Sentence examples for mutation screening from from inspiring English sources

Mutation screening from exons 8 through 13 was performed for 816 wild type patients except 1 patient in group 1A, 1 patient in group 1B and 2 in group 2 because the amount of RNA was not sufficient and a new biopsy was denied.

human peptide transporter (SLC15A1) and human glypican5 (GPC5) for mutation screening from this region.

The patient had a normal karyotype, and mutation screening from a peripheral blood sample revealed no gene fusions of FIP1L1-PDGFRα and ETV6-PDGFRβ.

A study of over 45,000 women referred for BRCA1 and BRCA2 mutation screening from 2006 to 2008, found that 13 16 % of African Americans, Native Americans and Hispanics possess disease-causing mutations and a high rate of variants of unknown significance [ 17].

The first study that reported an association between PALB2 mutations and breast cancer risk came from a large case-control mutation screening initiative from the UK involving familial breast cancer cases and unaffected controls from the UK.

Mutation screening started from whole-genome amplified (WGA) DNA for coding exons 1-9 and from genomic DNA for exons 10-14.

Genes may have been identified from mutation screens or from studies of natural variation.

Novel flowering-time genes may be identified in Brachypodium itself from mutation screens or from the analysis of different ecotypes.

Genomic sequences required for mutation screening were inferred from the following cDNAs or EST: Genbank accession AF259801 and TIGR tentative consensus accessions TC126316 and TC126421 for eIF4E genes and TIGR tentative consensus accessions TC167837, TC 156946, TC 165028 and TC155154 for eIF4G genes.

In the positional and brain-expressed candidate genes KIAA0767 and KIAA1646, we searched for variants in the complete exons and adjacent splice-junctions as well as in parts of the 5'- and 3'-untranslated regions by means of a systematic mutation screening in individuals from chromosome 22q-linked pedigrees.

This hypothesis is supported by a recent retrospective study from France of all 165 index cases who had undergone CDH1 mutation screening in their region from 2006 to 2012.