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A biomechanical model was developed, previously reported, based on inertial sensor data and upper limb (UL) anthropometric data.
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The objective of this study is to further develop previously reported mechanistic predictive model that simulates boron removal in full-scale seawater reverse osmosis (RO) desalination processes to take into account the effect of membrane fouling.
We have developed and previously reported on a therapeutic vaccination strategy for indolent B-cell lymphoma that combines local radiation to enhance tumor immunogenicity with the injection into the tumor of a TLR9 agonist.
The methodology that we have developed and previously reported for quantitative SPECT [2, 7 9] has been adapted for imaging the 177Lu distribution in vivo, with appropriate modifications for the radionuclide.
Our first patient presented with the novel manifestation of infantile spasms at the age of 3months, while the second developed the previously reported initial onset of tonic seizures with static developmental delay, but subsequently manifested the novel finding of electrical status epilepticus in sleep at the age of 15years.
Spheroids were developed as previously reported [53].
Serial propagation of cells in the absence of serum was developed as previously reported [ 25].
Isogenic doxorubicin-resistant sublines were developed as previously reported [ 14, 17] at the concentrations of 7.5 nM (Jurkat/7.5 nM DOX) and 15 nM (Jurkat/15 nM DOX) in Jurkat cells, as well as 5 nM (H9/5 nM DOX) and 10 nM (H9/10 nM DOX) in H9 cells.
Therefore, effects of fluoxetine on estrous cyclicity and behavior of Sprague Dawley female rats were smaller and required longer to develop than previously reported in Fischer female rats.
The unique structure of 3,5-disubstituted quinolines (2) was developed from the previously reported 4- 2,7-phenanthrolin-9-yl phenol 4- 2,7-phenanthrolin-9-yl phenol 4- 2,7-phenanthrolin-9-yl phenol 4- 2,7-phenanthrolin-9-yl phenol 4- 2,7-phenanthrolin-9-yl phenol
A novel potent and selective aminophenol scaffold for fXa inhibitors was developed from a previously reported benzimidazole-based naphthylamidine template.
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