Exact(1)
In this analysis, all years in which an author was active were analyzed from the year of first publication until 2012.
Similar(59)
The fractions collected were tested for depilatory activity and the active fractions were analyzed on SDS-PAGE [27].
For the drug-available sessions, the number of nose pokes in the active and inactive holes, number of infusions and number of ineffective nose pokes in the active hole were analyzed.
Active species were analyzed using an optical probe in front of narrow blind holes with diameters of 3 5 mm and a penetration depth of 30 mm.
Structural, chemical, electrochemical and thermal properties of the phase purity and the structural characterization of the synthesized cathode active electrodes were analyzed by X-ray powdiffractiontion (XRD) using a Rigaku D/Max 2200 system, and Cu Kα radiation.
Average peak areas of active components were analyzed after triplicate analysis.
Histomorphometric differences between the two active treatments were analyzed using an independent simple t test and analysis of variance (ANOVA).
Different concentrations of purified SLY (P353L) protein were used to treat hBMECs for 10 min, and active GTPases were analyzed using pull-down assays.
Burned areas were detected by means of fuzzy classification of spectral indices derived from Landsat satellite images while spatial patterns of active fires were analyzed based on MODIS dataset.
The respective binding modes of proposed active drugs were analyzed using 3D protein ligand interaction fingerprints, which map out the intermolecular interactions between the ligand and protein binding pocket [74, 75].
The active fractions were analyzed by SDS-PAGE [27].
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