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The binding affinities of the peptides to duplex DNA are shown to be related to the structural changes that they induce.
Details of single-spore (NZFS 2411, NZFS 2421, NZFS 2425, NZFS 2426 and NZFS 2432) and multispore (NZFS 171 and NZFS 2418) isolates of A. sp. nov. (New Zealand Forest Research Institute Culture Collection) used to obtain DNA are shown in Table 1.
Recent surprising findings about the driving forces for natural assemblies, such as DNA, are shown and a representative thermodynamic data for synthetic complexes and assemblies are highlighted to equip the reader with an up-to-date knowledge of promising strategies for the rational design of self-assembling systems in water.
Representative bivariate plots of cyclin B1 versus DNA are shown in Figure 7A.
Histogram data indicating percentage of cells with sub-diploid DNA are shown and are mean ± SD of three independent observations.
The results of ROC analysis in the stool DNA are shown in Figure 2. Table 4 shows the sensitivity/specificity of each gene for colon cancer detected in stool DNA samples.
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Only the backbone of the forward strand DNA is shown.
A primarily intercalative mode of binding of NHM with DNA is shown.
Consequently, as soon as a piece of junk DNA is shown to have a function, some scientists will say (logically enough) that it's not junk.
The largest-occurring lung tissue DNA putative adducts were 90% similar (n = 50), while putative adducts in esophagus tissue DNA were shown to be 80 and 84% similar to central and peripheral lung tissue DNA respectively.
Heteroplasmy of mitochondrial DNA was shown even in Bathymodiolus [50].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com