The reasons for these differences may be diverse and include varying clinical practices, different attitudes, cultural backgrounds and, not least, changes in practice developing over time.
8 9 Factors that may have caused dissimilar prevalence estimates include varying definitions of MAU and different study methodologies.
This may be due to serum collection that can include varying degrees of neutrophil lysis and release of defensins which are reported to decrease LF activity [ 35].
Multiple possibilities may be in play, including varying tissue or developmental requirements for the general factors or sensitivities to their perturbations, and potentially non-identical ribosome composition in different cells [29,31].
At any given age in a population, there is a range of healthspan phenotypes, including varying mobility, which may be predictive of how long an individual animal will live [ 13, 21].
There may be differences in the behaviors of individual pyrethroid metabolites that result in unknown enzymatic or proteomic impacts, including varying effects on the signaling for meiotic controls.
High-resolution imaging techniques, including TEM and atomic force microscopy, enable identification and classification of aggregates, which may include protofibrils, amyloid fibrils containing varying numbers of strands, and amorphous aggregates.
However, a variety of factors may be related to the inconsistent findings, the most important of which may include small numbers of participants, varying overall exposure levels, use of various detection methods for biomarkers and endogenous hormones, and differing age, sex, and unmeasured exposures to chemicals affecting hormone homeostasis.
Atop the plinth and forming the remainder of the base are one or more circular moldings that have varying profiles; these may include a torus (a convex molding that is semicircular in profile), a scotia (with a concave profile), and one or more fillets, or narrow bands.
