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Controlled drug delivery of bioactive molecules continues to be an essential component of engineering strategies for tissue defect repair.
While an understanding of single molecules continues to be important, the focus is on understanding the whole metabolic network at a systems-level.
The latrunculin class of bioactive small molecules continues to command attention as their chemical structures and biological properties have been explored for nearly three decades [ 1].
It is easy to show that, if α = m S f D 2 f D 1, such a proportionality between the starch content and the number of S molecules continues to hold true throughout the degradation process.
On the other hand, the fact that biosurfactants are characterized by a vast structural diversity and display a broad range of properties may also explain why this group of molecules continues to entice scientific curiosity (Marchant and Banat 2012).
The advantages of using biochemical QIBs over morphological in the assessment of cytostatic molecules continues to gain acceptance [ 6], including patient stratification and prognostic impact before therapy is initiated [ 7].
Similar(53)
As metabolic engineering methods and strategies continue to develop and diversify, production yields of target molecules continue to improve.
Electrostatic repulsion between protein molecules and steric hindrance in the pore entrance significantly reduce the probability of CAT protein molecules continuing to enter the pores.
Promising therapeutic molecules continue to emerge and exert their influence through a variety of mechanisms.
Insulin-related molecules continue to attract great interest in vaccine development.
As databases of small molecules continue to grow and become more open, it is important to develop the tools to search them efficiently.
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