Post-compression transmission electron microscopic analysis revealed anisotropic deformation mechanisms.
Microscopic analysis revealed changes in cell surface architecture and reduced thickness upon DTBP treatment.
Fluorescent microscopic analysis revealed significant cell-to-cell heterogeneity in biopolymer accumulation.
Electron microscopic analysis revealed that this pattern was due to the accumulation of DGL-α in dendritic spine heads.
Electron microscopic analysis revealed dilatation of T-tubules and degeneration of mitochondria in cardiomyocytes of Bmx/CA mice, which are similar to the changes observed in mice with decreased neuregulin-ErbB signaling.
She also offered hard evidence: a book of stamps that microscopic analysis revealed to be the source of the stamps on the three letters.
Atomic force microscopic analysis revealed funnel-shaped pore channels in the shell layer which may contribute to the entrapment of HB-VLPs.
Microscopic analysis revealed that cells grew both attached to the substrate and in suspension, forming three-dimensional structures like mammalian stem cell aggregates.
In addition, microscopic analysis revealed that the characteristic dislocation microstructure of a virgin specimen fatigued at constant plastic strain amplitude is never observed after prestraining.
Flow cytometric and scanning electron microscopic analysis revealed d-peptide B disrupts mouse myeloma membrane construction, whereas no cytotoxic effect on normal leukocytes was observed.
Field emission scanning electron microscopic analysis revealed that the average grain size of the thin films decreased with an increase in the Ti Cd molar ratio.
