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So, WHO took control and said, "This is a very dangerous epidemic, it can be stopped only by stopping transportation between Point A and Point B". So, flights were grounded, and because of the existence of WHO labs throughout the world collected samples, they did research, and the DNA of the SARS was decoded.
"But when they came back to take cell samples, they didn't explain properly to the Lackses what was going on," says Skloot.
Not only did they do the blood samples, they did a developmental study, and they also confirmed that the chemicals that they're finding in our bodies are the ones that are causing developmental delays.
Although bacteria were present in a few urine samples, they did not interfere with the scoring [see also Supplemental Material (doi 10.1289/ehp.1001959)].
Even though they presented compelling evidence for the presence of three divergent ITS2 types among their samples, they did not envision in their article the possibility that cryptic Pocillopora species may be present but rather decided to attribute the observed molecular diversity to interspecific hybridization.
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With few specimens to test, some companies are taking the virus samples they do have -- or just viral RNA snippets, which are safer to use -- and in the laboratory are putting them in specimens taken from people without SARS to see if the tests can detect the virus.
On top of that, some of the top design talent lives outside the U.S. and don't have a showroom or office here, and so the samples they do have are far away and unavailable at a moment's notice when an editor decides to add a plus look to a fashion story.
Two illustrations of this are that, first, fixed and unfixed cells cluster together based upon differentiation stage, not based upon degree of fixation, second, even though hESC and d5CXCR4+ are unfixed, unstained samples, they do not cluster together.
Therefore, while normal PCs or a second malignant clone may be present in these samples, they do not represent a clonal population that can be detected by Ig HC V region PCR.
In addition, although these methods can demonstrate the presence of estrogenic chemicals in environmental samples, they do not address whether chemicals are being absorbed and producing an effect at the organismal level.
Although relative quantification methods are useful to compare the same proteins between multiple biological samples, they do not provide the possibility to directly compare the data with other datasets or compare different proteins within a dataset with each other and they, by definition, do not provide absolute quantitative data.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com