Exact(1)
A further addition of nanoparticles (from 0.5 wt.% to 1.5 wt.%) into the capsules matrix resulted in an increase in the initial-release rate (IRR, from 3.17 to 4.17 μS/cm min) and maximum release level (MRL, from 36 to 52 μS/cm).
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Two theoretical studies have evaluated the potential risk of vaccine Al in infants, by reference to an oral "minimal risk level" (MRL) extrapolated from animal studies.
With algebra-derived MRL parameters from ARL constants, using the initial distribution of enzyme species, the dynamics of all of the elements and reaction rates upon glucose impulse were simulated in the hybrid ARL/MRL models using a stiff ODE solver (ode15s in Matlab).
This study uses national data from the Malaria Reference Laboratory (MRL) and data from probably the largest hub-and-spoke distribution system for intravenous artesunate in the UK.
For example, in the aminoglycoside (AMG) class of antimicrobial compounds, MRLs range from 50 μg/kg for gentamicin in bovine/porcine muscle to 20 000 μg/kg for apramycin in bovine kidney.
The other samples (RVS 12 and 13 for chlorpyrifos, RVS 15 for deltamethrin, RVS 11 for fenvalerate and RVS 10, 11, and 15 for diazinon) that exceeded their MRL were either from cafeteria or street food vending sites.
Cytokine-induced signaling in cells from MRL and lpr mice was comparable at 5 weeks of age, prior to disease development, but differences became apparent at 10 weeks, when lpr mice began to show symptoms.
In preparation for subsequent phospho-profiling experiments, we stained splenocytes from MRL and lpr mice at varying stages of disease (5 20 weeks) with antibodies specific to surface markers considered relevant to disease progression: B220, CD11b, Ly6C, Ly6G, Gr-1, CD19, IgM, CD21, CD3, TCRβ, TCRγδ, CD4, and CD8 [31], [31].
In order to evaluate autophagic activity in central T cells, we quantified autophagic compartments on thymus sections obtained from MRL lpr/lpr and NZB/W lupus-prone mice.
The protocol for the extraction of MRL rate constants from ARL models follows a series of steps as shown in Figure 6, which are described in detail below.
MRL/ lpr mice differ from MRL mice with respect to a mutation involving the Fas gene [ 26]; however, negative selection in the thymus does not seem to be impaired in either strain [ 27].
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