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1 basilar-membrane peak velocity toward scala tympani.
2 muscles (MEMs): the stapedius and the tensor tympani.
3 , promontory, round window niche, and chorda tympani.
4 eliver stimuli to the perilymph in the scala tympani.
5 o sodium in the contralateral, intact chorda tympani.
6 taste neurons projecting through the chorda tympani (27%) and greater superficial petrosal nerves (1
7 ogical studies suggest convergence of chorda tympani and glossopharyngeal afferent axons onto single
8 recordings from two taste nerves, the chorda tympani and glossopharyngeal, revealed depressed respons
10 found that the terminal fields of the chorda tympani and greater superficial petrosal nerves and over
11 d in comparison with controls in both chorda tympani and lingual nerves after both procedures, though
12 ical observations were made on feline chorda tympani and lingual nerves proximal and distal to transe
13 of the greater superficial petrosal, chorda tympani, and glossopharyngeal nerves at adulthood that a
15 e fibers, sprouting of fibers into the scala tympani, and improvement of electrically evoked auditory
17 nchronous with peak BM velocity toward scala tympani but at 80-90 dB sound pressure level (in decibel
18 ed within neurons located close to the scala tympani compared with those located close to the scala v
20 ccurred after combined section of the chorda tympani (CT) and greater superficial petrosal nerves.
22 us taste mixtures on responses of the chorda tympani (CT) nerve in the hamster (Mesocricetus auratus)
25 ce exhibited significant increases in chorda tympani (CT) nerve responses to sweet compounds after LA
28 responsive to bitter stimuli than the chorda tympani (CT) nerve, and this is particularly true for so
31 e greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves terminate
32 e greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves were labe
33 e greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves were visu
34 cally enlarged terminal fields of the chorda tympani (CT), greater superficial petrosal (GSP), and gl
36 ctin ricin was applied to the hamster chorda tympani (CT), producing anterograde degeneration of its
40 d from cells with evoked responses to chorda tympani (CT; which innervates taste buds on the rostral
41 ats with bilateral transection of the chorda tympani (CTX), bilateral transection of the glossopharyn
42 ore and after glossopharyngeal (GLX), chorda tympani (CTX), or combined glossopharyngeal and chorda t
43 ng was reduced in the dextran-labeled chorda tympani fibers and terminals as well as adjacent non-lab
44 epithelium, beginning embryonically, chorda tympani fibers are misdirected and innervate inappropria
45 ions as a chemoattractant that allows chorda tympani fibers to distinguish their fungiform papillae t
47 luding (a) numbers and type of active chorda tympani fibers, (b) compensatory responses to NaCl-solut
49 ietary manipulation on the developing chorda tympani field was evident when it occurred from E3 to da
50 TX), or combined glossopharyngeal and chorda tympani (GLX + CTX) transection, as well as after sham s
54 expression of either factor disrupted chorda tympani innervation patterns either before or during the
58 sitive endings and both stapedial and tensor tympani motoneurons, indicating that serotonin neurons t
59 on three groups of brainstem neurons: tensor tympani motoneurons, stapedius motoneurons, and medial o
61 ter injections of Fluorogold into the tensor tympani muscle, a column of labeled TTMNs was identified
64 evealed those NST subnuclei receiving chorda tympani nerve (CT) afferents, those connecting with the
65 ion was examined in rats in which the chorda tympani nerve (CT) and/or glossopharyngeal nerve (GL) wa
67 y confirmed cross-regeneration of the chorda tympani nerve (CT) into the posterior tongue in the abse
72 he glossopharyngeal nerve than in the chorda tympani nerve and involved all taste qualities; response
73 rats after unilateral axotomy of the chorda tympani nerve and/or maintenance on a sodium-restricted
76 l in combination with the labeling of chorda tympani nerve fibers with biotinylated dextran in golden
77 ere also group-related differences in chorda tympani nerve function, with OE mice showing a greater r
78 salt taste responses from the intact chorda tympani nerve in sodium-restricted rats in which a gusta
79 ungiform taste bud degeneration after chorda tympani nerve injury has been well documented in rats, h
81 Neither the glossopharyngeal nor the chorda tympani nerve is necessary for normal sensitivity to low
82 imulate afferent taste signals in the chorda tympani nerve of male and female rats and that these sig
84 restriction combined with unilateral chorda tympani nerve section leads to a rapid and specific decr
85 athogen-free rats received unilateral chorda tympani nerve section or sham section followed by dietar
87 the age when the nerves were cut, the chorda tympani nerve terminal field expanded to a volume four t
88 of injured peripheral axons, and the chorda tympani nerve terminal field organization in the nucleus
89 d persistent reduction of the labeled chorda tympani nerve terminal field volume and density in the N
90 sured the integrated responses of the chorda tympani nerve to 500 mM concentrations of NaCl, Na2SO4,
91 Electrophysiological responses of the chorda tympani nerve to NaCl were blunted by estrogen treatment
98 ental periods, terminal fields of the chorda tympani nerve within the nucleus of the solitary tract w
99 ming the anterior edge of the tongue (chorda tympani nerve) from a cold temperature can evoke sweetne
101 act (SHAM) and bilaterally transected chorda tympani nerves (CTX) received conditioned taste aversion
102 neurons in both glossopharyngeal and chorda tympani nerves differed in their relative sensitivities
103 al fields of the glossopharyngeal and chorda tympani nerves in the nucleus of the solitary tract (NST
104 gical recordings from the lingual and chorda tympani nerves proximal to the repair allowed characteri
105 sion that, for transected lingual and chorda tympani nerves, epineurial suturing is the preferred app
106 for nicotine and denatonium, and for chorda tympani neurons, some similarity to quinine was found on
108 nucleus had previously been named the tensor tympani part of the motor trigeminal nucleus (5TT) in ro
114 the basilar membrane and the fluid in scala tympani (ST) has been explored in both active and passiv
116 for all of the amiloride-insensitive chorda tympani taste nerve response to Na+ salts and part of th
121 that innervates the anterior tongue (chorda tympani), the posterior tongue (glossopharyngeal), or pa
122 oups: bilateral GL transection (GLX), chorda tympani transection (CTX), SHAM surgery, and combined tr
123 resent studies examined the effect of chorda tympani transection (neoCTX) of neonates on adult prefer
124 tracer pseudorabies virus into single tensor tympani (TT) muscles, and identified transynaptically la
125 all taste qualities; responses in the chorda tympani were more depressed to sweet and umami stimuli t
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