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This approach allows simultaneous illumination of the contributions of voltage and calcium-driven instability to total cellular instability as a function of cycle-length.
The approach allows simultaneous detection of pharmacologically active compounds and their metabolites [4, 19], supporting pharmacokinetic (PK) and pharmacodynamic (PD) developments in the pharmaceutical industry, e.g., contributing to PK screening [23, 24].
While that approach allows simultaneous evaluation of bivariate relationships, the separate PCAs and correlation circles allow for simultaneous examination of covariation among multiple immune indices.
This approach allows simultaneous quantification of precursor cell number and cell renewal, and is amenable for live-imaging and genetic analysis (Fig 1D, and below).
This approach allows simultaneous but separate modeling of the daily within-person fluctuations and the between-person differences to yield both within-person and between-person factor structures.
We have shown that this approach allows simultaneous visualization of the transfection of tibial cranial muscle and knee joint area in the same mouse.
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This approach allowed simultaneous mechanical testing and imaging of collagen fibers without traditional destructive fixation methods.
This approach allowed simultaneous multi-tissue regulation and CNS-directed stable transgene expression without detectably perturbing the endogenous miRNA pathway.
This approach allowed simultaneous detection of 10 CV autoantibodies targeting the structural myocardial proteins, the neurohormonal regulatory proteins, the vascular proteins, and the proteins associated with apoptosis and coagulation.
This approach allowed simultaneous detection of the substrate and the product without interference by other compounds.
This approach allowed simultaneous real-time qPCR analyses of the mRNA levels of 84 relevant genes, normalized to five different reference targets (β2-microglobulin, hypoxanthine phosphoribosyltransferase 1, ribosomal protein L13a, GAPDH and β-actin).
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