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ProteomicsGCN2 Adapts Protein Synthesis to Scavenging-Dependent Growth
Compared protein synthesis in Gcn2 WT vs Gcn2 KO murine PDAC cells (KRPC) in amino acid-replete or leucine-free media.
ORGANISM(S): Mus musculus (Mouse) 
2022-10-13 | PXD028143 | Pride
Gcn2 Macropinocytosis Pdac 
UnknownHepatitis C virus incidence trend and its risk factors among people who inject drugs in Hai Phong, Vietnam.
Not available
S-EPMC12508010 | biostudies-literature
UnknownProspective Evaluation of Magnetic Resonance Imaging and [18F]Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography at Diagnosis and Before Maintenance Therapy in Symptomatic Patients With Multiple Myeloma Included in the IFM/DFCI 2009 Trial: Results of the IMAJEM Study.
Not available
S-EPMC5578392 | biostudies-literature
UnknownInterface morphology effect on the spin mixing conductance of Pt/Fe3O4 bilayers.
Not available
S-EPMC6141513 | biostudies-literature
UnknownImportance of the ion-pair interactions in the OPEP coarse-grained force field: parametrization and validation.
Not available
S-EPMC4239435 | biostudies-literature
UnknownUnexpected Single-Ligand Occupancy and Negative Cooperativity in the SARS-CoV-2 Main Protease.
Not available
S-EPMC10865365 | biostudies-literature
ProteomicsLRRK2G2019S acts as a dominant interfering mutant in the context 1 of iron overload
A key pathological feature of Parkinson’s Disease (PD) is the loss of neuromelanin, an iron chelator within the dopaminergic neurons, which results in iron toxicity thought to result in selective neuronal vulnerability. This implicated iron handling pathways as an early target of research in PD. Giv...
ORGANISM(S): Mus musculus (Mouse) 
2026-04-27 | PXD071594 | Pride
Parkinson's disease Proteomics Lrrk2 
UnknownInterpersonal neural synchrony when predicting others' actions during a game of rock-paper-scissors.
Not available
S-EPMC9334613 | biostudies-literature
TranscriptomicsTranscription profiling of human promyelocytic NB4 cells treated with all-trans retinoic acid
Gene expression profiles of promyelocytic NB4 cells treated with all-trans retinoic acid (ATRA, 1 microM) during short periods of time (1h30 and 3h) were performed and compared to untreated cells (vehicule control, 0,02% ethanol).
ORGANISM(S): Homo sapiens 
2009-02-04 | E-BASE-7 | biostudies-arrayexpress
UnknownIntracellular Proteins Targeting with Bi-Functionalized Magnetic Nanoparticles Following their Endosomal Escape.
Not available
S-EPMC11962688 | biostudies-literature
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