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In both cases, the dose, dosage interval, and start date and times of dosing were described.
In both cases, the dose used in the calculation was a worker's estimated average daily dose (milligrams), calculated as one-half of his estimated shift dose (reflecting the 3-day-on/3-day-off pattern of work).
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In both cases the tomosynthesis dose was about nine times the radiography dose.
In both cases, the ion dose was well beyond the traditional static limit (1 × 10 primary ions cm 2 s–1); the step mode dose is estimated at ∼2.5 × 10 primary ions cm 2 s–1, corresponding to an etch rate of ∼200 nm/s based on atomic force microscopy measurements in similar previous work, assuming similar sputter rates.
In both cases, the drugs dose-dependently prevented the dexamethasone-dependent effect on Aβ 1 40 and 1 42 formation (Fig. 3A D).
In both cases, the high-dose group saw smaller changes from baseline than the conventional group.
In both cases the transposase dose-response curve matched the predicted power law relationship.
Similar results with the same tumour model were obtained with two different photosensitisers, Photofrin and ce6; in both cases, the chosen PDT only dose was in the moderate/halfway cure range and the adjuvant γ-inulin treatment increased the level of tumour cures to fully or highly curative range by reducing the recurrence rate.
In both cases the manufacturers assumed that doses of docetaxel could be calculated on the basis of a mean BSA of 1.7 m2 for all patients (male and female).
In both cases the effect of ATOH8 was dose-dependent.
In both cases, the patients were administered diagnostic doses of 99mTc radiopharmaceuticals (lower counting rate and dead-time conditions than post-Lu therapy scanning).
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CEO of Professional Science Editing for Scientists @ prosciediting.com