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Regardless of their heritability, these modifications provide important information crucial for genomic stability and proper DNA methylation; so, for the purpose of this review, we continue to refer to them as epigenetic marks.
Oxidative phosphorylation (OXPHOS), a main source of mitochondrial ROS, depends on respiratory super complexes in mitochondria [ 10], whose reversible phosphorylation and other forms of posttranslational modifications provide important layers of regulation [ 11].
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Therefore, biomarkers of disease modification provide important data about the likelihood of success or failure of new therapies under development.
Thus, the identification of proteins responsible for these modifications will provide important insights for cancer treatment.
Covalent modifications to cytosine provide important epigenetic information required for normal embryo development.
Therefore characterizing the identity and the nature of post-translational modifications of these nucleosomes may provide important clues to the molecular mechanisms of the histone eviction process.
Additionally, both the in vitro inhibition data and computational modeling results provide important information for the modification of andrographolide derivatives as selective inhibitors of UGT2B7.
Indeed, the process of determining the parameter modifications required to accurately simulate different mouse models will provide important quantitative information regarding their integrative metabolic phenotypes and the differences between mouse models.
It can provide important information about the surface changes of the metal after modification with the oil.
The results provide important information for process intensification of inhibitor removal from the pretreated materials and strain modifications for enhancing the capacity for degradation.
Gene profiling studies provide important information for key molecules relevant to a disease but are less informative of protein-protein interactions, post-translational modifications and regulation by targeted subcellular localization.
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