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1 , promontory, round window niche, and chorda tympani.
2  and basally streaming flows along the scala tympani.
3 eliver stimuli to the perilymph in the scala tympani.
4  basilar-membrane peak velocity toward scala tympani.
5 muscles (MEMs): the stapedius and the tensor tympani.
6 o sodium in the contralateral, intact chorda tympani.
7  taste neurons projecting through the chorda tympani (27%) and greater superficial petrosal nerves (1
8 ogical studies suggest convergence of chorda tympani and glossopharyngeal afferent axons onto single
9 recordings from two taste nerves, the chorda tympani and glossopharyngeal, revealed depressed respons
10                     Specifically, the chorda tympani and greater superficial petrosal nerve terminal
11 found that the terminal fields of the chorda tympani and greater superficial petrosal nerves and over
12 d in comparison with controls in both chorda tympani and lingual nerves after both procedures, though
13 ical observations were made on feline chorda tympani and lingual nerves proximal and distal to transe
14 h greatest density in cells lining the scala tympani and lower density in neural target tissue.
15  of the greater superficial petrosal, chorda tympani, and glossopharyngeal nerves at adulthood that a
16                 The glossopharyngeal, chorda tympani, and greater superficial petrosal nerves were la
17 e fibers, sprouting of fibers into the scala tympani, and improvement of electrically evoked auditory
18 hyme, including the spiral limbus, the scala tympani, and strial fibrocytes.
19 nchronous with peak BM velocity toward scala tympani but at 80-90 dB sound pressure level (in decibel
20 expression in other cell types of the chorda tympani circuit.
21 ed within neurons located close to the scala tympani compared with those located close to the scala v
22                                       Chorda tympani (CT) and glossopharyngeal (IXth) nerves relay ta
23 ccurred after combined section of the chorda tympani (CT) and greater superficial petrosal nerves.
24 llowing electrical stimulation of the chorda tympani (CT) nerve in rats.
25 us taste mixtures on responses of the chorda tympani (CT) nerve in the hamster (Mesocricetus auratus)
26                                   The chorda tympani (CT) nerve innervates lingual taste buds and is
27                                       Chorda tympani (CT) nerve responses of lean mice to sweet compo
28 ce exhibited significant increases in chorda tympani (CT) nerve responses to sweet compounds after LA
29   Neurophysiological responses of the chorda tympani (CT) nerve to lingual stimulation with sugars, o
30 ide (100 muM) treatment and bilateral chorda tympani (CT) nerve transection.
31 stomosed to the distal portion of the chorda tympani (CT) nerve using fibrin glue (IX-CT rats).
32 responsive to bitter stimuli than the chorda tympani (CT) nerve, and this is particularly true for so
33 ectrophysiological responses from the chorda tympani (CT) nerve, which transmits activity from lingua
34 ed taste receptor cells (TRCs) and by chorda tympani (CT) taste nerve recordings.
35                                       Chorda tympani (CT) transection reduced average discrimination
36 e greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves terminate
37 e greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves were labe
38 e greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves were visu
39 cally enlarged terminal fields of the chorda tympani (CT), greater superficial petrosal (GSP), and gl
40             The central fibers of the chorda tympani (CT), greater superficial petrosal nerve (GSP),
41 ctin ricin was applied to the hamster chorda tympani (CT), producing anterograde degeneration of its
42 n, temperature, touch, etc.), and the chorda tympani (CT), which conducts taste information.
43                      In contrast, the chorda tympani (CT), which innervates anterior tongue taste bud
44 er superficial petrosal (GSP) and the chorda tympani (CT).
45 d from cells with evoked responses to chorda tympani (CT; which innervates taste buds on the rostral
46 ats with bilateral transection of the chorda tympani (CTX), bilateral transection of the glossopharyn
47 ore and after glossopharyngeal (GLX), chorda tympani (CTX), or combined glossopharyngeal and chorda t
48 ng was reduced in the dextran-labeled chorda tympani fibers and terminals as well as adjacent non-lab
49  epithelium, beginning embryonically, chorda tympani fibers are misdirected and innervate inappropria
50 ions as a chemoattractant that allows chorda tympani fibers to distinguish their fungiform papillae t
51                   Responses of single chorda tympani fibers to mixtures of taste stimuli were studied
52 luding (a) numbers and type of active chorda tympani fibers, (b) compensatory responses to NaCl-solut
53 tracellular space by primary afferent chorda tympani fibers.
