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The biochemical markers of bone turnover were analyzed in multivariate analysis.
Bone mass and its turnover were analyzed by histomorphometry.
Bone mass and bone turnover were analyzed by histomorphometry.
To better understand the sex-related differences in LV remodeling, some indices of the myocardial ECM turnover were analyzed.
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Therefore, the potential role of bcl-2 in the regulation of HIF-1α protein turnover was analyzed.
In addition, MS-KIF18A protein turnover was analyzed in presence or absence of estrogen applying metabolic labeling with Met/Cis-S35 on MBA-15 cells.
To determine if transport and retrieval is coincidental or a requirement for ERAD, the D1, D2, and D3 variants were expressed moderately from the PRC1 (CPY) promoter and turnover was analyzed by cycloheximide chase and immunoblotting.
Staff turnover was analyzed by comparing the e-mail addresses between the two data collection points.
Bone turnover markers were analyzed by the research team using standardized commercial ELISA kits.
To assess metabolic turnover, extracted intracellular metabolites were analyzed after labeling for between 1 and 30 min.
To specifically address type I collagen turnover, biomarkers for degradation (ICTP) and neosynthesis (CICP) were analyzed in conditioned media.
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