Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice. - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q30479847

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What non-neuronal mechanisms should be studied to understand epileptic seizures?LGI proteins in the nervous system.Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis Dysfunctional ADAM22 implicated in progressive encephalopathy with cortical atrophy and epilepsy Autoantibodies to epilepsy-related LGI1 in limbic encephalitis neutralize LGI1-ADAM22 interaction and reduce synaptic AMPA receptors Loss of zebrafish lgi1b leads to hydrocephalus and sensitization to pentylenetetrazol induced seizure-like behavior.The temporal and spatial expression pattern of the LGI1 epilepsy predisposition gene during mouse embryonic cranial development.Basal ganglia T1 hyperintensity in LGI1-autoantibody faciobrachial dystonic seizures.Focal CA3 hippocampal subfield atrophy following LGI1 VGKC-complex antibody limbic encephalitis mTORC1 Is a Local, Postsynaptic Voltage Sensor Regulated by Positive and Negative Feedback Pathways.LGI2 truncation causes a remitting focal epilepsy in dogs.Essential roles of leucine-rich glioma inactivated 1 in the development of embryonic and postnatal cerebellum.Mutant LGI1 inhibits seizure-induced trafficking of Kv4.2 potassium channels Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF Epilepsy as a neurodevelopmental disorder.The LGI1-ADAM22 protein complex directs synapse maturation through regulation of PSD-95 function LGI1 acts presynaptically to regulate excitatory synaptic transmission during early postnatal development.LGI Proteins and Epilepsy in Human and Animals Neuronal autoantigens--pathogenesis, associated disorders and antibody testing Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling The expanding spectrum of clinically-distinctive, immunotherapy-responsive autoimmune encephalopathies.The very large G protein coupled receptor (Vlgr1) in hair cells.LGI1 tunes intrinsic excitability by regulating the density of axonal Kv1 channels.Motor cortex and hippocampus are the two main cortical targets in LGI1-antibody encephalitis.Arrested glutamatergic synapse development in human partial epilepsy.Models and detection of spontaneous recurrent seizures in laboratory rodents.Putting the Horse Before the Cart: Looking to Presynaptic Mechanisms in Genetic Models.Epilepsy gene LGI1 regulates postnatal developmental remodeling of retinogeniculate synapses.Chemical corrector treatment ameliorates increased seizure susceptibility in a mouse model of familial epilepsy.Homozygous Deletion of the LGI1 Gene in Mice Leads to Developmental Abnormalities Resulting in Cortical Dysplasia.Leucine-rich glioma inactivated 1 (Lgi1), an epilepsy-related secreted protein, has a nuclear localization signal and localizes to both the cytoplasm and the nucleus of the caudal ganglionic eminence neurons.Structural basis of epilepsy-related ligand-receptor complex LGI1-ADAM22.The Enlightened Brain: Novel Imaging Methods Focus on Epileptic Networks at Multiple Scales.Celecoxib Ameliorates Seizure Susceptibility in Autosomal Dominant Lateral Temporal Epilepsy.Clinical characteristics and short-term prognosis of LGI1 antibody encephalitis: a retrospective case study.The Nogo Receptor Ligand LGI1 Regulates Synapse Number and Synaptic Activity in Hippocampal and Cortical Neurons

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

http://www.wikidata.org/entity/Q30479847

description

2010 nî lūn-bûn

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2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2010 թվականի հուլիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Electroclinical characterizati ...... -inactivated 1-deficient mice.

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Electroclinical characterizati ...... -inactivated 1-deficient mice.

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Electroclinical characterizati ...... -inactivated 1-deficient mice.

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Electroclinical characterizati ...... a-inactivated 1-deficient mice

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Céline Dinocourt

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Eric Leguern

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Michel Baulac

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Richard Miles

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Sophie Rivaud-Péchoux

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Stéphanie Baulac

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Vincent Navarro

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P2860

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

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

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

LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

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

A common protein interaction domain links two recently identified epilepsy genes

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

Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission

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

A novel gene causing a mendelian audiogenic mouse epilepsy

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10.1093/BRAIN/AWQ171

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9

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133

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Desdemona Fricker

Giovanni Provenzano

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2929330

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