54 ietary manipulation on the developing chorda tympani field was evident when it occurred from E3 to da
55 TX), or combined glossopharyngeal and chorda tympani (GLX + CTX) transection, as well as after sham s
56                                   The chorda tympani, greater superficial petrosal, and glossopharyng
57      In the rat gustatory system, the chorda tympani, greater superficial petrosal, and glossopharyng
58                    Contraction of the tensor tympani in response to both auditory and non-auditory st
59 expression of either factor disrupted chorda tympani innervation patterns either before or during the
60 s well as electrode arrays with a full scala tympani insertion, higher modiolar distance, and shallow
61       NBF was least often seen in full scala tympani insertions, but there was no significant associa
62                                   The tensor tympani is believed to contract in response to self-gene
63                                   The tensor tympani is one of two middle ear muscles that regulates
64 ditory stimulation is mediated by the tensor tympani motoneurons (TTMNs).
65 sitive endings and both stapedial and tensor tympani motoneurons, indicating that serotonin neurons t
66 on three groups of brainstem neurons: tensor tympani motoneurons, stapedius motoneurons, and medial o
67 onin neurons innervated stapedial and tensor tympani motoneurons.
68 ter injections of Fluorogold into the tensor tympani muscle, a column of labeled TTMNs was identified
69 or trigeminal nucleus innervating the tensor tympani muscle.
70 rom rat glossopharyngeal (n = 30) and chorda tympani (n = 22) neurons.
71 evealed those NST subnuclei receiving chorda tympani nerve (CT) afferents, those connecting with the
72 ion was examined in rats in which the chorda tympani nerve (CT) and/or glossopharyngeal nerve (GL) wa
73                     Rats that had the chorda tympani nerve (CT) bilaterally transected showed an aver
74 y confirmed cross-regeneration of the chorda tympani nerve (CT) into the posterior tongue in the abse
75 as focused on neural responses of the chorda tympani nerve (CT) to taste stimuli.
76                                       Chorda tympani nerve (CT) transection (CTX) raises sodium chlor
77                                   The chorda tympani nerve (CT), one of three nerves that convey gust
78                   Recordings from the chorda tympani nerve (CT), which transmits taste information fr
79         Electrical stimulation of the chorda tympani nerve (CT; innervating taste buds on the rostral
80 timulation of GAD65(+) TBCs increased chorda tympani nerve activity and activated gustatory neurons i
81 he glossopharyngeal nerve than in the chorda tympani nerve and involved all taste qualities; response
82  rats after unilateral axotomy of the chorda tympani nerve and/or maintenance on a sodium-restricted
83                     In contrast, many chorda tympani nerve branches were observed near the epithelial
84                                       Chorda tympani nerve branching was reduced in NT4 overexpressin
85 l in combination with the labeling of chorda tympani nerve fibers with biotinylated dextran in golden
86 ere also group-related differences in chorda tympani nerve function, with OE mice showing a greater r
87  salt taste responses from the intact chorda tympani nerve in sodium-restricted rats in which a gusta
88 ungiform taste bud degeneration after chorda tympani nerve injury has been well documented in rats, h
89 5, or at adulthood, while leaving the chorda tympani nerve intact.
