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The ability of each type of fingerprint to predict similarity between molecules was determined using logistic regression, receiver operating characteristic (ROC) curves, and a range of measures of predictive success taken from the information retrieval and machine learning literatures.
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Quantity of molecules was determined by normalisation with linearized plasmid.
Expression of adhesion molecules was determined by flow cytometry.
Ligand-receptor interaction between these molecules is determined by the O-fucose-β1,3-N-acetylglucosaminyl-transferase, Fringe, which determines the Notch-bearing cell's reaction to its binding partners [10].
The structures of proteins and other biological molecules are determined by the delicate balance between several molecular interactions [1 3].
In normal circumstances, intestinal permeability to water-soluble molecules is determined by the presence of tight junctions between intestinal epithelial cells [ 65].
In the first step, a series of possible precursor molecules is determined for the target molecule.
Soluble adhesion molecules were determined by ELISA technique.
On the other hand, a reading register for binding an N-terminus MSA-221 40 MSA-221 40044) to peptide 1–9 of the HLA-DRβ1 molecule was determined between residues F and S according to data reported by Patarroyo et al. (2011).
Restriction enzyme cut sites were detected as gaps in linear DNA molecules, and the size of each restriction fragment between adjacent cut sites was determined.
By increasing the number of chloroform molecules inside the cavity, it was determined that the most stable complex between 6b and chloroform molecules is 6b·CHCl3.
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