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In this study, 38 CRC specimens and 38 peritumor specimens (as control; at a distance more than 10 mm from the tumor edge) were obtained from CRC patients with complete clinicopathologic data of specimens recorded.
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To our knowledge, this is one of limited number of studies that used non-neoplastic bladder tissue specimens as controls.
Using corresponding cryopreserved tissue specimens as controls, we show that formalin fixation and paraffin embedding does not interfere with the formaldehyde based dimethyl labeling.
Compressive strength test was conducted on control specimens as well as concrete specimens revived through the two cooling systems.
Rougher surface quality of the samples had higher bonding values as compared to those of control specimens as well as those sanded with 100 and 240 grits.
Moreover, with BCS, the current standard of care and an ever-growing need to extract normal host tissue DNA and RNA from the same small BCS specimen as control samples for the many high-resolution genetic and epigenetic assays now being performed on breast tumors [ 9]; there is renewed concern about the molecular normalcy of morphologically normal peritumor mammary tissue.
PA specimens (Valplast) of 40 × 10 × 2 mm and equally measuring PMMA specimens (Palapress) as control were fabricated.
An equal number of PMMA specimens served as control.
Every extraction was carried out without specimens as negative control, and we confirmed no amplification of the negative control in the PCR step.
One specimen served as control while the other two specimens were strengthened using CFRP fabric and NSM bars such that they have equivalent capacity at first yielding.
The other three specimens were considered as control specimens.
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