The epilepsy gene LGI1 encodes a secreted glycoprotein that binds to the cell surface (Q24309543)

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Ana Ayerdi-Izquierdo

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José Manuel Morante-Redolat

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Vicente Herranz-Pérez

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Kristy Favell

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Philip A Barker

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Jordi Pérez-Tur

Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras

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language of work or name

English

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publication date

1 December 2006

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published in

Human Molecular Genetics

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volume

15

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issue

23

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page(s)

3436-45

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cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Increased expression of LGI1 gene triggers growth inhibition and apoptosis of neuroblastoma cells.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Cyclooxygenase variants: the role of alternative splicing

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Alkaline phosphatase fusions of ligands or receptors as in situ probes for staining of cells, tissues, and embryos

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Alkaline phosphatase fusion proteins for molecular characterization and cloning of receptors and their ligands

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Localization of a gene for partial epilepsy to chromosome 10q

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Suppression of the cell proliferation and invasion phenotypes in glioma cells by the LGI1 gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

LGI1, a putative tumor metastasis suppressor gene, controls in vitro invasiveness and expression of matrix metalloproteinases in glioma cells through the ERK1/2 pathway

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

A common protein interaction domain links two recently identified epilepsy genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

LGI1 mutations in temporal lobe epilepsies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

LGI1 mutations in autosomal dominant partial epilepsy with auditory features

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021

Expression studies in gliomas and glial cells do not support a tumor suppressor role for LGI1.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL421

7 January 2021