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1 H), that is found in cells and fibers of the terminal nerve.
2 e the populations of GnRH cells found in the terminal nerve and midbrain, which appear to be neuromod
5 cally, the neuromodulatory GnRH cells of the terminal nerve arise from the cranial neural crest, and
7 ls motor and sensory neurons projecting to a terminal nerve branch before experimental manipulation o
8 g motor neurons preferentially reinnervate a terminal nerve branch to muscle as opposed to skin, a pr
9 nsory neuron that regenerated an axon into a terminal nerve branch to muscle might represent either a
10 h the exception of the primary olfactory and terminal nerve fibers, labeled only for NADPH-d, yielded
11 y regions that represent the typical path of terminal nerve fibers, nor were we able to locate a term
12 y of olfactory receptor neurons and that the terminal nerve functions to modulate the odorant sensiti
13 ed in the olfactory bulb (OB; but not in the terminal nerve ganglion cells [TNgc]), ventral telenceph
20 bulb; however, unlike species that possess a terminal nerve, lampreys have no immunoreactive cells or
22 tigate the role of actin in vertebrate nerve terminals, nerve-muscle preparations from garter snake (
23 ere found in the olfactory pit and along the terminal nerve on E34-E36 and were not seen in the foreb
26 of gnathostomes have been found to possess a terminal nerve, some components of which demonstrate imm
27 uromodulatory GnRH cells of the midbrain and terminal nerve, thus providing additional evidence for s
29 active (ir) perikarya in the olfactory bulbs-terminal nerve, ventral telencephalon, caudal preoptic a
30 lore the possibility that lampreys possess a terminal nerve, we examined the distribution of these pe
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