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In isoflurane anaesthetised rats extracellular recordings were made from neurons in the spinal trigeminal nucleus with meningeal afferent input.
Whole-cell recordings were made from neurons cultured from 4 separate SMA embryos and 5 wild-type embryos.
Recordings were made from neurons with Flag-D2S staining that were also GFP+ (AAV-D2L).
Electrophysiological recordings were made from neurons in live slices from both rats and GAD67-GFP mice.
Patch-clamp recordings were made from neurons in layer IV using infrared illumination and differential interference contrast optics.
Electrophysiological recordings were made from neurons located in the first ten sensilla chaetica located at the tip of the galea on the honeybee's proboscis.
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Intracellular recordings were made from 167 neurons in human tissue and from 73 neurons in monkey tissue samples.
Recordings were made from pyramidal neurons in the CA1 region, using glass pipettes containing CsMeSO4 internal solution (as above) and neurons voltage clamped at −70 mV unless otherwise stated.
Whole cell voltage clamp recordings were made from dopamine neurons in the SNc from wild type (WT) and GFP-D2 knock-in mice.
Optical recordings can be made from many neurons at once, revealing more of the "big picture" of how the retina responds to light.
Whole-cell voltage clamp electrophysiological recordings were made from dopamine neurons in the SNc identified by a location lateral to the medial terminal nucleus of the accessory optic tract.
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