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Minor differences in the ranking and range of TCDD blood concentrations occur when comparing estimated peak concentrations using the one compartment classical pharmacokinetic model to blood concentrations measured in 1982.
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23 Table 2 describes the application of PK/PD models to blood pressure, heart rate, and contractility effects.
We used residence-specific environmental lead measurements from three epidemiologic datasets as inputs for the IEUBK model to predict blood lead levels, and compared these predictions with blood lead levels of children living at these residences.
This research will investigate blood inventory management in a hospital, and develop a mathematical model to manage blood ordering and issuing.
To overcome these limitations and ease the use of toxicokinetic modeling in epidemiologic studies, we developed a simplified model to simulate blood POP levels across childhood and validated it to 45 months of age using blood levels of children enrolled in two longitudinal birth cohorts.
His lab uses zebrafish as a model to understand blood cell development and, in recent years, has made inspiring breakthroughs in the treatment of blood diseases and cancer, helping to establish zebrafish as a powerful model for translational research.
Establishment of an appropriate animal model to study blood pressure effects of lead will require careful assessment of dietary interactions with lead, unstressed blood pressure monitoring with standardized techniques, and documentation of biologically effective lead burden.
Objectives: We developed a toxicokinetic model to simulate blood POP levels in children from two longitudinal birth cohorts and aimed to validate it against blood levels measured at 6, 16, and 45 months of age.
In this paper, we propose a two-dimensional nonlinear "multiring" model to compute blood flow in axisymmetric elastic arteries.
In order to tackle these challenges, we developed a new Allen Cahn (AC) equation and likelihood model to segment blood vessels in angiograms.
Data of IVIM imaging (12 b-values ranging from 0 to 1000 s/mm, 12 repetitions) were fitted with a bi-exponential model to extract blood volume fraction (f) and pseudo-diffusion coefficient (D*).
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