Detalhe da pesquisa
1.
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.
Am J Hum Genet
; 111(3): 509-528, 2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38412861
2.
Recurrent chromosomal imbalances provide selective advantage to human embryonic stem cells under enhanced replicative stress conditions.
Genes Chromosomes Cancer
; 60(4): 272-281, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33336840
3.
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants.
Clin Genet
; 99(2): 259-268, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33131045
4.
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene.
medRxiv
; 2023 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37292950
5.
Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen-glucose Deprivation.
Neurotherapeutics
; 19(2): 550-569, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35289376
6.
CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells.
Sci Rep
; 7(1): 16650, 2017 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29192200
7.
Identification of long non-coding RNAs involved in neuronal development and intellectual disability.
Sci Rep
; 6: 28396, 2016 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27319317