Sentence examples for mutations and display from inspiring English sources

Exact(1)

This was consistent with data from the The Cancer Genome Atlas (TCGA) database, in which the proneural subgroup of glioblastoma was found to be enriched with IDH mutations and display hypermethylation in a large number of loci [ 28].

Similar(59)

HPV+ and HPV− tumors also exhibit differences in tumor biology, with HPV+ tumors having fewer p53 mutations and displaying reduced association with tobacco and alcohol consumption [ 17, 18].

It inputs raw sequence data (fastq format), identifies drug resistance and lineage specific mutations, and displays related outputs (see screenshots in Additional file 1: Figure S2).

Since almost all chloroplast transcriptomes responded rather sensitively to mutations and displayed complex expression patterns, the characteristic expression signatures of groups I and II or simple quantification of changes in transcript levels could not be used to identify specific defects in chloroplast RNA metabolism.

A study using the APP J20 transgenic mouse – bearing the Swedish and Indiana mutations and displaying increased β-secretase cleavage and increased Aβ42/Aβ40 concentration ratios [ 13] – revealed the presence of SDS-stable monomers through tetramers of Aβ throughout the life of the mice [ 41].

These transgenic mice co-express a total of five familial AD mutations ("5XFAD") and display early (2 months) plaque formation, impaired cognition (4 months), and neuronal cell death (9 months) [35].

The girl's 47-year-old father had the same THRA mutation and displayed short stature with a height 3.77 SDs below normal and acquired hearing loss due to otosclerosis (6, 8).

The Arabidopsis pex4-1 mutant is caused by a Pro123Leu missense mutation and displays a variety of phenotypes suggestive of peroxisome deficiencies, including sucrose dependence, IBA resistance, inefficient PTS2 processing [ 13], PTS1 import defects [ 14], and elevated membrane-associated PEX5 [ 33].

This CRC subgroup has an extremely low frequency of TP53 mutation, and displays overexpression of MDM2 and normal expression of p21, suggesting that deregulation of p53 pathway in this CRC subgroup may be due to other alternative mechanisms than TP53 mutation.

Table of intein mutations and surface display levels for directed evolution round 2 and a Western blot of the MESNA release reaction for the secreted 4 4 20 and GFP as wild-type intein fusion proteins.

As a model, we used Tg2576 mice, which overexpress a human APP transgene containing the Swedish FAD mutation (K670N/M671L), and display the slowest amyloid pathology [ 9] of all the models analyzed by Meyer-Luehmann et al. [ 16].

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