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Impaired neural development in a zebrafish model for Lowe syndrome

Human molecular genetics, 2012-04, Vol.21 (8), p.1744-1759

2012

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A zebrafish-centric approach to antiepileptic drug development

Disease models & mechanisms, 2021-07, Vol.14 (7)

Baraban, Scott C

2021

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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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Network Properties Revealed during Multi-Scale Calcium Imaging of Seizure Activity in Zebrafish

eNeuro, 2019-01, Vol.6 (1), p.ENEURO.0041-19.2019

2019

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Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish

PloS one, 2016-03, Vol.11 (3), p.e0151148-e0151148

2016

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Cell therapy for neurological disorders: Progress towards an embryonic medial ganglionic eminence progenitor-based treatment

Frontiers in neuroscience, 2023-04, Vol.17, p.1177678-1177678

2023

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Lhx6 Directly Regulates Arx and CXCR7 to Determine Cortical Interneuron Fate and Laminar Position

Neuron (Cambridge, Mass.), 2014-04, Vol.82 (2), p.350-364

2014

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Host brain environmental influences on transplanted medial ganglionic eminence progenitors

Scientific reports, 2024-02, Vol.14 (1), p.3610-3610, Article 3610

2024

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NPAS1 represses the generation of specific subtypes of cortical interneurons

Neuron (Cambridge, Mass.), 2014-12, Vol.84 (5), p.940-953

2014

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Large-Scale Phenotype-Based Antiepileptic Drug Screening in a Zebrafish Model of Dravet Syndrome

eNeuro, 2015-07, Vol.2 (4), p.ENEURO.0068-15.2015

2015

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Clemizole and trazodone are effective antiseizure treatments in a zebrafish model of STXBP1 disorder

Epilepsia open, 2022-09, Vol.7 (3), p.504-511

2022

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A novel zebrafish model of hyperthermia-induced seizures reveals a role for TRPV4 channels and NMDA-type glutamate receptors

Experimental neurology, 2012-09, Vol.237 (1), p.199-206

2012

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Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening

Frontiers in pharmacology, 2018-06, Vol.9, p.573-573

2018

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Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy

Nature neuroscience, 2005-08, Vol.8 (8), p.1059-1068

2005

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Phenotype-Based Screening of Synthetic Cannabinoids in a Dravet Syndrome Zebrafish Model

Frontiers in pharmacology, 2020-04, Vol.11, p.464-464

2020

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Reduction of seizures by transplantation of cortical GABAergic interneuron precursors into Kv1.1 mutant mice

Proceedings of the National Academy of Sciences - PNAS, 2009-09, Vol.106 (36), p.15472-15477

2009

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Bidirectional homeostatic plasticity induced by interneuron cell death and transplantation in vivo

Proceedings of the National Academy of Sciences - PNAS, 2014-01, Vol.111 (1), p.492-497

2014

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Animal models in epilepsy research: legacies and new directions

Nature neuroscience, 2015-03, Vol.18 (3), p.339-343

2015

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Emerging epilepsy models: insights from mice, flies, worms and fish

Current opinion in neurology, 2007-04, Vol.20 (2), p.164-168

Baraban, Scott C

2007

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In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish

iScience, 2021-06, Vol.24 (6), p.102558-102558, Article 102558

2021

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PAFAH1B1 haploinsufficiency disrupts GABA neurons and synaptic E/I balance in the dentate gyrus

Scientific reports, 2017-08, Vol.7 (1), p.8269-10, Article 8269

2017

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Zebrafish as a model for studying genetic aspects of epilepsy

Disease models & mechanisms, 2010-03, Vol.3 (3-4), p.144-148

2010

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Phenotypic analysis of catastrophic childhood epilepsy genes

Communications biology, 2021-06, Vol.4 (1), p.680-680, Article 680

2021

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Olig1 function is required to repress dlx1/2 and interneuron production in Mammalian brain

Neuron (Cambridge, Mass.), 2014-02, Vol.81 (3), p.574-587

2014

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Clemizole and modulators of serotonin signalling suppress seizures in Dravet syndrome

Brain (London, England : 1878), 2017-03, Vol.140 (3), p.669-683

2017

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Impaired neural development in a zebrafish model for Lowe syndrome

A zebrafish-centric approach to antiepileptic drug development

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

Network Properties Revealed during Multi-Scale Calcium Imaging of Seizure Activity in Zebrafish

Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish

Cell therapy for neurological disorders: Progress towards an embryonic medial ganglionic eminence progenitor-based treatment

Lhx6 Directly Regulates Arx and CXCR7 to Determine Cortical Interneuron Fate and Laminar Position

Host brain environmental influences on transplanted medial ganglionic eminence progenitors

NPAS1 represses the generation of specific subtypes of cortical interneurons

Large-Scale Phenotype-Based Antiepileptic Drug Screening in a Zebrafish Model of Dravet Syndrome

Clemizole and trazodone are effective antiseizure treatments in a zebrafish model of STXBP1 disorder

A novel zebrafish model of hyperthermia-induced seizures reveals a role for TRPV4 channels and NMDA-type glutamate receptors

Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening

Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy

Phenotype-Based Screening of Synthetic Cannabinoids in a Dravet Syndrome Zebrafish Model

Reduction of seizures by transplantation of cortical GABAergic interneuron precursors into Kv1.1 mutant mice

Bidirectional homeostatic plasticity induced by interneuron cell death and transplantation in vivo

Animal models in epilepsy research: legacies and new directions

Emerging epilepsy models: insights from mice, flies, worms and fish

In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish

PAFAH1B1 haploinsufficiency disrupts GABA neurons and synaptic E/I balance in the dentate gyrus

Zebrafish as a model for studying genetic aspects of epilepsy

Phenotypic analysis of catastrophic childhood epilepsy genes

Olig1 function is required to repress dlx1/2 and interneuron production in Mammalian brain

Clemizole and modulators of serotonin signalling suppress seizures in Dravet syndrome

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