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As in main Figure 1D, each row represents a uniquely modified H3 N-terminal peptide species (residues 1 50 for H3S and 7 50 for H3F), and each dotted horizontal line beneath a bolded residue represents a site where the specified modification was identified.
Each row in the table represents a single, discrete, and uniquely modified H3 N-terminal peptide, and each dotted horizontal line beneath a bolded residue represents a site where the specified modification was identified.
Polymer modification was identified by the master curves of phase angle and rheological black diagrams.
Structure prediction by X-ray simulations was performed and the band structure due to triple bond modification was identified.
This modification was identified in some but not all the PrP chains from the PrPSc of given specie and it was present in the PrPSc of all species tested [10].
The K618R modification was identified in colorectal cancer patients, however the clinical data are rather incomplete.
The desirable modification was identified as restraining of the Bacteroides fragilis flora.
Indeed, and by using peptide mapping MS, this particular modification was identified as amidated proline (AP; P-NH2) and quantified to be present at a level <2 % in GP2013, while being below the limit of detection in originator rituximab.
While no effect modification was identified for HRQoL in the HART trial [ 96], interaction analysis in the COACH trial showed that the intervention was only effective on time to death/readmission and reduced mortality rates in patients without depression [ 100].
The essential components of each element requiring modification were identified and recorded and a template was developed for discipline-specific modification.
The changes in structural and textural properties because of sulfate modification were identified.
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