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Only cases identified as having stage 3 (50 75%) or 4 (75–100%) fatty degeneration of the muscle were selected for this study.
For electron microscopic examination, three areas of the harvested muscle were selected.
Eleven genes represented by tags that were differentially expressed between untrained and trained skeletal muscle were selected for real time qRT-PCR validation.
During TURB, tumour fragments comprising both visible urothelium and underlying muscle were selected for RNA extraction and immediately stored in liquid nitrogen at −80 °C.
Heart and skeletal muscle were selected as vital target organs because they are among the ones most affected by the endogenous aging process and are almost fully composed of postmitotic cells.
The tibialis anterior and the distal part of vastus medialis muscle were selected for this study because of the relatively extensive body of data available on its structure and behaviour particularly suitable for conduction velocity (CV) measurements [ 25].
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The McKibben artificial muscle was selected as the muscle suit actuator because of its light weight, simple structure, softness, waterproof finish and power-to-weight ratio [18].
When the best reconstructing muscle was selected, R2 was 0.31±0.17 for X and 0.32±0.10 for Y (Table 1).
When a single best reconstructing muscle was selected, the percent of correct reconstructions was 65.9±11.4 (Table 1), and the average percent correct for any single muscle was 51.6±12.5 (Table 2).
The brachioradialis muscle was selected for this study because the PPT measurement of this muscle is relatively easy.
Since the mean number of MUPs of the triceps muscle was too low (≤ 2), the brachialis muscle was selected as a control.
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