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In addition, we stratified the regression models of sickness and disability following dropout across the quintiles of the propensity score for high school dropout.
The combination of theoretical models were the empowerment model, theories of planned behaviour and personal models of sickness [ 37], the empowerment model and the discovery learning theory [ 38], the social cognitive theory and the social ecological theory [ 50], the self-efficacy and self-management theories [ 55] and the cognitive theory and operant reinforcement theory [ 56].
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An alternative approach would be to examine the inflammatory cytokine response to docetaxel administration alone in a mouse model of sickness behavior.
Importantly, this model of sickness behavior does not contradict the development of hypersensitivity to noningestive stimuli through classical conditioning.
Consequently, analytical approaches to modeling of sickness absence duration should take into account both event dependence and heterogeneity to avoid obtaining biased estimates of the parameters of interest [ 11, 12].
There is also some evidence suggesting that NO modulates the function of hypothalamic arcuate nucleus (ARC) in an animal model of sickness anorexia induced by bacterial endotoxin lipopolysaccharide (LPS) injection [ 17]. iNOS-dependent NO formation inhibits orexigenic NPY-containing arcuate neurons that are excited by ghrelin.
Look for signs of sickness.
Animal models of serum sickness, a circulating immune complex disease, have been shown to develop cellular infiltrates in the uvea [7].
[ 1- 10] Most previous studies examined Karasek's demands-, control- (and support-) model[ 11] and Siegrist's effort-reward imbalances model[ 12] as predictors of sickness absence or were inspired by these models.[ 13] Other aspects have also been discussed and applied (organizational justice, leadership).
Table 2, fully adjusted model, shows higher odds of sickness absence for those who received the treatment combinations drug treatment, psychotherapy and physiotherapy (OR 1.67, 95% CI 1.25 to 2.25), compared with those who did not.
Intravenous administration of DB289 should be evaluated in mouse models of late-stage sleeping sickness.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com