Detalhe da pesquisa
1.
Microglia maintain structural integrity during fetal brain morphogenesis.
Cell;
187(4): 962-980.e19, 2024 Feb 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38309258
2.
Grey matter heterotopia subtypes show specific morpho-electric signatures and network dynamics.
Brain;
147(3): 996-1010, 2024 03 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37724593
3.
Pathogenic MTOR somatic variant causing focal cortical dysplasia drives hyperexcitability via overactivation of neuronal GluN2C N-methyl-D-aspartate receptors.
Epilepsia;
2024 May 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38717560
4.
Early suppression of excitability in subcortical band heterotopia modifies epileptogenesis in rats.
Neurobiol Dis;
177: 106002, 2023 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36649744
5.
Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsy.
Hum Mol Genet;
28(22): 3755-3765, 2019 11 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31411685
6.
Direct and Collateral Alterations of Functional Cortical Circuits in a Rat Model of Subcortical Band Heterotopia.
Cereb Cortex;
29(10): 4253-4262, 2019 09 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30534979
7.
Spontaneous epileptiform activity in a rat model of bilateral subcortical band heterotopia.
Epilepsia;
60(2): 337-348, 2019 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30597542
8.
Correct Laminar Positioning in the Neocortex Influences Proper Dendritic and Synaptic Development.
Cereb Cortex;
28(8): 2976-2990, 2018 08 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29788228
9.
TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway.
Proc Natl Acad Sci U S A;
111(6): 2337-42, 2014 Feb 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24469796
10.
Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.
Epilepsia;
57(4): 648-59, 2016 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26873267
11.
Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.
PLoS Genet;
9(9): e1003752, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24039599
12.
Normotopic cortex is the major contributor to epilepsy in experimental double cortex.
Ann Neurol;
76(3): 428-42, 2014 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25074818
13.
Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero.
Brain;
136(Pt 8): 2457-73, 2013 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23831613
14.
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.
Brain;
136(Pt 11): 3378-94, 2013 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24056535
15.
A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene.
Hum Mol Genet;
19(24): 4895-905, 2010 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20876615
16.
H19 acts as a trans regulator of the imprinted gene network controlling growth in mice.
Development;
136(20): 3413-21, 2009 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19762426
17.
Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome.
J Neurosci;
28(7): 1745-55, 2008 Feb 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18272695
18.
Size of Subcortical Band Heterotopia Influences the Susceptibility to Hyperthermia-Induced Seizures in a Rat Model.
Front Cell Neurosci;
13: 473, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31680876
19.
Spared cognitive and behavioral functions prior to epilepsy onset in a rat model of subcortical band heterotopia.
Brain Res;
1711: 146-155, 2019 05 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30689978
20.
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations.
J Vis Exp;
(130)2017 12 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29286390