Detalhe da pesquisa
1.
Transcriptional Dysregulation and Impaired Neuronal Activity in FMR1 Knock-Out and Fragile X Patients' iPSC-Derived Models.
Int J Mol Sci
; 24(19)2023 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37834379
2.
Regulation of impulsive and aggressive behaviours by a novel lncRNA.
Mol Psychiatry
; 26(8): 3751-3764, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31907380
3.
Corrigendum to: DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome.
Hum Mol Genet
; 31(12): 2106-2107, 2022 Jun 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34918050
4.
Netrin G1: its downregulation in the nucleus accumbens of cocaine-conditioned mice and genetic association in human cocaine dependence.
Addict Biol
; 23(1): 448-460, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28074533
5.
Medium throughput bisulfite sequencing for accurate detection of 5-methylcytosine and 5-hydroxymethylcytosine.
BMC Genomics
; 18(1): 96, 2017 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28100169
6.
Molecular convergence of neurodevelopmental disorders.
Am J Hum Genet
; 95(5): 490-508, 2014 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-25307298
7.
Implication of LRRC4C and DPP6 in neurodevelopmental disorders.
Am J Med Genet A
; 173(2): 395-406, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27759917
8.
A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.
Am J Med Genet A
; 170A(5): 1225-35, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26789910
9.
Investigation of genes important in neurodevelopment disorders in adult human brain.
Hum Genet
; 134(10): 1037-53, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26194112
10.
Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities.
Am J Hum Genet
; 91(6): 1128-34, 2012 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23217328
11.
iPSC-derived models for anorexia nervosa research.
Trends Mol Med
; 30(4): 339-349, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38472034
12.
Homozygous ALS-linked mutations in TARDBP/TDP-43 lead to hypoactivity and synaptic abnormalities in human iPSC-derived motor neurons.
iScience
; 27(3): 109166, 2024 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38433895
13.
Excitatory neuron-specific suppression of the integrated stress response contributes to autism-related phenotypes in fragile X syndrome.
Neuron
; 111(19): 3028-3040.e6, 2023 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37473758
14.
SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST/NRSF, network organization and primate-specific evolution.
Hum Mol Genet
; 19(14): 2841-57, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20457675
15.
FOXG1 dose tunes cell proliferation dynamics in human forebrain progenitor cells.
Stem Cell Reports
; 17(3): 475-488, 2022 03 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35148845
16.
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome.
Hum Mol Genet
; 18(8): 1405-14, 2009 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19218269
17.
Methylation of the tyrosine hydroxylase gene is dysregulated by cocaine dependence in the human striatum.
iScience
; 24(10): 103169, 2021 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34693223
18.
A Multistep Workflow to Evaluate Newly Generated iPSCs and Their Ability to Generate Different Cell Types.
Methods Protoc
; 4(3)2021 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34287353
19.
Auto-qPCR; a python-based web app for automated and reproducible analysis of qPCR data.
Sci Rep
; 11(1): 21293, 2021 10 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34716395
20.
Midbrain organoids with an SNCA gene triplication model key features of synucleinopathy.
Brain Commun
; 3(4): fcab223, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34632384