Sentence examples for variants is particularly from inspiring English sources

Mining sequence data for pharmacogenetic variants is particularly appealing in pediatric patients as it serves as an example of predictive and individualized medicine.

The question of mutability to a phenotype in a pool of variants is particularly relevant to Ctf/CIN phenotypes because of their functional relationship to oncogenesis, where a presumably random mutation initiates a CIN phenotype.

Given that the low transmission of visible light in organic tissue is one of the major obstacles in optogenetics, red-shifted ChR variants are particularly important, as longer wavelength light allows deeper tissue penetration.

These alienation variants are particularly relevant for adolescent health research as the feeling of empowerment and having supportive social relations, are important aspects of a positive youth development [2, 3, 6].

In Caucasians two such variants are particularly common: 2282del4 and R501X with originally reported carrier rates in general population of ∼2 and 6%, respectively [2].

The variants are particularly relevant to the development of hip OA in females.

Moreover, these variants are particularly more sensitive to low dox levels.

It is possible that genetic factors modify the association between EPT and MD, and that certain genetic variants are particularly important in determining MD in hormone users.

The non-synonymous SNPs (nsSNPs), also called missense variants, are particularly important since they result in an alteration of the amino acid sequence of the encoded protein.

There are, therefore, striking similarities between the D-repeat and rs143383 associations; the obvious similarity is that when it comes to lower-limb OA, both variants are particularly relevant to knee disease, but when it comes to early development, the hip is the main repository of the genetic effect.

Prematurely truncating mutations (by frameshift or nonsense variants) are particularly common in SDHD, and one study found that these mutations were associated with a significantly increased risk of phaeochromocytoma or sympathetic PGL compared to missense mutations that were not predicted to impair protein stability (Ricketts et al. 2010).