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Duck et al. [ 10] in their study on a community sample supported a two-factor model with factors representing positive and reverse-worded items.
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Samowitz, W.S. et al. Evaluation of a large, population-based sample supports a CpG island methylator phenotype in colon cancer.
Considering only the posterior sample supporting a divergence point (1123 samples), no branch shows evidence of strong heterotachy, although the posterior distribution across branches is significantly different from the uniform prior (p-value < 0.001).
Findings in both the clinical and standardization samples supported a six-factor model including Semantic Memory, Verbal Reasoning, Constructional Praxis, Visual Reasoning, Working Memory, and Processing Speed factors.
Findings in both the clinical and standardization samples supported a four-factor model containing auditory memory, visual memory, working memory, and learning factors.
Using the L90M assay as an example, the resulting distribution of collated ΔCTs from the pre-ARV era wildtype samples supported a ΔCT cutoff of 10.5 cycles for L90M clinical testing (ΔCTs ranged from 12.0 28.0 cycles) (Figure 3).
The 4 remaining urine samples supported a significantly better growth than HV urine (p = 0.0371).
Biopsy specimens were obtained from the head, ears, and paws, and analysis of these samples supported a diagnosis of mural folliculitis and mild plasma cell pododermatitis.
A similar trend was observed in the breast tissues (an ~16-fold increase in RBM6 expression in the chimeric negative tumour sample and an ~25-fold increase in the chimeric positive tumour sample), supporting an expression correlation between RBM6 expression and that of the RBM6-RBM5 chimerand andemonstratingng that the phenomenon was not tissue-specific.
Conclusions: Studies enrolling independent samples support a positive association between weight status and EAH among children; studies addressing causality are needed.
Also, our data provides the first genomic evidence in clinical samples supporting a conventional model for the emergence of acquired resistance whereby resistance emerges through a selective, clonal outgrowth of small populations of pre-existing, chemoresistant tumor cells [3].
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