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The mutational analysis of the kinase domain of EGFR revealed the presence of mutations in 2.6% of 77 gastric carcinomas.
The identity of the constructs and the presence of mutations were verified by DNA sequencing (Evrogen, Moscow, Russia).
To determine the presence of mutations in the NXF2 gene of patients with nonobstructive azoospermia.
H-ras and p53 genes were examined for presence of mutations using direct DNA sequencing.
When IM was added to IS3si treatment, the repression of cell viability was observed regardless of the presence of mutations within ABL1 kinase domain (Fig. 2d f).
In particular, the findings show that too few women with ovarian cancer are tested for the presence of mutations that could be used to guide health care decisions.
The first are tests designed to detect the presence of mutations in the human genome that are associated with specific diseases.
The presence of mutations was analyzed for an association with hematologic phenotypes, survival, and cardiovascular events.Detectable somatic mutations were rare in persons younger than 40 years of age but rose appreciably in frequency with age.
Shifted bands were sequenced to confirm the presence of mutations.
DNA sequencing analysis verified the presence of mutations in corresponding XP genes (Fig. 1A and 1B).
Additionally, the genotypic presence of mutations is not necessarily associated with clinical resistance.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com