Sentence examples for microscopy studies allowed from inspiring English sources

Microscopy studies allowed us to observe the size distribution of P3HT fraction in PMMA matrix as P3HT PMMA ratio changes.

Second, microscopy studies allowed us to distinguish two types of crystals in the blend samples, which have the short interplanar distances in the stacking direction (along the b axis of P3HT crystal) to be 0.417 (that is characteristic of ball-like structures, see Fig. 5a and Fig. 7) and 0.445 nm (characteristic of lamella structure shown in Fig. 5b), respectively.

Postmortem cytological studies of leptomeninges imprints reveal the presence of trypomastigotes of Trypanosoma sp. Histopathological and electron microscopy studies allowed us to identify an amastigote stage and to reject the involvement of other opportunistic microorganisms as the etiological agent of the SOL.

The electron microscopy studies allow us to address the issue of whether microglia are involved in the phagocytosis of degenerating synapses.

This is in good agreement with the zeolite ZSM-5 dispersion data described earlier by Sprung and Weckhuysen, although the single molecule fluorescence microscopy study now allows to obtain much higher spatial resolution, as illustrated in Fig. 30h.

In confocal microscopy studies, specific BODIPY-TMR-CGP binding allowed clear visualization of β1-adrenoceptors in live cells.

Fluorescence microscopy studies of YOYO-1 stained dsDNA allowed for real-time observation of the digestion from which the enzyme clipping rate and apparent processivity were deduced.

In particular there is a lack of confocal microscopy studies, which have the benefit of allowing us to discriminate clearly between the Ca2+ signals emanating from endothelial cells and smooth muscle cells, while allowing the integrity of the endothelium:vascular smooth muscle interface to remain intact.

Recent electron microscopy (EM) studies have allowed major breakthroughs in understanding the architecture of the regulatory particle, revealing that the additional modules provide a structural framework to position critical, ubiquitin-interacting subunits and thus allow the 26S proteasome to function as a universal degradation machine for a wide variety of protein substrates.

Total internal reflection fluorescence microscopy (TIRF-Microscopy) allows the observation of individual secretory vesicles in real-time during exocytosis.

Quantitative electron microscopy studies have confirmed the loss of the synapses (Jeffrey et al., 2000; Siskova et al., 2009) and allow a study of the morphological events.