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Fig. 6 The CV RMSE for different subsets of the final model as a function of MP.
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Scaffold pore size and distribution changed significantly as a function of BL-MP loading.
Genetic experiments indicate that SWI/SNF recruitment is an essential function of MP and that SWI/SNF ATPase activity is necessary for reprogramming.
The tumour uptake concentration data ([B]) as a function of peptide mass (Mp) was fitted to the sigmoid-shaped one-site competition curve: B M p = B unsp + B spec 1 + M p ED 50, (1).
When we compared the buccolingual thickness at the apex as a function of increasing SN-MP, we found a negative relationship, with the thickness decreasing with an increase in SN-MP (R = −0.64, p = 0.000), which is consistent with the findings of previous studies [7 10].
Results of the pooled analyses by Hardell [ 1- 3] on the risk of overall head tumours in exposed subjects compared to that of non-MP-users, as a function of the use of different MP types, (no. of cases and controls with ≥ 10-year use or latency): OR; 95%CI.
The relation for A0 Mp) as a function of the peptide mass Mp changes for the maximum (achievable) specific activity Asp at both sides of the equation: A 0 M p = M p × A sp = B 0.03 D B M p a ~ m S m ← m. (3).
The factors controlling the formation and the function of MP are not completely understood.
Mp was investigated as a function of the twist pitch lp and the field amplitude Bm.
Reflectivity measurements were also used to demonstrate that the effective refractive index of MP-Ge can be adjusted as a function of layer porosity.
Figure 6 shows that the CV RMSE of the individual subsets as a function of temperature increases for all sets of high temperatures (MP >250 °C).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com