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The differences in apoB between genotypes remained significant after controlling for age, cigarette smoking status, and BMI, by a general factorial model of variance (P=0.032).
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However, we can say that the relationship between adult intelligence and DNMT3L genotype remained significant, by both the additive and dominant models, following sequential exclusion of the highest MHT scores over a large span of the data; from the maximum possible score of 76 down to a score of 67 using the additive model and down to a score of 59 using the dominant model.
The difference in the TC, LDL-C, and non-HDL-C between the II and DD/ID genotype groups remained significant (P < 0.05), with lower estimated marginal mean values in II carriers than in the DD/ID groups.
However, correlations between emotional abuse and the LEIDS-R outcomes for each genotype separately remained significant, consistent with the results for the triallelic classification.
This association between TLR4 genotype and outcome remained significant (adjusted OR 2.9 [95% CI 1.2 to 6.7]), after adjustment for maternal age and chronic hypertension in our multivariable model (Figure 1a).
After adjustment for age, duration of diabetes, body mass index, systolic blood pressure, HbA1c, and serum creatinine, triglycerides, and total cholesterol in multivariate logistic-regression models, the association between this AR genotype and stroke remained significant.
Differences between all groups remained significant.
Analysis of the most frequent ethnic group in the study population, that is, Caucasians, showed that the relationship between 3435CC genotype and lower AUC remained significant in premenopausal women (AUC ± s.e. values (μg h l 1): 2816±149 and 5094±1050 for 3435CC (n=10) vs 3435CT and 3435TT (n=30), respectively, Mann Whitney test P=0.004).
In contrast, with high gf task performance entered as a covariate, all the reported associations between COMT val met genotype and regional fMRI activity remained significant.
Notably, with high gf task performance entered as a covariate, all the reported associations between COMT val met genotype and regional fMRI activity remained significant (see Table 1).
Phylogenetic signal for the birth death phylogeny remained significant for Genotype 1 (Figs S4A and S5A).
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