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Tetracyclines are effective but slow-acting antimalarial drugs whose mechanism of action remains uncertain. To characterize the antimalarial mechanism of tetracyclines, we evaluated their stage-specific activities, impacts on parasite transcription, and effects on two predicted organelle targets, th...
ORGANISM(S): Plasmodium falciparum 
To determine the transcriptome sub-lethal dose response profile for adult Lumbricus rubellus exposued to Cadmium.
ORGANISM(S): synthetic 
Copy number variation in two SJL sub-strains of an experimental autoimmune encephalomyelitis (EAE) rodent model of Multiple Sclerosis (MS)
ORGANISM(S): Mus musculus 
To determine the developmental and seasonal variation in transcript expression within a terrestial sentinal, the earthworm Lumbricus rubellus.
ORGANISM(S): synthetic_DNA 
To determine the transcriptome sub-lethal dose response profile for adult Lumbricus rubellus exposued to Atrazine.
ORGANISM(S): Lumbrius rubellus 
To determine the transcriptome sub-lethal dose response profile for adult Lumbricus rubellus exposued to Fluoranthene.
ORGANISM(S): Lumbrius rubellus 
Recent work has shown that cytotoxic T cells play a central role in immune-mediated control of cancers1-3, and monoclonal antibodies that target inhibitory receptors on T cells can induce significant clinical benefit in patients despite advanced disease4-6. However, many of the regulatory pathways t...
ORGANISM(S): Mus musculus 
In this study, we used an interdisciplinary approach, combining biophysics and systems biology, to design a microfluidic chip for the multiplexed detection and separation of pathogen cells from immune cells combined with proteomic profiling using mass spectrometry. Our nanochip design includes preci...
ORGANISM(S): Klebsiella pneumoniae subsp. pneumoniae 
2026-03-21 | PXD058426 | Pride
Methicillin resistance in Staphylococcus aureus depends on the production of mecA, which encodes penicillin-binding protein 2A (PBP2A), an acquired peptidoglycan transpeptidase with reduced susceptibility to beta-lactam antibiotics. Here, we show that preventing the expression of wall teichoic acids...
ORGANISM(S): Staphylococcus aureus 
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