Detalhe da pesquisa
1.
CNV profiles of Chinese pediatric patients with developmental disorders.
Genet Med
; 23(4): 669-678, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33402738
2.
Downregulation of ARHGDIA contributes to human glioma progression through activation of Rho GTPase signaling pathway.
Tumour Biol
; 2016 Oct 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27726098
3.
MicroRNA-26a regulates glucose metabolism by direct targeting PDHX in colorectal cancer cells.
BMC Cancer
; 14: 443, 2014 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-24935220
4.
Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies.
Nat Med
; 30(2): 470-479, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38253798
5.
PGK1 contributes to tumorigenesis and sorafenib resistance of renal clear cell carcinoma via activating CXCR4/ERK signaling pathway and accelerating glycolysis.
Cell Death Dis
; 13(2): 118, 2022 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35121728
6.
Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening.
Cell Discov
; 8(1): 109, 2022 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36229437
7.
Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement.
Mol Genet Genomic Med
; 9(4): e1624, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33724704
8.
Novel compound heterozygous pathogenic variants in ASCC1 in a Chinese patient with spinal muscular atrophy with congenital bone fractures 2 : Evidence supporting a "Definitive" gene-disease relationship.
Mol Genet Genomic Med
; 8(5): e1212, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32160656
9.
Clinical and Genetic Analysis of CHD7 Expands the Genotype and Phenotype of CHARGE Syndrome.
Front Genet
; 11: 592, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32625235
10.
Loss of hnRNPA2B1 inhibits malignant capability and promotes apoptosis via down-regulating Lin28B expression in ovarian cancer.
Cancer Lett
; 475: 43-52, 2020 04 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32006618
11.
Using a Large Margin Context-Aware Convolutional Neural Network to Automatically Extract Disease-Disease Association from Literature: Comparative Analytic Study.
JMIR Med Inform
; 7(4): e14502, 2019 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31769759
12.
Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature.
Mol Cytogenet
; 12: 49, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31827621
13.
PGRMC1 Is a Novel Potential Tumor Biomarker of Human Renal Cell Carcinoma Based on Quantitative Proteomic and Integrative Biological Assessments.
PLoS One
; 12(1): e0170453, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28107520
14.
The Overexpression of IQGAP1 and ß-Catenin Is Associated with Tumor Progression in Hepatocellular Carcinoma In Vitro and In Vivo.
PLoS One
; 10(8): e0133770, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26252773