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However, we compare different variants and study their closure properties.
Fortunately, we increasingly have the tools for these purposes, both to characterize variants and study them in a high-throughput manner.
In all the studies, interaction associations between the MUTYH variants and study code (for each individual study) were estimated and similarly between MUTYH variants and hormone replacement therapy (HRT) among female participants in three studies (the Scottish SOCCS studies and the studies – Croitoru et al, 2004; Cleary et al, 2009).
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R156 R165 (2008)Insightful review of initial findings from GWAS, the heritability that they do and do not explain, and potential for progress from other GWAS, identification of rare variants, and studies of epigenetics and gene expression and function.
These two issues contribute to the challenge of identifying the possible causative variants, and studying their effects in populations of non-European ancestry.
In this study, we have manipulated the copy number of native motor complexes on a physiological type of cargo, by incubating cellular extracts with RNA variants, and studied the consequences on motility in a defined in vitro setting using high spatiotemporal resolution imaging.
A tremendous amount of genomics research will be required before clinical utility is established with high confidence on some genetic variants, and studies that include a genomic component may, in aggregate, require the study of very large numbers of individuals before such utility can be established.
The potential interaction between each genetic variant and study design (CIS vs. invasive carcinoma) was evaluated with the interaction model by additionally including interaction term between genotypes and study design.
However all of their predicted sites (Ser18, Ser157, Ser316, Ser383, Thr242 and Thr432) are conserved between the two variants and their study did not distinguish between the two variant forms.
TJ helped to draft the manuscript and participated in the design of both the molecular variants and the study.
DHK helped to draft the manuscript and participated in the design of both the molecular variants and the study.
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