(Q28244922)

1

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E Brodtkorb

2

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T Piepoli

3

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G Finocchiaro

4

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O K Steinlein

https://scigraph.springernature.com/pub.10.1007/s10048-005-0216-5

5

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language of work or name

English

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publication date

May 2005

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published in

Neurogenetics

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volume

6

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page(s)

59-66

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issue

2

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exact match

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cites work

LGI1 mutations in autosomal dominant partial epilepsy with auditory features

1 reference

https://api.crossref.org/works/10.1007%2FS10048-005-0216-5

Autosomal dominant partial epilepsy with auditory features: defining the phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-005-0216-5

LGI1 mutations in temporal lobe epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-005-0216-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-005-0216-5

Expression and tissue localization of membrane-type 1, 2, and 3 matrix metalloproteinases in human astrocytic tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-005-0216-5

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

21 January 2018

1 reference

12 December 2020

Mutation and cancer: statistical study of retinoblastoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism

1 reference

12 December 2020

A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures

1 reference

12 December 2020

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

1 reference

12 December 2020

Expression of the LGI1 gene product in astrocytic gliomas: downregulation with malignant progression.

1 reference

12 December 2020

Structural diversity of leucine-rich repeat proteins

1 reference

12 December 2020

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

12 December 2020

Physical and functional characterization of the human LGI1 gene and its possible role in glioma development

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10.

1 reference

12 December 2020

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

1 reference

12 December 2020

Expression of extracellular matrix degrading enzymes during migration of xenografted brain cells.

1 reference

12 December 2020

Matrix metalloproteinases

1 reference

12 December 2020

Loss of heterozygosity on chromosomes 10q, 9p, 17p and 13q in malays with malignant glioma.

1 reference

12 December 2020

Autosomal dominant partial epilepsy with auditory features: description of a new family.

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24.

1 reference

12 December 2020

A common protein interaction domain links two recently identified epilepsy genes

1 reference

12 December 2020

Principles of tumor suppression

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of genetic information in central nervous system tumors common to children and young adults.

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytogenetics and Molecular Genetics of Malignant Gliomas and Medulloblastoma

1 reference

12 December 2020

Localization of a gene for partial epilepsy to chromosome 10q

1 reference

12 December 2020

Loss of heterozygosity for 10q loci in human gliomas

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of the promoter, genomic structure, and mouse ortholog of LGI1.

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice.

1 reference

12 December 2020

Significant evidence for linkage of febrile seizures to chromosome 5q14-q15.

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The leucine-rich repeat as a protein recognition motif

1 reference

12 December 2020

A novel gene causing a mendelian audiogenic mouse epilepsy

1 reference

12 December 2020

Metastasis suppressors alter the signal transduction of cancer cells

1 reference

12 December 2020

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

1 reference

12 December 2020