In conclusion, the genomes of mutans streptococci display remarkable differences, especially among different species.
Somatic cells and pluripotent cells display remarkable differences in most aspects of cell function.
By antimicrobial activity tests, peptides representing paralogs in the same family of cecropin and moricin families, displayed remarkable differences against 10 tested bacteria.
There are two genes (ileRS1 and ileRS2) in P. fluorescens which display remarkable differences.
In spite of their similarities, these proteins display remarkable differences both in length and amino acid composition of the carboxyl-terminal region (Fig. 1), which could underlie different structural and/or functional roles.
Although all the animals described above had comparable AQP4-specific antibody titres in their serum (data not shown), they displayed remarkable differences in the formation of additional lesions: After intrastriatal injection of CXCL2 and supplementation of the immune system with NMO-IgG, 2/9 animals displayed small perivascular lesions with AQP4 loss and neutrophil infiltration.
However, individual compartments of mucosal components of the immune system display remarkable differences with respect to dominant antibody isotypes, virus phenotypes, densities and origins of cells involved in innate and specific immunity, presence or absence of inductive sites, and routes of immunizations that induce humoral and cellular responses.
Candidate D displays many remarkable differences from M in the sectoral harmonics while candidate E shows anomalous coefficients, particularly at degrees n = 11−13.
Scanning electron microscopy showed clearly more accumulations of cellular blood elements and an increased aggregation of leukocytes on the UC-surface, compared to AO and TR, which in between displayed no remarkable differences.
As shown in Figure 6, the SERS spectra of LasRLBD forming a complex with either C12-HSL or C4-HSL, resemble that of ligand-free LasRLBD but display some remarkable differences: reduction in SERS intensity at 448, 690, and 788 correspondingnding to the C-terminal cysteine and appearance of additional peaks at 408, 1405 and 1630 cm 1.
