Sentence examples for mutations in question from inspiring English sources

First, researchers have to establish that the mutations in question actually are essential to the tumors' growth, said Dr. Bruce Evan Johnson, a lung cancer researcher at Dana-Farber and an author of the new paper.

As the authors rightly point out, to date the somatic mutations in question and under investigation have only been elucidated from PBMCs of MS patients.

First, general-population screening data are not available for these diseases in this population; consequently, statistics are often derived from targeted study populations enriched in the mutations in question.

For ~4 % of all the missense/nonsense mutations reported in the literature during 2012, it was necessary for the HGMD Curators to contact the original authors to obtain correction and/or clarification of the nature or precise location of the mutations in question.

Several of the TERC mutations have previously been assayed for telomerase activity in an in vitro fibroblast line system using co-transfection of plasmids bearing TERT and TERC with the mutations in question and these results have been noted (Table I).

The laboratory could not give the findings with 100percentt certainty because the mutation in question could be less common in other parts of Africa.

Then, as that species diversified to occupy new ecological niches with the assistance of the mutation in question, it would come to be found in a group of species that had a common ancestor.

Modification of Wolbachia action by the host is controlled by one nuclear locus with two alleles, one being the wild-type, the other the mutation in question.

Our study systematically enlarges on these concepts and shifts the focus to the evolutionary fate of Wolbachia-infections. We allow for the whole range of host modification with effects from 0% to 100% and further introduce a survival cost incurred by those males carrying the mutation in question.

Importantly, however, the ethnic background of the family or the individual where the mutation is found cannot be always indicative for the likely mechanism that resulted in the mutation in question.

This group was heterogeneous, consisting of members of BRCA1, BRCA2 and other cancer predisposing mutation families, some of whom carried the mutation in question and some of whom did not.