Sentence examples for clamp I from inspiring English sources

Throughout the baseline period and for the last 40 min of each step of the clamp (i.e. steady state periods), oxygen consumption (VO2) and carbon dioxide production (VCO2) were measured using indirect calorimetry (Deltatrac II; Datex-Ohmeda Dinision Instrumentarium canopy Helsinki Finland), in canopy mode for healthy volunteers and in respiratory mode for mechanically ventilated patients.

I don't mean its actual efficiency but the fact that the eraser, which resembles an elongated Chiclet, pulls out of the distinctive flat ferrule by means of a tiny clamp (I'm sure there is a name for this piece of pencil hardware) and can be extended and slotted back into the ferrule for longer life or, better yet, reversed, providing fresh edges for your precision erasure needs.

I don't mean its actual efficiency but the fact that the eraser, which resembles an elongated Chiclet, pulls out of the distinctive flat ferrule by means of a tiny clamp (I'm sure there is a name for this piece of pencil hardware) and can be extended and slotted back into the ferrule for longer life — or, better yet, reversed, providing fresh edges for your precision erasure needs.

AfThereon Delisht.

Then neurons were held in current clamp (I = 0) for the remainder of the experiment.

Therefore, the A subunit binds two clamp subunits, with the A domain binding to the clamp I subunit and the A' domain binding to the clamp III subunit.

Whole cell current clamp (I-Clamp) recordings were obtained from matGC and 4wpiGC.

The final two measurements during the morning clamps (i.e. t = 105 and t = 165 min) and the afternoon clamps (i.e. t = 390 and t = 450 min) were averaged for analysis.

Then, using my circular saw and clamps, I cut the shelves, managing to get them to come out the same length -- a task that would have been easier with a table saw, but I don't have one.

In a subset of neurons expressing ChR2-YFP-NavII-III (on-cell, 10/17 cells = 59%; current-clamp I = 0, 9/17 cells = 53%), this allowed the production of single action potentials using long-duration high-intensity blue light stimulation (Figure 5F).

This light source is routinely used to evoke spikes in ChR2-YFP-positive cells in our laboratory, but even long, 500 ms flashes never produced an action potential in ChR2-YFP-NavII-III-expressing cells (Figure 5A; on-cell and current-clamp I = 0 recording configurations, n = 5).