The limitations of crystallographic analysis can be overcome by advanced NMR spectroscopy, which makes it possible to study multiple protein conformations simultaneously, over time scales ranging from picoseconds to milliseconds.
This variability makes it essential to study multiple clones of cells or independently derived mutants to ensure that the effects observed are due to the mutation of interest, and not dependent on other effects of the genetic background.
Given the central role of treatment with pharmaceutical agents in modern medicine, it remains crucial to study multiple global populations as well as more drugs [ 10].
Instead, it is important to study multiple scales of biological systems and identify potential signal transduction chains between molecules, cells, organs, and complex traits such as clinical syndromes.
The strength of the method described below is that it (i) can efficiently study multiple output measures derived from the output images, (ii) can robustly identify parameter interactions, and (iii) checks the reliability of the result.
Second, it is important to study multiple cases across Canada in order to establish local level variations in addition to common factors that influence families' decisions to initiate, continue, and terminate care.
It is fine to study multiple pitches at the same time.
However, the complexity of teaching and learning can make it difficult to isolate and study multiple factors and their effects.
Archaeology is in a unique position to address this issue, because it can be used to study multiple ancient civilizations over long periods of time and before the existence of written records.
This finding implies that it may be important to study multiple transporters in the case of chemotherapeutic resistance.
It is therefore important to study multiple surgeons with different levels of experience and to define a stopping rule.
