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Exact(16)
For example, mutations in the anticodon region of a tRNA gene can result in a tRNA that sometimes inserts an amino acid at an erroneous stop codon; if the original mutation is caused by a stop codon, which arrests translation at that point, then a tRNA anticodon change can insert an amino acid and allow translation to continue normally to the end of the mRNA.
We conclude that the observed clinical severity of the cTnT Δ160E mutation is caused by a combination of direct sarcomeric disruption coupled to a profound dysregulation of Ca2 + homeostasis at the cellular level that results in a unique and highly progressive pattern of ventricular remodeling.
The vigEP812 mutation is caused by a P{EP} insertion within the vig coding region (Figure S3A) that results in severe reduction of the VIG protein (Figure 3A).
Analysis of the progeny phenotype demonstrated that the vasaAS mutation does not modify PEV (Figure S3C), indicating that the suppression observed with the vigEP812 mutation is caused by a reduction in the levels of VIG.
It has been revealed that Yaa mutation is caused by a translocation of a portion of the X chromosome containing TLR7 onto the Y chromosome [ 3, 4].
Whereas in L er-0 the old3 mutation is caused by a single gene defect, two genes are needed for the same phenotype in Col-0.
Similar(44)
Users should use a criterion, usually a cutoff value, to determine whether the mutation is causing splicing defects.
However, since each generation introduces up to 4.5 deleterious mutations [ 149], it might be as well that a de novo mutation is causing the disease.
Mutant lines complemented with the wild-type CTU2 construct showed reversion to wild type-like lateral root formation, confirming that the ctu2-2 mutatisn is causing this developmental defect.
The oxt6 mutation was caused by a T-DNA insertion into a gene encoding a polyadenylation factor subunit homolog, CPSF30.
To bolster the case that the mutation was causing disease, the scientists also showed that the AKT protein is overactive in the abnormal cells.
More suggestions(15)
mutation is affected
mutation is resulted
transformation is caused
mutation is affecting
mutation is linked
mutation is labeled
mutation is parametrised
mutation is known
mutation is implemented
mutation is shown
mutation is located
mutation is considered
mutation is required
mutation is done
mutation is identified
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