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parallel fiber

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Fibra paralela

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A parallel fiber results from the bifurcation of a cerebellar granule cell axon in the molecular layer into two diametrically opposed branches, that are oriented parallel to the long axis of the folium.
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Figure 47-14D shows that most reverberating pathways are constituted of many parallel fibers.
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The axon of a cerebellar granule cell splits to form a parallel fiber which innervates Purkinje cells.
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The branches of the T are straight and run long distances; thus, they are called parallel fibers.
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The dendrites of Golgi cells receive input from the parallel fibers.
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Figure 46-14D shows that most reverberating pathways are constituted of many parallel fibers.
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This method is similar to the way parallel fiber responses are monitored in the cerebellar cortex.
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These parallel fibers form thousands of excitatory Granule-cell-Purkinje-cell synapses onto the dendrites of Purkinje cells.
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The magnitude of the Purkinje cell response to stimulation of a “beam” of parallel fibers is monitored.
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This dendritic field is oriented at right angles to the parallel fibers.
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What is special about activation of the parallel fibers?
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The parallel fibers and ascending axon synapses from the same granule cell fire in synchrony which results in excitatory signals.
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These parallel fibers form thousands of excitatory granule-cell–Purkinje-cell synapses onto the intermediate and distal dendrites of Purkinje cells using glutamate as a neurotransmitter.
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Sensory information relayed from the pons through the mossy fibers to the granule cells is then sent along the parallel fibers to the Purkinje cells for processing.
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Parallel fibers pass orthogonally through the Purkinje neuron's dendritic arbor, with up to 200,000 parallel fibers forming a Granule-cell-Purkinje-cell synapse with a single Purkinje cell.
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Since multiple (~200,000) granule cells synapse onto a single Purkinje cell, the effects of each parallel fiber can be altered in response to a “teacher signal” from the climbing fiber input.
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This figure shows a section of skin innervated by a large number of parallel pain fibers.
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Purkinje cells show two distinct forms of electrophysiological activity: Simple spikes occur at rates of 17 – 150 Hz (Raman and Bean, 1999), either spontaneously or when Purkinje cells are activated synaptically by the parallel fibers, the axons of the granule cells.
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These parallel fibers make relatively weaker excitatory (glutamatergic) synapses to spines in the Purkinje cell dendrite, whereas climbing fibers originating from the inferior olivary nucleus in the medulla provide very powerful excitatory input to the proximal dendrites and cell soma.
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These modified fibers, called intrafusal fibers, run parallel to the normal, or extrafusal, fibers.
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Now, we conceive the tetrahedron ABCD as consisting of fibers parallel to one of its edges, AB.
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Often associated with splitting tear parallel to tendon fibers.
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It was found that the the major amount of the double shear strength parallel to grain in the joint is provided by parallel to fiber crushing resistance of the Guadua.
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Wood tends to split or shear between its fibers (usually parallel to the beam axis).
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Its superficial fibers are bipennate, but the deep fibers are parallel.
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When a muscle’s name includes the term rectus (straight), its fibers run parallel to that imaginary line.
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