Detalhe da pesquisa
1.
Identification and validation of a DNA methylation-driven gene-based prognostic model for clear cell renal cell carcinoma.
BMC Genomics
; 24(1): 307, 2023 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37286941
2.
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing.
Hum Genet
; 142(6): 835-847, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37095353
3.
m6A-immune-related lncRNA prognostic signature for predicting immune landscape and prognosis of bladder cancer.
J Transl Med
; 20(1): 492, 2022 10 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36309694
4.
16S rRNA gene sequencing reveals altered composition of gut microbiota in postoperative individuals with renal stones.
Lett Appl Microbiol
; 75(2): 271-280, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35306682
5.
Proteasome inhibition induces macrophage apoptosis via mitochondrial dysfunction.
J Biochem Mol Toxicol
; 35(11): e22894, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34418242
6.
Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21.
Prenat Diagn
; 41(3): 316-322, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33000500
7.
[Application of whole exome sequencing technology in fetuses with congenital structural abnormalities].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(9): 900-906, 2021 Sep 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-34487541
8.
All-trans-retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3ß signaling pathway.
J Cell Biochem
; 121(11): 4386-4396, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31961017
9.
Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.
Prenat Diagn
; 40(7): 803-812, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32267001
10.
Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography.
Prenat Diagn
; 40(10): 1290-1299, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32436246
11.
Comprehensive study of altered proteomic landscape in proximal renal tubular epithelial cells in response to calcium oxalate monohydrate crystals.
BMC Urol
; 20(1): 136, 2020 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-32867742
12.
Risk factors associated with fetal pleural effusion in prenatal diagnosis: a retrospective study in a single institute in Southern China.
J Obstet Gynaecol
; 40(4): 443-447, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31809620
13.
Whole genome assembly and functional portrait of hypervirulent extensively drug-resistant NDM-1 and KPC-2 co-producing Klebsiella pneumoniae of capsular serotype K2 and ST86.
J Antimicrob Chemother
; 74(5): 1233-1240, 2019 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30843067
14.
A smart preparation strategy for point-of-care cellular counting of trace volumes of human blood.
Anal Bioanal Chem
; 411(13): 2767-2780, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30976894
15.
CSN6 and Rab34 Are Involved in Androgen Receptor Trafficking in Mouse Testicular Sertoli Cells.
Cell Physiol Biochem
; 47(6): 2360-2368, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29991022
16.
First record of two ectoparasitic ciliates of the genus Trichodina (Ciliophora: Trichodinidae) parasitizing gills of an invasive freshwater fish, Micropercops swinhonis, in Tibet.
Parasitol Res
; 117(7): 2233-2242, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29804193
17.
Non-Genomic Action of Androgens is Mediated by Rapid Phosphorylation and Regulation of Androgen Receptor Trafficking.
Cell Physiol Biochem
; 43(1): 223-236, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28854419
18.
Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract.
Nephrol Dial Transplant
; 32(10): 1665-1675, 2017 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28387813
19.
Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
Arch Gynecol Obstet
; 296(5): 929-940, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28905115
20.
[Application of chromosomal microarray analysis for fetuses with ventricular septal defects].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(5): 699-704, 2017 Oct 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-28981937