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Graph showing nanocomposite distribution in tissues of rats after repeated doses in a 28-day oral toxicity study.
A three-dimensional finite-element computer model was used to describe the stress/strain distribution in tissues of the lower leg during pressure stimulation.
The study investigated the effects of applications of three ammonium fertilizers (NH4NO3, [NH4]2SO4, and NH4Cl) and two chelators (ethylene-diamine-tetraacetic acid, EDTA, and nitrilotriacetic acid, NTA) on soil microbial community structure, and the biomass and metal distribution in tissues of king grass (Pennisetum sinese Roxb), in soils contaminated with Cd, Pb, and Zn.
Figure 8 Graph showing nanocomposite distribution in tissues of rats 14 days after single oral dose administration.. Zinc distribution in rats after single dose of Tween-80-coated zinc-aluminium-levodopa layered double hydroxide nanocomposite (ZAL), tissue collected 14 days after treatment with 2,000 mg/kg (X) and 100 mL/kg of PBS (Z).
FMT enables real-time three-dimensional quantitation of fluorochrome distribution in tissues of live animals [ 27- 30].
As mentioned before, microglial cells in all studied nervous tissues do not express MECP2 at a detectable level, whereas resident macrophages from other tissues, in particular, hepatic Kupffer cells, do express it.As MECP2 is primarily visible in the chromocenters of mouse cells, we studied MECP2 distribution in tissues of a species, which does not possess chromocenters in interphase nuclei.
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A study investigating the distribution of ABV in tissues of PDD-positive birds has demonstrated ABV antigen in follicular cells, which may point toward vertical transmission (9 ).
One of the earliest studies addressed the issue by injecting fixed and stained tumor cells into the left side of the heart in rabbits and determining their subsequent distribution in tissue sections of several organs.
was used for comparing the distribution of S. Typhi in tissues of newborn mice, survival of S. Typhi strains in peripheral human mononuclear cells, in human blood, chlorinated tap water, raw sewage and surface water.
The distribution of BSE infectivity in tissues of greater kudu contrasts with that in tissues of BSE-infected cattle (24, 25 ) but is more like the distribution found in genetically susceptible sheep infected with scrapie or experimental BSE (26 – 26 ).
Peroxisome proliferators-activated receptor (PPAR) gene family members exhibit distinct patterns of distribution in tissues and differ in functions.
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