Exact(2)
Regulatory agencies commonly demand that Bt cultivars express Cry toxins at a dose that will impose near completely recessive resistance, that is, be high enough to kill nearly all heterozygous resistant insects.
The 50% inhibitory concentration, IC50 (a dose that will reduce the activity of the virus by approximately 50%) was calculated by using the formula: EXP (LN (Conc > 50%% ) − ((signal > 50%% − 50 ) / (signal > 50%% − signal < 50%% ) * LN (conc > 50%% / conc < 50%% ) ) ) Using an automated excel worksheet developed by Professors Maes and Cos of Antwerp University.
Similar(55)
The dose-category-specific rates provide some suggestion of a trend with increasing dose that will be examined below.
As used in this project, a biological threshold is the transition point (observed or expected) between the highest dose that will not elicit a given biological effect, and the lowest dose that will.
It's simply the smallest dose that will produce a desired outcome and anything beyond is wasteful.
The corrected sentences appear below: The human respiratory infectious dose 50 (dose that will produce an infection in 50% of exposed persons) is unknown but has been estimated to be 8,000 to 10,000 spore-bearing particles <5 μm in diameter (7).
The dose that will accumulate over a given period (say, 50 years) from exposure to a given source of radiation is called the committed dose, or dose commitment.
Thus, in vivo trials were conducted on five healthy pig oesophaguses to determine the maximal thermal dose that will not induce a perforation of the oesophagus or surrounding tissues.
We observed that depending on the cell or tissue of interest and the fluorescent marker used, a different optimal level of photobleaching may be required, which can be determined experimentally as the minimum photobleaching dose that will quench fluorescence of the reporter to a significant extend, without damaging the organism.
Further investigations need to optimize the antibiotic dose that will not significantly decrease the surface hardness below a clinically acceptable limit.
Phase I oncology clinical trials are designed to identify the optimal dose that will be recommended for phase II trials.
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