Exact(1)
Current theory is that changes in patterns of DNA methylation and histone modification alter the conformation of chromatin and accessibility of the DNA to transcriptional machinery, either by directly introducing steric hindrance or indirectly causing surrounding chromatin to adopt an "open" or "closed" conformation.
Similar(59)
These markers are represented by altered enzymatic activity, changes in protein expression or posttranslational modification, altered gene expression, protein or lipid metabolites, or a combination of these parameters [ 1].
Thus, it is worth exploring whether the attenuation of alveolar repair process or epigenetic modification altering WNT signaling will be candidates for clinical implications.
Pathways leading to pectin biosynthesis and modification altered on epidermal cells transiting to a TC fate (Additional file 13).
To probe whether the c7G modification altered the structure of DNA, the X-ray and NMR (at 15 °C) structures of 5′-d[CGCGAATTC- c7G -CG] were solved.
Adenosine-to-inosine (A-to-I) RNA editing is a widespread posttranscriptional modification, altering the sequence of RNA from that encoded in the DNA.
Although other epigenetic processes such as histone modification, altered chromatin structure, and noncoding RNA may also be important, DNA methylation is the most established heritable epigenetic mark.
Thus, epigenetic phenomena such as histone modification (altered nucleosome conformation) [ 60] or remodeling of chromatin (change of nucleosome position) [ 61] are commonly a required step to achieve gene expression in response to external stimuli.
Our data thus argue that TDP-43 truncation, modification, altered autoregulation or aggregates are not a prerequisite for toxicity and age-related neurodegeneration, which is also supported by data in other model systems (28, 41, 43– 43).
FAMAp:FAMA LGK was tested for its ability to complement fama lethality and defects in GC differentiation, and FAMAp:FAMA LGK -YFP was monitored to determine whether the LC E→LGKmodification altered FAMA's expression, stability or subcellular localization.
These modifications alter chromatin structure through noncovalent interactions within and between nucleosomes, leading to changes in macromolecular organization and promoter accessibility.
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