Further studies are in progress to characterize the expression levels of this 59-kDa serine protease in V. cholerae strains of both El Tor and classical biotypes.
These distinct binding patterns implied that these antibodies may recognize different sites of the target molecule, which are unequally exposed in the different ELISA formats, and work is now in progress to characterize these clones further.
Further studies are in progress to characterize these polymeric fractions.
Additional studies are in progress to characterize nucleotide sequences of all CPV isolates from this case.
Further studies are in progress to characterize some of these biomarkers to shed light on the basis for their selection.
Work is in progress to characterize the role of these proteins, including using localization with GFP fusions and knockdowns.
Studies are in progress to characterize the neuraminidase, M2, and HA2 proteins to determine the molecular basis responsible for antigenicity differences observed within isolates from this outbreak.
More detailed spectroscopic and theoretical studies are in progress to characterize the other redox states of 1– 3 and to clarify the electronic structures of radical species based on thea n − and related bis- and tris(dioxolenes).
Therefore, efforts are in progress to fully characterize these unknown sequences and to determine their identity and relationship to the immune response of holothurians.
We have already shown that a large fragment of EML3 binds tightly to DYNLL and studies are in progress to further characterize the DYNLL-EML3 interaction and to determine its possible function.
Further studies are in progress to better characterize the muscle involvement in these three mouse lineages using MRI.
