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The frequency of c-CBL mutation was highest in large cell carcinoma (14.7%; 5 of 34 patients) followed by squamous carcinoma (6.3%; 2 of 32 patients) and the least was observed in adenocarcinoma (AD) (1.8%; 1 of 53 patients), although these rates were not statistically significant (p = 0.292).
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The prevalence of the pfmdr1 86Y mutation was higher after treatment with AQ+SP than after SP, p = 0.002.
Frequency of L1014S point mutation was high for An.
The frequency of p.N34S mutation was higher in the group with severe disease (15/164; 9.1 %) and with alcoholic etiology (21/229; 9.2 %).
In our study of patients with advanced disease, the serum ferritin cutoff for the diagnosis of HFE-HH mutation was high at 2,685 ng/mL.
Also, the frequency of mutation was higher in exon 2 than exon 1 (3 cases in exon 2 compared with 1 case for exon 1).
In this study, we demonstrated that frequency of KRAS mutation was higher in LST-G than in LST-NG or polypid tumors.
The incidence of the EGFR driver mutation was higher in Asian NSCLC; 32% in Asians while 7% in non-Asians (Mitsudomi and Yatabe, 2007).
As shown in Table 3 > -wrap-foot>, the frequency of frameshift mutation was higher in PG carcinomas (66%) than in NPG carcinomas (0%).
Specifically, the frequency of L444P mutation was higher in the late onset PD (LOPD) cases compared with that in control subjects.
The frequency of the exon 3 T to C mutation was higher in cancer patients than in controls (odds ratio 3.8; 95% confidence intervals 1.8 8.0).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com