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UnknownProbing the glass transition in reversible cross-linked polymer composites.
Not available
S-EPMC9064213 | biostudies-literature
UnknownHeterologous Expression and Delivery of Biologically Active Exendin-4 by Lactobacillus paracasei L14.
Not available
S-EPMC5072737 | biostudies-literature
UnknownMacroscopically Ordered Piezo-Potential in All-Polymetric Solid Electrolytes Responding to Li Anode Volume Changes for Dendrites Suppression.
Not available
S-EPMC12786380 | biostudies-literature
ProteomicsPROTAC repurposing uncovers a noncanonical binding surface that mediates chemical degradation of nuclear receptors
MD-224 is a PROTAC that induces degradation of the human protein MDM2. However, we have found that it also induces degradation of a subset of nuclear receptors. DIA was performed to assess the overall specificity of MD-224 in 293T cells and the colorectal cancer cell line SNU-C4.
ORGANISM(S): Homo sapiens (Human) 
2025-09-18 | PXD066110 | Pride
Dia proteomics Pxr Protac Mdm2 Nuclear receptor Md-224 
UnknownA nanoprobe for fluorescent monitoring of microRNA and targeted delivery of drugs.
Not available
S-EPMC8695329 | biostudies-literature
UnknownIn-situ ²²³Ra-doped calcium-alginate composite microspheres: a high-LET and immunoactivating platform for α-particle radioembolization in hepatocellular carcinoma.
Not available
S-EPMC12869965 | biostudies-literature
UnknownPhosphorus removal performance and population structure of phosphorus-accumulating organisms in HA-A/A-MCO sludge reduction process.
Not available
S-EPMC5060981 | biostudies-literature
UnknownDiagnostic and prognostic value of systemic immune-inflammation index for heart failure: a systematic review and meta-analysis.
Not available
S-EPMC12414965 | biostudies-literature
UnknownAdrenomedullin Expression Is Associated With the Severity and Poor Prognosis of Interstitial Lung Disease in Dermatomyositis Patients.
Not available
S-EPMC9200949 | biostudies-literature
GenomicsGenome-Wide Association Studies in Upper Gastrointestinal Cancers (Asian)

This project aims to conduct genome-wide association studies (GWAS) in two anatomically different upper gastrointestinal (UGI) cancer sites in two populations with distinctly different disease rates and genetic profiles. One population has very high rates for both esophageal squamous cel...

phs000361.v1.p1 | EGA
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