Disruption of LGI1-linked synaptic complex causes abnormal synaptic transmission and epilepsy (Q30482626)

13 September 2017

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

1 reference

A disintegrin and metallopeptidase domain 23

13 September 2017

1 reference

Leucine-rich repeat LGI family, member 1

GOA release 2020-03-11

1 reference

A disintegrin and metallopeptidase domain 22

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

Yuko Fukata

1

1 reference

13 September 2017

Kathryn L Lovero

2

1 reference

13 September 2017

Tsuyoshi Iwanaga

3

1 reference

13 September 2017

Atsushi Watanabe

4

1 reference

13 September 2017

Norihiko Yokoi

5

1 reference

13 September 2017

Katsuhiko Tabuchi

6

1 reference

13 September 2017

Ryuichi Shigemoto

7

1 reference

13 September 2017

Roger A Nicoll

8

1 reference

13 September 2017

Masaki Fukata

9

1 reference

13 September 2017

language of work or name

English

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publication date

2 February 2010

1 reference

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

13 September 2017

1 reference

13 September 2017

107

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13 September 2017

8

1 reference

13 September 2017

3799-3804

1 reference

LGI1-associated epilepsy through altered ADAM23-dependent neuronal morphology

13 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

LGI1 and LGI4 bind to ADAM22, ADAM23 and ADAM11

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

Loss of inhibitory neuron AMPA receptors contributes to ataxia and epilepsy in stargazer mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

Efficient ADAM22 surface expression is mediated by phosphorylation-dependent interaction with 14-3-3 protein family members

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

Molecular constituents of neuronal AMPA receptors

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

Ataxia and peripheral nerve hypomyelination in ADAM22-deficient mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

Genetic mechanisms that underlie epilepsy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

The biology of epilepsy genes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

Deletion of the K(V)1.1 potassium channel causes epilepsy in mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

Endogenous serine protease inhibitor modulates epileptic activity and hippocampal long-term potentiation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840530

Functional analysis of secreted and transmembrane proteins critical to mouse development.

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0914537107

Seizures and reduced life span in mice lacking the potassium channel subunit Kv1.2, but hypoexcitability and enlarged Kv1 currents in auditory neurons

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0914537107

21 January 2018

Identifiers

DOI

10.1073/PNAS.0914537107

1 reference

13 September 2017

0 references

1 reference

13 September 2017

PubMed publication ID

20133599

1 reference