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This relationship reveals that both the complex-lamellar and the continuity flow conditions impose geometrical constraints.
The structure activity relationship revealed that 2-benzylbenzimidazole scaffold with hydrogen bonding acceptor on phenyl ring appears as a pharmacophore.
Structure activity relationship revealed that the nature of Ring X and substitution at position R influences the activity.
Structure activity relationship revealed that the nature of both Ring A and Ring B influences the activity.
Vector error calculation between the virtually simulated intermaxillary position and the intraoperative intermediate intermaxillary relationship revealed high accuracy.
The primary structure activity relationship revealed that substituents on the ring A were not beneficial for the activity.
Furthermore, as the subsequent analysis will show the relationship reveals to be unstable.
Structure activity relationship revealed that the role of methoxy groups are important.
A historical perspective on the physician-patient relationship reveals an evolving richness in the concepts of autonomy and neutrality.
This relationship reveals the effect of complexity of structure of blends in the energetic reaction involving Ca(NO3 2 incorporation processes.
The G V) relationship revealed that the fast inactivation of Nav1.8 was shifted in a hyperpolarizing direction (Fig. 4E).
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CEO of Professional Science Editing for Scientists @ prosciediting.com