveil a heterooligomeric basis for subtypes of alpha-dendrotoxin-sensitive K+ channels in bovine brain. , 1994, Biochemistry.
[72] J. H. Collins,et al. Tityustoxin K alpha blocks voltage-gated noninactivating K+ channels and unblocks inactivating K+ channels blocked by alpha-dendrotoxin in synaptosomes. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[73] M. Garcia-Calvo,et al. Subunit composition of the high conductance calcium-activated potassium channel from smooth muscle, a representative of the mSlo and slowpoke family of potassium channels. , 1994, The Journal of biological chemistry.
[74] L. Kolmakova-Partensky,et al. Intimations of K+ channel structure from a complete functional map of the molecular surface of charybdotoxin. , 1994 .
[75] O. McManus,et al. Purification and reconstitution of the high-conductance, calcium-activated potassium channel from tracheal smooth muscle. , 1994, The Journal of biological chemistry.
[76] S. Olesen,et al. Selective activation of Ca(2+)-dependent K+ channels by novel benzimidazolone. , 1994, European journal of pharmacology.
[77] O. McManus,et al. Maxikdiol: a novel dihydroxyisoprimane as an agonist of Maxi-K channels , 1994 .
[78] A. van Dorsselaer,et al. Synthesis and characterization of kaliotoxin. Is the 26-32 sequence essential for potassium channel recognition? , 1993, The Journal of biological chemistry.
[79] K. Wüthrich,et al. Nuclear magnetic resonance solution structure of dendrotoxin K from the venom of Dendroaspis polylepis polylepis. , 1993, Journal of molecular biology.
[80] C. Miller,et al. Mechanism of charybdotoxin block of a voltage-gated K+ channel. , 1993, Biophysical journal.
[81] A. Harvey,et al. Structural features important for the biological activity of the potassium channel blocking dendrotoxins , 1993, British journal of pharmacology.
[82] M. Garcia-Calvo,et al. Purification, characterization, and biosynthesis of margatoxin, a component of Centruroides margaritatus venom that selectively inhibits voltage-dependent potassium channels. , 1993, The Journal of biological chemistry.
[83] C. Shieh,et al. Segmental exchanges define 4-aminopyridine binding and the inner mouth of K+ pores , 1993, Neuron.
[84] J. Arch,et al. Comparison of the airways relaxant and hypotensive potencies of the potassium channel activators BRL 55834 and levcromakalim (BRL 38227) in vivo in guinea‐pigs and rats , 1993, British journal of pharmacology.
[85] L. Salkoff,et al. mSlo, a complex mouse gene encoding "maxi" calcium-activated potassium channels. , 1993, Science.
[86] Ronald L. Davis. Mushroom bodies and drosophila learning , 1993, Neuron.
[87] O. McManus,et al. An activator of calcium-dependent potassium channels isolated from a medicinal herb. , 1993, Biochemistry.
[88] U. Hellman,et al. A potassium channel toxin from the secretion of the sea anemone Bunodosoma granulifera. Isolation, amino acid sequence and biological activity. , 1993, Biochimica et biophysica acta.
[89] H. Rochat,et al. P05, a new leiurotoxin I-like scorpion toxin: synthesis and structure-activity relationships of the alpha-amidated analog, a ligand of Ca(2+)-activated K+ channels with increased affinity. , 1993, Biochemistry.
[90] O. McManus,et al. Synthetic charybdotoxin-iberiotoxin chimeric peptides define toxin binding sites on calcium-activated and voltage-dependent potassium channels. , 1993, Biochemistry.
[91] G. Yellen,et al. The internal quaternary ammonium receptor site of Shaker potassium channels , 1993, Neuron.
[92] N. Sigal,et al. Voltage-gated potassium channels regulate calcium-dependent pathways involved in human T lymphocyte activation , 1993, The Journal of experimental medicine.
[93] D. Marion,et al. Sequence-specific 1H-NMR assignment and secondary structure of black mamba dendrotoxin I, a highly selective blocker of voltage-gated potassium channels. , 1993, European journal of biochemistry.
[94] M. Crest,et al. Synthesis and Characterization of Kaliotoxin , 1993 .
[95] G. Edwards,et al. The pharmacology of ATP-sensitive potassium channels. , 1993, Annual Review of Pharmacology and Toxicology.
[96] J. Dolly,et al. Characterization of monoclonal antibodies against voltage-dependent K+ channels raised using alpha-dendrotoxin acceptors purified from bovine brain. , 1992, Biochemistry.
