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The role of terminal and bridging oxygen species is also addressed.
In the present study, we investigated the role of terminal capping (i.e. N-terminal acetylation and C-terminal amidation) on polymorphic Aβ16 21 amyloid oligomer and protofibrils via molecular dynamics (MD) simulations.
Based upon the DFT and TDDFT calculated results of push pull porphyrin sensitizers, named as YD20, YD21, YD22, 2Flu ZnP COOH, and 2Flu ZnP CN COOH, the role of terminal groups in the modification of their electronic structures and related properties are investigated.
The second finding deserving discussion is the role of terminal drop in functional decline [ 15- 18].
Several conflicting reports have been published dealing with the role of terminal galactose residues in modulating IgG activity [11].
To our knowledge, this is the first report that evaluates the role of terminal drop in functional decline among older adults.
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The role of such terminal groups was studied and the results showed that depending on the nature of the terminal groups the monolayers present distinct isotherms due to the different interactions with the water subphase.
Here, the role of the terminal hydrophobic clusters was investigated by means of amino acid substitutions or deletions.
To verify the role of the terminal hydroxyl group in 1 binding to CPA, 2-benzyl-5-benzyloxy-4-oxopentanoic acid 2 was also synthesized and evaluated.
It takes into account the passive as well as active role of a terminal primary source, wall-mounted auxiliary source, open duct radiation impedance, and the effects of mean flow and damping.
Our data strengthen evidence for a role of this terminal complement component in druse pathogenesis.
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