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1 th intact taste systems and after unilateral chorda-lingual nerve transection.
2 ional PM-MA dynamics with various methods of chorda preservation during MVR to assess their impact on
3 ng, rupture of chorda tendinae, and valve or chorda tendinae thickness.
4 ion, valvular nodular thickening, rupture of chorda tendinae, and valve or chorda tendinae thickness.
5 hat all taste neurons projecting through the chorda tympani (27%) and greater superficial petrosal ne
6                                              Chorda tympani (CT) and glossopharyngeal (IXth) nerves r
7 eness occurred after combined section of the chorda tympani (CT) and greater superficial petrosal ner
8 stry following electrical stimulation of the chorda tympani (CT) nerve in rats.
9 rogeneous taste mixtures on responses of the chorda tympani (CT) nerve in the hamster (Mesocricetus a
10                                          The chorda tympani (CT) nerve innervates lingual taste buds
11                                              Chorda tympani (CT) nerve responses of lean mice to swee
12 Lean mice exhibited significant increases in chorda tympani (CT) nerve responses to sweet compounds a
13          Neurophysiological responses of the chorda tympani (CT) nerve to lingual stimulation with su
14  amiloride (100 muM) treatment and bilateral chorda tympani (CT) nerve transection.
15 was anastomosed to the distal portion of the chorda tympani (CT) nerve using fibrin glue (IX-CT rats)
16 e more responsive to bitter stimuli than the chorda tympani (CT) nerve, and this is particularly true
17 ding electrophysiological responses from the chorda tympani (CT) nerve, which transmits activity from
18 polarized taste receptor cells (TRCs) and by chorda tympani (CT) taste nerve recordings.
19                                              Chorda tympani (CT) transection reduced average discrimi
20      The greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves te
21 ion, the greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves we
22 s of the greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves we
23 dramatically enlarged terminal fields of the chorda tympani (CT), greater superficial petrosal (GSP),
24                    The central fibers of the chorda tympani (CT), greater superficial petrosal nerve
25 oxic lectin ricin was applied to the hamster chorda tympani (CT), producing anterograde degeneration
26 on (pain, temperature, touch, etc.), and the chorda tympani (CT), which conducts taste information.
27                             In contrast, the chorda tympani (CT), which innervates anterior tongue ta
28 e greater superficial petrosal (GSP) and the chorda tympani (CT).
29 differed from cells with evoked responses to chorda tympani (CT; which innervates taste buds on the r
30 ry in rats with bilateral transection of the chorda tympani (CTX), bilateral transection of the gloss
31 red before and after glossopharyngeal (GLX), chorda tympani (CTX), or combined glossopharyngeal and c
32 pani (CTX), or combined glossopharyngeal and chorda tympani (GLX + CTX) transection, as well as after
33 orded from rat glossopharyngeal (n = 30) and chorda tympani (n = 22) neurons.
34 Physiological studies suggest convergence of chorda tympani and glossopharyngeal afferent axons onto
35 ogical recordings from two taste nerves, the chorda tympani and glossopharyngeal, revealed depressed
36                            Specifically, the chorda tympani and greater superficial petrosal nerve te
37     We found that the terminal fields of the chorda tympani and greater superficial petrosal nerves a
38 ncreased in comparison with controls in both chorda tympani and lingual nerves after both procedures,
39 rphological observations were made on feline chorda tympani and lingual nerves proximal and distal to
40 re p75 expression in other cell types of the chorda tympani circuit.
41  staining was reduced in the dextran-labeled chorda tympani fibers and terminals as well as adjacent
42 lingual epithelium, beginning embryonically, chorda tympani fibers are misdirected and innervate inap
43 y functions as a chemoattractant that allows chorda tympani fibers to distinguish their fungiform pap
44                          Responses of single chorda tympani fibers to mixtures of taste stimuli were
45 ors including (a) numbers and type of active chorda tympani fibers, (b) compensatory responses to NaC
46  the extracellular space by primary afferent chorda tympani fibers.
47 f the dietary manipulation on the developing chorda tympani field was evident when it occurred from E
48    Overexpression of either factor disrupted chorda tympani innervation patterns either before or dur
49 eling revealed those NST subnuclei receiving chorda tympani nerve (CT) afferents, those connecting wi
50 timulation was examined in rats in which the chorda tympani nerve (CT) and/or glossopharyngeal nerve
51                            Rats that had the chorda tympani nerve (CT) bilaterally transected showed
52 ogically confirmed cross-regeneration of the chorda tympani nerve (CT) into the posterior tongue in t
53 earch has focused on neural responses of the chorda tympani nerve (CT) to taste stimuli.
