Detalhe da pesquisa
1.
Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency.
PLoS Genet
; 19(10): e1010952, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37782669
2.
Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy.
PLoS Genet
; 11(6): e1005347, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26125563
3.
Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy.
PLoS Genet
; 10(7): e1004454, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25010494
4.
A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice.
PLoS Genet
; 6(8)2010 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20700442
5.
Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.
Hum Mol Genet
; 18(9): 1633-41, 2009 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19254928
6.
Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4.
Hum Mol Genet
; 17(12): 1738-49, 2008 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18316356
7.
Development of a new genetic model for absence epilepsy: spike-wave seizures in C3H/He and backcross mice.
J Neurosci
; 25(13): 3452-8, 2005 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-15800200
8.
Stargazer--a mouse to seize!
Epilepsy Curr
; 5(5): 161-5, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16175212
9.
A targeted mutation in Cacng4 exacerbates spike-wave seizures in stargazer (Cacng2) mice.
Proc Natl Acad Sci U S A
; 102(6): 2123-8, 2005 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-15677329
10.
Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive threshold.
Hum Mol Genet
; 12(9): 975-84, 2003 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12700166
11.
Phenotypic heterogeneity in the stargazin allelic series.
Mamm Genome
; 14(8): 506-13, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12925883