(Q33987529)

30 July 2017

title

LGI2 truncation causes a remitting focal epilepsy in dogs (English)

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30 July 2017

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5

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6

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10

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16

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14

Kerstin Lindblad-Toh

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Tarja Jokinen

2

object named as

Tarja S Jokinen

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30 July 2017

Masaki Fukata

3

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Yuko Fukata

object named as

Yuko Fukata

4

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Eija H. Seppälä

1

object named as

Eija H Seppälä

1 reference

30 July 2017

Sami K Kilpinen

7

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30 July 2017

Frank Steffen

8

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30 July 2017

Elisabeth Dietschi

9

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30 July 2017

Ranja Eklund

11

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30 July 2017

Xiaochu Zhao

12

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30 July 2017

Jennifer J Rilstone

13

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30 July 2017

Berge A Minassian

15

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30 July 2017

publication date

28 July 2011

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30 July 2017

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30 July 2017

volume

7

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30 July 2017

issue

7

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30 July 2017

page(s)

e1002194

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Creative Commons Attribution 4.0 International

30 July 2017

copyright license

start time

28 July 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.

1 reference

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

5 July 2018

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Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Adam22 is a major neuronal receptor for Lgi4-mediated Schwann cell signaling

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Leucine-rich glioma inactivated 3 induces neurite outgrowth through Akt and focal adhesion kinase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

LGI1-associated epilepsy through altered ADAM23-dependent neuronal morphology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Prevalence and characteristics of epilepsy in the Belgian shepherd variants Groenendael and Tervueren born in Denmark 1995-2004

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

LGI1 and LGI4 bind to ADAM22, ADAM23 and ADAM11

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Systematic bioinformatic analysis of expression levels of 17,330 human genes across 9,783 samples from 175 types of healthy and pathological tissues

5 July 2018

1 reference

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Leucine-rich glioma inactivated 3 associates with syntaxin 1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

PLINK: a tool set for whole-genome association and population-based linkage analyses

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Benign familial juvenile epilepsy in Lagotto Romagnolo dogs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Postnatal growth and morphological development of the brain: a species comparison

5 July 2018

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5 July 2018

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Developmental remodelling of the lemniscal synapse in the ventral basal thalamus of the mouse.

5 July 2018

1 reference

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The claw paw mutation reveals a role for Lgi4 in peripheral nerve development

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Expanded repeat in canine epilepsy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Mutations in EFHC1 cause juvenile myoclonic epilepsy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

LGI1 mutations in temporal lobe epilepsies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Morphometric study of human cerebral cortex development

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145619

Sacred disease secrets revealed: the genetics of human epilepsy

5 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002194

Electroencephalography findings in healthy and Finnish Spitz dogs with epilepsy: visual and background quantitative analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002194

Mouse LGI3 gene: expression in brain and promoter analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002194

Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002194

AnADAMTS17Splice Donor Site Mutation in Dogs with Primary Lens Luxation

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21829378

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21829378

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1002194

1 reference

30 July 2017

1 reference

30 July 2017

1 reference