Suggestions(2)
Exact(1)
Figure 5 demonstrates that the CG KI mice and Fmr1 KO mice show a relatively linear progression in deficits as a function of CGG repeat length toward the Fragile X Full Mutation range for spatial and temporal processing.
Similar(59)
The MIC required for isolates with this mutation ranges from 1 μg/mL to 4 μg/mL.
The detection rate for AR mutations in Complete AIS (CAIS) range from 66·7%to83%3%, whereas for Partial AIS (PAIS) patients, the detection rate for AR mutations range from 13·6%to28%8%. 3, 4 AIS is characterized by a clinical spectrum ranging from phenotypically female patients (CAIS) to decreased virilization (PAIS) in 46,XY individuals with normal or elevated androgen levels.
In genomewide studies of polymorphisms in Drosophila, estimated selection coefficients for single mutations range from 0.000012 to 0.02 (Jensen et al. 2008).
Transmission rates for nonfunctional mutations ranged from 13to90%0% for the other 12 gRNA-e lines.
Loomis et al. generated PacBio long reads for expanded CGG-repeat FMR1 alleles in full mutation range [41].
Finally, many parameters, such as population size, crossover rate, mutation rate, range for fuzzy sets, and number of fuzzy rules, which control the GFS could affect the results.
In NSCLC of any histology, pooled frequencies of EGFR mutations ranged from 8.4% to 35.9% for ever/heavy smokers and from 37.6% to 62.5% for never/light smokers, depending on ethnicity (supplementary Table S3, available at Annals of Oncology online).
This resulted in small changes to the estimated relative risks for all LoF mutations ranging from 1.67 (95% CI: 1.34 2.09) to 2.42 (95% CI: 1.97 2.99).
While this would limit our ability to analyze specific codon mutations, we are able to increase the statistical significance for the codon mutation ranges.
A similar mechanism of pathogenesis has also been suggested for FXTAS, which is caused by a CGG expansion in the 5′UTR of the Fragile X mental retardation 1 (FMR1) gene within the pre-mutation range (55 200 repeats) for fragile X syndrome.
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