Map Scn2a

Map of recombinant DNA constructs expressed in ScN2a cells using the

Expression of CD4PrP in ScN2a cells 4 Map of the MHM2PrP and CD4PrP

Map of recombinant DNA constructs expressed in ScN2a cells using the

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Selective loss of Scn2a in ventral tegmental area dopaminergic neurons

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JCI Insight Scn2a severe hypomorphic mutation decreases excitatory

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Opposing Effects on NaV12 Function Underlie Differences Between SCN2A

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Scn2a insufficiency alters spontaneous neuronal Ca2 activity in

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A Nonsense Mutation of the Sodium Channel Gene SCN2A in a Patient with

Schematic drawing of SCN2A indicating the location of studied

Frontiers Functional analysis of a novel de novo SCN2A variant in a

SCN2A channelopathies Mechanisms and models Hedrich 2019

Schematic drawing of SCN2A indicating the location of studied

The AutismAssociated Gene Scn2a Contributes to Dendritic Excitability

Frontiers Disruption of the autismassociated gene SCN2A alters

The AutismAssociated Gene Scn2a Contributes to Dendritic Excitability

Understanding the SCN2A mystery therapeutic responses in a

Scn2a insufficiency alters spontaneous neuronal Ca2 activity in

Frontiers Functional analysis of a novel de novo SCN2A variant in a

Scn2a knockout increases AP excitability with intact axonal

Functional Characterization of a De Novo SCN2A Mixed Variant Linked to

Diagram showing the structure of the SCN2A protein and the locations of

A case of recurrent encephalopathy with SCN2A missense mutation Brain

The AutismAssociated Gene Scn2a Contributes to Dendritic Excitability

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Scn2a gainoffunction mutation aggravates EAE disease course

Boosting SCN2A expression reduces seizures in mice The Transmitter

Rare dysfunctional SCN2A variants are associated with malformation of

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Scn2a heterozygosity in granule cells alone impairs VOR gaindown

Physical and functional convergence of the autism risk genes Scn2a and

De novo SCN2A mutation in a Chinese infant with severe earlyonset

SCN2A Wikipedia

Selective loss of Scn2a in ventral tegmental area dopaminergic neurons

Opposing Effects on NaV12 Function Underlie Differences Between SCN2A

SCN2A variants are associated with malformation of cortical development

JCI Insight Scn2a severe hypomorphic mutation decreases excitatory

Selective loss of Scn2a in ventral tegmental area dopaminergic neurons

Missense mutation of the sodium channel gene SCN2A causes Dravet

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Scn2a insufficiency alters spontaneous neuronal Ca2 activity in

Physical and functional convergence of the autism risk genes Scn2a and

Selective loss of Scn2a in ventral tegmental area dopaminergic neurons

Scn2a haplodeficiency in dorsal telencephalic excitatory but in those

Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with

Scn2a gainoffunction mutation aggravates EAE disease course

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SCN2A mutation is associated with infantile spasms and bitemporal

Rare dysfunctional SCN2A variants are associated with malformation of

Scn2a insufficiency alters spontaneous neuronal Ca2 activity in

Selective loss of Scn2a in ventral tegmental area dopaminergic neurons

SCN2A Wikipedia

Frontiers Disruption of the autismassociated gene SCN2A alters

A pathogenic Scn2a nonsense mutation inactivated the mutated allele a

Functional and pharmacological evaluation of a novel SCN2A variant

Decoding SCN2A Variants Bridging Genetics and Phenotypes in Autism

Functional and pharmacological evaluation of a novel SCN2A variant

Physical and functional convergence of the autism risk genes Scn2a and

Figure 3 from A DeNovo SCN2A Mutation Identified in a Chinese Patient

Selective loss of Scn2a in ventral tegmental area dopaminergic neurons

SFARI SCN2A variants result in opposite effects on sodium channel

SCN2A contributes to oligodendroglia excitability and development in

A Novel Splicing SCN2A Mutation in an Adolescent With LowFunctioning

Novel SCN2A mutation in a family associated with juvenileonset

The AutismAssociated Gene Scn2a Contributes to Dendritic Excitability

PPT State of the Science in Autism on the path to precision medicine

Progress in Understanding and Treating SCN2AMediated Disorders Trends

Frontiers SCN2ARelated Epilepsy The Phenotypic Spectrum Treatment

SCN2ANav12

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Voltage Gated Sodium Channel Genes in Epilepsy Mutations Functional

Impaired cerebellar plasticity hypersensitizes sensory reflexes in

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IJMS Free FullText A Complex Genomic Rearrangement Resulting in

Sanders Lab Publications

The Genetics of SCNA2 FamilieSCN2A Foundation

SCN1A mutation database

Model mice hint at sodium channel genes contribution to autism The

A matter of space and time Emerging roles of diseaseassociated

Progress in Understanding and Treating SCN2AMediated Disorders Trends

Sodium channel epilepsies and neurodevelopmental disorders from

Paradoxical hyperexcitability from NaV12 sodium channel loss in

SCN2ARelated Disorders

Special Issue Ion Channels and Genetic Epilepsy Journal of

Sanders Lab Code

SCN2Arelated epilepsy of infancy with migrating focal seizures report

Frontiers Case Report Prenatal imaging and genetic integrated

A Novel Epilepsy Mutation in the Sodium Channel SCN1A Identifies a

Progress in Understanding and Treating SCN2AMediated Disorders Trends

Paradoxical hyperexcitability from NaV12 sodium channel loss in

Sodium channelopathies of skeletal muscle and brain Physiological

SCN1A gainoffunction paralogs and the Philadelphia variant Beyond

黄卓课题组与合作团队在Advanced Science杂志在线发表了题为 “The DEC2-SCN2A axis is essential ...

Advanced Science The DEC2SCN2A axis is essential

Paradoxical hyperexcitability from NaV12 sodium channel loss in

SCN3A a sodium channel in epilepsy and brain malformations Beyond

SCN2ARelated Disorders

More than meets the eye A conserved sensorimotor reflex helps unravel

Full article Voltagegated sodium channels Action players with many faces

SCN2Aepilepsie Kinderneurologie

A Complex Genomic Rearrangement Resulting in Loss of Function of SCN1A

Characterization of 5 untranslated regions of the voltagegated sodium

The phenotypic spectrum of SCN2Arelated epilepsy European Journal of

Paradoxical hyperexcitability from NaV12 sodium channel loss in

Advanced Science The DEC2SCN2A axis is essential

SCN1A Channels a Wide Range of Epileptic Phenotypes Report of Novel

Impaired cerebellar plasticity hypersensitizes sensory reflexes in

Understanding the basis of SCN2Arelated sensory hypersensitivity in

Sodium Current SCN2A Epilepsy

SCN2A Epilepsy Electrophysiology

Map SCN2A Expression in Mouse Brain

SCN Neuropeptide

SCN1A Gene

SCN2A Ribbon

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