Detalhe da pesquisa
1.
CancerImmunityQTL: a database to systematically evaluate the impact of genetic variants on immune infiltration in human cancer.
Nucleic Acids Res
; 49(D1): D1065-D1073, 2021 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33010176
2.
Hepatocellular carcinoma risk variant modulates lncRNA HLA-DQB1-AS1 expression via a long-range enhancer-promoter interaction.
Carcinogenesis
; 42(11): 1347-1356, 2021 11 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34665859
3.
Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese population.
Arch Toxicol
; 95(3): 1117-1128, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33474615
4.
AWESOME: a database of SNPs that affect protein post-translational modifications.
Nucleic Acids Res
; 47(D1): D874-D880, 2019 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30215764
5.
N6-methyladenosine mRNA methylation of PIK3CB regulates AKT signalling to promote PTEN-deficient pancreatic cancer progression.
Gut
; 69(12): 2180-2192, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32312789
6.
Genetic variants in m6A modification genes are associated with esophageal squamous-cell carcinoma in the Chinese population.
Carcinogenesis
; 41(6): 761-768, 2020 07 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32047883
7.
Evaluation of polymorphisms in microRNA-binding sites and pancreatic cancer risk in Chinese population.
J Cell Mol Med
; 24(3): 2252-2259, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31880394
8.
ANKLE1 N6 -Methyladenosine-related variant is associated with colorectal cancer risk by maintaining the genomic stability.
Int J Cancer
; 146(12): 3281-3293, 2020 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31509622
9.
Functional characterization of a low-frequency V1937I variant in FASN associated with susceptibility to esophageal squamous cell carcinoma.
Arch Toxicol
; 94(6): 2039-2046, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32388819
10.
A functional variant in the boundary of a topological association domain is associated with pancreatic cancer risk.
Mol Carcinog
; 58(10): 1855-1862, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31237042
11.
A novel coiled-coil domain containing-related gene signature for predicting prognosis and treatment effect of breast cancer.
J Cancer Res Clin Oncol
; 149(15): 14205-14225, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37558766
12.
Estrogen receptor α inhibits Caveolin 1 translation by promoting m6A-dependent miR199a-5p maturation to confer nab-paclitaxel resistance.
Am J Cancer Res
; 13(12): 6210-6225, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38187046
13.
Genome-wide enhancer-gene regulatory maps link causal variants to target genes underlying human cancer risk.
Nat Commun
; 14(1): 5958, 2023 09 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37749132
14.
Genome-wide gene-bisphenol A, F and triclosan interaction analyses on urinary oxidative stress markers.
Sci Total Environ
; 807(Pt 1): 150753, 2022 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34619205
15.
Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer.
Chin Med J (Engl)
; 135(11): 1348-1357, 2022 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35830250
16.
Pan-Cancer Analysis of Microbiome Quantitative Trait Loci.
Cancer Res
; 82(19): 3449-3456, 2022 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35972351
17.
Aberrant RNA Splicing Is a Primary Link between Genetic Variation and Pancreatic Cancer Risk.
Cancer Res
; 82(11): 2084-2096, 2022 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35363263
18.
Aberrant MCM10 SUMOylation induces genomic instability mediated by a genetic variant associated with survival of esophageal squamous cell carcinoma.
Clin Transl Med
; 11(6): e485, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34185429
19.
A genetic variant conferred high expression of CAV2 promotes pancreatic cancer progression and associates with poor prognosis.
Eur J Cancer
; 151: 94-105, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33975060
20.
Colorectal cancer risk variant rs7017386 modulates two oncogenic lncRNAs expression via ATF1-mediated long-range chromatin loop.
Cancer Lett
; 518: 140-151, 2021 10 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34274452