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Genetic DNA testing for neonatal diabetes revealed no pathogenic mutation in common KCNJ11, ABCC8 and INS genes.
They had one mutation in common, a substitution of aspartate in position 112 to glutamate (Asp112 → Glu).
One feature of the evolved xyloglucan binders is that all contained one mutation in common (aspartate to glutamate in position 112) compared to XG-34.
Further association analysis using wild O. marmoratus (N = 68) and O. profundicola (N = 34) stocks revealed that they only had a single 430-bp insertion Y chromosome-specific mutation in common.
Finally, we propose that the roles of normal specific and mutation in common AS variants should be examined in addition to cancer-specific transcripts; analyses of these absent AS transcripts may further aid in the understanding of the cancer physiology.
Similar(54)
But two patients with the same type of cancer might have only five mutations in common.
Genetic sequencing, which entered the popular lexicon with the launch of the Human Genome Project, in 1990, allows for the opposite type of search: comparing the entire genomes of people who suffer from an unknown disorder, to see if they have genetic mutations in common.
E6-3 and E6-4 share three mutations, but have no mutations in common with the lineage that produced E6-1 and E6-2.
The reason is that most variants do not have any mutations in common (of the 105 different amino acid mutations, only 12 occur in more than one variant).
Although two isolates share the same frameshift mutation in CAN1, they do not share any other mutations in common, suggesting that these inactivating events occurred independently.
Comparison of our V-D-J rearrangements with the two anti-DNA specific antibodies revealed very few somatic mutations in common, however.
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