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Examples of such molecules are the matrix metalloprotease (MMP -13 and the insulin-like growth factor binding protein (IGFBP)-5.

Such off-target binding may cross target structure and fold categories, such as when an ion channel inhibitor is found also to modulate GPCRs, and we consider examples of such molecules at the close of the section.

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An example of such molecules is growth hormone releasing factor 1 29 NH2-acetate, or sermorelin, that recently became available to practitioners for use in longevity medicine (Merriam et al 2001).

Activity of such molecules could vary between individuals (for example through genetic variation) linking the variation in the responses at the population level with the observed correlations.

A grid of such molecules can be used for computer memory.

Killer cell immunoglobulin-like receptors (KIRs) are a well-studied example of such inhibitory molecules.

Examples of such genes include those involved in generation of bioactive molecules such as NOS2A, IL-6, TNF, and IL-1β, the chemokines CCL2, and matrix metallopeptidases.

Examples of such public goods produced by bacterial pathogens include quorum-sensing molecules, siderophores, extracellular polymeric matrix, and exotoxins; for cancer cells, examples include growth and invasion factors, angiogenesis factors, and immune suppression factors (Pepper 2008).

Examples of such junctions from the analysis performed here are cholesterol and sphingiosine, molecules whose biosynthesis and function are lineage-specific.

The increased expression of anti-apoptotic proteins such as Bcl-XL, cFLIP, or XIAP and the reduced expression of pro-apoptotic molecules such as caspases and Bid are just some examples of such protective signals [ 13].

While the very possibility of designing a small molecule inhibitor for such interactions was once doubted, there are examples of such inhibitors that are currently marketed products and many more inhibitors in various stages of research and development.

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