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In this study, we use a separate, unrelated outgroup of individuals with progressive supranuclear palsy (PSP), a neurodegenerative condition with no known etiological overlap with ASD, as a control population.
hESC-derived hNSCs (Liu et al., 2012) were used as a control population.
As a control population, we analyzed 42 healthy, cancer-free blood donors with normal values for blood counts, C-reactive protein and liver enzymes.
Options for testing the validity of Family Stream migrants as a control population for Skill Stream migrants are constrained in our context due the dynamic nature of Australian migration policy and the limited data that are available.
Finally, we conducted a limited out-of-sample test for the validity of Family Stream migrants as a control population for Skill Stream migrants by calculating treatment effects from CSAM cohort 1 to cohort 2. Although some policy variation between cohorts 1 and 2 of CSAM is inevitable, it is reasonable to suppose that this variation is relatively minor.
The group of transplant recipients who were never viremic served as a control population (figure 2A, white circles).
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However, defective release of vascular plasminogen activator was observed on several occasions in all five subjects as compared with a control population of 125 persons (0.04 Committee on Thrombolytic Agents [CTA] units/ml plasma as compared with 0.21 CTS units/ml).
Notwithstanding, the nuclei of CD4+ T-cells treated with TSA displayed significantly lower levels of NFκB as compared to a control population.
This highlights the importance of using a control population as when compared with our general pregnant population PET rates differ between T2DM and controls.
We deliberately chose a control population with choledocholithiasis as opposed to a purely healthy control population in an effort to minimize selection bias.
Thirty healthy donors recruited from laboratory personnel were included as a normal control population.
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