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A distinct sodium channel voltage-sensor locus determines insect selectivity of the spider toxin Dc1a

Nature communications, 2014-07, Vol.5 (1), p.4350-4350, Article 4350

2014

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Precise spatiotemporal control of voltage-gated sodium channels by photocaged saxitoxin

Nature communications, 2021-07, Vol.12 (1), p.4171-9, Article 4171

2021

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Structural basis for voltage-sensor trapping of the cardiac sodium channel by a deathstalker scorpion toxin

Nature communications, 2021-01, Vol.12 (1), p.128-13, Article 128

2021

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Maladaptive activation of Nav1.9 channels by nitric oxide causes triptan-induced medication overuse headache

Nature communications, 2019-09, Vol.10 (1), p.4253-13, Article 4253

2019

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Multiple pore conformations driven by asynchronous movements of voltage sensors in a eukaryotic sodium channel

Nature communications, 2013-01, Vol.4 (1), p.1350-1350, Article 1350

2013

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Polymer-tetrodotoxin conjugates to induce prolonged duration local anesthesia with minimal toxicity

Nature communications, 2019-06, Vol.10 (1), p.2566-14, Article 2566

2019

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Impaired cortico-striatal excitatory transmission triggers epilepsy

Nature communications, 2019-04, Vol.10 (1), p.1917-1917, Article 1917

2019

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In vivo spatiotemporal control of voltage-gated ion channels by using photoactivatable peptidic toxins

Nature communications, 2022-01, Vol.13 (1), p.417-13, Article 417

2022

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CD8 + T cells stimulate Na-Cl co-transporter NCC in distal convoluted tubules leading to salt-sensitive hypertension

Nature communications, 2017-01, Vol.8 (1), p.14037-14, Article 14037

2017

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Insulin inhibits glucagon release by SGLT2-induced stimulation of somatostatin secretion

Nature communications, 2019-01, Vol.10 (1), p.139-139, Article 139

2019

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Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment

Nature communications, 2013, Vol.4 (1), p.2410-2410, Article 2410

2013

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Staphylococcus aureus produces pain through pore-forming toxins and neuronal TRPV1 that is silenced by QX-314

Nature communications, 2018-01, Vol.9 (1), p.37-37, Article 37

2018

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Molecular basis for class Ib anti-arrhythmic inhibition of cardiac sodium channels

Nature communications, 2011-06, Vol.2 (1), p.351, Article 351

2011

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Mesoscale infraslow spontaneous membrane potential fluctuations recapitulate high-frequency activity cortical motifs

Nature communications, 2015-07, Vol.6 (1), p.7738-7738, Article 7738

2015

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Spider venom-derived peptide induces hyperalgesia in Na v 1.7 knockout mice by activating Na v 1.9 channels

Nature communications, 2020-05, Vol.11 (1), p.2293

2020

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Structural modelling and mutant cycle analysis predict pharmacoresponsiveness of a Na(V)1.7 mutant channel

Nature communications, 2012, Vol.3, p.1186-1186

2012

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Structural mapping of Nav1.7 antagonists

Nature communications, 2023-06, Vol.14 (1), p.3224-3224, Article 3224

2023

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AKAPs-PKA disruptors increase AQP2 activity independently of vasopressin in a model of nephrogenic diabetes insipidus

Nature communications, 2018-04, Vol.9 (1), p.1411-11, Article 1411

2018

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Structural basis for modulation of human NaV1.3 by clinical drug and selective antagonist

Nature communications, 2022-03, Vol.13 (1), p.1286-1286, Article 1286

2022

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Cardiac radiotherapy induces electrical conduction reprogramming in the absence of transmural fibrosis

Nature communications, 2021-09, Vol.12 (1), p.5558-5558, Article 5558

2021

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Synergistic effects of ion transporter and MAP kinase pathway inhibitors in melanoma

Nature communications, 2016-08, Vol.7 (1), p.12336-19, Article 12336

2016

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Endogenous opioids contribute to insensitivity to pain in humans and mice lacking sodium channel Nav1.7

Nature communications, 2015-12, Vol.6 (1), p.8967-8967, Article 8967

2015

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The complete structure of an activated open sodium channel

Nature communications, 2017-02, Vol.8 (1), p.14205-14205, Article 14205

2017

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Wnt5a induces renal AQP2 expression by activating calcineurin signalling pathway

Nature communications, 2016-11, Vol.7 (1), p.13636-13636, Article 13636

2016

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An aptamer-based depot system for sustained release of small molecule therapeutics

Nature communications, 2023-04, Vol.14 (1), p.2444-2444, Article 2444

2023

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A distinct sodium channel voltage-sensor locus determines insect selectivity of the spider toxin Dc1a

Precise spatiotemporal control of voltage-gated sodium channels by photocaged saxitoxin

Structural basis for voltage-sensor trapping of the cardiac sodium channel by a deathstalker scorpion toxin

Maladaptive activation of Nav1.9 channels by nitric oxide causes triptan-induced medication overuse headache

Multiple pore conformations driven by asynchronous movements of voltage sensors in a eukaryotic sodium channel

Polymer-tetrodotoxin conjugates to induce prolonged duration local anesthesia with minimal toxicity

Impaired cortico-striatal excitatory transmission triggers epilepsy

In vivo spatiotemporal control of voltage-gated ion channels by using photoactivatable peptidic toxins

CD8 + T cells stimulate Na-Cl co-transporter NCC in distal convoluted tubules leading to salt-sensitive hypertension

Insulin inhibits glucagon release by SGLT2-induced stimulation of somatostatin secretion

Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment

Staphylococcus aureus produces pain through pore-forming toxins and neuronal TRPV1 that is silenced by QX-314

Molecular basis for class Ib anti-arrhythmic inhibition of cardiac sodium channels

Mesoscale infraslow spontaneous membrane potential fluctuations recapitulate high-frequency activity cortical motifs

Spider venom-derived peptide induces hyperalgesia in Na v 1.7 knockout mice by activating Na v 1.9 channels

Structural modelling and mutant cycle analysis predict pharmacoresponsiveness of a Na(V)1.7 mutant channel

Structural mapping of Nav1.7 antagonists

AKAPs-PKA disruptors increase AQP2 activity independently of vasopressin in a model of nephrogenic diabetes insipidus

Structural basis for modulation of human NaV1.3 by clinical drug and selective antagonist

Cardiac radiotherapy induces electrical conduction reprogramming in the absence of transmural fibrosis

Synergistic effects of ion transporter and MAP kinase pathway inhibitors in melanoma

Endogenous opioids contribute to insensitivity to pain in humans and mice lacking sodium channel Nav1.7

The complete structure of an activated open sodium channel

Wnt5a induces renal AQP2 expression by activating calcineurin signalling pathway

An aptamer-based depot system for sustained release of small molecule therapeutics

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