Sentence examples for of remarkable activity from inspiring English sources

Exact(1)

The decades between 1610 and 1670, referred to in the history of mathematics as "the precalculus period," were a time of remarkable activity in which researchers throughout Europe contributed novel solutions and competed with each other to arrive at important new methods.

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Our experiments disclosed a remarkable activity of PJ-34 on disruption of the bipolar clustering of supernumerary centrosomes in mammary MDA-231 cancer cells, causing distorted multi-polar spindles as early as 6 hours after PJ-34 application, followed by massive cell death within 48-72 hours.

NCI selected, 7-chloro-3-{[ 4-chlorophenyl) methylidene] amino}-2-phenylquinazolin-4(3H)-one 12, with GI50 value of −5.59 M, TGI value of −5.12 M, and LC50 value of −4.40 M showed remarkable activity against CNS SNB-7-chloro-3-{[ 4-chlorophenyl

If selection in the phase I trial had been confined to patients with activating mutations or amplifications of c-MET, the remarkable activity in NSCLC patients with EML4-ALK fusion may have been missed.

The NDCs-supported Pd catalysts prepared from 1,10-phenanthroline exhibited a remarkable activity of 55.6 mmol gPd−1 min−1, which may be related to the higher amount of nitrogen of the support with a higher contribution of quaternary nitrogen species.

The unique properties of NQTrp and its remarkable activity in vitro and in vivo make it a promising lead for the development of small molecule inhibitors of oligomerization for the treatment of AD. 1,4-naphthoquinon-2-yl-L-tryptophan (NQTrp) was synthesized from L-tryptophan and 1,4-naphthoquione by a one step synthesis according to the protocol by Shrestha-Dawadi et al. [39].

Thus, the remarkable activity of imatinib as monotherapy may not be observed in most cancer settings.

In early clinical studies, remarkable activity of single agents targeting VEGF-A has been observed (Martin and Schilder, 2007).

Therefore, the remarkable activity of the Pt80Pd20 aerogel indicates the best balance between the free energies of adsorption of oxygen-containing reaction species.

The compounds thus synthesized can be considered as decarbonyl analogues of the anticancer alkaloid luotonin A and were evaluated in a DNA relaxation assay for their ability to inhibit human topoisomerase I. Interestingly, two of the compounds showed a remarkable activity that is comparable to that of the standard drug camptothecin.

The fact that experiences influence subsequent behaviour is evidence of an obvious but nevertheless remarkable activity called remembering.

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