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Consistently with previous reports, these steps consist of a succession of newly ingested non-degraded RB, phagocytic vacuoles containing partly degraded RB with electronically dense inclusions, and then late vacuoles filled with electronically dense RB degradation remnants.
The three steps consist of aggregation, optimization, and control.
The third, fourth, and fifth lifting steps consist of non-separable 2D structures, and the same goes for the fifth to the 11th steps.
Successive iterative steps consist of a pair of fourth-order system of equations forming a proper sequence of sets of 2-D problems converging to a 3-D problem.
Finally, since macro steps consist of only finitely many micro steps whose number is known at compile-time, one can determine tight bounds on the reaction time by a simplified worst-case execution time analysis [11 14].
The final steps consist of rearranging the long-vectors and in its initial form and computing an inverse Fourier transform in order to come back to the time-distance-component domain.
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One of the metabolic steps consists of the decarboxylation of the α-keto acids of leucine, isoleucine, and valine, respectively.
The second and the third steps consisted of cloning the EYFPBax and ECFPBax cDNA.
The final steps consisted of 20 25 cycles of 94° (5 sec).
All washing steps consisted of 1 minute of flow, followed by 5 minutes of incubation.
The following steps consisted of masking the repeats, vector and organelle sequences.
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