Detalhe da pesquisa
1.
A common single nucleotide variant in the cytokine receptor-like factor-3 (CRLF3) gene causes neuronal deficits in human and mouse cells.
Hum Mol Genet
; 32(24): 3342-3352, 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37712888
2.
Mecp2 deletion results in profound alterations of developmental and adult functional connectivity.
Cereb Cortex
; 33(12): 7436-7453, 2023 06 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36897048
3.
A viral toolkit for recording transcription factor-DNA interactions in live mouse tissues.
Proc Natl Acad Sci U S A
; 117(18): 10003-10014, 2020 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32300008
4.
Functions of Gtf2i and Gtf2ird1 in the developing brain: transcription, DNA binding and long-term behavioral consequences.
Hum Mol Genet
; 29(9): 1498-1519, 2020 06 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32313931
5.
Altered neuronal physiology, development, and function associated with a common chromosome 15 duplication involving CHRNA7.
BMC Biol
; 19(1): 147, 2021 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34320968
6.
Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models.
Hum Mol Genet
; 28(20): 3443-3465, 2019 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31418010
7.
Translational profiling of hypocretin neurons identifies candidate molecules for sleep regulation.
Genes Dev
; 27(5): 565-78, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23431030
8.
Abnormal Microglia and Enhanced Inflammation-Related Gene Transcription in Mice with Conditional Deletion of Ctcf in Camk2a-Cre-Expressing Neurons.
J Neurosci
; 38(1): 200-219, 2018 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29133437
9.
Using animal models to evaluate the functional consequences of anesthesia during early neurodevelopment.
Neurobiol Learn Mem
; 165: 106834, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29550366
10.
Antisense reduction of tau in adult mice protects against seizures.
J Neurosci
; 33(31): 12887-97, 2013 Jul 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-23904623
11.
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors.
J Neurosci
; 33(7): 2732-53, 2013 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-23407934
12.
Characterization of early markers of disease in the mouse model of mucopolysaccharidosis IIIB.
J Neurodev Disord
; 16(1): 16, 2024 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38632525
13.
Mice lacking Astn2 have ASD-like behaviors and altered cerebellar circuit properties.
bioRxiv
; 2024 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38405978
14.
Oxytocin-induced birth causes sex-specific behavioral and brain connectivity changes in developing rat offspring.
iScience
; 27(2): 108960, 2024 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38327784
15.
Antecedent glycemic control reduces severe hypoglycemia-induced neuronal damage in diabetic rats.
Am J Physiol Endocrinol Metab
; 304(12): E1331-7, 2013 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23592483
16.
A comprehensive assay of social motivation reveals sex-specific roles of autism-associated genes and oxytocin.
Cell Rep Methods
; 3(6): 100504, 2023 06 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37426756
17.
Extensive characterization of a Williams Syndrome murine model shows Gtf2ird1 -mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior.
bioRxiv
; 2023 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36711815
18.
Extensive characterization of a Williams syndrome murine model shows Gtf2ird1-mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior.
Genes Brain Behav
; 22(4): e12853, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37370259
19.
Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits.
bioRxiv
; 2023 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36909558
20.
Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits.
Cell Rep
; 42(11): 113411, 2023 11 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37952155