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α-Conotoxins to explore the molecular, physiological and pathophysiological functions of neuronal nicotinic acetylcholine receptors

Neuroscience letters, 2018-07, Vol.679, p.24-34

2018

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Discovery, Synthesis, and Structure–Activity Relationships of Conotoxins

Chemical reviews, 2014-06, Vol.114 (11), p.5815-5847

2014

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N‑Terminal Liver-Expressed Antimicrobial Peptide 2 (LEAP2) Region Exhibits Inverse Agonist Activity toward the Ghrelin Receptor

Journal of medicinal chemistry, 2019-01, Vol.62 (2), p.965-973

2019

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Nicotinic acetylcholine receptor inhibitors derived from snake and snail venoms

Neuropharmacology, 2017-12, Vol.127, p.196-223

2017

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Use of Venom Peptides to Probe Ion Channel Structure and Function

The Journal of biological chemistry, 2010-04, Vol.285 (18), p.13315-13320

2010

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Conus venom peptide pharmacology

Pharmacological reviews, 2012-04, Vol.64 (2), p.259-298

2012

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Predatory and Defensive Strategies in Cone Snails

Toxins, 2024-02, Vol.16 (2), p.94

2024

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Inhibitory Glycine Receptors: An Update

The Journal of biological chemistry, 2012-11, Vol.287 (48), p.40216-40223

2012

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Conotoxins: Chemistry and Biology

Chemical reviews, 2019-11, Vol.119 (21), p.11510-11549

2019

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A Combined Transcriptomics and Proteomics Approach Reveals the Differences in the Predatory and Defensive Venoms of the Molluscivorous Cone Snail Cylinder ammiralis (Caenogastropoda: Conidae)

Toxins, 2021-09, Vol.13 (9), p.642

2021

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ConoServer: updated content, knowledge, and discovery tools in the conopeptide database

Nucleic acids research, 2012-01, Vol.40 (Database issue), p.D325-D330

2012

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Deep Venomics Reveals the Mechanism for Expanded Peptide Diversity in Cone Snail Venom

Molecular & cellular proteomics, 2013-02, Vol.12 (2), p.312-329

2013

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Evolution of separate predation- and defence-evoked venoms in carnivorous cone snails

Nature communications, 2014-03, Vol.5 (1), p.3521-9, Article 3521

2014

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Synthesis and Biological Activity of Novel α-Conotoxins Derived from Endemic Polynesian Cone Snails

Marine drugs, 2023-06, Vol.21 (6), p.356

2023

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Backbone Cyclization Turns a Venom Peptide into a Stable and Equipotent Ligand at Both Muscle and Neuronal Nicotinic Receptors

Journal of medicinal chemistry, 2020-11, Vol.63 (21), p.12682-12692

2020

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Comparative Venomics Reveals the Complex Prey Capture Strategy of the Piscivorous Cone Snail Conus catus

Journal of proteome research, 2015-10, Vol.14 (10), p.4372-4381

2015

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Towards an integrated venomics approach for accelerated conopeptide discovery

Toxicon (Oxford), 2012-09, Vol.60 (4), p.470-477

2012

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Pharmacology of predatory and defensive venom peptides in cone snails

Molecular bioSystems, 2017, Vol.13 (12), p.2453-2465

2017

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Transcriptomic Messiness in the Venom Duct of Conus miles Contributes to Conotoxin Diversity

Molecular & cellular proteomics, 2013-12, Vol.12 (12), p.3824-3833

2013

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Honeybee CaV4 has distinct permeation, inactivation, and pharmacology from homologous NaV channels

The Journal of general physiology, 2024-05, Vol.156 (5)

2024

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Proteomic insight into the venom composition of the largest European rear-fanged snake, Malpolon monspessulanus monspessulanus

Toxicon X, 2022-09, Vol.15, p.100130-100130, Article 100130

2022

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Transcriptomic-Proteomic Correlation in the Predation-Evoked Venom of the Cone Snail, Conus imperialis

Marine drugs, 2019-03, Vol.17 (3), p.177

2019

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Venomics Reveals Venom Complexity of the Piscivorous Cone Snail, Conus tulipa

Marine drugs, 2019-01, Vol.17 (1), p.71

2019

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Pmu1a, a novel spider toxin with dual inhibitory activity at pain targets hNaV1.7 and hCaV3 voltage‐gated channels

The FEBS journal, 2023-07, Vol.290 (14), p.3688-3702

2023

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Preferential use of unobstructed lateral portals as the access route to the pore of human ATP-gated ion channels (P2X receptors)

Proceedings of the National Academy of Sciences - PNAS, 2011-08, Vol.108 (33), p.13800-13805

2011

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α-Conotoxins to explore the molecular, physiological and pathophysiological functions of neuronal nicotinic acetylcholine receptors

Discovery, Synthesis, and Structure–Activity Relationships of Conotoxins

N‑Terminal Liver-Expressed Antimicrobial Peptide 2 (LEAP2) Region Exhibits Inverse Agonist Activity toward the Ghrelin Receptor

Nicotinic acetylcholine receptor inhibitors derived from snake and snail venoms

Use of Venom Peptides to Probe Ion Channel Structure and Function

Conus venom peptide pharmacology

Predatory and Defensive Strategies in Cone Snails

Inhibitory Glycine Receptors: An Update

Conotoxins: Chemistry and Biology

A Combined Transcriptomics and Proteomics Approach Reveals the Differences in the Predatory and Defensive Venoms of the Molluscivorous Cone Snail Cylinder ammiralis (Caenogastropoda: Conidae)

ConoServer: updated content, knowledge, and discovery tools in the conopeptide database

Deep Venomics Reveals the Mechanism for Expanded Peptide Diversity in Cone Snail Venom

Evolution of separate predation- and defence-evoked venoms in carnivorous cone snails

Synthesis and Biological Activity of Novel α-Conotoxins Derived from Endemic Polynesian Cone Snails

Backbone Cyclization Turns a Venom Peptide into a Stable and Equipotent Ligand at Both Muscle and Neuronal Nicotinic Receptors

Comparative Venomics Reveals the Complex Prey Capture Strategy of the Piscivorous Cone Snail Conus catus

Towards an integrated venomics approach for accelerated conopeptide discovery

Pharmacology of predatory and defensive venom peptides in cone snails

Transcriptomic Messiness in the Venom Duct of Conus miles Contributes to Conotoxin Diversity

Honeybee CaV4 has distinct permeation, inactivation, and pharmacology from homologous NaV channels

Proteomic insight into the venom composition of the largest European rear-fanged snake, Malpolon monspessulanus monspessulanus

Transcriptomic-Proteomic Correlation in the Predation-Evoked Venom of the Cone Snail, Conus imperialis

Venomics Reveals Venom Complexity of the Piscivorous Cone Snail, Conus tulipa

Pmu1a, a novel spider toxin with dual inhibitory activity at pain targets hNaV1.7 and hCaV3 voltage‐gated channels

Preferential use of unobstructed lateral portals as the access route to the pore of human ATP-gated ion channels (P2X receptors)

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