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In demographic data collection, it is accepted that mobile populations and individuals are poorly represented, whether in rich, more developed, populations or in the global South.
Equally importantly, our study demonstrates the need for and role of evidence from different socio-historical contexts in clarifying empirically driven hypotheses from long-term economically developed populations.
Thus, while VavNULL mice showed severely reduced populations of both developing and mature T cells [29], Vav1WT chimera mice developed populations of thymocytes and peripheral T lymphocytes similar to WT mice (Fig. 4A,B), although the total number of thymocytes generated in such RAG-chimera is typically somewhat lower, as compared to WT (Fig. 4A and data not shown).
Immigrant genotypes, however, have a low likelihood of becoming established in already developed populations [ 41, 46, 47].
It is therefore conceivable that optimal CVD risk stratification differs amongst patients with RA from developing populations compared to those from developed populations.
Reported data on atherogenesis in the general population and diseases such as RA derive almost exclusively from developed populations [ 23, 24].
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A previously developed population balance approach was extended in order to include particle energy balance effects.
The zero one kinetics was employed for the nucleation rate, with the model comprising a set of rigorously developed population balance equations.
A system exhibiting zero-one kinetics was employed, with the model comprising a set of rigorously developed population balance equations to predict monomer conversion, PSD and MWD.
In order to evaluate the previously developed population models, some model modifications needed to be made.
During cycle 1, the previously developed population pharmacokinetic model adequately described the non-linear pharmacokinetic profile of indisulam.
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