Sentence examples for genomic changes caused from inspiring English sources

Genomic changes caused by Agrobacterium-mediated transformation have been reported.

The differences in BAF between orthoxenografts at passage 1 and passage 4 that were not compatible with progressive stromal removal were interpreted as structural genomic changes caused by the successive engraftments (highlighted in Supplementary Fig S4A and B).

Learning more about the most common forms of DNA breakage is important because the genomic changes caused by these breaks are driving forces behind both cancer and evolution, including the evolution of drug resistance in bacteria.

Cumulative evidence has suggested that progressive genomic changes cause the cellular phenotype to progress from the preneoplastic stage to HCC [ 40].

Effectors, avirulence genes and other pathogenicity-related factors often cluster in repeat-rich regions and there are numerous examples implicating TE-mediated mechanisms in the genomic changes causing altered virulence or host-specificity (Kang et al. 2001; Sacristán et al. 2009; van de Wouw et al. 2010; Xue et al. 2012).

This means that the genomic changes that caused wMelPop to become pathogenic must have occurred between wMelCS and wMelPop.

An important consideration therefore is not the genomic changes that cause an increased frequency of plastome reorganization, but what genome changes allow such major plastome changes to persist without being eliminated as deleterious.

The genomic and environmental contributions to transcriptome reorganization indicated a negative epistatic relationship, that is, a negatively compensative relation of the transcriptional changes caused by the two contributors.

Identifying the specific genomic changes that cause gene expression variation is a vital step in understanding phenotypic diversity and the genetic architecture of complex traits.

Approximately 70% of mutant alleles are of missense type; the remainder are null mutations (deletion/insertion causing frame shifting, nonsense, and splice site mutations), large genomic rearrangements, and synonymous or intronic changes causing aberrant splicing.

These changes cause downregulation of Erk pathways.