Various scenarios of different numbers of individual samples, different numbers of pooled samples containing various numbers of individual specimens, the relationships between chemical analytical error and other sources of sample variance, have been compared by simulating random sampling from computer generated populations using realistic measures of variation from ongoing monitoring activities.
In the excision specimen the relationship was stronger (P < 0.0001); median RFS was about 18 months for patients with Ki67 in the highest tertile, as compared with more than 7 years for the other two tertiles.
Non-linear finite element analyses for 3-D models of plane-sided SE(B) and PCVN specimens define the relationship between ˜σw and J from which the variation of fracture toughness across different crack configurations is predicted.
Due to the variation in compressive strength and strain at peak stress of different specimens, the stress strain relationships were compared in a normalized manner.
Compared to the EBR specimens, the bond slip relationships derived for the NSM specimens at ambient temperature presented (i) similar stiffness and (ii) higher values of maximum shear stress.
Applying real-time RT-PCR, we investigated the miR-31, miR-143 and miR-145 expression in 98 primary CRC specimens, along with the corresponding normal mucosa specimens, and analyze the relationship of their expression with clinicopathological features.
It is also demonstrated that one truncated cone specimen test can replace several tests using conventional cylindrical specimens to study the relationship between dynamic recrystallized grain size and saturated stress.
Using microarray, we quantified the expression profile of 237 IFN related genes in 87 CH liver biopsy specimens to clarify the relationship between IFN pathway and viral elimination, and to predict patients' clinical outcome.
This research simulated the insertion of epidural catheters in cadaveric specimens and observed the relationship between the relevant structures.
We also used independent sets of GBM specimens to analyze the relationship of subcellular localization of FABP7 with patient outcome and EGFR expression, and to seek possible mechanisms underlying the functions of FABP7 in GBM.
