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Electron microscopy analysis demonstrated that LASV GPC pseudotyped virus appeared structurally similar to native virion.
X-ray diffraction and high-resolution transmission electron microscopy analysis demonstrated the nanowire have preferred orientation along [1 1 0] direction.
Confocal microscopy analysis demonstrated punctate distribution of MMP9, MMP9) on the surface as shown in (a).
Immunofluorescence microscopy analysis demonstrated that VPA induced the formation of LC3B puncta in both LNCaP and PC-3 cells (Fig. 1E).
There was no histological evidence of glomerular pathology but electron microscopy analysis demonstrated thin basement membrane disease and effacement of podocyte foot processes.
Fluorescence microscopy analysis demonstrated that production of the fusion protein resulted in the formation of peroxisome extensions akin to those observed in H. polymorpha dnm1 cells.
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The fluorescence microscopy analysis demonstrates that CNT/DNA-Cy5 conjugates were distributed within the cytoplasm and did not affect cell morphology.
Time-course microscopy analysis demonstrates that the cytotoxicity of nanotube/surfactant conjugates is related to the toxicity of the surfactant molecules attached on the nanotube surfaces.
Transmission electron microscopy analysis demonstrates that the alloy consists of micrometre-scale α-Mg solid solution dendrites and nanometre-scale amorphous matrix (80 530 nm in thickness).
Scanning electron microscopy and transmission electron microscopy analysis demonstrate that the flake-like MnO2 thickness (about less than 10 nm) and uniformly distributed on the porous graphene/CNTs framework.
A proposed core shell model coupled with transmission electron microscopy analysis demonstrates that the FV is distributed more heterogeneously with increasing ISRO, which is beneficial for multiplying the shear bands.
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