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Intermediate precision was tested by repeated analysis of PG in pure form using the concentrations shown in Table 3 for a period of 3 successive days.
Intermediate precision was tested by repeated analysis of ALD in pure form using the concentrations shown in Table 4 over a period of three successive days.
It was performed through repeated analysis of SER in pure form, using the concentrations shown in Table 2 for a period of 3 successive days.
Intermediate precision: intermediate precision was tested by replicate analysis of the three drugs in pure form using the concentrations shown in (Table 3) for a period of 3 successive days.
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Intermediate precision: Intermediate precision was evaluated through repeated analysis of MTP and FDP in pure form applying the proposed method, using the concentrations showed in Table 4 for a period of 3 successive days.
It was performed through repeated analysis of SER either in pure form or in tablets, using the concentrations showed in Table 3 for a period of 3 successive days.
Inhibitors were used at the concentration shown in parentheses (μM).
Furthermore, mean risks of the number of the PGE compounds in given home posed comparable risks as those estimates using the PGE concentrations, shown in Table 4.
PK parameters in each brain region calculated using the concentration profiles are shown in Table 2.
If Λ < − v ∞, then by using the concentration compactness principle of Lions, one shows that Λ is the principle eigenvalue of S with a positive eigenfunction Φ 0 : S Φ 0 = λ 0 Φ 0, Φ 0 ∈ H 2 ( R N ), Φ 0 > 0. 3. The spectrum of S in ( − ∞, − v ∞ ), namely σ ( S ) ∩ ( − ∞, − v ∞ ), is at most a countable set, which we denote by Λ = λ 0 < λ 1 < λ 2 < ⋯, .
Models using PM2.5 concentrations showed similar results for CD4+, CD3+, and CD19+, whereas associations for CD8+ disappeared.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com