Sentence examples for mutation in question from inspiring English sources

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

Most patients who have cancers with the mutation in question have no idea; to find them, large groups of cancer patients must have their tumors genetically tested.

For instance, you could sequence a patient's genome and then create an entire organoid with the mutation in question to test whether it was the root cause of the condition.

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.

The mutation in question has been found in as many as one-third of all Parkinson's cases among Ashkenazi (European descent) Jews and North African Arabs, whose common Semitic origin places the two ethnic groups closer together, genetically speaking, then some might think.

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.

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.

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).

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.