International Journal of General Systems, Год журнала: 2025, Номер unknown, С. 1 - 31
Опубликована: Июнь 5, 2025
Язык: Английский
International Journal of General Systems, Год журнала: 2025, Номер unknown, С. 1 - 31
Опубликована: Июнь 5, 2025
Язык: Английский
Knowledge-Based Systems, Год журнала: 2025, Номер unknown, С. 113314 - 113314
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
1Intelligent Systems with Applications, Год журнала: 2025, Номер 25, С. 200470 - 200470
Опубликована: Янв. 5, 2025
Язык: Английский
Процитировано
0Research Square (Research Square), Год журнала: 2025, Номер unknown
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0Journal of Translational Medicine, Год журнала: 2025, Номер 23(1)
Опубликована: Апрель 15, 2025
The intricate shared genetic architecture underlying allergic disorders-including asthma, atopic dermatitis, contact rhinitis, conjunctivitis, urticaria, anaphylaxis, and eosinophilic esophagitis-remains incompletely characterized. Our study employed genomic structural equation modeling (Genomic SEM) to define the common factor representing of disorders. Coupled with diverse post-GWAS analytical methods, we aimed discover susceptible loci investigate associations external traits. Furthermore, explored enriched pathways, cellular layers, elements, investigated putative plasma protein biomarkers. Polygenic risk score (PRS) analyses, leveraging our integrated GWAS data, were conducted assess chromosomal-level for A well-fitted SEM revealing We identified a total 2038 genome-wide significant SNP (p < 5e-8), including 31 previously unreported loci. Fine-mapping variants gene sets pinpointed 2 causal candidate genes. Genetic correlation analyses further illuminated multiple traits, notably psychiatric Preliminary findings four Notably, this presents first comprehensive characterization disorders through analysis an unmeasured composite phenotype, providing novel insights into etiological pathways across these conditions.
Язык: Английский
Процитировано
0Engineering Applications of Artificial Intelligence, Год журнала: 2025, Номер 153, С. 110768 - 110768
Опубликована: Апрель 22, 2025
Язык: Английский
Процитировано
0International Journal of Applied Earth Observation and Geoinformation, Год журнала: 2025, Номер 140, С. 104605 - 104605
Опубликована: Май 19, 2025
Язык: Английский
Процитировано
0Deleted Journal, Год журнала: 2025, Номер 7(6)
Опубликована: Май 23, 2025
Язык: Английский
Процитировано
0Journal of Translational Medicine, Год журнала: 2025, Номер 23(1)
Опубликована: Май 23, 2025
Sphingosine-1-phosphate receptor 3 (S1PR3) has been implicated in promoting tumor progression various cancers. However, the role and molecular mechanisms of S1PR3 oral squamous cell carcinoma (OSCC) remain poorly understood. The aims this study were to investigate function OSCC its potential as a therapeutic target. expression was determined through qPCR, Western blotting analysis, immunohistochemistry (IHC), TCGA database. correlation between clinical prognosis analyzed using database IHC. effects on proliferation cycle investigated CCK-8 assay, colony formation EdU incorporation xenograft mouse model. which affects explored RNA-seq array. combining antagonist with cisplatin growth examined assays. overexpressed upregulation correlated unfavorable clinicopathological characteristics adverse prognosis. Targeting reduced AKT phosphorylation, led downregulation WEE1, kinase involved regulation. This resulted reducing CDC2 disrupting G2/M checkpoint inhibiting proliferation. Furthermore, combination exhibited synergistic inhibitory when combined cisplatin. These findings reveal critical for regulating via AKT/WEE1/CDC2 pathway, thus offering basis developing treatment strategies patients.
Язык: Английский
Процитировано
0International Journal of General Systems, Год журнала: 2025, Номер unknown, С. 1 - 31
Опубликована: Июнь 5, 2025
Язык: Английский
Процитировано
0