A single acidic residue can guide binding site selection but does not govern QacR cationic-drug affinity.

The two EU missions EUSEC and EUPOL were basically concerned with the reform of the security sector in general and the reform of the army and the police in particular to

This study was carried out to understand the inluence of a selected antiarrhythmic drug on the pharmacodynamics and pharmacokinetics of an antidiabetic drug in

The lower nephrotoxicity is probably due to a reduced accumulation of the drug in the renal cortex as with a single larger dose, more of the drug is excreted and not reabsorbed in

The evaluation of blood drug measurement alone, except in cases of extreme low adherence and variability of drug intake, is not enough for the recognition of incorrect drug intake,

This change of paradigm is crucial to the understanding of the toxic mechanisms underlying not only the parent compound (pharmaceutical drug) but also the biological

Having in mind that routinely used tests to identify pneumococci may not be sufficient when atypical isolates are found, and that it is important to correctly identify

Following the intramuscular administration of tolfenamic acid as a single drug and in combination with moxifloxacin in the male and female rats, peak plasma

shows the location of the binding sites on the surface of the protein structure and Table 3 shows the volume, depth and drug score for cruzain and Llacys1.. Three pockets were