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High-content screening (HCS) has become a powerful tool in drug discovery; however, their reliance on indirect readouts and surrogate markers limits their ability to directly assess drug-protein interactions at endogenous levels, particularly in subcellular contexts. Here, we report the development ...
ORGANISM(S): Homo sapiens (Human) 
2025-09-08 | PXD059271 | Pride
This study is about high content screening small molecule compound as radiosensitizer. Two compounds were got finally from a chemical bank. Our data indicate cancer cell lines became more sensitive to radiation after treatment with both two compounds respectively. In order to know the mechanism, mic...
ORGANISM(S): Homo sapiens 
Upon contact with a biomaterial, cells and surrounding tissues respond in a manner dictated by the physicochemical and mechanical properties of the material. Traditionally, cellular responses are monitored using invasive analytical methods that report the expression of genes or proteins. These analy...
ORGANISM(S): Homo sapiens 
High-content, targeted RNA-seq screening in organoids for drug discovery in colorectal cancer
Integrated time-series analysis and high-content CRISPR screening delineate the dynamics of macrophage immune regulation
Screening and transcriptomic analysis of high growth and lipid-content mutants of Crypthecodinium cohnii using acetyl-CoA carboxylase inhibitor sethoxydim
Unbiased phenotypic screens in patient-relevant disease models offer the potential to detect therapeutic targets for rare diseases. In this study, we developed a high-throughput screening assay to identify molecules that correct aberrant protein trafficking in adaptor protein complex 4 (AP-4) defici...
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD042950 | Pride
Integrated time-series analysis and high-content CRISPR screening delineate the dynamics of macrophage immune regulation [RNA-seq]
Integrated time-series analysis and high-content CRISPR screening delineate the dynamics of macrophage immune regulation [ATAC-seq]
Pooled CRISPR Screening of High-content Cellular Phenotypes by Ghost Cytometry
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