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Most DPP data originated from studies of pre-diabetic whites, with only sparse evidence of the effect of DPP in African Americans (AAs) in community settings.
These animals originated from studies undertaken between 2005 and 2007 that sought to improve the efficiency of SCNT by addressing issues related to mitochondrial heteroplasmy and chromatin remodelling at the point of nuclear transfer.
However, most of these findings originated from studies that relied upon DPR production not through RAN translation, but through AUG-initiated translation of a synthetic non-repetitive RNA sequence.
To test the accuracy of the models, we used published measured plasma concentration data that originated from studies of manual (bolus and short infusion) and computer-controlled (target-controlled infusion [TCI] and long infusion) propofol dosing schemes.
These developments marked the rise of computational biology as a field, and they originated from studies centred on protein crystallography, in which scientists found computers indispensable for carrying out laborious Fourier analyses to determine the three-dimensional structure of proteins.
Although the method we applied originated from studies of infectious diseases, it is unknown whether Farr's Law applies to epidemics of a non-infectious origin.
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Their chemistry originates from studies on molecular mechanisms of bioluminescence and has a history of over 30 years.
Most studies investigating the relationship between the genotypic characteristics of hepatitis B virus (HBV) and the clinical or epidemiological aspects of HBV infection originate from studies of patients with chronic rather than acute hepatitis B.
Therefore, our knowledge about cardiovascular effects mainly originates from studies using HRT, whereby the progestogen effects were assessed according to clinical endpoints, metabolic effects and influence on vascular markers in vitro or in vivo, respectively.
However, uncontrolled field studies had significantly higher effect sizes, probably due to all cases in this category originating from studies to understand the effect of a non-native predator on prey.
These datasets originate from studies of mRNAs that are actively being translated in response to cells over-expressing eIF4E or cells with an activated oncogenic AKT: eIF4E signaling pathway, respectively.
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