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In a curative growth assay, weight increase is measured in animals first deprived of a vitamin and then given various quantities of it.
All tablets were characterized for assay, weight variation, hardness and friability and were found to meet the pharmacopoeial standards.
In contrast, for the PM the data drives the assay weight as well as group assignment of the assays.
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Two classical in vivo assays, the rodent uterine wet weight assay and the vaginal cornification assay, have traditionally been used for testing estrogenic activity of compounds.
From the lists we selected genes to study in further detail to determine whether p50 and/or Bcl-3 showed increased binding to κB binding sites using chromatin immunoprecipitation (ChIP) assays in weight bearing and unloaded mouse plantar flexor muscles.
In chronic P. promelas assays, reduced weight and survival was present when concentrations were 2920 mg/L or greater.
Other measurement time points, different anti-FXa assays and weight of the animals complicate direct comparisons [ 16, 17].
The objective of this study is to describe spatiotemporal and ground reaction force changes in a rat medial meniscus transection (MMT) model of knee OA and to compare these gait measures with assays of weight bearing and tactile allodynia.
Similar TCID50 values were observed among the three strains in the in vitro assay ((3.83±0.22)×10 TCID50/g lung weight in the BALB/c mice, (2.62±1.45)×10 TCID50/g lung weight in the C57BL/6 mice and (1.22±1.19)×10 TCID50/g lung weight in the ICR mice).
Prior to PES, the propranolol cohorts and phenytoin cohorts were put through a battery of behavioral assays, weekly weights were acquired and whole-body plethysmography was performed.
The formulations were assessed on assay, dissolution, friability, weight variation and disintegration time.
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