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Using this method, we quantified the amounts of TG in mouse liver and found that the measured total mass of TG correlated with that obtained by enzymatic methods.
Using the LC-MS method, we quantified the levels of hmC and mC in parallel using the isotope-labeled derivative [D2]-hmC.
In addition, through using a real-time polymerase chain reaction method, we quantified hydrocarbon-degrading bacterial traits based on their catabolic genes (i.e. alkB (alkane monooxygenase), nah (naphthalene dioxygenase) and tol (xylene monooxygenase) genes).
Using a large-scale computer-assisted imaging method, we quantified endocrine cell mass and islet cellular composition.
In the second method, we quantified the number of catalytic turnovers based on fluorescence intensity trajectories of individual zeolite domains.
Using this method, we quantified expression per genome in the allotetraploid (T2) and its diploid progenitors (D3 and D4) for seven different genes or gene families (table 1).
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Using the replacement cost method, we quantify the direct consumptive value of aquatic species and sites for indigenous subsistence in three Australian tropical river catchments where negligible data exists on indigenous water values and the extensive use of wild resources for food, art, craft and medicines.
Methods: We quantified miRNA expression in urinary sediment of 56 CKD patients who underwent kidney biopsy.
Methods: We quantified markers of inflammation in 1,163 serum samples from 580 men.
In Methods, we quantified the cold-hot annotation of each TCM medicinal by assigning a seven-level cold-hot score to it.
In order to examine the consensus across multiple sources and prediction methods we quantified the overlap of drug drug-event associations or drug drug-event associations
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