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Lipase units are defined as the µmols of ρ-nitrophenol released per minute per ml of sample.
The TK1 activity is expressed as pmol of dTMP formed per minute per mL of serum.
Chitotriosidase activity was measured as nanomoles of substrate hydrolysed per minute per mL (nmol/mL/hr).
*Mean enzyme activity expressed in μmoles benzoylcholine hydrolyzed per minute per mL of serum.
DPP4 activity in plasma was expressed as the amount of cleaved AMC per minute per ml (nmol/min/ml).
Glomerular filtration rate was estimated by fitting a linear least-squares regression to the logarithmically transformed counts per minute per ml (c.p.m. ml−1) vs time data.
Similar(48)
Caspase 3 activity was converted to μmols of p-nitroaniline release per minute (min) per millilitre (mL) of a placental cell lysate or a positive control [ 20].
Plasma sPLA2 activity, expressed as nanomoles per minute per millilitre (nmol/min per mL), was measured by selective fluorometric assay as previously described [ 17].
The arterial input function was derived from the time-attenuation curve from ROIs comprising both anterior cerebral arteries in cross section, and the rCBF (in millilitre per minute per 100 mL) was calculated using a deconvolution approach.
Chosen units are in milliliters per minute per 100 ml for K m, K s, and K s ( c ) ; SUV for c t + ; and percentage for RI (from which the respective slope and intercept units follow).
Forearm balances for glucose, FFAs, and insulin were calculated as follows: balance = ([A] – [V]) ⋅ F, where [A] and [V] are arterial and venous concentrations and F is forearm blood flow in milliliters per minute per 100 mL forearm volume.
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