about
Potential developmental neurotoxicity of pesticides used in EuropeA nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizuresMice with a targeted disruption of the Cl-/HCO3- exchanger AE3 display a reduced seizure thresholdMice with deficiency of G protein gamma3 are lean and have seizuresMutations in LGI1 cause autosomal-dominant partial epilepsy with auditory featuresDevelopmental neurotoxicity of pyrethroid insecticides: critical review and future research needsA missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful miceSodium channels SCN1A, SCN2A and SCN3A in familial autismFunctional evaluation of human ClC-2 chloride channel mutations associated with idiopathic generalized epilepsiesTilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causationUsing mouse models of autism spectrum disorders to study the neurotoxicology of gene-environment interactionsNeuronal carbonic anhydrase VII provides GABAergic excitatory drive to exacerbate febrile seizuresRole of voltage-gated calcium channels in epilepsy.Unraveling monogenic channelopathies and their implications for complex polygenic diseaseMouse behavioral assays relevant to the symptoms of autism.Functional properties and differential neuromodulation of Na(v)1.6 channels.Pharmacogenomics in the treatment of epilepsy.Epilepsy in Irish Wolfhounds.Sacred disease secrets revealed: the genetics of human epilepsy.Genetic forms of epilepsies and other paroxysmal disordersGene expression, genetics, and genomics in epilepsy: some answers, more questions.The neurobiology of epilepsy.BACE1 regulates voltage-gated sodium channels and neuronal activity.Canine epilepsy genetics.Sodium Channel Mutations in GEFS(+) Produce Persistent Inward Current.Increased neuronal firing in computer simulations of sodium channel mutations that cause generalized epilepsy with febrile seizures plus.Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation.Modeling brain dynamics using computational neurogenetic approach.Depolarization block of neurons during maintenance of electrographic seizures.Inbred or Outbred? Genetic Diversity in Laboratory Rodent Colonies.Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant mice.Calcium triggers reversal of calmodulin on nested anti-parallel sites in the IQ motif of the neuronal voltage-dependent sodium channel NaV1.2.No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies
P2860
Q21245813-CC5DF7BE-312D-4E40-849C-F9B795717FECQ24313526-9C9585E8-3E78-485F-8B55-C70FA8A04952Q24535556-EA5BB16C-1234-4744-8AAA-EB620F999A81Q24562837-E81B970E-1CC8-49AF-AB69-B0B37EB46B96Q24643177-1F01E8A8-57E2-4417-AFB5-A7E76FA4C927Q24814126-A89EFC73-1C09-4710-8F76-D76DE48C61C8Q27346832-A941E804-225B-4E23-B4E7-BB0EDBDE814DQ28212831-9A19EDF4-0A78-423A-9FEC-FBC2C313FA62Q28271976-4F956A95-EB72-4B04-B24B-B76D6DEC1E57Q28385221-9D16CBB8-B163-4BC0-927A-D70B8FEA6C92Q28392778-049B6093-E9A9-4C69-819F-C38E6F4D2AC2Q28512731-4F378E18-2AC3-49F3-A433-239E94A48190Q30427731-E0F1CDCB-A635-4837-BA51-B53F4C83DD27Q33905030-90BA0CF6-77EA-4961-8EAA-0F6EF7C80539Q34699041-75B8C8A3-9257-4A6A-8E61-A407D826DD7FQ34791973-8232D028-611B-4853-835E-BC83BE6F960AQ35574947-762D46FB-5733-44B5-8B2F-8335598566A0Q35899400-DA45AD2A-CD5D-4569-821C-E99AFCA187CFQ36210058-B932E743-7AD9-453C-B546-937CCDE8E0ECQ36805699-8C6D2497-2ED6-432E-8A37-B67137D500E0Q36850241-59A092A8-AA10-4368-90EB-1621982E29E4Q36873536-9FECA146-79DD-461F-A1C2-D5B5E6CB161BQ37355641-BD6BF71D-589D-400B-A1ED-75E0D588AC97Q37950831-E61DD9AA-A190-412B-B7AD-EDBF0B535F92Q40466621-497823E7-9A96-4BFE-A50A-9CE372B5616AQ40542880-97004F4C-8707-4164-99C9-A8B257DAAB1BQ43168798-C075A6FC-D68C-4F89-980D-636BEAD2836FQ43240962-2BB8D1EC-10AC-49D6-BE2E-47730D262B32Q44475051-77969557-04FA-457B-8903-6C4F66F30CD4Q47192676-9F6DDDC9-53F6-44A8-BC4A-848603026972Q48325327-9D888FCC-CADE-4476-ACED-836403D5F20FQ51084792-8DE24F8A-5A3F-4364-ABB7-01ED40545CAAQ52955807-BF51592F-1FAB-4643-82BA-8F3C3DE94AA4Q57982315-C2B33226-1801-4C92-97E1-C37A2D34F47A
P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Identification of epilepsy genes in human and mouse
@ast
Identification of epilepsy genes in human and mouse
@en
Identification of epilepsy genes in human and mouse
@nl
type
label
Identification of epilepsy genes in human and mouse
@ast
Identification of epilepsy genes in human and mouse
@en
Identification of epilepsy genes in human and mouse
@nl
prefLabel
Identification of epilepsy genes in human and mouse
@ast
Identification of epilepsy genes in human and mouse
@en
Identification of epilepsy genes in human and mouse
@nl
P2860
P1476
Identification of epilepsy genes in human and mouse
@en
P2093
P2860
P304
P356
10.1146/ANNUREV.GENET.35.102401.091142
P577
2001-01-01T00:00:00Z