Detalhe da pesquisa
1.
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
2.
[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
3.
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
4.
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
5.
Genetic tests aid in counseling of fetuses with cerebellar vermis defects.
Prenat Diagn
; 40(10): 1228-1238, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32386258
6.
A genetic approach to the etiologic investigation of isolated intrauterine growth restriction.
Am J Obstet Gynecol
; 225(6): 695-696, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34358481
7.
Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma.
BMC Med Genomics
; 17(1): 96, 2024 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38650036
8.
Prenatal diagnosis and outcomes in fetuses with duplex kidney.
Int J Gynaecol Obstet
; 2024 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38189110
9.
Prenatal Diagnosis of PPP2R1A-Related Neurodevelopmental Disorders Using Whole Exome Sequencing: Clinical Report and Review of Literature.
Genes (Basel)
; 14(1)2023 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36672867
10.
Identification of Alternative Splicing and LncRNA Genes in Brain Tissues of Fetal Mice at Different Developmental Stages.
Comb Chem High Throughput Screen
; 26(1): 58-82, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-35400338
11.
Genetic Analysis and Sonography Characteristics in Fetus with SHOX Haploinsufficiency.
Genes (Basel)
; 14(1)2023 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36672881
12.
Genetic diagnosis of fetal microcephaly at a single tertiary center in China.
Front Genet
; 14: 1112153, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37229200
13.
ASXL3 gene mutations inhibit cell proliferation and promote cell apoptosis in mouse cardiomyocytes by upregulating lncRNA NONMMUT063967.2.
Biochem Biophys Rep
; 35: 101505, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37435360
14.
Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2.
Mol Neurobiol
; 60(6): 2986-3003, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36763283
15.
Genome-wide identification and expression analysis of the MYC transcription factor family and its response to sulfur stress in cabbage (Brassica oleracea L.).
Gene
; 814: 146116, 2022 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34942321
16.
Effects of Plant Hormones, Metal Ions, Salinity, Sugar, and Chemicals Pollution on Glucosinolate Biosynthesis in Cruciferous Plant.
Front Plant Sci
; 13: 856442, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35574082
17.
Physicochemical and biological factors determining the patchy distribution of soil water repellency among species of dominant vegetation in loess hilly region of China.
Front Plant Sci
; 13: 908035, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36275577
18.
Identification of differential microRNAs and messenger RNAs resulting from ASXL transcriptional regulator 3 knockdown during during heart development.
Bioengineered
; 13(4): 9948-9961, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35435106
19.
Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis.
Mol Cytogenet
; 15(1): 27, 2022 Jun 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35765027
20.
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.
Genome Med
; 14(1): 123, 2022 10 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36307859