[97] J. Reuben,et al. Selective blockers of voltage-gated K+ channels depolarize human T lymphocytes: mechanism of the antiproliferative effect of charybdotoxin. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[98] M. Rogawski,et al. Charybdotoxin, dendrotoxin and mast cell degranulating peptide block the voltage-activated K+ current of fibroblast cells stably transfected with NGK1 (Kvl.2) K+ channel complementary DNA , 1992, Neuroscience.
[99] J. W. Goh,et al. Effect of charybdotoxin and leiurotoxon I on potassium currents in bullfrog sympathetic ganglion and hippocampal neurons , 1992, Brain Research.
[100] B. A. Johnson,et al. Determination of the three-dimensional structure of iberiotoxin in solution by 1H nuclear magnetic resonance spectroscopy. , 1992, Biochemistry.
[101] Chul-Seung Park,et al. Interaction of charybdotoxin with permeant ions inside the pore of a K+ channel , 1992, Neuron.
[102] R. North,et al. Calcium-activated potassium channels expressed from cloned complementary DNAs , 1992, Neuron.
[103] R. Latorre,et al. Mode of action of iberiotoxin, a potent blocker of the large conductance Ca(2+)-activated K+ channel. , 1992, Biophysical journal.
[104] O. McManus,et al. Mechanism of iberiotoxin block of the large-conductance calcium-activated potassium channel from bovine aortic smooth muscle. , 1992, Biochemistry.
[105] T. Skarzynski,et al. Crystal structure of α-dendrotoxin from the green mamba venom and its comparison with the structure of bovine pancreatic trypsin inhibitor , 1992 .
[106] A. Brown,et al. A single nonpolar residue in the deep pore of related K+ channels acts as a K+:Rb+ conductance switch. , 1992, Biophysical journal.
[107] A. Brown,et al. Differences between the deep pores of K+ channels determined by an interacting pair of nonpolar amino acids , 1992, Neuron.
[108] R. North,et al. Multiple subunits of a voltage-dependent potassium channel contribute to the binding site for tetraethylammonium , 1992, Neuron.
[109] M. Lazdunski,et al. Scyllatoxin, a blocker of Ca(2+)-activated K+ channels: structure-function relationships and brain localization of the binding sites. , 1992, Biochemistry.
[110] H. Rochat,et al. Kaliotoxin, a novel peptidyl inhibitor of neuronal BK-type Ca(2+)-activated K+ channels characterized from Androctonus mauretanicus mauretanicus venom. , 1992, The Journal of biological chemistry.
[111] C. Roumestand,et al. Refined structure of charybdotoxin: common motifs in scorpion toxins and insect defensins. , 1991, Science.
[112] A. Brown,et al. Internal and external TEA block in single cloned K+ channels. , 1991, The American journal of physiology.
[113] R. North,et al. Identification of amino acid residues involved in dendrotoxin block of rat voltage-dependent potassium channels. , 1991, Molecular pharmacology.
[114] G. Grover,et al. Specific block of the anti-ischemic actions of cromakalim by sodium 5-hydroxydecanoate. , 1991, Circulation research.
[115] O. McManus. Calcium-activated potassium channels: Regulation by calcium , 1991, Journal of bioenergetics and biomembranes.
[116] A. VanDongen,et al. Patterns of internal and external tetraethylammonium block in four homologous K+ channels. , 1991, Molecular pharmacology.
[117] S. Hausdorff,et al. Design, synthesis, and functional expression of a gene for charybdotoxin, a peptide blocker of K+ channels. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[118] C. Deutsch,et al. Characterization of high affinity binding sites for charybdotoxin in human T lymphocytes. Evidence for association with the voltage-gated K+ channel. , 1991, The Journal of biological chemistry.
[119] R. MacKinnon,et al. Mutations affecting internal TEA blockade identify the probable pore-forming region of a K+ channel , 1991, Science.
[120] C. Roumestand,et al. Three-dimensional structure of natural charybdotoxin in aqueous solution by 1H-NMR. Charybdotoxin possesses a structural motif found in other scorpion toxins. , 1991, European journal of biochemistry.
[121] C. Lévêque,et al. Polypeptide components of the apamin receptor associated with a calcium activated potassium channel , 1990, FEBS letters.
[122] J. Findlay,et al. Alpha-dendrotoxin acceptor from bovine brain is a K+ channel protein. Evidence from the N-terminal sequence of its larger subunit. , 1990, The Journal of biological chemistry.
[123] A. Patchett,et al. Synthesis and structural characterization of charybdotoxin, a potent peptidyl inhibitor of the high conductance Ca2(+)-activated K+ channel. , 1990, The Journal of biological chemistry.
