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1 sed by anterior taste buds innervated by the chorda tympani nerve.
2 ter compounds, was cross-reinnervated by the chorda tympani nerve.
3 netic stimulation of GAD65(+) TBCs increased chorda tympani nerve activity and activated gustatory ne
4 ed in the glossopharyngeal nerve than in the chorda tympani nerve and involved all taste qualities; r
5 n adult rats after unilateral axotomy of the chorda tympani nerve and/or maintenance on a sodium-rest
8 eling revealed those NST subnuclei receiving chorda tympani nerve (CT) afferents, those connecting wi
9 timulation was examined in rats in which the chorda tympani nerve (CT) and/or glossopharyngeal nerve
11 ogically confirmed cross-regeneration of the chorda tympani nerve (CT) into the posterior tongue in t
17 ith intact (SHAM) and bilaterally transected chorda tympani nerves (CTX) received conditioned taste a
18 ividual neurons in both glossopharyngeal and chorda tympani nerves differed in their relative sensiti
19 conclusion that, for transected lingual and chorda tympani nerves, epineurial suturing is the prefer
20 al level in combination with the labeling of chorda tympani nerve fibers with biotinylated dextran in
21 te: warming the anterior edge of the tongue (chorda tympani nerve) from a cold temperature can evoke
22 there were also group-related differences in chorda tympani nerve function, with OE mice showing a gr
23 ctional salt taste responses from the intact chorda tympani nerve in sodium-restricted rats in which
24 terminal fields of the glossopharyngeal and chorda tympani nerves in the nucleus of the solitary tra
28 FFAs stimulate afferent taste signals in the chorda tympani nerve of male and female rats and that th
30 hysiological recordings from the lingual and chorda tympani nerves proximal to the repair allowed cha
35 sodium restriction combined with unilateral chorda tympani nerve section leads to a rapid and specif
36 ified pathogen-free rats received unilateral chorda tympani nerve section or sham section followed by
38 ess of the age when the nerves were cut, the chorda tympani nerve terminal field expanded to a volume
39 tenance of injured peripheral axons, and the chorda tympani nerve terminal field organization in the
40 cant and persistent reduction of the labeled chorda tympani nerve terminal field volume and density i
41 We measured the integrated responses of the chorda tympani nerve to 500 mM concentrations of NaCl, N
42 s of the geniculate ganglion project via the chorda tympani nerve to innervate taste buds in fungifor
50 evelopmental periods, terminal fields of the chorda tympani nerve within the nucleus of the solitary