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Subsequent to wax removal, each specimen was divided into a control half and an experimental half.
Each specimen was divided along the midsagittal plane, and a Masson trichrome histologic section was prepared.
The cross-sectional area of each specimen was divided by the peak tensile load at failure to calculate stress at fracture (MPa).
The value of the critical distance was normalised (L*) meaning that the chosen critical distance for each specimen was divided by the adhesive layer length (Eq. 8).
After homogenization, the specimen was divided into three parts.
Each biopsy specimen was divided in two fragments, for myoblast isolation and for RNA extraction.
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Each test specimen is divided into two parts and then solution of silver nitrate AgNO3 was poured on each section according to the standard UNI 79287 (UNI 79287 1978).
Returning light from the specimen is divided into two pathways by the beam splitter.
In this study the sentinel nodes as well as each lymph node of the neck dissection specimen were divided along the equatorial plane into two halves, which then were embedded in paraffin.
Each of the six fresh specimens was divided into three conditions: normal, single staple, and double staples.
Each of the specimens was divided into 2 equal parts, half for histopathologic analysis, and half for preparation of decontaminated suspensions for culture and microscopic examination (3, 5 – 7 ).
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