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For those samples that were redundant across the databases, the union of the observed point mutations was reported for the co-mutated genes.
Recently, a high frequency of NR5A1 gene mutations was reported in a small group of women with POI.
The detection of FLT3 mutations was reported previously [34].
The presence of double PIK3CA mutations was reported elsewhere.
The concomitant occurrence of PIK3CA and KRAS mutations was reported previously in CRC and other human cancer types [ 21, 35].
Similarly, a higher prevalence of FBXW7 and PHF6 mutations was reported in adult T-ALL 10, 17, 18.
Similar(50)
To date, no other CNVs have been described in the ATP1A2 but only point mutations are reported.
In 2012, Somatic DDX41 mutations were reported in the study of sporadic acute myeloid leukemia (AML) syndrome by Ding et al. (2012).
Soon after, DNMT3A mutations were reported in AML cohorts from others, with frequencies as high as 22.1% (Ley et al., 2010).
Furthermore, small de novo mutations were found to be overrepresented among glutamatergic postsynaptic proteins [59] and genes harbouring detrimental de novo mutations were reported to be enriched in networks affecting protein interactions [65].
Mitochondrial DNA (mtDNA) mutations are reported in different tumors.
More suggestions(15)
mutations was analyzed
mutations was verified
mutations was based
mutations was performed
mutations was confirmed
mutations was demonstrated
mutations was determined
mutations was produced
mutations was observed
mutations was designated
mutations was estimated
mutations were reported
mutations was found
mutations was calculated
mutations was visualized
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