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UnknownResolving therapy resistance mechanisms in multiple myeloma by multiomics subclone analysis.
Not available
S-EPMC10733835 | biostudies-literature
UnknownA meta-analysis of crop response patterns to nitrogen limitation for improved model representation.
Not available
S-EPMC6797162 | biostudies-literature
UnknownTowards Probing Conformational States of Y2 Receptor Using Hyperpolarized 129Xe NMR.
Not available
S-EPMC9919357 | biostudies-literature
UnknownBorophenes made easy.
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S-EPMC8565903 | biostudies-literature
UnknownEstablishment of closed 35S ribosomal RNA gene chromatin in stationary Saccharomyces cerevisiae cells.
Not available
S-EPMC11551728 | biostudies-literature
UnknownFetal bovine serum: how to leave it behind in the pursuit of more reliable science
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S-EPMC12371577 | biostudies-literature
UnknownT-bet suppresses proliferation of malignant B cells in chronic lymphocytic leukemia.
Not available
S-EPMC11307267 | biostudies-literature
UnknownThe SAGE study: Global observational analysis of glycaemic control, hypoglycaemia and diabetes management in T1DM.
Not available
S-EPMC8518876 | biostudies-literature
ProteomicsRiboflavin metabolism shapes FSP1-driven ferroptosis resistance
Membrane protection against oxidative damage is tightly buffered by glutathione peroxidase 4 (GPX4), and endogenous radical-trapping antioxidants such as ubiquinone, vitamin E and K. Deficiencies in these protective systems have been linked to the accumulation of phospholipid peroxidation and ferrop...
ORGANISM(S): Homo sapiens (Human) 
2025-10-31 | PXD061038 | Pride
Riboflavin Ferroptosis Fsp1 Cell death Vitamin b2 
ProteomicsInvestigating N-terminal shedding of GPR125 in GPR125 overexpressing HEK293T cells using N- and C-terminal enrichment and different cleavage strategies
The study was conducted to elucidate potential cleavage sites of GPR125 which are known to undergo N-terminal shedding through autoproteolysis in a region different to other GRPs. To do these different enzymatic strategies as well as enrichment of both N-terminal and C-terminal peptides, was conduct...
ORGANISM(S): Homo sapiens (Human) 
2026-08-31 | PXD083139 | Pride
Gpr125 Scx C-terminal Lysate Hek293t Enrichment Lc-msms Adra3 N-terminal Medium 
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