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Charybdotoxin
Slow Inactivation in Voltage Gated Potassium Channels Is Insensitive to the Binding of Pore Occluding Peptide Toxins
Glycine311, a Determinant of Paxilline Block in BK Channels: a Novel Bend in the BK S6 Helix Yu Zhou Washington University School of Medicine in St
Ion Channels: Structural Basis for Function and Disease
Synergistic Antinociception by the Cannabinoid Receptor Agonist Anandamide and the PPAR-Α Receptor Agonist GW7647
Centipede KCNQ Inhibitor Sstx Also Targets KV1.3
Potassium Channel Kcsa
Natural Modulators of Large-Conductance Calcium
Purification, Sequence, and Model Structure of Charybdotoxin, a Potent
A Four-Disulphide-Bridged Toxin, with High Affinity Towards Voltage-Gated
Charybdotoxin Chtx - #11CHA001 - CAS : 95751-30-7 Product Information
The Block of Shaker K Channels by -Conotoxin PVIIA Is State Dependent
Trans-Toxin Ion-Sensitivity of Charybdotoxin-Blocked
Design and Synthesis of Cysteine‑Rich Peptides
Mode of Action of Iberiotoxin, a Potent Blocker of the Large Conductance Ca2 -Activated K+ Channel Sebastian Candia, Maria L
Binding of -Conotoxin-PVIIA to Open and Closed Shaker K-Channels Are
Dendrotoxin and Charybdotoxin Increase the Cytosolic Concentration of Free Ca2÷ in Cerebrocortical Synaptosomes: an Effect Not Shared by Apamin
UK-78282, a Novel Piperidine Compound That Potently
Masarykova Univerzita V Brně
Top View
11100.Full.Pdf
Toxins Targeting the KV1.3 Channel: Potential Immunomodulators for Autoimmune Diseases
Bkca Channels As Targets for Cardioprotection
A Potent and Kv1.3-Selective Analogue of the Scorpion Toxin
Therapeutic Potential of Venom Peptides
Item Name Catalog Number Quantity A-803467 A-105 10 Mg A
Modulation of Acetylcholine Release at Mouse Neuromuscular Junctions by Interaction of Three Homologous Scorpion Toxins with K+ Channels 1H
Modification by Charybdotoxin and Apamin Of
Charybdotoxin (C7802)
The Charybdotoxin Receptor of a Shaker K+ Channel: Peptide and Channel Residues Mediating Molecular Recognition Steve A
Ion Channels Product Listing | Edition 1
Paxilline Inhibits BK Channels by an Almost Exclusively Closed-Channel Block Mechanism Yu Zhou Washington University School of Medicine in St
Charybdotoxin Blocks Dendrotoxin-Sensitive Voltage-Activated K+ Channels
For Peer Review Only Journal: Expert Opinion on Therapeutic Targets
Potassium Channels in T Lymphocytes: Toxins to Therapeutic Immunosuppressants
Charybdotoxin Blocks Voltage-Gated K + Channels in Human and Murine T Lymphocytes
Evidence for Two Calcium-Dependent Potassium Conductances in Lizard Motor Nerve Terminals
Structure-Function Relationship of Bifunctional Scorpion Toxin Bmbktx1
Role of Potassium Ion Channels (K+ Channels) on Proliferation and Development of Colonic Cancer
The Charybdotoxin Family of K+ Channel-Blocking Peptides Review
Structural and Functional Study of Potassium Channel Inhibitor Hstx1
Design, Synthesis, and Functional Expression of a Gene for Charybdotoxin, a Peptide Blocker of K+ Channels CHUL-SEUNG PARK, SHARON F
Suppression of Potassium Conductance by Droperidol Has
Molecular Mechanisms of Resin Acids and Their Derivatives on the Opening of a Potassium Channel
Structural Determinants of Lolitrems for Inhibition of BK Large Conductance Ca2+-Activated K+ Channels☆
Wo 2007/009462 A2
Molecular Cloning of a Glibenclamide-Sensitive, Voltage-Gated Potassium Channel Expressed in Rabbit Kidney
Solution Structure and Proposed Binding Mechanism of a Novel
Clinical Expression of Perennial Ryegrass (Lolitrem-B) Intoxication In
Centipedes Subdue Giant Prey by Blocking KCNQ Channels
A Role for BK Channels in Heart Rate Regulation in Rodents
NIH Public Access Author Manuscript Eur J Pharmacol