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That is, if there are n measured frequencies, we pick n frequencies at random (with possible repetitions) and measure CP and CD, then reiterate many times to obtain a distribution, from which we extract the covariance matrix.
For all measured frequencies, we find unambiguous subtle anomalies in the dielectric constant and dielectric loss.
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To address these hypotheses, we measured frequencies of activated (CD38+ HLA-DR+), regulatory (CD4+CD25+CD127dim), HIV-specific, and CMV-specific T cells in a large cohort of HIV controllers.
To address these hypotheses, we measured frequencies of activated (CD38+ HLA-DR+), regulatory (CD4+CD25+CD127dim), HIV-specific, and CMV-specific T cells among HIV controllers and 3 control populations: HIV-infected individuals with treatment-mediated viral suppression (ART-suppressed), untreated HIV-infected "non-controllers" with high levels of viremia, and HIV-uninfected individuals.
We developed a virtual mouse vocal organ that creates appropriate syllable sequences based on age-related changes in several features that we measured: frequency, bandwidth, duration, inter-syllable interval, syllable probability and the sequential pattern (transitional probability).
We measured frequency of reporting of each of the 'hassles'hassles
We measured frequency and breadth of community participation, and perceptions about participation.
We measured frequency tuning in spiking receptors following previously described methods (Lyons-Warren et al., 2012).
We measured frequency and temporal parameters from 230 great calls (mean: 13.5 calls per animal; range: 2 27).
We measured frequency specific changes in evoked spatiotemporal patterns of neural activation in response to non-painful electrical stimuli in adults with and without ADHD.
We measured frequency and duration of agonistic encounters of the resident mouse for the first 3 min upon introducing the intruder.
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CEO of Professional Science Editing for Scientists @ prosciediting.com