Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome

Interneuron desynchronization precedes seizures in a mouse model of Dravet syndrome

(2020) Conny H. Tran et al.   JOURNAL OF NEUROSCIENCE

GluN2A NMDA Receptor Enhancement Improves Brain Oscillations, Synchrony, and Cognitive Functions in Dravet Syndrome and Alzheimer’s Disease Models

(2020) Jesse E. Hanson et al.   Cell Reports

Convulsive seizures and some behavioral comorbidities are uncoupled in the Scn1a A1783V Dravet syndrome mouse model

(2020) Saja Fadila et al.   EPILEPSIA

Augmented Reticular Thalamic Bursting and Seizures in Scn1a-Dravet Syndrome

(2019) Stefanie Ritter-Makinson et al.   Cell Reports

In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations

(2019) Andreea Nissenkorn et al.   PLoS One

Mitochondrial Regulation of the Hippocampal Firing Rate Set Point and Seizure Susceptibility

(2019) Boaz Styr et al.   NEURON

Disordered breathing in a mouse model of Dravet syndrome

(2019) Fu-Shan Kuo et al.   eLife

Hippocampal deletion of NaV1.1 channels in mice causes thermal seizures and cognitive deficit characteristic of Dravet Syndrome

(2019) Rachael E. Stein et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndrome

(2019) Kevin M Goff et al.   eLife

Single‐cell RNA‐Seq characterization of anatomically identified OLM interneurons in different transgenic mouse lines

(2019) Jochen Winterer et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Impairment of sharp-wave ripples in a murine model of Dravet Syndrome

(2019) Christine S. Cheah et al.   JOURNAL OF NEUROSCIENCE

A more efficient conditional mouse model of Dravet syndrome: Implications for epigenetic selection and sex-dependent behaviors

(2019) Aaron D. Williams et al.   JOURNAL OF NEUROSCIENCE METHODS

Epilepsy and neuropsychiatric comorbidities in mice carrying a recurrent Dravet syndrome SCN1A missense mutation

(2019) Ana Ricobaraza et al.   Scientific Reports

Classes and continua of hippocampal CA1 inhibitory neurons revealed by single-cell transcriptomics

(2018) Kenneth D. Harris et al.   PLOS BIOLOGY

A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome

(2018) Morgana Favero et al.   JOURNAL OF NEUROSCIENCE

Selective NaV1.1 activation rescues Dravet syndrome mice from seizures and premature death

(2018) Kay L. Richards et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Gene expression profiling in a mouse model of Dravet syndrome

(2018) Nicole A. Hawkins et al.   EXPERIMENTAL NEUROLOGY

Altered hippocampal interneuron activity precedes ictal onset

(2018) Mitra L Miri et al.   eLife

Serotonin enhances excitability and gamma frequency temporal integration in mouse prefrontal fast-spiking interneurons

(2017) Jegath C Athilingam et al.   eLife

Screening of conventional anticonvulsants in a genetic mouse model of epilepsy

(2017) Nicole A. Hawkins et al.   Annals of Clinical and Translational Neurology

Unaltered Network Activity and Interneuronal Firing During Spontaneous Cortical Dynamics In Vivo in a Mouse Model of Severe Myoclonic Epilepsy of Infancy

(2016) Angela Michela De Stasi et al.   CEREBRAL CORTEX

Dissecting the phenotypes of Dravet syndrome by gene deletion

(2015) Moran Rubinstein et al.   BRAIN

TheSCN1AMutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype

(2015) Heng Meng et al.   HUMAN MUTATION

Dendritic integration: 60 years of progress

(2015) Greg J Stuart et al.   NATURE NEUROSCIENCE

Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome

(2015) Moran Rubinstein et al.   NEUROBIOLOGY OF DISEASE

Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development

(2015) Ming-Shian Tsai et al.   NEUROBIOLOGY OF DISEASE

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

(2014) Akshitkumar M. Mistry et al.   NEUROBIOLOGY OF DISEASE

Impaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome

(2014) C. Tai et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism

(2013) Yu Liu et al.   ANNALS OF NEUROLOGY

Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of Dravet syndrome

(2013) Camille Liautard et al.   EPILEPSIA

Mapping genetic modifiers of survival in a mouse model of Dravet syndrome

(2013) A. R. Miller et al.   GENES BRAIN AND BEHAVIOR

Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome

(2013) Ikuo Ogiwara et al.   HUMAN MOLECULAR GENETICS

Variable Dendritic Integration in Hippocampal CA3 Pyramidal Neurons

(2013) Judit K. Makara et al.   NEURON

Transient Sodium Current at Subthreshold Voltages: Activation by EPSP Waveforms

(2012) Brett C. Carter et al.   NEURON

Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome

(2012) C. S. Cheah et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Blueprint for the Spatiotemporal Origins of Mouse Hippocampal Interneuron Diversity

(2011) L. Tricoire et al.   JOURNAL OF NEUROSCIENCE

Voltage-gated sodium channel isoform-specific effects of pompilidotoxins

(2010) Emanuele Schiavon et al.   FEBS Journal

Molecular Identity of Dendritic Voltage-Gated Sodium Channels

(2010) A. Lorincz et al.   SCIENCE

TheSCN1Avariant database: a novel research and diagnostic tool

(2009) Lieve RF Claes et al.   HUMAN MUTATION