Detalhe da pesquisa
1.
Proximal telomeric decompaction due to telomere shortening drives FOXC1-dependent myocardial senescence.
Nucleic Acids Res
; 2024 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38634789
2.
Trisomy 21-driven metabolite alterations are linked to cellular injuries in Down syndrome.
Cell Mol Life Sci
; 81(1): 112, 2024 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38433139
3.
MicroRNA-338-3p as a therapeutic target in cardiac fibrosis through FGFR2 suppression.
J Clin Lab Anal
; 36(8): e24584, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35792028
4.
PGAM1 deficiency ameliorates myocardial infarction remodeling by targeting TGF-ß via the suppression of inflammation, apoptosis and fibrosis.
Biochem Biophys Res Commun
; 534: 933-940, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33168191
5.
FLNC and MYLK2 Gene Mutations in a Chinese Family with Different Phenotypes of Cardiomyopathy.
Int Heart J
; 62(1): 127-134, 2021 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33455984
6.
A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities.
Fetal Pediatr Pathol
; 40(3): 256-261, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31805817
7.
CD36 Enhances Vascular Smooth Muscle Cell Proliferation and Development of Neointimal Hyperplasia.
Arterioscler Thromb Vasc Biol
; 39(2): 263-275, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30567481
8.
Ankyrin repeat domain 1: A novel gene for cardiac septal defects.
J Gene Med
; 21(4): e3070, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30659708
9.
Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease.
Prenat Diagn
; 38(6): 406-413, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29573438
10.
In vitro remodeling and structural characterization of degradable polymer scaffold-based tissue-engineered vascular grafts using optical coherence tomography.
Cell Tissue Res
; 370(3): 417-426, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28887711
11.
Population pharmacokinetics and safety of eptifibatide in healthy Chinese volunteers and simulations on the dose regimens approved for a Western population.
Int J Clin Pharmacol Ther
; 53(8): 658-66, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26104033
12.
Corrigendum for Xia Y, Yang Y, Huang S, et al (2018) https://doi.org/10.1002/pd.5249.
Prenat Diagn
; 39(4): 328, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30916817
13.
Single-cell RNA-seq uncovers distinct pathways and genes in endothelial cells during atherosclerosis progression.
Front Mol Biosci
; 10: 1176267, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37325477
14.
PRP significantly promotes the adhesion and migration of vascular smooth muscle cells on stent material.
Eur J Med Res
; 28(1): 581, 2023 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38071348
15.
Saturation of radiation trapping and lifetime measurements in three-level laser crystals.
Opt Express
; 20(23): 25613-23, 2012 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23187380
16.
Upregulation of the Long Non-coding RNA LINC01480 Is Associated With Immune Infiltration in Coronary Artery Disease Based on an Immune-Related lncRNA-mRNA Co-expression Network.
Front Cardiovasc Med
; 9: 724262, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35557532
17.
SGLT2 inhibitor dapagliflozin reduces endothelial dysfunction and microvascular damage during cardiac ischemia/reperfusion injury through normalizing the XO-SERCA2-CaMKII-coffilin pathways.
Theranostics
; 12(11): 5034-5050, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35836807
18.
Identification and characterization of novel elastin gene mutations in eleven families with supravalvular aortic stenosis.
Front Genet
; 13: 1059640, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36518217
19.
Integrated Strategies of Diverse Feature Selection Methods Identify Aging-Based Reliable Gene Signatures for Ischemic Cardiomyopathy.
Front Mol Biosci
; 9: 805235, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35300115
20.
Atypical deletion of Williams-Beuren syndrome reveals the mechanism of neurodevelopmental disorders.
BMC Med Genomics
; 15(1): 79, 2022 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35379245