Sentence examples for microscopic analysis demonstrates from inspiring English sources

Gross and electron microscopic analysis demonstrates that polycaprolactone (PCL -derived kidney vascular corrosion casts are able to caPCL -derivedchitecture of normal renal tissue and can serve as a sacrificial template for the creation of a collagen-based vascular scaffold.

Furthermore, flow cytometric and microscopic analysis demonstrates that ROS production is significantly greater in Wolbachia-infected mosquito cells and is associated with endosymbiont-containing vacuoles located in the host cell cytoplasm.

Fluorescence microscopic analysis demonstrates that SC/D-F9 of S. crispus induced cell death of all four breast and prostate cancer cells by apoptosis as depicted by strong reaction of these cells with the Annexin V antibody (green), compared to control (DMSO-treated) cells.

Immunostaining for DGL-α resulted in a widespread punctate pattern at the light microscopic level, whereas high-resolution electron microscopic analysis demonstrated that this pattern is due to accumulation of the enzyme adjacent to postsynaptic specializations of several distinct morphological types of glutamatergic and GABAergic synapses.

Microscopic analysis demonstrated a dose-dependent stimulatory angiogenic effect of microglial cells on vessel branching (Fig 5B C).

Microscopic analysis demonstrated that DMSO had no apparent effect on the melanoma cells after at least one week in culture.

Confocal laser scanning microscopic analysis demonstrated that a portion of the liposome-coupled antigens were taken up and processed beyond the MHC class II compartment.

Confocal microscopic analysis demonstrated the presence of GluR2/3 and GluR4 receptor units as discrete puncta in the inner plexiform and outer plexiform layers, but these could not be colocalized on the surface of microglial cells in rotational views (Fig 6D).

Confocal laser scanning microscopic analysis demonstrated that antigens coupled to the surface of unsaturated-fatty-acid-based liposomes received processing at both MHC class I and class II compartments, while most of the antigens coupled to the surface of saturated-fatty-acid-based liposomes received processing at the class II compartment.

Microscopic analysis demonstrated that aortic allografts from recipients treated with donor apoptotic cells exhibited considerably lower amounts of locally deposited IgG (end-titer 1∶25) and C3d compared to grafts from recipients untreated (IgG end-titer 1∶400), or injected with BALB/c splenocytes alive (IgG end-titer 1∶400) or necrotic (IgG end-titer 1∶200).

Indeed, microscopic analysis demonstrated that less than 0.5% of the cells were still engaged in mating (data not shown).