[124] R. MacKinnon,et al. Mutations affecting TEA blockade and ion permeation in voltage-activated K+ channels. , 1990, Science.
[125] G. Edwards,et al. Structure-activity relationships of K+ channel openers. , 1990, Trends in pharmacological sciences.
[126] G. Kaczorowski,et al. Characterization of high affinity binding sites for charybdotoxin in synaptic plasma membranes from rat brain. Evidence for a direct association with an inactivating, voltage-dependent, potassium channel. , 1990, The Journal of biological chemistry.
[127] H. Kuroda,et al. Solution synthesis of charybdotoxin (ChTX), a K+ channel blocker. , 1990, Biochemical and biophysical research communications.
[128] G. Giménez-Gallego,et al. Purification and characterization of a unique, potent, peptidyl probe for the high conductance calcium-activated potassium channel from venom of the scorpion Buthus tamulus. , 1990, The Journal of biological chemistry.
[129] L. Kaczmarek,et al. Cloning and expression of cDNA and genomic clones encoding three delayed rectifier potassium channels in rat brain , 1990, Neuron.
[130] M. Lazdunski,et al. Leiurotoxin I (scyllatoxin), a peptide ligand for Ca2(+)-activated K+ channels. Chemical synthesis, radiolabeling, and receptor characterization. , 1990, The Journal of biological chemistry.
[131] M. Lazdunski,et al. Purification and pharmacological characterization of peptide toxins from the black mamba (Dendroaspis polylepis) venom. , 1990, Toxicon : official journal of the International Society on Toxinology.
[132] G. Kaczorowski,et al. Characterization of high affinity binding sites for charybdotoxin in sarcolemmal membranes from bovine aortic smooth muscle. Evidence for a direct association with the high conductance calcium-activated potassium channel. , 1989, The Journal of biological chemistry.
[133] M. Blaustein,et al. Rat brain dendrotoxin receptors associated with voltage-gated potassium channels: dendrotoxin binding and receptor solubilization. , 1989, Molecular pharmacology.
[134] R. MacKinnon,et al. Functional modification of calcium-activated potassium channel by trimethyloxonium , 1989 .
[135] M. Lazdunski,et al. Dendrotoxin-binding brain membrane protein displays a K+ channel activity that is stimulated by both cAMP-dependent and endogenous phosphorylations. , 1989, Biochemistry.
[136] U. Quast,et al. In vitro and in vivo comparison of two K+ channel openers, diazoxide and cromakalim, and their inhibition by glibenclamide. , 1989, The Journal of pharmacology and experimental therapeutics.
[137] M. Cahalan,et al. Charybdotoxin blocks voltage-gated K+ channels in human and murine T lymphocytes , 1989, The Journal of general physiology.
[138] M. Lazdunski,et al. Polypeptide constitution of receptors for apamin, a neurotoxin which blocks a class of Ca2+‐activated K+ channels , 1989 .
[139] J. Dolly,et al. Dendrotoxin acceptor from bovine synaptic plasma membranes. Binding properties, purification and subunit composition of a putative constituent of certain voltage-activated K+ channels. , 1989, The Biochemical journal.
[140] R Latorre,et al. Varieties of calcium-activated potassium channels. , 1989, Annual review of physiology.
[141] A. Breeze,et al. Interactions between discrete neuronal membrane binding sites for the putative K+-channel ligands beta-bungarotoxin, dendrotoxin and mast-cell-degranulating peptide. , 1989, European journal of biochemistry.
[142] R. MacKinnon,et al. Charybdotoxin block of Shaker K+ channels suggests that different types of K+ channels share common structural features , 1988, Neuron.
[143] D. Wemmer,et al. Solution structure of apamin determined by nuclear magnetic resonance and distance geometry. , 1988, Biochemistry.
[144] M. Blaustein,et al. Four polypeptide components of green mamba venom selectively block certain potassium channels in rat brain synaptosomes. , 1988, Molecular pharmacology.
[145] G. Giménez-Gallego,et al. Purification and characterization of a unique, potent inhibitor of apamin binding from Leiurus quinquestriatus hebraeus venom. , 1988, The Journal of biological chemistry.
[146] M. Lazdunski,et al. Purification and subunit structure of a putative K+-channel protein identified by its binding properties for dendrotoxin I. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[147] M. Lazdunski,et al. Existence of different populations of the dendrotoxin I binding protein associated with neuronal K+ channels. , 1988, Biochemical and biophysical research communications.
