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Chloride channels: often enigmatic, rarely predictable

Annual review of physiology, 2010-01, Vol.72 (1), p.95-121

2010

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Sharks are the preferred scraping surface for large pelagic fishes: Possible implications for parasite removal and fitness in a changing ocean

PloS one, 2022-10, Vol.17 (10), p.e0275458

2022

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Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice

Neurobiology of disease, 2014-05, Vol.65, p.1-11

2014

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Shallow subtidal marine benthic communities of Nachvak Fjord, Nunatsiavut, Labrador: A glimpse into species composition and drivers of their distribution

PloS one, 2023-11, Vol.18 (11), p.e0293702-e0293702

2023

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Unexpected Efficacy of a Novel Sodium Channel Modulator in Dravet Syndrome

Scientific reports, 2017-05, Vol.7 (1), p.1682-9, Article 1682

2017

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First quantification of subtidal community structure at Tristan da Cunha Islands in the remote South Atlantic: from kelp forests to the deep sea

PloS one, 2018-03, Vol.13 (3), p.e0195167

2018

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Altered neurological and neurobehavioral phenotypes in a mouse model of the recurrent KCNB1-p.R306C voltage-sensor variant

Neurobiology of disease, 2024-05, Vol.194, p.106470-106470, Article 106470

2024

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Direct evidence of impaired neuronal Na/K-ATPase pump function in alternating hemiplegia of childhood

Neurobiology of disease, 2018-07, Vol.115, p.29-38

2018

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Scanning mutagenesis of the voltage-gated sodium channel NaV1.2 using base editing

Cell reports (Cambridge), 2023-06, Vol.42 (6), p.112563-112563, Article 112563

2023

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Remote seamounts are key conservation priorities for pelagic wildlife

Conservation letters, 2024-01, Vol.17 (1), p.n/a

2024

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Functional consequences of a KCNT1 variant associated with status dystonicus and early‐onset infantile encephalopathy

Annals of clinical and translational neurology, 2019-09, Vol.6 (9), p.1606-1615

2019

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Functional and pharmacological evaluation of a novel SCN2A variant linked to early‐onset epilepsy

Annals of clinical and translational neurology, 2020-09, Vol.7 (9), p.1488-1501

2020

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Enhanced slow inactivation contributes to dysfunction of a recurrent SCN2A mutation associated with developmental and epileptic encephalopathy

The Journal of physiology, 2021-09, Vol.599 (18), p.4375-4388

2021

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Evolutionary and functional divergence between the cystic fibrosis transmembrane conductance regulator and related ATP-binding cassette transporters

Proceedings of the National Academy of Sciences - PNAS, 2008-12, Vol.105 (48), p.18865-18870

2008

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Selective Targeting of Gain-of-Function KCNQ1 Mutations Predisposing to Atrial Fibrillation

Circulation. Arrhythmia and electrophysiology, 2013-10, Vol.6 (5), p.960-966

2013

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Cryptic prokaryotic promoters explain instability of recombinant neuronal sodium channels in bacteria

The Journal of biological chemistry, 2021-01, Vol.296, p.100298, Article 100298

2021

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Alternative splicing potentiates dysfunction of early-onset epileptic encephalopathy SCN2A variants

The Journal of general physiology, 2020-03, Vol.152 (3)

2020

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Isolation and Characterization of a High Affinity Peptide Inhibitor of ClC-2 Chloride Channels

The Journal of biological chemistry, 2009-09, Vol.284 (38), p.26051-26062

2009

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The novel sodium channel modulator GS‐458967 (GS967) is an effective treatment in a mouse model of SCN8A encephalopathy

Epilepsia (Copenhagen), 2018-06, Vol.59 (6), p.1166-1176

2018

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Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties

The Journal of general physiology, 2023-10, Vol.155 (10), p.1

2023

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CaMKII modulates sodium current in neurons from epileptic Scn2a mutant mice

Proceedings of the National Academy of Sciences - PNAS, 2017-02, Vol.114 (7), p.1696-1701

2017

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Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders

Brain (London, England : 1878), 2024-08, Vol.147 (8), p.2761-2774

2024

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Cellular and behavioral effects of altered NaV1.2 sodium channel ion permeability in Scn2aK1422E mice

Human molecular genetics, 2022-08, Vol.31 (17), p.2964-2988

2022

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Scanning mutagenesis of the voltage-gated sodium channel Na V 1.2 using base editing

Cell reports (Cambridge), 2024-06, Vol.43 (6), p.114327

2024

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State-dependent Inhibition of Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channels by a Novel Peptide Toxin

The Journal of biological chemistry, 2007-12, Vol.282 (52), p.37545-37555

2007

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Chloride channels: often enigmatic, rarely predictable

Sharks are the preferred scraping surface for large pelagic fishes: Possible implications for parasite removal and fitness in a changing ocean

Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice

Shallow subtidal marine benthic communities of Nachvak Fjord, Nunatsiavut, Labrador: A glimpse into species composition and drivers of their distribution

Unexpected Efficacy of a Novel Sodium Channel Modulator in Dravet Syndrome

First quantification of subtidal community structure at Tristan da Cunha Islands in the remote South Atlantic: from kelp forests to the deep sea

Altered neurological and neurobehavioral phenotypes in a mouse model of the recurrent KCNB1-p.R306C voltage-sensor variant

Direct evidence of impaired neuronal Na/K-ATPase pump function in alternating hemiplegia of childhood

Scanning mutagenesis of the voltage-gated sodium channel NaV1.2 using base editing

Remote seamounts are key conservation priorities for pelagic wildlife

Functional consequences of a KCNT1 variant associated with status dystonicus and early‐onset infantile encephalopathy

Functional and pharmacological evaluation of a novel SCN2A variant linked to early‐onset epilepsy

Enhanced slow inactivation contributes to dysfunction of a recurrent SCN2A mutation associated with developmental and epileptic encephalopathy

Evolutionary and functional divergence between the cystic fibrosis transmembrane conductance regulator and related ATP-binding cassette transporters

Selective Targeting of Gain-of-Function KCNQ1 Mutations Predisposing to Atrial Fibrillation

Cryptic prokaryotic promoters explain instability of recombinant neuronal sodium channels in bacteria

Alternative splicing potentiates dysfunction of early-onset epileptic encephalopathy SCN2A variants

Isolation and Characterization of a High Affinity Peptide Inhibitor of ClC-2 Chloride Channels

The novel sodium channel modulator GS‐458967 (GS967) is an effective treatment in a mouse model of SCN8A encephalopathy

Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties

CaMKII modulates sodium current in neurons from epileptic Scn2a mutant mice

Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders

Cellular and behavioral effects of altered NaV1.2 sodium channel ion permeability in Scn2aK1422E mice

Scanning mutagenesis of the voltage-gated sodium channel Na V 1.2 using base editing

State-dependent Inhibition of Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channels by a Novel Peptide Toxin

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