We justify the procedure here because: 1) the modifications are limited to items within the same factor; 2) the modifications were limited to error correlations for sequential items, and 3) only 10 of the 406 error correlations among the 29 items were freed.
Because the modifications were only observed in Chlamydomonas Rubisco, they might account for the differences in kinetic properties between the algal and plant enzymes.
This was surprising because the modification was not near an anchor residue.
The analysis of PTMs, on the other hand, is challenging because those modifications are usually in low abundance, complex or transient in nature.
Indeed, this finding is consistent with the observation that post-translational modifications of proteins only rarely contribute to the cognate T cell epitopes bound to class II MHC [15], [16], [17], perhaps because these modifications are removed in lysosomes.
This is because the gene modifications are crafted based on knowledge of what genes do, in contrast to the shotgun approach of traditional breeding or using chemicals or radiation to induce mutations.
The modification was required because, in some species, the proportion of bridging females was equal to zero, and the SDI index is undefined when the minimal value (the denominator) is zero.
Because the payment amount under the modification is less than what the borrower previously paid, the computer assesses a late fee.
The modification is convenient because of mild reactions and wide applicability.
The modification is required because of the intricacies of DVB-T2 signal in case the CFO is equal to, or more than, three times subcarrier spacing in the presence of Rayleigh channel and with strong noise.
