Sentence examples for mutations after a from inspiring English sources

These mismatches will give rise to mutations after a round of replication that can be deleterious or silent.

The 2006b variant appears to have emerged from an earlier strain that had accumulated more mutations after a long period of stasis.

Our results do, however, argue against a hypothesis that has often been raised in the literature: too much stability is bad, so selection for constant stability actively favors destabilizing mutations after a stabilizing mutation.

Genetic variants responsible for changes in mean YFP expression as small as 3% relative to the wild-type genotype were then successfully mapped despite their significant impact on fitness and confirmed using allele replacement, showing that BSA-seq is a powerful method for identifying small effect mutations after a mutagenesis screen.

An early study from Senegal showed that 12.5% had one or more drug resistance mutations after a median of 30 months on ART [ 26], whereas a recent study from Côte d'Ivoire found 22% resistance after a median of 37 months on ART [ 27].

Here, we examine the influence of experimental design and mutational properties on the mapping success of BSA-seq when the density of segregating sites is low, with the goal of providing a general framework for large-scale mapping of small effect mutations after a mutagenesis screen.

To determine the average number of family members diagnosed with a Fragile X Mental Retardation-1 (Fmutationafter after a proband receives the initial diagnosis of fragile X syndrome (FXS).

To clarify, this result provides a quantitative prediction of the ratio of the frequency of a neutral mutation after a generation to the rate of such mutations.

While the discussion so far has focused on known BRCA mutation carriers, it is important to emphasise that simply relying on the presence or absence of a BRCA mutation after a genetic test is an inadequate assessment of a woman's likely future cancer risks.

These proposals are supported by results showing the elimination of a severe mtDNA mutation after a number of generations (Fan et al. 2008), or by low nonsynonymous/synonymous substitution (dN/ dS) ratios observed in mtDNA sequences over generations (Stewart et al. 2008).

In 1998 Schott et al. [ 73] found two NKX2.5 mutations after mapping a chromosomal locus in families with ASDII.