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As metabolic engineering methods and strategies continue to develop and diversify, production yields of target molecules continue to improve.
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.
Upon addition of dissolvent or crosslinking agents, SPI molecules continue to aggregate and form various structures such as microspheres, hydrogels and polymer blends [ 42, 43].
As chemical repositories of small molecules continue to grow and become more open (Chen et al., 2005, 2007; Irwin and Shoichet, 2005), it becomes increasingly important to develop the tools to search them efficiently.
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Controlled drug delivery of bioactive molecules continues to be an essential component of engineering strategies for tissue defect repair.
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.
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.
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