The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
about
PPAR-alpha agonists as novel antiepileptic drugs: preclinical findingsIncreased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fearSeizures and enhanced cortical GABAergic inhibition in two mouse models of human autosomal dominant nocturnal frontal lobe epilepsy.Nicotinic Receptors: Role in Addiction and Other Disorders of the Brain.Genetic testing in the epilepsies--report of the ILAE Genetics CommissionNovel Mutations in Synaptic Transmission Genes Suppress Neuronal Hyperexcitation in Caenorhabditis elegans.Genes associated with idiopathic epilepsies: a current overview.The nicotinic acetylcholine receptor alpha 4 subunit contains a functionally relevant SNP Haplotype.Mutational analysis of CHRNB2, CHRNA2 and CHRNA4 genes in Chinese population with autosomal dominant nocturnal frontal lobe epilepsyEpi4K: gene discovery in 4,000 genomes.Role of genetics in the diagnosis and treatment of epilepsy.Channelopathies in idiopathic epilepsy.Animal models for autosomal dominant frontal lobe epilepsy: on the origin of seizures.Alpha7 neuronal nicotinic receptors as a drug target in schizophrenia.The molecular biology of genetic-based epilepsies.The role of nicotinic acetylcholine receptors in autosomal dominant nocturnal frontal lobe epilepsy.Neuronal nicotinic receptors in sleep-related epilepsy: studies in integrative biology.Distinctive effects of nicotinic receptor intracellular-loop mutations associated with nocturnal frontal lobe epilepsy.Nicotine Elicits Convulsive Seizures by Activating Amygdalar Neurons.Mice expressing the ADNFLE valine 287 leucine mutation of the Β2 nicotinic acetylcholine receptor subunit display increased sensitivity to acute nicotine administration and altered presynaptic nicotinic receptor function.Pleiotropic functional effects of the first epilepsy-associated mutation in the human CHRNA2 gene.Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.Nocturnal frontal lobe epilepsy.Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study.
P2860
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P2860
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
description
2005 nî lūn-bûn
@nan
2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@ast
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@en
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@en-gb
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@nl
type
label
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@ast
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@en
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@en-gb
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@nl
prefLabel
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@ast
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@en
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@en-gb
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@nl
P2093
P1476
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits
@en
P2093
Daniel Bertrand
Elaine Hughes
Frances Elmslie
John Trounce
Ortrud K Steinlein
Sonia Bertrand
Thomas Sander
P304
P356
10.1016/J.NBD.2005.05.013
P407
P577
2005-12-01T00:00:00Z