liver_mass_children

height

weight

<p>Vector of genders (either 'Male' or 'Female').</p>

gender

<p>For individuals under 18, predict the liver mass from height, weight, and
gender, using equations from Ogiu et al.</p>

Functions and data tables for simulation and statistical analysis
of chemical toxicokinetics ("TK") as in Pearce et al. (2017)
<doi:10.18637/jss.v079.i04>. Chemical-specific in vitro
data have been obtained from relatively high throughput
experiments. Both physiologically-based ("PBTK") and empirical
(e.g., one compartment) "TK" models can be parameterized for
several hundred chemicals and multiple species. These models are
solved efficiently, often using compiled (C-based) code. A Monte
Carlo sampler is included for simulating biological variability
(Ring et al., 2017 <doi:10.1016/j.envint.2017.06.004>)
and measurement limitations. Calibrated methods are included for
predicting tissue:plasma partition coefficients and volume of
distribution
(Pearce et al., 2017 <doi:10.1007/s10928-017-9548-7>).
These functions and data provide a set of tools for
in vitro-in vivo extrapolation ("IVIVE") of high throughput
screening data (e.g., Tox21, ToxCast) to real-world exposures via
reverse dosimetry (also known as "RTK")
(Wetmore et al., 2015 <doi:10.1093/toxsci/kfv171>).

John Wambaugh

httk

High-Throughput Toxicokinetics

Robert Pearce

Caroline Ring

Greg Honda

Jimena Davis

Nisha Sipes

Barbara Wetmore

Woodrow Setzer

liver_mass_children function

Predict liver mass for children. — liver_mass_children

Predict liver mass for children.

State of Data and AI Literacy Report 2025

liver_mass_children: Predict liver mass for children.

Description

Usage

Arguments

Value