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The presence of the hyperexpression Her-2/neu in cases of "++" reaction is conducted with the help of hybridization method in situ using the fluorescent marker FISH (fluorescent in situ hybridization).
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This indicates that analysis of plasma can be used as a good early nonlethal diagnostic marker of fish intoxication by transition metal ions.
The results of this study emphasized the importance of comet assay and MN test and suggest its broader application as an early biological marker of fish exposure to genotoxic and clastogenic pollutants in aquatic environments.
The association between high Ery-Hg and low MI risk is most likely because Ery-Hg is a marker of fish intake.
We measured total Hg in erythrocytes (Ery-Hg) and long-chain n-3 polyunsaturated fatty acids in plasma (P-PUFA; an exposure marker for fish intake).
Moreover, there is no evidence of the practice to preserve genetic diversity as measured from neutral genetic markers increases fish performance or population viability outside of populations that experience strong inbreeding depression, and limited data that genetic diversity increases the potential for populations to adapt to changing environments.
Mitochondrial DNA (mtDNA) sequences of cytochrome b (cyt b) and 16S rRNA (16S) genes are amongst the most widely used genetic markers for fish species identification [3], [4].
Identification of QTL related to growth is the basis for application of genetic markers in fish breeding.
Given the lack of DNA markers for FISH analysis, detailed molecular karyotype analyses of radish have not yet been conducted.
We therefore aimed to investigate the diagnostic performance of combined applications of the four most broadly available urine markers cytology, FISH, uCyt+, and NMP22 in a large cohort of patients undergoing surveillance for NMIBC.
For the other five elephant-specific markers, RNA-FISH was not conducted in human and mouse because they were close to loci already included in this study.
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