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One set of chick brains was perfused for immunohistochemistry while a second was sampled for quantitative RT-PCR.
A recent study showed that the conjugation of QDs with cell-penetrating lipopeptides and the subsequent injection into intact embryonic chick brains helped to identify and monitor neural stem cells as they migrate in the developing brain [78].
In the present study, 50-MHz radiation, similarly modulated as a sinusoid, was found to produce changes in calcium-ion efflux from chick brains exposed in vitro in a Crawford cell.
One model of Ca2+ efflux has described a "windowing" phenomenon, similar to that previously described in chick brains in which efflux reaches a maximum at discrete EMF windows [33], [34].
Similar(56)
Equalizing the electric field intensity within chick brain immersed in buffer solution at different carrier frequencies.
A kinectin cDNA clone containing a 4.7-kilobase insert was isolated from an embryonic chick brain cDNA library by immunoscreening with a panel of monoclonal antibodies.
We have previously shown that 16-Hz, sinusoidal electromagnetic fields can cause enhanced efflux of calcium ions from chick brain tissue, in vitro, in two intensity regions centered on 6 and 40 Vp-p/m.
Presented here are the numerical relationships between incident power densities that produce the same average electric field intensity within a chick brain half immersed in buffered saline solution and exposed to a uniform electromagnetic field at carrier frequencies of 50, 147, and 450 MHz.
Adey and colleagues reported that RF electromagnetic fields influenced Ca2+ within tissues following experiments measuring 45Ca2+ fluxes in excised chick brain [7].
The majority of these results can be traced to one or two groups who used a very specific biological preparation; whole or excised chick brain.
Limited knowledge about the functions of IgLONs mainly derives from studies in rat and chick brain, the tissues where they are primarily expressed [17], [28], [29].
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