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In a follow-up study, high-temperature LC, enabling lower organic modifier concentrations, was demonstrated [ 43].
A clear increase of intestinal concentrations was demonstrated after administration of a five-fold higher dose (31 454 μg/g).
The role of elevated zinc concentrations was demonstrated to affect gene expression in cancer cells at posttranscriptional level [ 39].
The antiproliferative effect of nanomolar SR31747A concentrations was demonstrated in vitro on a series of various established animal cell lines Labit-Le Bouteillerr et al, 1998).
Similarly, the intraindividual reproducibility of NAA, Cho and Glx concentrations was demonstrated by our group [ 40] and by others [ 41, 42].
Activation of cell-specific signaling pathways by low TGF-β1 concentrations was demonstrated with a prominent activation of the Rho/ROCK pathway in fibrosis-derived cells, whereas the Smad pathway was predominantly activated in normal cells.
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Significant reduction of stress concentrations were demonstrated.
Full activation of the as-grown dopant concentrations is demonstrated by combined SIMS and Hall experiments, and corroborated using a contactless spectroscopic ellipsometry approach.
The simulations without clamped metabolite concentrations are demonstrated in Figure 8A C.
The ability of FSC to quantify absolute concentrations is demonstrated using lipid mixtures.
Equivalent blood concentrations were demonstrated between 80 mg/m2 oral and 30 mg/m2 intravenous, and between 60 mg/m2 oral and 25 mg/m2 intravenous [ 3].
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