54                                              Chorda tympani nerve (CT) transection (CTX) raises sodiu
55                                          The chorda tympani nerve (CT), one of three nerves that conv
56                          Recordings from the chorda tympani nerve (CT), which transmits taste informa
57                Electrical stimulation of the chorda tympani nerve (CT; innervating taste buds on the
58 netic stimulation of GAD65(+) TBCs increased chorda tympani nerve activity and activated gustatory ne
59 ed in the glossopharyngeal nerve than in the chorda tympani nerve and involved all taste qualities; r
60 n adult rats after unilateral axotomy of the chorda tympani nerve and/or maintenance on a sodium-rest
61                            In contrast, many chorda tympani nerve branches were observed near the epi
62                                              Chorda tympani nerve branching was reduced in NT4 overex
63 al level in combination with the labeling of chorda tympani nerve fibers with biotinylated dextran in
64 there were also group-related differences in chorda tympani nerve function, with OE mice showing a gr
65 ctional salt taste responses from the intact chorda tympani nerve in sodium-restricted rats in which
66       Fungiform taste bud degeneration after chorda tympani nerve injury has been well documented in
67 15), P25, or at adulthood, while leaving the chorda tympani nerve intact.
68         Neither the glossopharyngeal nor the chorda tympani nerve is necessary for normal sensitivity
69 FFAs stimulate afferent taste signals in the chorda tympani nerve of male and female rats and that th
70                                          The chorda tympani nerve of Snap25 conditional knockout mice
71                                              Chorda tympani nerve recordings demonstrated that p75(-/
72                           After axotomy, the chorda tympani nerve regenerated but was initially unres
73                  During sonidegib treatment, chorda tympani nerve responses to lingual chemical stimu
74       Electrophysiological recordings of the chorda tympani nerve reveal nearly abolished ammonium an
75  sodium restriction combined with unilateral chorda tympani nerve section leads to a rapid and specif
76 ified pathogen-free rats received unilateral chorda tympani nerve section or sham section followed by
77                    Thus, it appears that the chorda tympani nerve terminal field defaults to its earl
78 ess of the age when the nerves were cut, the chorda tympani nerve terminal field expanded to a volume
79 tenance of injured peripheral axons, and the chorda tympani nerve terminal field organization in the
80 cant and persistent reduction of the labeled chorda tympani nerve terminal field volume and density i
81  We measured the integrated responses of the chorda tympani nerve to 500 mM concentrations of NaCl, N
82 s of the geniculate ganglion project via the chorda tympani nerve to innervate taste buds in fungifor
83        Electrophysiological responses of the chorda tympani nerve to NaCl were blunted by estrogen tr
84                   In Experiment 1, rats with chorda tympani nerve transection (CTX) acquired a LiCl-c
85                                     In rats, chorda tympani nerve transection (CTX) greatly increases
86                                              Chorda tympani nerve transection (CTX) has been useful t
87                                              Chorda tympani nerve transection eliminated all labeled
88                    The terminal field of the chorda tympani nerve was assessed 35 d following nerve s
89                 After CTX in adult rats, the chorda tympani nerve was labeled with biotinylated dextr
90 evelopmental periods, terminal fields of the chorda tympani nerve within the nucleus of the solitary
91 te: warming the anterior edge of the tongue (chorda tympani nerve) from a cold temperature can evoke
92 sed by anterior taste buds innervated by the chorda tympani nerve.
93 ter compounds, was cross-reinnervated by the chorda tympani nerve.
94 ith intact (SHAM) and bilaterally transected chorda tympani nerves (CTX) received conditioned taste a
95 ividual neurons in both glossopharyngeal and chorda tympani nerves differed in their relative sensiti
96  terminal fields of the glossopharyngeal and chorda tympani nerves in the nucleus of the solitary tra
97 hysiological recordings from the lingual and chorda tympani nerves proximal to the repair allowed cha
98  conclusion that, for transected lingual and chorda tympani nerves, epineurial suturing is the prefer
99 nd only for nicotine and denatonium, and for chorda tympani neurons, some similarity to quinine was f
100 s a specific deficit in both the neural (via chorda tympani recording) and behavioral responses to ad
101                                          The chorda tympani responses to mineral salts were monitored
102                                          The chorda tympani responses to NaCl, KCl, NH4Cl and CaCl2 w
103              The order of effectiveness was: chorda tympani section > trigeminal section > thermal in
104 ed rat fungiform taste receptor cells and by chorda tympani taste nerve recordings.
105 ccounts for all of the amiloride-insensitive chorda tympani taste nerve response to Na+ salts and par
106 ta, and extracellularly, surrounding labeled chorda tympani terminal fibers and boutons in the NST.
107 ndent factors determine the formation of the chorda tympani terminal field during later development.
108 is required for a permanent expansion of the chorda tympani terminal field in the offspring.
109 al exhibited enlarged and irregularly shaped chorda tympani terminal fields.
110 gery groups: bilateral GL transection (GLX), chorda tympani transection (CTX), SHAM surgery, and comb
111   The present studies examined the effect of chorda tympani transection (neoCTX) of neonates on adult
112 volved all taste qualities; responses in the chorda tympani were more depressed to sweet and umami st
113 ctioned that innervates the anterior tongue (chorda tympani), the posterior tongue (glossopharyngeal)
114 volumes of the greater superficial petrosal, chorda tympani, and glossopharyngeal nerves at adulthood
115                        The glossopharyngeal, chorda tympani, and greater superficial petrosal nerves
116                                          The chorda tympani, greater superficial petrosal, and glosso
117             In the rat gustatory system, the chorda tympani, greater superficial petrosal, and glosso
118 r chain, promontory, round window niche, and chorda tympani.
119 onses to sodium in the contralateral, intact chorda tympani.

 
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