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Staging of investigated specimens was based on morphological aspects due to chronologically heterogeneous late development.
Histological examination of the tissue specimens was based on a Cresyl-Violet staining.
Assessment of NAFLD specimens was based on the criteria described by Matteoni [ 7].
The histologic classification of the tumour specimens was based on World Health Organization criteria (World Health Organization, 1982).
Our manual identification of unidentified specimens was based on ventral centroid size, ventral RWs 1, 2, 4, 5, 6, and if available, apertural centroid size and apertural RWs 1, 2, 4, 5.
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The standard floating roller peel specimens were based on the ASTM standard D3167 [1].
The pull-out specimens were based on RILEM recommendations, and the beam specimens were tested under a simply supported four-point loading condition.
As mentioned earlier, for the single-lap shear tests, the specimens were based on short lengths of RC T-beams and stainless steel bonded on uncracked concrete regions.
The MDCT specimens are based on the conventional DCT test concept relative to a notched specimen with cylindrical shape (Nieto et al. 2014), allowing the pulling force to be applied in a simple way without the inconvenience of possible material local fractures at the pulling holes due to stress concentration, as would happen by conventional DCT concrete specimens.
The grading and histopathology subtyping of ESCC specimens were based on WHO criteria.
Microarray diagnostics of tumour specimens is based on gene expression measurement of a specific set of predictive or prognostic genes.
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