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The crust mantle boundary (Moho) is ubiquitously imaged, and we occasionally observe structures that may represent the base of the continental lithosphere or other thermal, chemical, or viscous boundaries in the upper mantle.
We occasionally observe these and other atypical shapes in cumulative distributions.
In addition, we occasionally observe patients with familial aggregation (48, 49).
Indeed, we occasionally observe hemifusion at neutral pH even with X31-HA WT virions (see Video 9).
We occasionally observe affected siblings or relatives with neurodegenerative diseases, which raises the possibility of involvement of genetic factors in these diseases.
We occasionally observe large gaps in sequence read profiles, possibly due to repetitive regions in the genome to which reads cannot be mapped uniquely, or to sequencing artifacts.
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We occasionally observed C60 molecules arranged in a line along the sidewall inside SWCNTs with large diameters/width (>7 nm), indicating that large diameter SWCNTs were sometimes flattened.
We occasionally observed this phenotype following TVC-specific misexpression of Vegfrdn, which significantly reduced cell sphericity and produced a small increase in the average fraction of TVC surface in contact with the epidermis (Fig. 5a c).
During the stretching of unit I of the dimer in either type of the experiments mentioned above, we occasionally observed a force peak having the force of about 0.5 0.7 nN when extension length reached 40 50 nm.
In highly blistered areas, we occasionally observed open/burst blisters (Fig. 2e).
Under the cap we occasionally observed small blood clots or patches of cloudy, presumably necrotic cells.
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