Detalhe da pesquisa
1.
Adaptive sequence divergence forged new neurodevelopmental enhancers in humans.
Cell
; 185(24): 4587-4603.e23, 2022 11 23.
Artigo
Inglês
| MEDLINE | ID: mdl-36423581
2.
Founder cells shape brain evolution.
Cell
; 184(8): 1965-1967, 2021 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-33861961
3.
Progenitor Hyperpolarization Regulates the Sequential Generation of Neuronal Subtypes in the Developing Neocortex.
Cell
; 174(5): 1264-1276.e15, 2018 08 23.
Artigo
Inglês
| MEDLINE | ID: mdl-30057116
4.
Astrocytes Assemble Thalamocortical Synapses by Bridging NRX1α and NL1 via Hevin.
Cell
; 164(1-2): 183-196, 2016 Jan 14.
Artigo
Inglês
| MEDLINE | ID: mdl-26771491
5.
The exon junction complex component EIF4A3 is essential for mouse and human cortical progenitor mitosis and neurogenesis.
Development
; 150(10)2023 05 15.
Artigo
Inglês
| MEDLINE | ID: mdl-37139782
6.
Non-muscle myosins control radial glial basal endfeet to mediate interneuron organization.
PLoS Biol
; 21(2): e3001926, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36854011
7.
A ubiquitous GC content signature underlies multimodal mRNA regulation by DDX3X.
Mol Syst Biol
; 20(3): 276-290, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38273160
8.
Dosage-dependent requirements of Magoh for cortical interneuron generation and survival.
Development
; 147(1)2020 01 13.
Artigo
Inglês
| MEDLINE | ID: mdl-31857347
9.
Local gene regulation in radial glia: Lessons from across the nervous system.
Traffic
; 21(12): 737-748, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33058331
10.
Enhancing our brains: Genomic mechanisms underlying cortical evolution.
Semin Cell Dev Biol
; 76: 23-32, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-28864345
11.
EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome.
Hum Mol Genet
; 26(12): 2177-2191, 2017 06 15.
Artigo
Inglês
| MEDLINE | ID: mdl-28334780
12.
Acute Lengthening of Progenitor Mitosis Influences Progeny Fate during Cortical Development in vivo.
Dev Neurosci
; 41(5-6): 300-317, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-32541147
13.
Mouse models of Casc3 reveal developmental functions distinct from other components of the exon junction complex.
RNA
; 23(1): 23-31, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27780844
14.
Haploinsufficiency for Core Exon Junction Complex Components Disrupts Embryonic Neurogenesis and Causes p53-Mediated Microcephaly.
PLoS Genet
; 12(9): e1006282, 2016 09.
Artigo
Inglês
| MEDLINE | ID: mdl-27618312
15.
Genomic divergence and brain evolution: How regulatory DNA influences development of the cerebral cortex.
Bioessays
; 38(2): 162-71, 2016 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-26642006
16.
Rbm8a haploinsufficiency disrupts embryonic cortical development resulting in microcephaly.
J Neurosci
; 35(18): 7003-18, 2015 May 06.
Artigo
Inglês
| MEDLINE | ID: mdl-25948253
17.
Generation of a Magoh conditional allele in mice.
Genesis
; 52(8): 752-8, 2014 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-24771530
18.
The EJC component Magoh regulates proliferation and expansion of neural crest-derived melanocytes.
Dev Biol
; 375(2): 172-81, 2013 Mar 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23333945
19.
Genetic interaction screens identify a role for hedgehog signaling in Drosophila border cell migration.
Dev Dyn
; 242(5): 414-31, 2013 May.
Artigo
Inglês
| MEDLINE | ID: mdl-23335293
20.
A human-specific enhancer fine-tunes radial glia potency and corticogenesis.
bioRxiv
; 2024 Apr 11.
Artigo
Inglês
| MEDLINE | ID: mdl-38645099