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KCC2 overexpression prevents the paradoxical seizure-promoting action of somatic inhibition

Nature communications, 2019-03, Vol.10 (1), p.1225-13, Article 1225

2019

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CACNA1D De Novo Mutations in Autism Spectrum Disorders Activate Cav1.3 L-Type Calcium Channels

Biological psychiatry (1969), 2015-05, Vol.77 (9), p.816-822

2015

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Designer receptor technology for the treatment of epilepsy

EBioMedicine, 2019-05, Vol.43, p.641-649

2019

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Combination antioxidant therapy prevents epileptogenesis and modifies chronic epilepsy

Redox biology, 2019-09, Vol.26, p.101278-101278, Article 101278

2019

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Single-molecule orientations determined by direct emission pattern imaging

Journal of the Optical Society of America. B, Optical physics, 2004-06, Vol.21 (6), p.1210

2004

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A Polybasic Plasma Membrane Binding Motif in the I-II Linker Stabilizes Voltage-gated CaV1.2 Calcium Channel Function

The Journal of biological chemistry, 2015-08, Vol.290 (34), p.21086-21100

2015

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Disruptor: Computational identification of oncogenic mutants disrupting protein-protein and protein-DNA interactions

Communications biology, 2023-07, Vol.6 (1), p.720-720, Article 720

2023

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C-Terminal Modulatory Domain Controls Coupling of Voltage-Sensing to Pore Opening in Cav1.3 L-type Ca2+ Channels

Biophysical journal, 2014-04, Vol.106 (7), p.1467-1475

2014

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Olanzapine: A potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogenetics

Science advances, 2019-04, Vol.5 (4), p.eaaw1567-eaaw1567

2019

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Functional Characterization of Spinocerebellar Ataxia Associated Dynorphin A Mutant Peptides

Biomedicines, 2021-12, Vol.9 (12), p.1882

2021

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Semiology, clustering, periodicity and natural history of seizures in an experimental occipital cortical epilepsy model

Disease models & mechanisms, 2018-12, Vol.11 (12)

2018

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Cell-type-specific tuning of Cav1.3 Ca2+-channels by a C-terminal automodulatory domain

Frontiers in cellular neuroscience, 2015-08, Vol.9

2015

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Gating defects of disease-causing de novo mutations in Cav1.3 Ca2+ channels

Channels (Austin, Tex.), 2018-01, Vol.12 (1), p.388-402

2018

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Dimethyl sulfoxide’s impact on epileptiform activity in a mouse model of chronic temporal lobe epilepsy

Epilepsy research, 2023-11, Vol.197, p.107235-107235, Article 107235

2023

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Imaging Nanometre-Sized Hot Spots on Smooth Au Films with High-Resolution Tip-Enhanced Luminescence and Raman Near-Field Optical Microscopy

Chemphyschem, 2008-02, Vol.9 (2), p.316-320

2008

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Orientation of Fluorescent Dyes in the Nano Channels of Zeolite L

The journal of physical chemistry. B, 2001-01, Vol.105 (1), p.25-35

2001

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Structural determinants of CaV1.3 L-type calcium channel gating

Channels (Austin, Tex.), 2012-05, Vol.6 (3), p.197-205

2012

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Characterization of the intrahippocampal kainic acid model in female mice with a special focus on seizure suppression by antiseizure medications

Experimental neurology, 2024-06, Vol.376, p.114749, Article 114749

2024

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C-terminal modulatory domain controls coupling of voltage-sensing to pore opening in Cav1.3 L-type Ca(2+) channels

Biophysical journal, 2014-04, Vol.106 (7), p.1467

2014

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In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsy

Brain (London, England : 1878), 2020-03, Vol.143 (3), p.891-905

2020

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A Novel Immobilization Method for Single Protein spFRET Studies

Biophysical journal, 2005-08, Vol.89 (2), p.L11-L13

2005

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Epilepsy Gene Therapy Using an Engineered Potassium Channel

The Journal of neuroscience, 2019-04, Vol.39 (16), p.3159-3169

2019

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Biochemical autoregulatory gene therapy for focal epilepsy

Nature medicine, 2018-09, Vol.24 (9), p.1324-1329

2018

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Loss of Ca v 1.3 ( CACNA1D ) function in a human channelopathy with bradycardia and congenital deafness

Nature neuroscience, 2011-01, Vol.14 (1), p.77-84

2011

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KCC2 overexpression prevents the paradoxical seizure-promoting action of somatic inhibition

CACNA1D De Novo Mutations in Autism Spectrum Disorders Activate Cav1.3 L-Type Calcium Channels

Designer receptor technology for the treatment of epilepsy

Combination antioxidant therapy prevents epileptogenesis and modifies chronic epilepsy

Single-molecule orientations determined by direct emission pattern imaging

A Polybasic Plasma Membrane Binding Motif in the I-II Linker Stabilizes Voltage-gated CaV1.2 Calcium Channel Function

Disruptor: Computational identification of oncogenic mutants disrupting protein-protein and protein-DNA interactions

C-Terminal Modulatory Domain Controls Coupling of Voltage-Sensing to Pore Opening in Cav1.3 L-type Ca2+ Channels

Olanzapine: A potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogenetics

Functional Characterization of Spinocerebellar Ataxia Associated Dynorphin A Mutant Peptides

Semiology, clustering, periodicity and natural history of seizures in an experimental occipital cortical epilepsy model

Cell-type-specific tuning of Cav1.3 Ca2+-channels by a C-terminal automodulatory domain

Gating defects of disease-causing de novo mutations in Cav1.3 Ca2+ channels

Dimethyl sulfoxide’s impact on epileptiform activity in a mouse model of chronic temporal lobe epilepsy

Imaging Nanometre-Sized Hot Spots on Smooth Au Films with High-Resolution Tip-Enhanced Luminescence and Raman Near-Field Optical Microscopy

Orientation of Fluorescent Dyes in the Nano Channels of Zeolite L

Structural determinants of CaV1.3 L-type calcium channel gating

Characterization of the intrahippocampal kainic acid model in female mice with a special focus on seizure suppression by antiseizure medications

C-terminal modulatory domain controls coupling of voltage-sensing to pore opening in Cav1.3 L-type Ca(2+) channels

In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsy

A Novel Immobilization Method for Single Protein spFRET Studies

Epilepsy Gene Therapy Using an Engineered Potassium Channel

Biochemical autoregulatory gene therapy for focal epilepsy

Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension

Loss of Ca v 1.3 ( CACNA1D ) function in a human channelopathy with bradycardia and congenital deafness

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