Detalhe da pesquisa
1.
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
Am J Hum Genet
; 108(9): 1669-1691, 2021 09 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34314705
2.
The gut microbiome modulates the susceptibility to traumatic stress in a sex-dependent manner.
J Neurosci Res
; 102(3): e25315, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38439584
3.
Multi-strain probiotics ameliorate Alzheimer's-like cognitive impairment and pathological changes through the AKT/GSK-3ß pathway in senescence-accelerated mouse prone 8 mice.
Brain Behav Immun
; 119: 14-27, 2024 Mar 26.
Artigo
Inglês
| MEDLINE | ID: mdl-38548184
4.
A luciferase reporter mouse model to optimize in vivo gene editing validated by lipid nanoparticle delivery of adenine base editors.
Mol Ther
; 31(4): 1159-1166, 2023 04 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36793209
5.
Triglyceride-glucose index as a potential predictor for in-hospital mortality in critically ill patients with intracerebral hemorrhage: a multicenter, case-control study.
BMC Geriatr
; 24(1): 385, 2024 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38693481
6.
Perineuronal Nets in the CNS: Architects of Memory and Potential Therapeutic Target in Neuropsychiatric Disorders.
Int J Mol Sci
; 25(6)2024 Mar 18.
Artigo
Inglês
| MEDLINE | ID: mdl-38542386
7.
Design, Synthesis, Antifungal Evaluation, Structure-Activity Relationship (SAR) Study, and Molecular Docking of Novel Spirotryprostatin A Derivatives.
Molecules
; 29(4)2024 Feb 15.
Artigo
Inglês
| MEDLINE | ID: mdl-38398616
8.
Involvement of spinal NADPH oxidase 4 and endoplasmic reticulum stress in morphine-tolerant rats.
J Neurochem
; 2023 Dec 08.
Artigo
Inglês
| MEDLINE | ID: mdl-38069511
9.
De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder.
Am J Hum Genet
; 106(4): 438-452, 2020 04 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32197073
10.
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects.
Am J Hum Genet
; 107(2): 311-324, 2020 08 06.
Artigo
Inglês
| MEDLINE | ID: mdl-32738225
11.
Dunaliella Ds-26-16 acts as a global regulator to enhance salt tolerance by coordinating multiple responses in Arabidopsis seedlings.
Planta
; 257(6): 110, 2023 May 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37149499
12.
Maximum likelihood synchronization algorithm correction for photon-counting communications with blocking loss.
Opt Express
; 31(17): 28320-28337, 2023 Aug 14.
Artigo
Inglês
| MEDLINE | ID: mdl-37710889
13.
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis.
Brain
; 145(8): 2687-2703, 2022 08 27.
Artigo
Inglês
| MEDLINE | ID: mdl-35675510
14.
Activation of Epac in the BLA disrupts reconsolidation and attenuates heroin-seeking behaviour.
Addict Biol
; 28(10): e13330, 2023 10.
Artigo
Inglês
| MEDLINE | ID: mdl-37753572
15.
[Periplaneta americana extract Câ ¡-3 induces senescence of leukemia K562 cells via SIRT1/mTOR signaling pathway].
Zhongguo Zhong Yao Za Zhi
; 48(11): 3039-3045, 2023 Jun.
Artigo
Chinês
| MEDLINE | ID: mdl-37381962
16.
Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness.
Hum Mol Genet
; 29(13): 2218-2239, 2020 08 03.
Artigo
Inglês
| MEDLINE | ID: mdl-32504085
17.
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders.
Am J Hum Genet
; 105(3): 631-639, 2019 09 05.
Artigo
Inglês
| MEDLINE | ID: mdl-31353024
18.
Expanding the phenotypic spectrum of ARCN1-related syndrome.
Genet Med
; 24(6): 1227-1237, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35300924
19.
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Genet Med
; 24(10): 2065-2078, 2022 10.
Artigo
Inglês
| MEDLINE | ID: mdl-35980381
20.
Lipid-Nanoparticle-Based Delivery of CRISPR/Cas9 Genome-Editing Components.
Mol Pharm
; 19(6): 1669-1686, 2022 06 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35594500