Sentence examples for mutations trigger the from inspiring English sources

Although different mutations trigger the retinal diseases studied, we observed commonalities in the miRNA expression pattern that appear to be associated with the PR cell death kinetics.

Even if ibm1 and ddm1 mutations trigger the hyper-methylation by different mechanisms, these pathways may converge on overlapping targets, with possible interactions of different layers of epigenetic marks.

Our results show that although different mutations trigger the retinal diseases studied, there are commonalities in the miRNA expression pattern that appear to be associated with the PR cell death kinetics.

Considering that the HFS missense mutations lead to CMG2 ER retention, an alternative possibility could have been that these mutations trigger the unfolded protein response (UPR; Ron & Walter, 2007), which in turn would cause the disease.

These results demonstrate for the first time that OPA1 mutation triggers the upregulation of NMDA receptors expression.

Its mutation triggers the differentiation of non-colored plastids into chromoplasts with an increased capacity to accumulate β-carotene in cauliflower and potato.

The discovery of the JAK2 mutation triggered the development of molecular-targeted therapies for the MPNs, with this especially applying to MF, given the lack of an appropriate therapy for many of these patients.

Failure of the mechanism of the oxidant-mediated inhibition of the catalytic action on Ras (i.e., by Ras Cys mutation) triggers the two simultaneous, but unrelated, signaling events that result in overactivation of wt Ras.

This study shows that nec1 mutation triggers the induction of H2O2 and SA, restricts Bgh microcolony formation and affects non-host resistance against Pseudomonas syringae applied at high inoculum density, whereas it has no effect on Bgh penetration efficiency or mlo-dependent race non-specific Bgh resistance.

Thus, these data support the hypothesis that CLN6 and CLN3 mutations trigger distinct processes that converge on a shared pathway, which is responsible for proper subunit c protein turnover and neuronal cell survival.

In a few hundred families worldwide scientists have pinpointed a few rare gene mutations which trigger the disease across many generations.