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1 e innervates neuromasts of the supraorbital, infraorbital, and otic lines, whereas the anteroventral
3 thalamus and cortex of awake rats while the infraorbital branch of the trigeminal nerve was stimulat
4 Several months after cauterization of the infraorbital branch of the trigeminal nerve, the tactile
9 n, the effect of neonatal transection of the infraorbital nerve (a major component of the trigeminal
10 model of chronic constriction injury to the infraorbital nerve (CCI-ION) to study whether CCI-ION ca
12 rent study examined the long-term effects of infraorbital nerve (ION) axoplasmic transport attenuatio
13 adult rats that sustained transection of the infraorbital nerve (ION) on P-0 or P-7 or implantation o
18 ither eliminated by transection of the right infraorbital nerve (IoN), or selectively altered by repe
21 natal lesion of the primary afferents in the infraorbital nerve causes the death of one-third of the
22 of acute receptive field changes, following infraorbital nerve cut, may contribute to some types of
23 eld shifts with those that did not, prior to infraorbital nerve cut, there was no difference in mean
26 One of the major consequences of neonatal infraorbital nerve damage is irreversible morphological
30 chronic constriction injury (CCI) of the rat infraorbital nerve in the rostral ventromedial medulla (
34 timuli delivered via a cuff electrode to the infraorbital nerve yielded robust sensory responses in V
37 Unilateral and bilateral sectioning of the infraorbital nerve, which innervates the whiskers, was t
42 lar isolation of 37 interpolaris cells, with infraorbital receptive fields, was maintained following
44 1.6% exhibited receptive field shifts to non-infraorbital regions after cutting the infraorbital nerv
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