[148] M. Navia,et al. Purification, sequence, and model structure of charybdotoxin, a potent selective inhibitor of calcium-activated potassium channels. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[149] M. Lazdunski,et al. The receptor site for the bee venom mast cell degranulating peptide. Affinity labeling and evidence for a common molecular target for mast cell degranulating peptide and dendrotoxin I, a snake toxin active on K+ channels. , 1988, Biochemistry.
[150] R. MacKinnon,et al. Mechanism of charybdotoxin block of the high-conductance, Ca2+- activated K+ channel , 1988, The Journal of general physiology.
[151] M. Lazdunski,et al. Two potent central convulsant peptides, a bee venom toxin, the MCD peptide, and a snake venom toxin, dendrotoxin I, known to block K+ channels, have interacting receptor sites. , 1987, Biochemical and biophysical research communications.
[152] C. Miller,et al. Purification of charybdotoxin, a specific inhibitor of the high-conductance Ca2+-activated K+ channel. , 1986, The Journal of biological chemistry.
[153] K. Magleby,et al. Single apamin-blocked Ca-activated K+ channels of small conductance in cultured rat skeletal muscle , 1986, Nature.
[154] C. Granier,et al. Molecular structure of rat brain apamin receptor: differential photoaffinity labeling of putative K+ channel subunits and target size analysis. , 1986, Biochemistry.
[155] M. Lazdunski,et al. Properties of the apamin-sensitive Ca2+-activated K+ channel in PC12 pheochromocytoma cells which hyper-produce the apamin receptor. , 1986, The Journal of biological chemistry.
[156] L. Possani,et al. Noxiustoxin, a short-chain toxin from the Mexican scorpion Centruroides noxius, induces transmitter release by blocking K+ permeability , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[157] J. Halliwell,et al. 4-Aminopyridine and dendrotoxin induce repetitive firing in rat visceral sensory neurones by blocking a slowly inactivating outward current , 1986, Neuroscience Letters.
[158] J. Halliwell,et al. Central action of dendrotoxin: selective reduction of a transient K conductance in hippocampus and binding to localized acceptors. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[159] M. Lazdunski,et al. The all-or-none role of innervation in expression of apamin receptor and of apamin-sensitive Ca2+-activated K+ channel in mammalian skeletal muscle. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[160] A. Harvey,et al. Dendrotoxins: snake toxins that block potassium channels and facilitate neurotransmitter release. , 1985, Pharmacology & therapeutics.
[161] R. Latorre,et al. Charybdotoxin, a protein inhibitor of single Ca2+-activated K+ channels from mammalian skeletal muscle , 1985, Nature.
[162] C. Granier,et al. Interactions of the neurotoxin apamin with a Ca2+-activated K+ channel in primary neuronal cultures. , 1984, Journal of Biological Chemistry.
[163] M. Lazdunski,et al. Apamin: a specific toxin to study a class of Ca2+-dependent K+ channels. , 1984, Journal de physiologie.
[164] D. G. Haylett,et al. High affinity binding of [125I]monoiodoapamin to isolated guinea‐pig hepatocytes , 1983, FEBS letters.
[165] B. Martin,et al. The primary structure of noxiustoxin: A K+ channel blocking peptide, purified from the venom of the scorpion Centruroides noxius Hoffmann , 1982 .
[166] E. Karlsson,et al. PROTEASE INHIBITOR HOMOLOGUES FROM MAMBA VENOMS: FACILITATION OF ACETYLCHOLINE RELEASE AND INTERACTIONS WITH PREJUNCTIONAL BLOCKING TOXINS , 1982, British journal of pharmacology.
[167] M. Lazdunski,et al. The Ca2+‐dependent slow K+ conductance in cultured rat muscle cells: characterization with apamin. , 1982, The EMBO journal.
[168] M. Lazdunski,et al. Specific binding and pharmacological interactions of apamin, the neurotoxin from bee venom, with guinea pig colon. , 1982, Life sciences.
[169] M. Lazdunski,et al. Preparation of a pure monoiodo derivative of the bee venom neurotoxin apamin and its binding properties to rat brain synaptosomes. , 1982, The Journal of biological chemistry.
[170] A. Maelicke,et al. Selective blockage of voltage-dependent K+ channels by a novel scorpion toxin , 1982, Nature.
[171] M. Lazdunski,et al. Apamin as a selective blocker of the calcium-dependent potassium channel in neuroblastoma cells: voltage-clamp and biochemical characterization of the toxin receptor. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[172] C. Granier,et al. Use of synthetic analogs for a study on the structure-activity relationship of apamin. , 1978, European journal of biochemistry.