Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice. (Q30479847)

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8 February 2020

title

Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice (English)

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8 February 2020

1

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8 February 2020

Giovanni Provenzano

3

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8 February 2020

Ivan Cohen

4

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8 February 2020

Desdemona Fricker

7

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8 February 2020

8

Michel Baulac

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8 February 2020

author name string

Vincent Navarro

2

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8 February 2020

Céline Dinocourt

5

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8 February 2020

Sophie Rivaud-Péchoux

6

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8 February 2020

Richard Miles

9

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8 February 2020

Eric Leguern

10

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8 February 2020

Stéphanie Baulac

11

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8 February 2020

language of work or name

English

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publication date

21 July 2010

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8 February 2020

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8 February 2020

volume

133

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issue

9

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8 February 2020

page(s)

2749-2762

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Disruption of LGI1-linked synaptic complex causes abnormal synaptic transmission and epilepsy

8 February 2020

cites work

1 reference

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Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability

20 June 2018

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20 June 2018

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Regional distribution of the leucine-rich glioma inactivated (LGI) gene family transcripts in the adult mouse brain

20 June 2018

1 reference

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LGI1-associated epilepsy through altered ADAM23-dependent neuronal morphology

20 June 2018

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Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy.

20 June 2018

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Lateral temporal lobe epilepsies: clinical and genetic features

20 June 2018

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LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.

20 June 2018

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LGI1 and LGI4 bind to ADAM22, ADAM23 and ADAM11

20 June 2018

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A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy

20 June 2018

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Epileptogenesis in the dentate gyrus: a critical perspective

20 June 2018

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Defining the expression pattern of the LGI1 gene in BAC transgenic mice

20 June 2018

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

20 June 2018

1 reference

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Effects of seizures on developmental processes in the immature brain

20 June 2018

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The epilepsy gene LGI1 encodes a secreted glycoprotein that binds to the cell surface

20 June 2018

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20 June 2018

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

20 June 2018

1 reference

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The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1

20 June 2018

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ADPEAF mutations reduce levels of secreted LGI1, a putative tumor suppressor protein linked to epilepsy

20 June 2018

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Fluoro-Jade C results in ultra high resolution and contrast labeling of degenerating neurons

20 June 2018

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LGI1 mutations in autosomal dominant partial epilepsy with auditory features

20 June 2018

1 reference

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A common protein interaction domain links two recently identified epilepsy genes

20 June 2018

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Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

20 June 2018

1 reference

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Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.

20 June 2018

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Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

20 June 2018

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A novel gene causing a mendelian audiogenic mouse epilepsy

20 June 2018

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Autosomal dominant partial epilepsy with auditory features: defining the phenotype

20 June 2018

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Experimental models of multifactorial epilepsies: the EL mouse and mice susceptible to audiogenic seizures

20 June 2018

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A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors

20 June 2018

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ZnT-3, a putative transporter of zinc into synaptic vesicles

20 June 2018

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Drug resistant ADLTE and recurrent partial status epilepticus with dysphasic features in a family with a novel LGI1mutation: electroclinical, genetic, and EEG/fMRI findings

20 June 2018

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Mass spectrometry identifies LGI1-interacting proteins that are involved in synaptic vesicle function in the human brain

26 November 2018

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A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes

26 November 2018

1 reference

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Expression profile of Lgi1 gene in mouse brain during development

26 November 2018

1 reference

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Two novel epilepsy-linked mutations leading to a loss of function of LGI1.

26 November 2018

1 reference

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The LGI1/epitempin gene encodes two protein isoforms differentially expressed in human brain

26 November 2018

1 reference

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Vlgr1 knockout mice show audiogenic seizure susceptibility.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929330

No evidence for a seriously increased malignancy risk in LGI1-caused epilepsy.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929330

Seizure anticipation in human neocortical partial epilepsy

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929330

Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929330

Maternally expressed PGK-Cre transgene as a tool for early and uniform activation of the Cre site-specific recombinase

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929330

26 November 2018

Identifiers

DOI

10.1093/BRAIN/AWQ171

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20659958 AND SRC:MED&resulttype=core&format=json

8 February 2020

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8 February 2020

PubMed publication ID

20659958

1 reference