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1 r chain, promontory, round window niche, and chorda tympani.
2 onses to sodium in the contralateral, intact chorda tympani.
3 hat all taste neurons projecting through the chorda tympani (27%) and greater superficial petrosal ne
4 Physiological studies suggest convergence of chorda tympani and glossopharyngeal afferent axons onto
5 ogical recordings from two taste nerves, the chorda tympani and glossopharyngeal, revealed depressed
6                            Specifically, the chorda tympani and greater superficial petrosal nerve te
7     We found that the terminal fields of the chorda tympani and greater superficial petrosal nerves a
8 ncreased in comparison with controls in both chorda tympani and lingual nerves after both procedures,
9 rphological observations were made on feline chorda tympani and lingual nerves proximal and distal to
10 volumes of the greater superficial petrosal, chorda tympani, and glossopharyngeal nerves at adulthood
11                        The glossopharyngeal, chorda tympani, and greater superficial petrosal nerves
12                                              Chorda tympani (CT) and glossopharyngeal (IXth) nerves r
13 eness occurred after combined section of the chorda tympani (CT) and greater superficial petrosal ner
14 stry following electrical stimulation of the chorda tympani (CT) nerve in rats.
15 rogeneous taste mixtures on responses of the chorda tympani (CT) nerve in the hamster (Mesocricetus a
16                                          The chorda tympani (CT) nerve innervates lingual taste buds
17                                              Chorda tympani (CT) nerve responses of lean mice to swee
18 Lean mice exhibited significant increases in chorda tympani (CT) nerve responses to sweet compounds a
19  amiloride (100 muM) treatment and bilateral chorda tympani (CT) nerve transection.
20 was anastomosed to the distal portion of the chorda tympani (CT) nerve using fibrin glue (IX-CT rats)
21 e more responsive to bitter stimuli than the chorda tympani (CT) nerve, and this is particularly true
22 polarized taste receptor cells (TRCs) and by chorda tympani (CT) taste nerve recordings.
23                                              Chorda tympani (CT) transection reduced average discrimi
24      The greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves te
25 ion, the greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves we
26 s of the greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves we
27 dramatically enlarged terminal fields of the chorda tympani (CT), greater superficial petrosal (GSP),
28                    The central fibers of the chorda tympani (CT), greater superficial petrosal nerve
29 oxic lectin ricin was applied to the hamster chorda tympani (CT), producing anterograde degeneration
30 on (pain, temperature, touch, etc.), and the chorda tympani (CT), which conducts taste information.
31                             In contrast, the chorda tympani (CT), which innervates anterior tongue ta
32 e greater superficial petrosal (GSP) and the chorda tympani (CT).
33 differed from cells with evoked responses to chorda tympani (CT; which innervates taste buds on the r
34 ry in rats with bilateral transection of the chorda tympani (CTX), bilateral transection of the gloss
35 red before and after glossopharyngeal (GLX), chorda tympani (CTX), or combined glossopharyngeal and c
36  staining was reduced in the dextran-labeled chorda tympani fibers and terminals as well as adjacent
37 lingual epithelium, beginning embryonically, chorda tympani fibers are misdirected and innervate inap
38 y functions as a chemoattractant that allows chorda tympani fibers to distinguish their fungiform pap
39                          Responses of single chorda tympani fibers to mixtures of taste stimuli were
40 ors including (a) numbers and type of active chorda tympani fibers, (b) compensatory responses to NaC
41  the extracellular space by primary afferent chorda tympani fibers.
42 f the dietary manipulation on the developing chorda tympani field was evident when it occurred from E
43 pani (CTX), or combined glossopharyngeal and chorda tympani (GLX + CTX) transection, as well as after
44                                          The chorda tympani, greater superficial petrosal, and glosso
45             In the rat gustatory system, the chorda tympani, greater superficial petrosal, and glosso
46    Overexpression of either factor disrupted chorda tympani innervation patterns either before or dur
47 orded from rat glossopharyngeal (n = 30) and chorda tympani (n = 22) neurons.
48 eling revealed those NST subnuclei receiving chorda tympani nerve (CT) afferents, those connecting wi
49 timulation was examined in rats in which the chorda tympani nerve (CT) and/or glossopharyngeal nerve
50                            Rats that had the chorda tympani nerve (CT) bilaterally transected showed
51 ogically confirmed cross-regeneration of the chorda tympani nerve (CT) into the posterior tongue in t
52 earch has focused on neural responses of the chorda tympani nerve (CT) to taste stimuli.
