Detalhe da pesquisa
1.
The complex etiology of autism spectrum disorder due to missense mutations of CHD8.
Mol Psychiatry
; 2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38438524
2.
Inhibiting proBDNF to mature BDNF conversion leads to ASD-like phenotypes in vivo.
Mol Psychiatry
; 2024 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38762692
3.
Multiple types of navigational information are independently encoded in the population activities of the dentate gyrus neurons.
Proc Natl Acad Sci U S A
; 119(32): e2106830119, 2022 08 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35930667
4.
Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism.
Cell
; 137(7): 1235-46, 2009 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-19563756
5.
Brain-specific heterozygous loss-of-function of ATP2A2, endoplasmic reticulum Ca2+ pump responsible for Darier's disease, causes behavioral abnormalities and a hyper-dopaminergic state.
Hum Mol Genet
; 30(18): 1762-1772, 2021 08 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34104969
6.
In utero Exposure to Valproic Acid throughout Pregnancy Causes Phenotypes of Autism in Offspring Mice.
Dev Neurosci
; 45(5): 223-233, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37044070
7.
Insight into the function of a unique voltage-sensor protein (TMEM266) and its short form in mouse cerebellum.
Biochem J
; 479(11): 1127-1145, 2022 06 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35574701
8.
Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism.
Proc Natl Acad Sci U S A
; 117(18): 10055-10066, 2020 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32312822
9.
Inflammatory Skin Disease Causes Anxiety Symptoms Leading to an Irreversible Course.
Int J Mol Sci
; 24(6)2023 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36983014
10.
Forebrain-specific deficiency of the GTPase CRAG/Centaurin-γ3 leads to immature dentate gyri and hyperactivity in mice.
J Biol Chem
; 296: 100620, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33811862
11.
Perturbation of monoamine metabolism and enhanced fear responses in mice defective in the regeneration of tetrahydrobiopterin.
J Neurochem
; 161(2): 129-145, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35233765
12.
Oligodendrocyte dysfunction due to Chd8 mutation gives rise to behavioral deficits in mice.
Hum Mol Genet
; 29(8): 1274-1291, 2020 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32142125
13.
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
Nature
; 537(7622): 675-679, 2016 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-27602517
14.
Suppression of DNA Double-Strand Break Formation by DNA Polymerase ß in Active DNA Demethylation Is Required for Development of Hippocampal Pyramidal Neurons.
J Neurosci
; 40(47): 9012-9027, 2020 11 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33087478
15.
Heterogeneity of microglial proton channel in different brain regions and its relationship with aging.
J Neurochem
; 157(3): 624-641, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33404063
16.
Obligatory roles of dopamine D1 receptors in the dentate gyrus in antidepressant actions of a selective serotonin reuptake inhibitor, fluoxetine.
Mol Psychiatry
; 25(6): 1229-1244, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30531938
17.
Neuronal degeneration and cognitive impairment can be prevented via the normalization of mitochondrial dynamics.
Pharmacol Res
; 163: 105246, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33086082
18.
Vasopressin escape and memory impairment in a model of chronic syndrome of inappropriate secretion of antidiuretic hormone in mice.
Endocr J
; 68(1): 31-43, 2021 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32879162
19.
Acquired Expression of Mutant Mitofusin 2 Causes Progressive Neurodegeneration and Abnormal Behavior.
J Neurosci
; 39(9): 1588-1604, 2019 02 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-30606759
20.
Neural symptoms in a gene knockout mouse model of Sjögren-Larsson syndrome are associated with a decrease in 2-hydroxygalactosylceramide.
FASEB J
; 33(1): 928-941, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30085884