Sentence examples for mutation but it from inspiring English sources

Both mutations occurred prior to the H274Y mutation but it is only in the past couple of years that they have come together in the same virus to produce a fully potent, drug-resistant strain.

It's difficult to know exactly what he's ­singing beneath the severe Speak & Spell-esque vocal mutation, but it's safe to assume this is Auto-Tune in extremis.

This not only speeds up the process, but also eliminates the need to integrate the reprogramming genes into the chromosome, which is one potential source of genetic mutation, but it's still not clear whether these cells contain fewer mutations than those reprogrammed using viruses.

Antibiotic resistance evolves naturally via natural selection through random mutation, but it could also be engineered by applying an evolutionary stress on a population.

30 Haploinsufficiency may result from a null mutation, but it is possible that there is still KCNQ4 function from the intact allele.

We have demonstrated a family with a possible autosomal recessive RP1L1 mutation, but it is important to note that we have found the mutation only in one family.

What is likely is that the A and M haplotypes vary elsewhere, too, and that some of those variations make a difference to protein composition, and thus to a mouse's success.It is a pity that the team studied silent mutations, but it is hardly a cause for criticism.

The KDM5D protein is, however, quite abundant according to PaxDB database (http://pax-db.org/#!protein/Q9BY66) which could also explain the high number of clustered mutations but it does not explain the Y chromosome link as the YDHS database does.

The structure of double mutant N71S/F124K combines the effects of the two individual single mutations, but it gives a greater selective enhancement of activity with CB1954 over nitrofurazone than either of these, and the highest specificity constant for CB1954 of all the mutations studied.

B-SIFT will fail to recognize most of these as being activating mutations, but it does in fact find many of these as deleterious mutations instead (EGFR L858R B-SIFT = −1, BRAF V600E B-SIFT = −1).

This might be the case for patient LH22, who had homozygous c.164C>T mutations, but it may not cause LCA in patient QT453 since QT453 had homozygous nonsense mutations (G1226X) in CRB1.