This study was designed to determine the involvement of microRNAs (miR), which are actively involved in the physiological function of stem cells.
For these reasons, they are effective and commonly used to help determine the involvement of various proteins in pesticide resistance13,14,15,16.
We carried out lethal time bioassays to determine the involvement of detoxification mechanisms in ivermectin resistance in the southern cattle tick, R. microplus.
Cells were pretreated with histamine receptor antagonists pyrilamine, ranitidine, cimetidine and thioperamide to determine the involvement of histamine receptors.
This study was designed to determine the involvement of histamine receptors in histamine-mediated effect on STAT1 phosphorylation.
To determine the involvement of tight-junction specific proteins (occludin, claudin-1 and 5, ZO-1 protein) in intercellular pathway opening by ultrasound.
In ongoing experiments, we apply this model to determine the involvement of the PrL on alcohol seeking behaviour in this task.
To classify secondary corneal amyloidosis (SCA) by its clinical appearance, to analyze the demographics of the patients, and to determine the involvement of lactoferrin.
The present study was designed to determine the involvement of central prostaglandin synthesis on the pressor and bradycardic effect of cytidine 5′-diphosphocholine (CDP-choline).
Lethal time bioassays with inhibitors in combination with ivermectin were carried out to determine the involvement of cytochrome P450, GST, esterases, and ABC transporters in the detoxification of ivermectin.
To determine the involvement of cation-chloride cotransporters (CCCs) in the K+-mediated transport of water against an experimentally applied osmotic gradient, we continued the experimental series described above with the inclusion of pharmacological agents.
