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However, for reasons of safety, the practicability of safe, risk-minimizing measurements should be demonstrated on healthy participants, first, which is a usual approach [ 18– 20].
First, the observed divergence in bill morphology should be demonstrated on additional independent populations to rule out the possibility that the pattern is caused by chance (criterion 1).
However, to establish causation in the determinism of responsiveness to immunotherapy, level of TA and TA presentation should be assessed before treatment and a predictive relationship should be demonstrated on the likelihood to respond to the respective treatment.
Similar(56)
The feasibility of embedded control in terms of computational power should be demonstrated through real tests on the embedded microcontroller.
Thus, as second step, not only the impact on users' satisfaction, but also on their knowledge should be demonstrated [ 6, 21, 22].
Of course, the effectiveness of antirheumatic treatment based on osteitis should be demonstrated.
However, the existence of these peptides as natural epitopes on tumour cells should be demonstrated.
Finally, an impact of such strategies on hard outcomes should be demonstrated before incorporation into routine clinical practice.
As already mentioned above, effects of the melanocyte system on aneurysm formation should be demonstrated directly by analyzing specific genetic variations in patients and controls.
In the future, the involvement of PLCβ in the regulation of Fhit by Gαq and their possible roles on cancer therapy should be demonstrated.
Power should be exercised and it should be demonstrated.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com