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Fraction 1 (19 mg) was identified as fucosterol (3).
Fraction 3 (8.0 mg) was identified as saringosterol (7) and fraction 4 (19 mg) as apo-9′-fucoxanthinone (8).
A biologically active dose of 1000 mg was identified in all three studies.
In this study, MG was identified as a marker for monitoring the onset, development, and remission of sepsis.
However, no subgroup for which dabigatran 110 mg offered any clinical or economic advantage over 150 mg was identified.
MG was identified as a better biomarker than the established routine markers (for example, CRP, PCT, IL-6, and sCD14-ST) for the identification of patients with sepsis.
Similar(49)
The metabolites generated after degradation of 50 mg/mL of MG were identified by GC/MS analysis (Fig. 5).
The metabolites generated after degradation of MG were identified by LC/MS and a plausible pathway of MG degradation has been elucidated.
In this study, pathways that are dysregulated in MG were identified by pathway enrichment analysis.
40 patients with recurrent pretreated MG were identified as being treated with fotemustine at doses ranging from 65 mg/m2 to 100 mg/m.
Relevant English-language articles on the efficacy, cardiovascular safety, or sexual function safety of alfuzosin 10 mg were identified via MEDLINE searches.
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