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- Furthermore, gamma-secretase cleavage of C99 and C83, the alpha-secretase derived APP C-terminal fragment
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- Furthermore, pretreatment of cells with MG132, a proteasome inhibitor, significantly inhibited geldanamycin-induced downregulation of GRK5
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- Furthermore, since the synthesis of oligonucleotides is more cost effective than that of peptides, our system may provide an alternative method to evaluate many candidate fusion inhibitory peptides
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- Future there will be an even higher deal of heterogeneity in
- Future work will be needed to model a comprehensive reaction scheme to explain the complete data-set of biochemical observations
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