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In this respect, a glycoform analysis of a Manase mutant could provide further information.
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Structure-guided functional investigation of cysteine mutants could provide the physiological implications of the disulfide bond and could allow us to design potential inhibitors for the better treatment of intestinal amebiasis.
Consequently, an analysis of the relevant mutants could provide important insights into the regulation of glycan synthesis.
Therefore, detailed comparisons of three-dimensional structures of wild-type PrPC and its mutants could provide valuable insights into the underlying molecular mechanism of prion conversions.
Experimental verification of the dimer mutants could provide a valuable tool for confirmation, falsification and/or model refinement.
Within this context, the cdipt mutants could provide an excellent platform for preclinical in vivo whole-organism studies evaluating the therapeutic potential of such compounds in ameliorating epithelial injury and inflammation.
If sufficiently stable, this mutant protein could provide important clues about the nuclear function of FBXO7 that is lost in PARK15.
Generation and maintenance of continuous genetic variation may lead to partial protection and escape mutants, which could provide a "pump" that generates more variants and "new" viruses.
Nevertheless, our 2GS data of third-generation mutants also could provide the literal effect of EMS mutagenesis throughout the individual genomes.
Consequently, if dHb neurons are born early on both left and right in tcf7l2 mutants, then this could provide an explanation for the increased presence of dHbl neurons in the right dHb.
Further studies on other BE mutants and their amylose CLD could provide evidence for or against this inference.
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