Sentence examples for most active position from inspiring English sources

In such applications, the mover position sensing method must be explicitly addressed since most active position sensing methods require traveling cables, which are also an obstacle for multi-car elevator systems.

The FRET reporters showed that the most active rotational position again corresponded to increased separation of the Box1 motifs.

This array also revealed that SIRT1 has a general preference for aromatic residues in the Z position, but this effect depends on the residue in the X position, with the most active substrates having either basic or hydrophobic residues in the X position.

Their 5-monosubstituted counterparts must have strongly electron-donating groups to effect significant GSH induction; however, aliphatic groups, the most active function group at this position, were only able to increase GSH by a maximum of 165 % (compound 5a).

The compound with an iodine substituent in position 5, denoted iodobikinin, was most active in inhibiting BIN2 activity in vitro and efficiently induced brassinosteroid-like responses in vivo.

We present results on representative slices having peak voxel of activation, whereas Montreal Neurological Institute (MNI) position of this most active voxel is listed in Table 2.

The MNI position of the most active voxel on the reconstructed data using the proposed Optshrink LR + S method (with smoothing) is same as that obtained with the original data.

But in the c-Abl ligand, the occurrence of bromine and fluorine at the R2 position is the most active.

Among these 3-cyanopyridine derivatives, the MICs of compound 5h against S. epidermidis and C. albicans were 15.6 mg/L, which revealed that compound 5h featured double fluoro substituents at meta- and para-position was the most active compound.

Substitution at the 7- and 8-positions provided the most active XAA analogues for human cells.

Mono-methyl XAA analogues with substitutions at the seventh and eighth positions were the most active in stimulating human leukocytes to produce IL-6 and IL-8; and for inhibition of tube formation by ECV304 human endothelial-like cells, while 5- and 6-substituted analogues were the most active in murine cell systems.