Detailed procedures are provided in Supplemental Material, "Histopathological evaluation".
Quantitative MR imaging did rarely correlate significantly with morphological MR scores and may possibly provide supplemental information for evaluation of cartilage transplant maturation [ 132, 178].
To evaluate the accuracy of the individual ocular PK predictions using the combined ocular/systemic TMDD model, we built an additional systemic PK model, which was shown to meet model evaluation criteria (Supplemental Table 2 and Supplemental Figure 2).
ISOpure can also play an important supplemental role to pathological evaluation of tumors by providing an independent assessment of cancerous RNA content.
Four months after delivery, the increased body weight associated with BPA exposure persisted in the F0 mice; no differences in food intake were measured during a 6-day evaluation [see Supplemental Material, Figure 1C (doi:10.1289/ehp.1001993)].
An example set of questions designed to troubleshoot PCR is presented in Supplemental Material A. For evaluation purposes, the class included two 80-min exams each written with a focus on conceptual information, data interpretation, and troubleshooting experimental procedures.
While glaucomatous structural damage can be assessed subjectively by clinically examining the optic nerve head (ONH) and peripapillary retinal nerve fibre layer (RNFL), the introduction of ocular imaging modalities into clinical management has allowed for supplemental objective and quantitative evaluation of ocular structure.
Once the entire body of scientific literature that examined the effect of O3 exposure on various health effects was identified, the U.S. EPA followed a detailed study selection process to identify those references most relevant (i.e., policy relevant) to the O3 NAAQS review and evaluate their overall quality (see Supplemental Material, "Study selection and evaluation of individual study quality").
Additional secondary measures are described in supplemental Appendix A. Safety evaluations on all patients receiving one or more doses of trial medication (safety set) included adverse event reporting, withdrawals, clinically relevant laboratory changes, 12-lead electrocardiogram, vital signs, and physical and neurological examinations.
