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Second, "design the right molecule": we aimed to define a set of tractable design and selection parameters to guide rational PET ligand design.
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Rather than inferring the structure from the tracking of single molecules, we aimed at reconstructing the structure itself, meaning that we tried to visualize the sub-spine actin organization.
With these molecules we aim to realize novel phases of matter, study controlled quantum chemistry, simulate interesting systems such as superconductors, and perhaps implement molecular states as qubits for quantum computation.
To characterize the neurorespiratory toxicity of this molecule at high doses, we aimed at investigating alterations in Sprague Dawley rat ventilation and brain electrical activity after baclofen administration and studied their reversal by GABA-receptor antagonists.
Thus, considering this study as a first step to further explore the utility of these molecules as tumour markers, we aimed to determine the levels of sEGFR and their ligands in the serum of healthy donors and compare them with the levels in patients of NSCLC and HNC.
We performed inhibition and induction screens in parallel since we aimed at identifying molecules that induce RBC vesiculation (induction screens) and molecules that inhibit vesiculation induced by ionomycin (inhibition screens).
We aimed to identify molecules that critically regulate IGF-1-induced anchorage-independent survival.
Here, we aimed to identify molecules associated with this unique phenotype.
In this study we aimed to identify small molecule and genetic enhancers of AON-dependent and independent exon skipping through the screening of small molecule libraries with annotated functions, in addition to cDNA and siRNA collections.
In the current study, we aimed to develop small molecule inhibitors of APE1 for cancer therapy.
We aimed to find key molecules associated with chemoresistance using gene expression profiling as a screening tool.
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CEO of Professional Science Editing for Scientists @ prosciediting.com