Detalhe da pesquisa
1.
Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early-onset long QT syndrome and sinoatrial node dysfunction.
Ann Noninvasive Electrocardiol
; 27(1): e12889, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34755423
2.
Single-cell transcriptome and cell-specific network analysis reveal the reparative effect of neurotrophin-4 in preantral follicles grown in vitro.
Reprod Biol Endocrinol
; 19(1): 133, 2021 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34481496
3.
Young and early-onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutations.
Ann Noninvasive Electrocardiol
; 26(4): e12840, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33949037
4.
Indicators and prediction models for the severity of Covid-19.
Int J Clin Pract
; 75(10): e14571, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34170611
5.
The Influence of Environmental Factors on Ovarian Function, Follicular Genesis, and Oocyte Quality.
Adv Exp Med Biol
; 1300: 41-62, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33523429
6.
Clinical outcomes after single-versus double-embryo transfers in women with adenomyosis: a retrospective study.
Arch Gynecol Obstet
; 304(1): 263-270, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33386415
7.
Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes.
Ann Noninvasive Electrocardiol
; 25(1): e12694, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31565860
8.
Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation.
BMC Med Genet
; 19(1): 148, 2018 08 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30129429
9.
Compound and heterozygous mutations of DSG2 identified by Whole Exome Sequencing in arrhythmogenic right ventricular cardiomyopathy/dysplasia with ventricular tachycardia.
J Electrocardiol
; 51(5): 837-843, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30177324
10.
Global crotonylome identifies EP300-regulated ANXA2 crotonylation in cumulus cells as a regulator of oocyte maturation.
Int J Biol Macromol
; 259(Pt 2): 129149, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38176486
11.
Dipotassium tetra-aqua-bis-(µ-citrato-κ(4) O:O',O'',O''')nickelate(II) tetra-hydrate.
Acta Crystallogr Sect E Struct Rep Online
; 69(Pt 9): m502-3, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24426997
12.
A salting-out assisted liquid-liquid extraction method for 25 emerging pesticides in follicular fluid.
J Chromatogr B Analyt Technol Biomed Life Sci
; 1229: 123897, 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37793248
13.
Reactivation of PPARα alleviates myocardial lipid accumulation and cardiac dysfunction by improving fatty acid ß-oxidation in Dsg2-deficient arrhythmogenic cardiomyopathy.
Acta Pharm Sin B
; 13(1): 192-203, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36815030
14.
Multi-Omics Analysis Reveals Translational Landscapes and Regulations in Mouse and Human Oocyte Aging.
Adv Sci (Weinh)
; 10(26): e2301538, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37401155
15.
Combination therapy of hydrogel and stem cells for diabetic wound healing.
World J Diabetes
; 13(11): 949-961, 2022 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36437861
16.
Gut microbiota dysbiosis-derived macrophage pyroptosis causes polycystic ovary syndrome via steroidogenesis disturbance and apoptosis of granulosa cells.
Int Immunopharmacol
; 107: 108717, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35334358
17.
NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte Maturation.
Front Endocrinol (Lausanne)
; 13: 907286, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35937804
18.
Single-cell transcriptome and translatome dual-omics reveals potential mechanisms of human oocyte maturation.
Nat Commun
; 13(1): 5114, 2022 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36042231
19.
NAT10-Mediated N4-Acetylcytidine of RNA Contributes to Post-transcriptional Regulation of Mouse Oocyte Maturation in vitro.
Front Cell Dev Biol
; 9: 704341, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34395433
20.
Identification of rare heterozygous linkage R965C-R1309H mutations in the pore-forming region of SCN5A gene associated with complex arrhythmia.
Mol Genet Genomic Med
; 9(5): e1613, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33764691