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Biochimica Et Biophysica Acta. Biomembranes|November 23, 2018
Electrophysiological characterization of Tityus obscurus β toxin 1 (To1) on Na<sup>+</sup>-channel isoformsDiogo Vieira Tibery, Leandro Ambrósio Campos, Caroline Barbosa Farias Mourão, et al.
Biomolecules|May 4, 2026
Electrophysiological Characterization of the Venom and Toxins from the Scorpion <i>Tityus championi</i> Targeting Voltage-Gated Sodium Channels and Molecular Modeling of Tch3, a Toxin with Therapeutic Potential for Pain ReliefGalit Akerman-Sánchez, Steve Peigneur, Kathleen Carleer, et al.
Protein Science : a Publication of the Protein Society|January 16, 2023
ScrepYard: An online resource for disulfide-stabilized tandem repeat peptidesJunyu Liu, Michael Maxwell, Thom Cuddihy, et al.
Bioorganic & Medicinal Chemistry|October 19, 2017
Astemizole analogues with reduced hERG inhibition as potent antimalarial compoundsJunjun Tian, Leen Vandermosten, Steve Peigneur, et al.
Toxins|August 24, 2018
<i>Phoneutria nigriventer</i> Spider Toxin PnTx2-1 (δ-Ctenitoxin-Pn1a) Is a Modulator of Sodium Channel GatingSteve Peigneur, Ana Luiza B Paiva, Marta N Cordeiro, et al.
Marine Drugs|September 25, 2019
Magnificamide, a β-Defensin-Like Peptide from the Mucus of the Sea Anemone <i>Heteractis magnifica</i>, Is a Strong Inhibitor of Mammalian α-AmylasesOksana Sintsova, Irina Gladkikh, Aleksandr Kalinovskii, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 30, 2016
Allosteric binding site in a Cys-loop receptor ligand-binding domain unveiled in the crystal structure of ELIC in complex with chlorpromazineMieke Nys, Eveline Wijckmans, Ana Farinha, et al.
Biophysical Journal|May 1, 2021
Potassium channel blocker crafted by α-hairpinin scaffold engineeringValentin M Tabakmakher, Andrei M Gigolaev, Steve Peigneur, et al.
The FEBS Journal|October 14, 2020
Scorpion toxin MeuNaTxα-1 sensitizes primary nociceptors by selective modulation of voltage-gated sodium channelsMarianne van Cann, Alexey Kuzmenkov, Jörg Isensee, et al.
European Journal of Medicinal Chemistry|August 13, 2017
Clathrodin, hymenidin and oroidin, and their synthetic analogues as inhibitors of the voltage-gated potassium channelsNace Zidar, Aleš Žula, Tihomir Tomašič, et al.
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