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Further, this NEMO modification contributes to TRAF6-mediated activation of NFκB.
H3K4 trimethylation is a marker of transcriptional active chromatin, and this modification contributes to gene activation [64].
What remains to be determined are how each histone modification contributes to chromatin configurations and the control of Pol II movement, which trans-acting factors lay down the marks, and whether the marks facilitate recruitment of additional factors during the three phases of transcription, and during co-transcriptional splicing.
Whether this modification contributes to the stability of cytosolic proteins such as THB1 is not known.
Moreover, epigenetic deregulation, especially histone modification, contributes to the deregulation of HOX genes in cancer.
Promoter methylation, along with histone modification, contributes to MT1G inactivation in thyroid tumorigenesis.
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We hypothesized that taxon-specific gene modification contributed to the evolutionary steps in coleoid cephalopod camera eye development.
Proteomics facilitates the identification of new biomarkers of chemical exposure and studies of mechanisms by which protein modification contribute to the adverse effects of environmental exposure [ 73, 74].
The conducted research has demonstrated that each of the proposed modifications contributes to increased age estimation precision according to the MAE metric.
Genetic modifications contribute to the occurrence of prolapse (proof level 2).
Structure of a typical bacterial cell, showing the cell wall, a plasmid, and other components that are susceptible to modifications contributing to the development of antibiotic resistance.
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