Detalhe da pesquisa
1.
Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy.
Ann Neurol
; 2022 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36534060
2.
Investigation of long interspersed element-1 retrotransposons as potential risk factors for idiopathic temporal lobe epilepsy.
Epilepsia
; 62(6): 1329-1342, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33826137
3.
Cognitive and behavioral effects of brief seizures in mice.
Epilepsy Behav
; 98(Pt A): 249-257, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31398689
4.
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Brain
; 136(Pt 10): 3140-50, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24014518
5.
Quantitative trait loci analysis reveals candidate genes implicated in regulating functional deficit and CNS vascular permeability in CD8 T cell-initiated blood-brain barrier disruption.
BMC Genomics
; 14: 678, 2013 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24090483
6.
Genome wide association studies (GWAS) and common forms of human epilepsy.
Epilepsy Behav
; 28 Suppl 1: S63-5, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23756483
7.
RNA Sequencing in Hypoxia-Adapted T98G Glioblastoma Cells Provides Supportive Evidence for IRE1 as a Potential Therapeutic Target.
Genes (Basel)
; 14(4)2023 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37107600
8.
Postmortem toxicology findings from the Camden Opioid Research Initiative.
PLoS One
; 18(11): e0292674, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37910493
9.
Quantitative trait locus on distal chromosome 1 regulates the occurrence of spontaneous spike-wave discharges in DBA/2 mice.
Epilepsia
; 53(8): 1429-35, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22612065
10.
Patient Perceptions and Potential Utility of Pharmacogenetic Testing in Chronic Pain Management and Opioid Use Disorder in the Camden Opioid Research Initiative.
Pharmaceutics
; 14(9)2022 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36145611
11.
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants.
Neurology
; 98(20): e2046-e2059, 2022 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35314505
12.
Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy.
Genes (Basel)
; 12(9)2021 09 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34573423
13.
Predisposition to epilepsy--does the ABCB1 gene play a role?
Epilepsia
; 51(9): 1882-5, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20491876
14.
Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice.
Epilepsia
; 51(9): 1707-13, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20831751
15.
The Molecular Genetic Interaction Between Circadian Rhythms and Susceptibility to Seizures and Epilepsy.
Front Neurol
; 11: 520, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32714261
16.
Isoliquiritigenin suppresses cocaine-induced extracellular dopamine release in rat brain through GABA(B) receptor.
Eur J Pharmacol
; 587(1-3): 124-8, 2008 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-18495107
17.
Genetic variants in the cocaine- and amphetamine-regulated transcript gene (CARTPT) and cocaine dependence.
Neurosci Lett
; 440(3): 280-3, 2008 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-18572320
18.
Association between polymorphisms in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) on chromosome 8p and schizophrenia.
Neuropsychobiology
; 57(1-2): 55-60, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18451639
19.
Quantitative trait locus for seizure susceptibility on mouse chromosome 5 confirmed with reciprocal congenic strains.
Physiol Genomics
; 31(3): 458-62, 2007 Nov 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-17698926
20.
Identification of three mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.
Gene
; 388(1-2): 135-47, 2007 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17156941