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Injected tendons (MB and PRP-MB) consistently demonstrated disruption of normal tendon morphology compared to control tendons (needlestick).
Finally, spectral-domain optical coherence tomography (SD-OCT) demonstrated disruption of the subfoveal photoreceptor inner segment outer segment (IS OS) junction with possible RPE perturbation (Fig. 4).
In three-dimensional cultures, AdECadEC-infected cells demonstrated disruption of tissue architecture, loss of cell cell adhesion, and the invasion of individual tumor cells into the stroma.
Cell studies using metastatic breast cancer cells demonstrated disruption of Src kinase involved in the cancer migration by albumin dasatinib nano-shell and generation of photoactivated oxidative stress by mTHPC-PLGA nano-core.
Chitin synthase gene A of the S. exigua (SeCHSA) is not expressed in the midgut, and our previous research using injection of SeCHSA dsRNA into S. exigua larvae demonstrated disruption of the larval development [20].
This was confirmed by a demonstrated disruption of both glucose and lipid metabolism at both doses.
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(a) Sagittal MDCT image demonstrates disruption of the posterior vertebral line, a small osseous fragment with displacement towards the thecal sac (arrow), and increased interspinous distance (double arrow).
b Oblique axial T2-weighted image demonstrates disruption of the low signal cervical stroma ring (short arrow) and shows the tumour extending into the right parametrium (long arrow).
Axial T2-weighted image demonstrates disruption of the target sign by a mass (block arrow), which extends posteriorly to invade the anterior wall of the vagina (arrows).
(b) Sagittal STIR image demonstrates disruption of the anterior (white asterisk) and posterior longitudinal ligaments (white arrow) and severe injury to the ligamentum flavum and intraspinous ligaments (black asterisk).
We here present a case of MEWDS both classic in appearance on posterior segment photography and angiography with SD-OCT studies clearly demonstrating disruption of the IS OS junction with preservation of other outer retinal layers.
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