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Both models demonstrated poor dextran accumulation compared to the liver as a positive control, suggesting that although several pathological features were observed, low vascular density and small blood vessel size led to relatively poor tumour perfusion.
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As shown in Fig. 1, the estimated model demonstrated poor fit of the data [χ (12, n = 383) = 485.47, P < 0.001, CFI = 0.464, RMSEA = 0.32 (90% CI 0.30 0.35)] likely due to a net effect of constructs in the model (i.e., too many paths being estimated relative to the sample size), not because of the structural relations specified.
Moreover, in support of biofilm formation and VPS production being required for infection and biofilm formation in vivo, analysis using the rabbit ileal loop model system demonstrated poor biofilm formation by the vps mutant (Kamruzzaman et al. 2010).
This impairment in learning and memory function is consistent with the neuropsychiatric studies of lupus-prone murine models which demonstrate poor performance in spatial memory tasks [53] [57].
Item 17 demonstrated poor fit to the Rasch model as evidenced by a statistically significant chi-square (p = 0.000607).
PC-PART items assessed as one scale, and original PC-PART domains evaluated as separate scales, demonstrated poor fit to the Rasch model.
The original 10-item version explained 61.3% variance by the first latent dimension (general self-efficacy), but three items demonstrated poor fit to the Rasch model and were deleted.
They demonstrated poor understanding of trigonometric identities.
However, the PDR demonstrated poor sensitivity in this patient population.
The CAM-ICU demonstrated good performance, while the 3 simple questions demonstrated poor performance.
Eleven (12%) patients demonstrated poor response.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com