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While microscopy identifies the highly infectious multibacillary patients, its diagnostic performance varies depending on the diligence and the work-load of the microscopist, it requires multiple specimens (and patient visits) which leads to significant drop-out of infectious patients, and takes several days to provide results under programmatic conditions [1].
In addition, smear microscopy identifies the most infectious TB patients.
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Ultrastructural immunocytochemical microscopy identified the NTPDase 1 on the parasite surface and in its subcellular cytoplasmic vesicles, mitochondria, kinetoplast and nucleus.
Fracture surface analysis of the SBM modified epoxy via scanning electron microscopy identified the toughening mechanism as cavitation of ∼100 nm spherical micelles, void growth of the epoxy and concomitant matrix shear yielding.
Microarchitectural analysis by scanning electron microscopy identified the production of particulate agglomerates when 10% of ethanol in the scCO2 stream was used and the ability to make porous membranes with different morphologies and mechanical properties depending on the programmed gradient mode and the entrainer percentage (2.5 5%) added to the scCO2 stream.
Confocal microscopy identified the eGFP labeled neuronal cell bodies and axons within the cultured left lung.
In agreement with these molecular findings, ultrastructural studies in vivo using electron microscopy identified the numerous bacteria occupying the apical cytoplasm of infected enterocytes which was otherwise composed almost entirely of free ribosomes and scattered mitochondria [ 29, 33].
Transmission electron microscopy identified the intracellular peri-nuclear accumulation of membrane bound organelles containing amorphous, electron dense material - phenotypic features suggestive of lipofuscin granules, at magnifications of both 7450X and 22300X in both normal and glaucomatous LC cells.
Schuette et al. (2009), using immuno-light and immuno-electron microscopy, identified the presence of callose in the spores of physcomitrella where it was deposited in the inner exospore layer near the expanded aperture region (local expansion of the intine layer) at the proximal pole, suggesting that callose is involved in aperture expansion during wall development (Fig. 2).
Comprehensive transmission electron microscopy analysis identifies the exposure planes of the cube-shaped ceria nanoparticles as {111} crystal planes.
The microscopy identified Mg4Al3Si4 as the most likely precipitate composition, with possibilities for compositional variation within a single precipitate.
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