Detalhe da pesquisa
1.
Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain.
Nature
; 629(8011): 384-392, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38600385
2.
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia.
Am J Hum Genet
; 104(5): 936-947, 2019 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30982608
3.
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Brain
; 144(5): 1435-1450, 2021 06 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33880529
4.
AUTS2 Regulates RNA Metabolism and Dentate Gyrus Development in Mice.
Cereb Cortex
; 31(10): 4808-4824, 2021 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34013328
5.
Clonal analysis reveals laminar fate multipotency and daughter cell apoptosis of mouse cortical intermediate progenitors.
Development
; 145(17)2018 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30217810
6.
The spectrum of brain malformations and disruptions in twins.
Am J Med Genet A
; 185(9): 2690-2718, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33205886
7.
Intermittent Hypoxia Disrupts Adult Neurogenesis and Synaptic Plasticity in the Dentate Gyrus.
J Neurosci
; 39(7): 1320-1331, 2019 02 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30587544
8.
Glial injury in neurotoxicity after pediatric CD19-directed chimeric antigen receptor T cell therapy.
Ann Neurol
; 86(1): 42-54, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31074527
9.
Intermediate progenitors and Tbr2 in cortical development.
J Anat
; 235(3): 616-625, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30677129
10.
New insights into the development of the human cerebral cortex.
J Anat
; 235(3): 432-451, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31373394
11.
Growth and folding of the mammalian cerebral cortex: from molecules to malformations.
Nat Rev Neurosci
; 15(4): 217-32, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24646670
12.
C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and Hippocampus.
J Neurosci
; 37(4): 960-971, 2017 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-28123028
13.
A dual-fluorescence reporter in the Eomes locus for live imaging and medium-term lineage tracing.
Genesis
; 55(8)2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28646547
14.
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia.
Brain
; 138(Pt 6): 1613-28, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25722288
15.
The protomap is propagated to cortical plate neurons through an Eomes-dependent intermediate map.
Proc Natl Acad Sci U S A
; 110(10): 4081-6, 2013 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23431145
16.
Genetic elimination of GABAergic neurotransmission reveals two distinct pacemakers for spontaneous waves of activity in the developing mouse cortex.
J Neurosci
; 34(11): 3854-63, 2014 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-24623764
17.
Glial localization of antiquitin: implications for pyridoxine-dependent epilepsy.
Ann Neurol
; 75(1): 22-32, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24122892
18.
Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas.
J Pathol
; 234(4): 436-40, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25143307
19.
Conditional ablation of Tbr2 results in abnormal development of the olfactory bulbs and subventricular zone-rostral migratory stream.
Dev Dyn
; 243(3): 440-50, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24550175
20.
Dynamic interactions between intermediate neurogenic progenitors and radial glia in embryonic mouse neocortex: potential role in Dll1-Notch signaling.
J Neurosci
; 33(21): 9122-39, 2013 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-23699523