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For zero external input the fixed point is stable and the neuron is said to be excitable.
We consider θ ∈ mod 2 π, and the neuron is said to fire when θ increases through π and is effectively reset to −π.
For (varsigmageqvarsigma_{1}=1) the 'reset potential' (v=-50) in (FSS) is immediately mapped to a non-negative number, and the neuron is therefore spiking at its maximal frequency of once in three iterations.
Similarly, the voltage stays in the left interval for two iterations and the neuron is spiking once in four iterations for (varsigma_{1}>varsigmageqvarsigma_{2}=frac {1}{2} 5-sqrt{17})).
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When the neuron fires, this means that its output has a non-zero value and the output of the neuron is transmitted to neurons in the next layer.
Further, tone responses were only included in analysis if the neuronal FR during each oddball stimulus exceeded 0.02 Hz, and the neuron was significantly tuned to the tone.
Administration of 10-10 M nesfatin-1 increased [Ca2+]i in a single neuron isolated from the PVN, and the neuron was subsequently shown to be immunoreactive to CRH.
When the neuron is activated, the receptors are turned down, and when the neuron is silent they are turned up (Hudspeth et al., 2000).
The space between the SGCs and the neurons is 20 nm, which allows for an effective control of the extracellular environment by both neurons and SGCs [20].
Using Image J, the nucleus and cytoplasm of the neuron were cropped and the pixels were counted (3-day-old animals, n = 20 animals, 10 neurons from each).
Saposin C is a lysosomal protein, and lysosomes in the neuron are located in the soma.
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