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The measured MeHg(I) concentrations was 3.7 236.6 ng g−1 (as Hg), and no EtHg(I) was detected.
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The [Ca2+] i concentration was estimated based on calibration curves as follows.
The first step is determining P i concentration was the generation of a standard curve correlating absorbance at 660 nM with known concentrations of P i in the colorimetric reagent as shown in Figure 4A.
Recovery of IGF-I concentrations was assessed by spiking assay buffer with either recombinant human IGF-I or recombinant rabbit IGF-I.
The intra-assay variability (precision) measured in rabbit serum displaying low, medium and high IGF-I concentrations was 2.55, 2.25 and 1.49%, respectively (Table 1; supplementary material Table S1).
Plasma HDL-cholesterol concentrations were significantly lower after the rTFA diet than after the control diet (−2.8%; P = 0.004), whereas no significant change in plasma apo A-I concentrations was found after the rTFA diet.
Thus, some recommendations for the design and sampling strategy of nutritional trials where IGF-I concentrations are measured are discussed.
Plasma IGF-I concentrations were lower (P<0.05) in low purebred offspring than in the other three calf groups.
To determine if serum IGF-I concentrations are similar in healthy adult subjects from the Samoan, Māori and European populations in New Zealand.
IGF-I concentrations are described as SD scores.
Unexpectedly, IGF-I concentrations were not affected by IGF-I genotype.
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