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We first examined whether uPAR and β1 integrin were physically associated by testing the ability of anti- β1 antibody to coimmunoprecipitate (co-IP) uPAR and of uPAR antibody to co-IP β1 integrin from cell lysates.
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The protection against the development of ALA was confirmed by analyzing the hepatomegaly associated and by testing liver function, in particular the determination of alanine aminotransferase (ALT), a pyridoxal cytoplasmic phosphate-dependent enzyme involved in cellular nitrogen metabolism, amino metabolism acid, and liver gluconeogenesis.
We next asked whether increased SNARE complex formation is associated with suppression by testing SRO7 overexpression plasmids for suppression of the sec9-4 growth defect.
We also investigated if the balance between pro-apoptotic and anti-apoptotic proteins was associated with DSS by testing the impact of Bcl-2/Bax and Bcl-XL/Bax ratios on survival outcome.
By using multiple levels of testing for significance of association, we aimed to reduce the risk of selecting false positives by further testing groups of highly associated candidate genes by testing for gene gene interactions in the curated literature that may lead to more refined analysis in replicate populations.
Several studies have addressed the identification of genetic loci associated with MAP susceptibility by testing candidate genes, by genome-wide linkage or association studies.
We tested whether this could be explained by a preference for a specific number of symbols associated with brain size by testing another random sample from the very same replicate populations as in the learning trials, but without the training.
We will check to see whether refusal or losses to follow-up is associated with sociodemographic characteristics by testing the statistical significance of differences between refusals and consenters, and those lost to follow-up versus those retained at 6 months in terms of age, sex and level of education.
We attempted to replicate the genetic association in ABAT using an adult Swedish GERD case-control cohort by testing the associated ABAT SNP together with surrounding SNPs but found no evidence for genetic association.
We tested whether this IGFBP3 polymorphism is associated with human narcolepsy-cataplexy by testing 130 trios using the transmission disequilibrium test (TDT).
As above, we characterized the nature of the 3-way interaction by testing the associated simple interactions, confirming it was also driven by CS+ trials (Fig. 4 C ).
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