Using this method, we were able to measure the pH at which both 1 and 2 start to become NMR-invisible.
By means of this method, we were able to estimate the coordinates of the receptive field centre, as well as the receptive field size, of each voxel.
Using this method we were free to generate about 2 octaves of notes enabling us to add a variety of music to our game.
Applying the PCR method, we were able to detect as low as 0.15 trypanosome ml−1.
Using this method, we were able to screen for CD8+ T-cell recognition of 1183 peptides expressed in hypocretin neurons and detect such cells in both NT1 patients and healthy controls.
Using this method, we were able to rapidly identify clinically actionable drug sensitivities for several ovarian cancers and high-grade serous tumors by testing two different drug concentrations and a library of 240 protein kinase inhibitor compounds.
Highlighting the universal applicability of our method, we were able to quantify and compare the hydrophobic adhesion for all strains, ranging from the short rod-shaped Plantibacter L1 (0.7 × 1.2 µm) to the chain-forming Bacillus L13 (1.4 × 3.7 μm).
Using this method, we were able to measure the spectra of electrons emitted solely as a result of Auger transitions and free of beam impact-induced background down to 0 eV.
With a mini-plot method we were able to assess the decomposition dynamic of chars with few operational costs.
With this method we were able to identify even minor speed changes in several angular positions for the chosen events.
Using the O18 diffusion method we were able to observe several deformation modes (diffusional creep, gliding at the interfaces, etc).