90  Neither the glossopharyngeal nor the chorda tympani nerve is necessary for normal sensitivity to low
91 imulate afferent taste signals in the chorda tympani nerve of male and female rats and that these sig
92                                   The chorda tympani nerve of Snap25 conditional knockout mice shows
93                                       Chorda tympani nerve recordings demonstrated that p75(-/-) mice
94                    After axotomy, the chorda tympani nerve regenerated but was initially unresponsive
95           During sonidegib treatment, chorda tympani nerve responses to lingual chemical stimulation
96 lectrophysiological recordings of the chorda tympani nerve reveal nearly abolished ammonium and sour
97  restriction combined with unilateral chorda tympani nerve section leads to a rapid and specific decr
98 athogen-free rats received unilateral chorda tympani nerve section or sham section followed by dietar
99             Thus, it appears that the chorda tympani nerve terminal field defaults to its early postn
100 the age when the nerves were cut, the chorda tympani nerve terminal field expanded to a volume four t
101  of injured peripheral axons, and the chorda tympani nerve terminal field organization in the nucleus
102 d persistent reduction of the labeled chorda tympani nerve terminal field volume and density in the N
103 sured the integrated responses of the chorda tympani nerve to 500 mM concentrations of NaCl, Na2SO4,
104 e geniculate ganglion project via the chorda tympani nerve to innervate taste buds in fungiform papil
105 Electrophysiological responses of the chorda tympani nerve to NaCl were blunted by estrogen treatment
106            In Experiment 1, rats with chorda tympani nerve transection (CTX) acquired a LiCl-conditio
107                              In rats, chorda tympani nerve transection (CTX) greatly increases the de
108                                       Chorda tympani nerve transection (CTX) has been useful to study
109                                       Chorda tympani nerve transection eliminated all labeled innerva
110             The terminal field of the chorda tympani nerve was assessed 35 d following nerve sections
111          After CTX in adult rats, the chorda tympani nerve was labeled with biotinylated dextran amin
112 ental periods, terminal fields of the chorda tympani nerve within the nucleus of the solitary tract w
113 ming the anterior edge of the tongue (chorda tympani nerve) from a cold temperature can evoke sweetne
114 anterior taste buds innervated by the chorda tympani nerve.
115 pounds, was cross-reinnervated by the chorda tympani nerve.
116 act (SHAM) and bilaterally transected chorda tympani nerves (CTX) received conditioned taste aversion
117  neurons in both glossopharyngeal and chorda tympani nerves differed in their relative sensitivities
118 al fields of the glossopharyngeal and chorda tympani nerves in the nucleus of the solitary tract (NST
119 gical recordings from the lingual and chorda tympani nerves proximal to the repair allowed characteri
120 sion that, for transected lingual and chorda tympani nerves, epineurial suturing is the preferred app
121  for nicotine and denatonium, and for chorda tympani neurons, some similarity to quinine was found on
122 e injected lipopolysaccharide into the scala tympani of mouse inner ears.
123 essures in scala vestibuli (P(SV)) and scala tympani (P(ST)) at the basal cochlea in cadaveric human
124 nucleus had previously been named the tensor tympani part of the motor trigeminal nucleus (5TT) in ro
125 cific deficit in both the neural (via chorda tympani recording) and behavioral responses to administr
126                                   The chorda tympani responses to mineral salts were monitored in the
127                                   The chorda tympani responses to NaCl, KCl, NH4Cl and CaCl2 were rec
128       The order of effectiveness was: chorda tympani section > trigeminal section > thermal injury =
129 e between the scala vestibuli (SV) and scala tympani (ST) found in the cochlea.
130 , Belgium) was used to segment out the scala tympani (ST) from the muCT images.
131  the basilar membrane and the fluid in scala tympani (ST) has been explored in both active and passiv
132 fungiform taste receptor cells and by chorda tympani taste nerve recordings.
133  for all of the amiloride-insensitive chorda tympani taste nerve response to Na+ salts and part of th
134  extracellularly, surrounding labeled chorda tympani terminal fibers and boutons in the NST.
135 actors determine the formation of the chorda tympani terminal field during later development.
136 ired for a permanent expansion of the chorda tympani terminal field in the offspring.
137 bited enlarged and irregularly shaped chorda tympani terminal fields.
138  that innervates the anterior tongue (chorda tympani), the posterior tongue (glossopharyngeal), or pa
139 oups: bilateral GL transection (GLX), chorda tympani transection (CTX), SHAM surgery, and combined tr
140 resent studies examined the effect of chorda tympani transection (neoCTX) of neonates on adult prefer
141 tracer pseudorabies virus into single tensor tympani (TT) muscles, and identified transynaptically la
142 all taste qualities; responses in the chorda tympani were more depressed to sweet and umami stimuli t
143 ment of the pumps' delivery ports into scala tympani with an orientation toward the cochlear apex.

 
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