Detalhe da pesquisa
1.
KDM5-mediated transcriptional activation of ribosomal protein genes alters translation efficiency to regulate mitochondrial metabolism in neurons.
Nucleic Acids Res
; 2024 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38597673
2.
Intellectual disability-associated disruption of O-GlcNAc cycling impairs habituation learning in Drosophila.
PLoS Genet
; 18(5): e1010159, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35500025
3.
The epigenetic regulator G9a attenuates stress-induced resistance and metabolic transcriptional programs across different stressors and species.
BMC Biol
; 19(1): 112, 2021 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34030685
4.
O-GlcNAcase contributes to cognitive function in Drosophila.
J Biol Chem
; 295(26): 8636-8646, 2020 06 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32094227
5.
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder.
PLoS Genet
; 13(10): e1006864, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29069077
6.
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.
Am J Hum Genet
; 98(1): 149-64, 2016 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26748517
7.
Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.
Am J Hum Genet
; 98(3): 541-552, 2016 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26942287
8.
BOD1 Is Required for Cognitive Function in Humans and Drosophila.
PLoS Genet
; 12(5): e1006022, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27166630
9.
CEP89 is required for mitochondrial metabolism and neuronal function in man and fly.
Hum Mol Genet
; 22(15): 3138-51, 2013 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23575228
10.
Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability.
Am J Hum Genet
; 91(1): 73-82, 2012 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22726846
11.
GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila.
J Med Genet
; 50(8): 507-14, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23644463
12.
Pre-Pulse Inhibition of an escape response in adult fruit fly, Drosophila melanogaster.
Res Sq
; 2024 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38343805
13.
Genetics, molecular control and clinical relevance of habituation learning.
Neurosci Biobehav Rev
; 143: 104883, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36152842
14.
From Rare Copy Number Variants to Biological Processes in ADHD.
Am J Psychiatry
; 177(9): 855-866, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32600152
15.
Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders.
Biol Psychiatry
; 86(4): 294-305, 2019 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31272685
16.
Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila.
PLoS One
; 14(2): e0211652, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30753188
17.
High-throughput Analysis of Locomotor Behavior in the Drosophila Island Assay.
J Vis Exp
; (129)2017 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29155762
18.
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Nat Genet
; 49(4): 515-526, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28191889
19.
De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila.
Eur J Hum Genet
; 24(8): 1145-53, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26757981
20.
Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders.
Front Neurosci
; 8: 331, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25414627