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Alcohol researchers have confined most experiments to laboratory animals and to test-tube cultures of cells.
We furthermore ascribe the longstanding contradiction between experiments and theory on the collapse pressure of SWCNTs to the presence of filling in most experiments to date, while empty SWCNTs follow the theoretically predicted collapse behaviour.
First, most experiments to date have used a linear utility function where the marginal return of a public good out of one unit of contribution of a private good is less than one.
For most experiments to detect nutrition affects at P < 0.05, they required a difference between treatments of 0.2 0.8 μm in cashmere mean fibre diameter and 15 42 g in clean cashmere production.
We co-transfected with a GFP plasmid in most experiments to fill the cells and allow visualization of dendrites and dendritic spines (Fig. 1A), and quantified spine shape and size from images of GFP distribution.
Both MRC5 and U2OS cell lines were subsequently used in parallel for most experiments to ascertain if any observed effects required the more reliable cell cycle checkpoints of primary cells (MRC5) and thus were not recapitulated in transformed cell lines such as the U2OS line that has stable p53- and pRb-dependent checkpoints but is defective for p16INK [24], [24].
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To accurately gauge its tiny tug, most experiments have to be carefully isolated from electrical and seismic disturbances and performed in a vacuum to minimize the push of atoms in the air.
3. Most experiments (at least those employed to derive mechanism) were performed in near rigor conditions.
Although exposure to lower physiological oxygen conditions (2 5%) has been documented to increase survival, proliferation and dopaminergic differentiation of cultured neurons, most experiments continue to be done predominantly at atmospheric oxygen levels.
In most experiments, six to eight images at 1.4 µm z-intervals were captured at 10 to 20 min time intervals.
Most experiments taken to support this notion, however, confounded variations of movement amplitudes with symmetry in starting locations and variations in target location.
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