Sentence examples for mutation is mostly from inspiring English sources

The mutation is mostly found in the Dutch population [ 8, 20], and it is absent or very rare in other populations [ 16- 19].

It has been reported that G → T somatic mutation is mostly observed in oxidative stress-associated tumours such as lung, breast, ovarian, gastric, and colon cancers.

Indeed, β-catenin mutation is mostly confined to endometrioid adenocarcinomas where it is predominantly expressed in the nucleus, whereas, in serous and mucinous OC, aberrant β-catenin expression is chiefly cytoplasmic.

In homozygous mutant females, oogenesis was stopped a little earlier than in germline clones, but the phenotype was nearly identical, indicating that the effect of the mutation is mostly germline-dependent (data not shown).

Although AβOs generated by the Osaka mutation are mostly intracellular, picomolar amounts are released from cells (ELISA data; this study).

K-ras mutation was frequently detected in tubulovillous adenomas (24 out of 40, 60%), while BRAF mutation was mostly observed in serrated adenomas (5 out of 8, 63%).

The scarcity of empirical studies testing the dominance effect of adaptive mutations is mostly due to the difficulty of identifying adaptive mutations and their fitness effects.

Current data related to somatic mutations is mostly buried in journals or scattered between several locus-specific databases (LSDBs) and general databases that have no or very limited connections between them.

This observation extends the utility of intolerance scores to indicating where pathogenic mutations are mostly likely to fall within genes.

The PEPD mutations are mostly characterized (nine out of 11) within the S4 segment, S4-S5 linkeregionon, and the cytosolic regions of domain III and domain IV of Nav1.7 except for R185H and R1007C (Fig. 2A and Table 1).

Even in more complex situations where more than two loci are involved and the dominance relationships are not complete, hybrids would still have larger eyes than the parental populations if different genetic changes were responsible for the eye reduction in the two populations and the eye-reducing mutations are mostly recessive.