53                                              Chorda tympani nerve (CT) transection (CTX) raises sodiu
54                                          The chorda tympani nerve (CT), one of three nerves that conv
55                Electrical stimulation of the chorda tympani nerve (CT; innervating taste buds on the
56 ed in the glossopharyngeal nerve than in the chorda tympani nerve and involved all taste qualities; r
57 n adult rats after unilateral axotomy of the chorda tympani nerve and/or maintenance on a sodium-rest
58                            In contrast, many chorda tympani nerve branches were observed near the epi
59                                              Chorda tympani nerve branching was reduced in NT4 overex
60 al level in combination with the labeling of chorda tympani nerve fibers with biotinylated dextran in
61 there were also group-related differences in chorda tympani nerve function, with OE mice showing a gr
62 ctional salt taste responses from the intact chorda tympani nerve in sodium-restricted rats in which
63       Fungiform taste bud degeneration after chorda tympani nerve injury has been well documented in
64 15), P25, or at adulthood, while leaving the chorda tympani nerve intact.
65         Neither the glossopharyngeal nor the chorda tympani nerve is necessary for normal sensitivity
66 FFAs stimulate afferent taste signals in the chorda tympani nerve of male and female rats and that th
67                  During sonidegib treatment, chorda tympani nerve responses to lingual chemical stimu
68  sodium restriction combined with unilateral chorda tympani nerve section leads to a rapid and specif
69 ified pathogen-free rats received unilateral chorda tympani nerve section or sham section followed by
70                    Thus, it appears that the chorda tympani nerve terminal field defaults to its earl
71 ess of the age when the nerves were cut, the chorda tympani nerve terminal field expanded to a volume
72 tenance of injured peripheral axons, and the chorda tympani nerve terminal field organization in the
73 cant and persistent reduction of the labeled chorda tympani nerve terminal field volume and density i
74  We measured the integrated responses of the chorda tympani nerve to 500 mM concentrations of NaCl, N
75        Electrophysiological responses of the chorda tympani nerve to NaCl were blunted by estrogen tr
76                   In Experiment 1, rats with chorda tympani nerve transection (CTX) acquired a LiCl-c
77                                     In rats, chorda tympani nerve transection (CTX) greatly increases
78                                              Chorda tympani nerve transection (CTX) has been useful t
79                                              Chorda tympani nerve transection eliminated all labeled
80                    The terminal field of the chorda tympani nerve was assessed 35 d following nerve s
81                 After CTX in adult rats, the chorda tympani nerve was labeled with biotinylated dextr
82 evelopmental periods, terminal fields of the chorda tympani nerve within the nucleus of the solitary
83 te: warming the anterior edge of the tongue (chorda tympani nerve) from a cold temperature can evoke
84 ter compounds, was cross-reinnervated by the chorda tympani nerve.
85 ith intact (SHAM) and bilaterally transected chorda tympani nerves (CTX) received conditioned taste a
86 ividual neurons in both glossopharyngeal and chorda tympani nerves differed in their relative sensiti
87  terminal fields of the glossopharyngeal and chorda tympani nerves in the nucleus of the solitary tra
88 hysiological recordings from the lingual and chorda tympani nerves proximal to the repair allowed cha
89  conclusion that, for transected lingual and chorda tympani nerves, epineurial suturing is the prefer
90 nd only for nicotine and denatonium, and for chorda tympani neurons, some similarity to quinine was f
91                                          The chorda tympani responses to mineral salts were monitored
92                                          The chorda tympani responses to NaCl, KCl, NH4Cl and CaCl2 w
93              The order of effectiveness was: chorda tympani section > trigeminal section > thermal in
94 ed rat fungiform taste receptor cells and by chorda tympani taste nerve recordings.
95 ccounts for all of the amiloride-insensitive chorda tympani taste nerve response to Na+ salts and par
96 ta, and extracellularly, surrounding labeled chorda tympani terminal fibers and boutons in the NST.
97 ndent factors determine the formation of the chorda tympani terminal field during later development.
98 is required for a permanent expansion of the chorda tympani terminal field in the offspring.
99 al exhibited enlarged and irregularly shaped chorda tympani terminal fields.
100 ctioned that innervates the anterior tongue (chorda tympani), the posterior tongue (glossopharyngeal)
101 gery groups: bilateral GL transection (GLX), chorda tympani transection (CTX), SHAM surgery, and comb
102   The present studies examined the effect of chorda tympani transection (neoCTX) of neonates on adult
103 volved all taste qualities; responses in the chorda tympani were more depressed to sweet and umami st

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