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Biopolymers|June 9, 2016
t-boc synthesis of huwentoxin-i through native chemical ligation incorporating a trifluoromethanesulfonic acid cleavage strategyParashar Thapa, Chino C Cabalteja, Edwin E Philips, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 13, 2021
Synthetic polypeptide crotamine: characterization as a myotoxin and as a target of combinatorial peptidesCeline Pompeia, Eduardo Osório Frare, Steve Peigneur, et al.
The Journal of Biological Chemistry|April 29, 2018
Gating modifier toxins isolated from spider venom: Modulation of voltage-gated sodium channels and the role of lipid membranesAkello J Agwa, Steve Peigneur, Chun Yuen Chow, et al.
Toxicon : Official Journal of the International Society on Toxinology|May 18, 2018
Synthesis, folding, structure and activity of a predicted peptide from the sea anemone Oulactis sp. with an ShKT foldBankala Krishnarjuna, Jessica Villegas-Moreno, Michela L Mitchell, et al.
Plos One|December 9, 2017
Synthesis of novel purpurealidin analogs and evaluation of their effect on the cancer-relevant potassium channel KV10.1Lien Moreels, Chinmay Bhat, Manuela Voráčová, et al.
Toxicon : Official Journal of the International Society on Toxinology|September 8, 2014
Discovery of a new subclass of α-conotoxins in the venom of Conus australisEline K M Lebbe, Steve Peigneur, Mohitosh Maiti, et al.
Biochemical Pharmacology|August 9, 2008
A common "hot spot" confers hERG blockade activity to alpha-scorpion toxins affecting K+ channelsYousra Abdel-Mottaleb, Gerardo Corzo, Marie-France Martin-Eauclaire, et al.
International Journal of Molecular Sciences|October 27, 2022
Research into the Bioengineering of a Novel α-Conotoxin from the Milked Venom of <i>Conus obscurus</i>Sean Wiere, Christopher Sugai, Michael J Espiritu, et al.
BMC Biology|June 12, 2025
Beyond venomous fangs: Uloboridae spiders have lost their venom but not their toxicityXiaojing Peng, Ludwig Dersch, Josephine Dresler, et al.
European Journal of Medicinal Chemistry|January 21, 2014
Substituted 4-phenyl-2-aminoimidazoles and 4-phenyl-4,5-dihydro-2-aminoimidazoles as voltage-gated sodium channel modulatorsNace Zidar, Žiga Jakopin, David J Madge, et al.
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