Sentence examples for mutation shown in from inspiring English sources

Intriguingly, the N451D mutation (shown in blue in Fig. 7a) alone decreased viral transduction of CHO and Pro5 cells (Fig. 6), but when this mutation is combined with the D532N change, viral transduction of CHO cells is synergistically improved.

Preliminary results indicate that the D532N mutation (shown in green in Fig. 7a) may be responsible for this dependence, as the D532N mutant exhibits enhanced viral binding to heparin and significantly increased transduction of CHO cells (data not shown and Fig. 6a, S2).

p.V600E mutation (control, shown in red) can be clearly distinguished from p.V600K mutation (shown in green) and p.V600R (shown in blue).

The decreased sucrose utilization by deletion of cra in EMY-69 was partially relieved by scrR mutation, shown in EMY-70 (Fig.  2c).

Not unexpectedly, the resonance perturbations resulting from the H361Y mutation are very similar (although not identical) to the perturbations resulting from the I522V mutation, shown in the previous supplemental figure.

However, the mutation shown in Figure 4 induces a further decrease of FRET efficiency, a result that is incompatible if complexin were unstructured (in the subsection headed "FRET Analysis").

Mutations shown in the table are more than the number of isolates that were sent for sequencing.

Altogether six of the mutations shown in table 1 were potentially deleterious, being a nonsense mutation, a frameshift insertion mutation, or a missense mutation with FI ≤ −2.0.

Two other tables provide a summary of the statistics in COSMIC for the selected gene and a summary of the mutations shown in the figure.

Several of the mutations shown in figure 4 were consistently present at or above the 1% abundance, without being eliminated by other fluctuations in the population.

As summarized in Fig. 3AB, mutations shown in green (Y61A, H47A, R159A, H259A, H281A, R304A, and F332A) had neither an effect on dimerization, autoproteolysis nor substrate cleavage.