Exact(4)
In genotyping SLC23A2 rs1715364 in the German study, the variant CC genotype was associated with an elevated OR for CLL, consistent with findings from the U.S. study.
In a population-based, prospective, Italian study, the variant alleles on 9p21 were not only found to influence the development but also the progression of carotid atherosclerosis [15].
In this study the variant rs3758539 was involved in the development of GDM [ 26].
In our study, the variant type ST701 (annotated as M. africanum in the spolDB4 database) (4 ) is also an M. orygis specific type and exactly matches that of a previous isolate of the oryx bacillus (SB0319) from the M. bovis spoligotype database (5 ).
Similar(56)
In previous study, the variants of HPV-16 E6 gene have been reported.
For the three families in the study, the variants shared between the affected and the unaffected members in the same family were removed.
Feng et al. [32] studies the variant problem to maximum the influence of the team.
Further study of the variant in other patient cohorts and exploration of the functional effects of TM6SF2 on inflammatory response will be needed to address this point.
The study demonstrates the variant and promising ways in which lead levels can be used to speak to us about the past.
The new study confirms the variant's role in diabetes, although the findings came about somewhat fortuitously.
In another study [24], the variant genotype AA of FOXP3 was also positively associated with tumor size, in triple negative breast cancer.
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