(Q36221618)

English

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

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

author name string

Christine S Cheah

1

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Frank H Yu

2

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Ruth E Westenbroek

3

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Franck K Kalume

4

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

John C Oakley

5

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Gregory B Potter

6

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

John L Rubenstein

7

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

William A Catterall

8

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

language of work or name

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publication date

20 August 2012

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

number of pages

6

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inferred from page(s)

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

109

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Europe PubMed Central

PMC publication ID

12 August 2017

36

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

14646-14651

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Pure haploinsufficiency for Dravet syndrome Na(V)1.1 (SCN1A) sodium channel truncating mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

Dravet syndrome: the long-term outcome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

The core Dravet syndrome phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

NaV1.1 channels and epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy

1 reference

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Dlx1&2 and Mash1 transcription factors control striatal patterning and differentiation through parallel and overlapping pathways.

1 reference

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1 October 2017

Generation of Cre-transgenic mice using Dlx1/Dlx2 enhancers and their characterization in GABAergic interneurons

1 reference

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1 October 2017

Inherited neuronal ion channelopathies: new windows on complex neurological diseases

1 reference

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1 October 2017

Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

The origin and specification of cortical interneurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

The VGL-Chanome: A Protein Superfamily Specialized for Electrical Signaling and Ionic Homeostasis

1 reference

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1 October 2017

Localization of voltage-gated ion channels in mammalian brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

An unexpected requirement for brain-type sodium channels for control of heart rate in the mouse sinoatrial node

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

An unexpected role for brain-type sodium channels in coupling of cell surface depolarization to contraction in the heart

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

Severe myoclonic epilepsy in infants--a review based on the Tokyo Women's Medical University series of 84 cases

1 reference

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1 October 2017

Sodium channel beta subunits: anything but auxiliary

1 reference

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1 October 2017

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

Modification of seizure activity by electrical stimulation. II. Motor seizure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

1 October 2017

Mortality in Dravet syndrome: search for risk factors in Japanese patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

22 September 2018

Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

22 September 2018

Type I and type II Na(+) channel alpha-subunit polypeptides exhibit distinct spatial and temporal patterning, and association with auxiliary subunits in rat brain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

22 September 2018

Localization of Ca2+ channel subtypes on rat spinal motor neurons, interneurons, and nerve terminals.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3437823

22 September 2018

Differential subcellular localization of the RI and RII Na+ channel subtypes in central neurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/22908258

12 December 2020

based on heuristic

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Identifiers

10.1073/PNAS.1211591109

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

2012PNAS..10914646C

0 references

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1 reference

https://api.fatcat.wiki/v0/release/n7a4gheenzhepdp6t2vfohayhi

24 November 2022

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

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