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We will discuss the variation in Section 4.6 when nodes can afford up to a certain level of demodulation cost.
Results show that the profile variables explain only 10% of the variation in Overall score, 10% of variation in Section 1 score, 7% of variation in Section 2 score, and 11% of variation in Section 3 score.
One of the biggest challenges in using phase microscopy for structural analysis of such clinically-prepared cell and tissue samples is decoupling the variation in section thickness from the actual structural changes within the cell or tissue.
To normalize EGFR homodimerization, EGFR or HER2 phosphorylation readouts for cellular content in each tissue section and the variation in section size, tubulin was used as an internal control.
Stereology avoids the need to correct for variation in section thickness and cell size of each case as established in the Abercrombie principle [ 28, 32], with confident, unbiased live counting of neurons at high magnification using 63 or 100× objectives.
However, if a fixed optical depth location inside the sample is chosen such that the variation in section thickness of the sample is outside the coherence length around this chosen location, then δp at this fixed optical depth location, and all the other preceding locations, will not be affected by the variations in sample thickness.
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Sampling of brain specimens is, however, manual work, and thus, a wide range of variation in sectioning levels, is generally seen.
We have explained Bolzano's method of idea-variation in section 3.6 with respect to single propositions.
Caesarean section: The Government is concerned about the variation in caesarean section rates between hospitals and has a programme in hand to address this and the reasons for the rise in caesarean section rate overall.
To our knowledge this is the first study to examine the variation in caesarean section rates among multiparous women with at least one previous caesarean section with a singleton cephalic fetus at term by intended mode of birth and to explore their maternal and neonatal outcomes.
He cites a 1978 paper that showed a link between the gene behind sickle cell disease and a variation in a section of junk DNA.
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