Detalhe da pesquisa
1.
Variants of the promoter of MYH6 gene in congenital isolated and sporadic patent ductus arteriosus: case-control study and cellular functional analyses.
Hum Mol Genet
; 33(10): 884-893, 2024 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38340456
2.
Tetralogy of Fallot: variants of MYH6 gene promoter and cellular functional analyses.
Pediatr Res
; 2023 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38135727
3.
A multicenter, randomized controlled study on the efficacy of agomelatine in ameliorating anhedonia, reduced motivation, and circadian rhythm disruptions in patients with major depressive disorder (MDD).
Ann Gen Psychiatry
; 22(1): 46, 2023 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37957751
4.
Identification and Functional Verification of CITED2 Gene Promoter Region in Patients with Patent Ductus Arteriosus.
Int J Mol Sci
; 24(22)2023 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38003393
5.
Identification and functional analysis of genetic variants of ISL1 gene promoter in human atrial septal defects.
J Gene Med
; 24(12): e3450, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36170181
6.
Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications.
Clin Genet
; 102(5): 391-403, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35882632
7.
Functional significance of novel variants of the MEF2C gene promoter in congenital ventricular septal defects.
Am J Med Genet A
; 188(8): 2397-2405, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35719119
8.
Targeting IRE1α-JNK-c-Jun/AP-1-sEH Signaling Pathway Improves Myocardial and Coronary Endothelial Function Following Global Myocardial Ischemia/Reperfusion.
Int J Med Sci
; 19(9): 1460-1472, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36035373
9.
Identification of variants of ISL1 gene promoter and cellular functions in isolated ventricular septal defects.
Am J Physiol Cell Physiol
; 321(3): C443-C452, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34260301
10.
Genetic analysis of the CITED2 gene promoter in isolated and sporadic congenital ventricular septal defects.
J Cell Mol Med
; 25(4): 2254-2261, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33439552
11.
GSA-Human: Genome Sequence Archive for Human.
Yi Chuan
; 43(10): 988-993, 2021 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34702711
12.
Novel mutations of TCTN3/LTBP2 with cellular function changes in congenital heart disease associated with polydactyly.
J Cell Mol Med
; 24(23): 13751-13762, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33098376
13.
Protein biomarkers and risk scores in pulmonary arterial hypertension associated with ventricular septal defect: integration of multi-omics and validation.
Am J Physiol Lung Cell Mol Physiol
; 319(5): L810-L822, 2020 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32877226
14.
The 2019 novel coronavirus resource.
Yi Chuan
; 42(2): 212-221, 2020 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32102777
15.
Rapid detection of PAH gene mutations in Chinese people.
BMC Med Genet
; 20(1): 135, 2019 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31382905
16.
Metabolomics and Biomarkers for Paroxysmal and Persistent Atrial Fibrillation.
J Am Heart Assoc
; 13(3): e032153, 2024 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38293949
17.
Metabolomics Analysis Identifies Differential Metabolites as Biomarkers for Acute Myocardial Infarction.
Biomolecules
; 14(5)2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38785939
18.
Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis.
Biomolecules
; 13(2)2023 02 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36830727
19.
Multiple therapies relieve long-term tardive dyskinesia in a patient with chronic schizophrenia: A case report.
World J Clin Cases
; 11(32): 7895-7899, 2023 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38073685
20.
Lysine crotonylation of SERCA2a correlates to cardiac dysfunction and arrhythmia in Sirt1 cardiac-specific knockout mice.
Int J Biol Macromol
; 242(Pt 4): 125151, 2023 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37270127