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A novel assay for surface DNA hybridization, which is free of sample and probe labeling, convenient and of low cost, sensitive and capable of differentiation of single-base mutations, is reported.
Statistics based on the distribution of variation within samples did not exhibit detectable patterns across populations or loci, and therefore, only Tajima's D [30] calculated from the total number of mutations is reported.
However, a number of patients with mutations in GUCA1A have reduced rod as well as cone function; whilst the disorder in most patients with Y99C and L151F mutations is reported as cone dystrophy with normal rod-mediated vision, some affected individuals from the same families have altered rod function and present as a cone-rod dystrophy [14], [16].
The frequency of the mutations is reported in Table 3.
Quantitative analysis of K-ras mutations is reported to provide a useful tool for diagnosing pancreatic cancer when the percentage of K-ras mutations is high (Tada et al, 2002a).
The frequency of complex mutations is reported to be higher in basal subtype breast cancers, including cases arising in carriers of germ-line BRCA1 mutations (Holstege et al, 2009; Manié et al, 2009).
Similar(53)
To date, no other CNVs have been described in the ATP1A2 but only point mutations are reported.
Recently, a high frequency of NR5A1 gene mutations was reported in a small group of women with POI.
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].
More suggestions(15)
mutant is reported
transfer is reported
mutations is performed
mutations is taken
mutations is known
mutations is shown
mutations is proposed
mutations is expected
mutations is given
mutations is recommended
mutations is maintained
mutations is likely
mutations is assumed
mutations is limited
mutations is estimated
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