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by
Yu, Qing, author.
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isobaric labeling technology. A portion of this dissertation describes the design and evaluation of several
by
Hoang, Trish T., author.
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pathway might be used to design ANG-based therapeutics. CHAPTER 4 outlines several future directions for
by
Babkin, Petr, author.
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susceptible to G5I142 inhibition. The relevance of this work for drug design directed towards GLUT5 is two
by
Gosavi, Pallavi M., author.
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activation. Thus, we demonstrated that self-assembly of peptides can present an excellent tool to design
by
Presley, Gerald, author.
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physiological changes. The same wafer culture design was then used to resolve changes in fungal secretomes
by
Alqahtani, Saad, author.
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major influence on both the selection of compounds for high-throughput screening and the design of lead
by
Smith, Thomas P., author.
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-binding site and opens new avenues for the use of boronic acids in the design of small-molecule therapeutics.
by
Akopian, Aram, author.
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Alıntı:
each side by a binding motif of Zif268. This design of the enzyme and its target site was further

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