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We modified the procedures described above for participants assigned to DAART.
To observe growth kinetics within the host, we modified the procedures of Uchiyama et al.[ 49].
In order to make the dual fluorescence assay more convenient, we modified the procedures of plasmid construction so as to speed up the workflow.
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We modified the procedure by allowing only such shifts that do not increase overtime consumption, therefore, leading to schedules with possibly both decreased makespan and lowered overtime costs.
In the work reported here, we have modified the procedure for obtaining the textural features and proposed the scribble boosting technique, which eliminates the main drawbacks of these earlier algorithms.
Most recently, several clinicians modified the procedure by further reducing the flap size needed for the procedure, moving the access site to the ridge crest, and limit the access window to an implant osteotomy created with osteotomes [11, 12].
We modified the procedure used by Sharan et al. [33] to merge CPIMs.
This experiment was conceptually the same as Experiment 1, but we modified the procedure and apparatus to allow more detailed examination of the cognitive processes involved.
We modified the procedure described above to accommodate cultured mammalian cells (see Materials and Methods) and established that the procedure could detect uptake of both white (FIG. 1C) and opaque (FIG. 1D) cells of C. albicans.
To further improve the local control, we modified the procedure described by Robbins et al from October 2002.
For this, we partially modified the procedure described by Izuta et al. (2007) [ 19].
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