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The wide homogeneity range for the NbB2 phase allows a similar ultra-thin B-rich tissue phase to form between thin (5 10 nm) columnar NbB2 −x grains also for films with a B/Nb atomic ratio of 1.8, as revealed here by analytical aberration-corrected scanning transmission electron microscopy.
Here, we derive the analytical aberrations when a cover slip is inserted between the sample and the immersion water, as it is the case in most in vivo recordings when a glass coverslip is used to stabilize the brain after exposing it through a craniotomy.
One tube 22, condition 2 was excluded because several analytical parameters showed aberrations that exceeded 3 standardized residuals, and we concluded that this tube did not contain a sample of appropriate quality.
High-resolution transmission electron microscopy was performed in a JEM-ARM200F probe aberration corrected analytical microscope with a resolution of 0.08 nm.
The HRTEM images were taken on an aberration-corrected analytical transmission electron microscopy (ARM200F).
For designing a system with this corrector, analytical expressions for the aberrations are required.
We describe the application of X-ray energy dispersive spectroscopy (XEDS) event-streamed spectral imaging (ESSI) in an aberration-corrected analytical electron microscope (AEM) as a reliable method for the acquisition of ultra-high spatial resolution elemental maps.
The high resolution is achieved via an analytical reconstruction method in which the aberrations of the spectrograph are calculated a priori from the magnetic field maps and used directly to correct the raw data.
Under the small aberration approximations, we give the analytical formula for characterizing the relationship between the sensor signal and the amplitude of the aberration mode.
The relatively small numbers of patients in each clinical subgroup did not allow us to identify association between specific aberrations and clinical characteristics at this time; this may require both more samples as well as novel analytical methods to analyze patterns of similar aberrations.
A better coverage of the genome allows for the identification of more numerous and smaller aberrations that cannot be detected with analytical tools of lower resolution.
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