Detalhe da pesquisa
1.
Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndrome.
Hum Mol Genet
; 29(15): 2461-2470, 2020 08 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32469049
2.
Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene.
Hum Mol Genet
; 24(9): 2662-72, 2015 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25634563
3.
Mass Spectrometry-Based Visualization of Molecules Associated with Human Habitats.
Anal Chem
; 88(22): 10775-10784, 2016 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27732780
4.
Normalized Clinical Severity Scores Reveal a Correlation between X Chromosome Inactivation and Disease Severity in Rett Syndrome.
Genes (Basel)
; 15(5)2024 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38790223
5.
Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndrome.
Genes Brain Behav
; 21(1): e12739, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33942492
6.
Behavioral and brain anatomical analysis of Foxg1 heterozygous mice.
PLoS One
; 17(10): e0266861, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36223387