Sentence examples for exploited for development of from inspiring English sources

Magnetic characterization suggests that these hybrid materials can be used for development of magnetic storage devices, while their multifunctional properties could be potentially exploited for development of a variety of catalysts and sensors.

Thus, apoptotic pathways might be significantly altered in cancer cells relative to untransformed cells, and these differences might present a therapeutic window that can be exploited for development of cancer drugs.

Our recent discovery of a Src inhibitor, RACK1, which works both to inhibit growth (by suppressing Src activity at G1 and mitotic checkpoints) and to induce death of colon cells, could be exploited for development of new and more powerful and selective strategies for treatment of human colon cancer.

Glyphosate, glufosinate, synthetic auxins, sulfonylurea, imidazolinones, triketones, isoxazoles, callistemone, cyclohexanediones, aryloxyphenoxypropionates and phenylpyrazolines are common herbicides for which herbicide tolerance (HT) mechanisms are well known and exploited for development of herbicide tolerant crops (Endo and Toki, 2013).

These results suggest that the root aqueous extract of C. edulis contain potent anti-viral agents against HSVs that can be exploited for development of an alternative remedy for HSV infections [50, 51].

DMC1 recombination requires hydrolysis of ATP, a feature that can be exploited for development of small molecule inhibitors.

For example, blocking receptor interaction could be exploited for the development of novel types of vaginal microbicide based on mini-CD4 molecules and on broadly neutralizing mini-antibodies, which also have potential for blocking mucosal infection [ 11] of women.

Their high surface to volume ratio can be exploited for the development of a new generation of chemical and biological sensors [1 3].

These properties can be exploited for the development of flow directing materials, e.g. wound dressings that prevent development of stress concentrators while augmenting transport of pharmaceuticals to the wound site, as well as transport of drainage away from the wound site, via convective flow.

However, when considering Hippo signalling upstream of YAP/TAZ, the Hippo community will first have to define whether loss or gain of specific PPIs can act as major drivers of cancer before PPIs upstream of YAP/TAZ can be exploited for the development of novel therapeutics.

Therefore, we provide in this manuscript insight into a new regulatory mechanism of cell homeostasis that could possibly be exploited for the development of novel clinical compounds, allowing the modulation of autophagy activity in human diseases.