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By increasing the oxalic acid concentration to 0.5 M (Fig. 2c), a nanoparticle array was completely formed.
In contrast, the intensity distribution in the NC array was completely different from that of the planar counterpart; strongly concentrated light intensity appeared in the NCs (Figure 5b,c,d).
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Although the gas flow in the NW array is completely turbulent, it could be observed that there still exists a laminar flow layer adjacent to the top of the NW array, where the flow velocity is much higher than that in the NW array.
Of note, the results detected by SNP array were completely concordant with those of the gene specific assays.
Alternate schemas include subretinal implants positioned in the remnant space between the RPE and the surviving retina and suprachoroidal implants where the stimulating array is completely positioned in the choroid, outside the retinal space altogether.
As already pointed out, all DNA samples were processed together, and the position on the arrays was completely randomized to account for slide and array position effect.
At 800 °C, the nanotube arrays are completely destroyed and only dense rutile crystallites are observed.
At 800°C, the nanotube arrays are completely destroyed and only dense rutile film is observed.
Similarly, genes found after the end of these two arrays are completely different, with the exception of homologous transposase genes (IS3 family) being found near the last cassette of both arrays.
Finally, probes that were absent in more than 25%% of all arrays were completely removed from the dataset, resulting in a final dataset of 15,740 probes and 24 arrays.
The number of focal adhesions was decreased for cells cultured on the 50-nm arrays and was completely absent for cells on the 100-nm and 200-nm arrays.
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