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N-linked glycosylation is the most frequent modification of secreted and membrane-bound proteins in eukaryotic cells, disruption of which is the basis of the congenital disorders of glycosylation (CDGs).
The major emendations in the final versions can be summarized as follows: #The most frequent modification is expansion of the original material.
The most frequent modification was the choice of chemotherapy regimen and the less frequent modification was the use of chemotherapy.
In the experimental group, for breast cancer the most frequent modification of practice concerned less extensive follow-up after treatment.
The most frequent modification was the collection of information on the average duration (in minutes) for mild, moderate, and strenuous LTPA (e.g., [ 65– 65]).
For patients who initiated second-line cART with a detectable HIV RNA, the most frequent modification was from NNRTI to a boosted PI-based (65%) cART (Table 1).
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Root etching was the most common biological modification, and the most frequent modifications are involved with the microenvironments of the surface to burial substrate.
Modifications were most often motivated by mycological results, and de-escalation was the most frequent change.
Cytosine methylation is the most frequent endogenous modification of DNA in eukaryotes and is involved in regulating gene expression [ 1].
Glycosylation is the most frequent posttranslational modification of proteins and lipids influencing inter- and intracellular communication and cell adhesion.
(65) Binary Cr-DNA adducts are the most frequent DNA modifications in the in vitro reductions of Cr VI).
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