Sentence examples for common imprint from inspiring English sources

On the other hand the resist was specially designed for the use in combination with Polydimethylsiloxane (PDMS) stamps, its negligible propensity to permeate into the stamp material under contact leads to an improved stamp life time compared to the use of common imprint resists.

This is due to the fact that potential selection will affect only certain loci, whereas population demography and -history will leave a common imprint across all neutral loci [ 24].

Two fundamental questions will naturally arise from this discovery: how common are imprinted genes of this type and how strong is the evidence for their existence in humans and other organisms?

However, KDM1B and transcription through DMRs account for genomic imprinting at defined regions and are not common to most imprinted regions.

Difficulties to identify new imprinted genes partially rely on the lack of strict characteristics of sequence, gene organization, etc., common to all imprinted genes and that could be used as criterion to identify new candidates.

INS may be the fourth marsupial imprinted gene to be associated with a DMR [ 47, 82, 83] and, if so, provides further evidence of a common origin of imprinting mechanisms in therian mammals.

This is likely due to the incomplete silencing of maternally imprinted alleles, which is a common phenomenon for imprinted loci [20], [21], [22].

Co-regulation of these genes could be mediated by common regulatory elements in imprinted regions or by imprinted microRNAs.

One problem surrounding any discussion of the loss of imprinting is common to all theories: we don't know how the acquisition of imprinted expression affects the subsequent evolution of imprinted genes.

It improved its search ability by distilling common features of known imprinted genes and contrasting them with characteristics of 552 genes that are never imprinted.

Our preliminary analyses also show, that common dysregulation patterns for imprinted genes throughout the genome can be described in SRS patients with different epigenetic alterations, suggesting that these patterns are associated with the clinical phenotype.