Sentence examples for future mutations from inspiring English sources

The mutation is then moved higher on the list, as well as future mutations of the mutation, until the spammer is reduced to sending gobbledygook.

In summary, the outcome of selection can be the consequence of two competing processes – selection for enhanced transmission through females and selection for reduced modification in males, where consecutive mutations work synergistically within each class (that is, they ease the spread of future mutations of similar effect) and antagonistically between classes.

Their fate then depends on local values of lCI, t, e, d, and c, as well as on the timing of mutational events: If a costly male mutant arrives first, spreads, and Wolbachia disappears as a result, then future mutations enhancing Wolbachia action (whether through increased transmission rate, increased rescue-function, or a 'nuclear rescue construct') necessarily are of no effect.

The current, and potentially future, mutations in DNAJB6-myopathy patients will be crucial guides in obtaining this knowledge.

One mechanism for this impact is that neutral genetic drift can change a protein's stability and so alter its tolerance to future mutations [ 26- 28].

The combination of in silico and in vitro testing can provide important predictive phenotype genotype guidance for future mutations in this gene.

If this was the case, then the very act of mutating would decrease the future mutation rate.

Since each hemagglutinin mutation potentially sculpts future mutation space, drift can follow many stochastic paths, undermining its unpredictability and underscoring the need for drift-insensitive vaccines.

We observed mutations in all 4 genes, hence we assume that future mutation analysis, be it by sequencing or any other technique, will include the PIK3CA, NRAS and BRAF genes.

The implications of these results for future mutation studies with the aim of increasing the oxygen tolerance of this enzyme are discussed.

Therefore, it may be useful to extend future mutation screenings of MFN2 to patients with early onset forms of hereditary motor neuropathy.