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1 ste buds is vallate > foliate > > palate > > fungiform.
2 cate differences in morphogenetic control of fungiform and circumvallate papilla development and numb
3 e number, morphology, and spatial pattern of fungiform and circumvallate papillae and associated tast
4 in the epithelial basement membrane of early fungiform and circumvallate papillae in regions where ta
5 les, tenascin and laminin, in the developing fungiform and circumvallate papillae of fetal, perinatal
6 educes the number of sour taste cells in the fungiform and circumvallate papillae of mice.
7 led to rapid loss of taste buds (TB) in both fungiform and circumvallate papillae, including disrupti
8                                           In fungiform and circumvallate papillae, the shift in tenas
9                                              Fungiform bud numbers in BDNF-OE mice are 35%, yet genic
10 spite a stereotyped patterned arrangement of fungiform buds as rows and columns on the tongue.
11  both wild-type and BDNF-OE mice exhibit, in fungiform buds, the same, "discrete" receptoneural patte
12 um of three types of gustatory papillae: the fungiform, circumvallate, and foliate.
13 e NT4/5 gene functions in the maintenance of fungiform gustatory papillae and raises the possibility
14 ignaling has established roles in supporting fungiform induction, development and patterning.
15 the tongue to stimulate either left or right fungiform, or left or right foliate papillae.
16 ng the development and spatial patterning of fungiform papilla and targeting of taste neurons to thes
17 , Wnt-beta-catenin signaling is critical for fungiform papilla and taste bud development.
18 lopment and maintenance of taste organs, the fungiform papilla and taste bud, and surrounding lingual
19                                              Fungiform papilla development progressed in half tongues
20 gue shape (E13) and results in a repatterned fungiform papilla distribution that does not respect nor
21                      We observed that during fungiform papilla formation in mice, Shh and components
22 nd morphogenetic roles for Shh in tongue and fungiform papilla formation, but also suggest that Shh f
23 ults demonstrate a prominent role for Shh in fungiform papilla induction and patterning and indicate
24 o system for studying mechanisms involved in fungiform papilla morphogenesis in patterns on the anter
25 ctopic dickkopf1 (Dkk1) blocks initiation of fungiform papilla morphogenesis.
26                                     However, fungiform papilla morphology, number and innervation are
27  cyclopamine, jervine, or blocking antibody, fungiform papilla numbers doubled on the dorsal tongue w
28  distinctive roles for Wnt5a in tongue size, fungiform papilla patterning and development are shown a
29 e number of PLCbeta2+ taste bud cells in the fungiform papilla was reduced in sucrose rats.
30    A requirement for normal Shh signaling in fungiform papilla, taste bud and filiform papilla mainte
31 nnervation to the dorsal anterior tongue and fungiform papilla.
32 ation only in taste buds, whereas 43% of the fungiform papillae also had additional labeled innervati
33       Here, we report that Shh expression in fungiform papillae and formation of normal mature fungif
34 cell responses of 120 taste cells of the rat fungiform papillae and soft palate maintained within the
35 oth transgenic lines had severe reduction in fungiform papillae and taste bud number, primarily in th
36 ological and immunohistochemical analyses of fungiform papillae and taste buds were also conducted.
37                                              Fungiform papillae and taste buds were reduced in number
38 gnaling has roles in forming and maintaining fungiform papillae and taste buds, most likely via stage
39 in causes massive overproduction of enlarged fungiform papillae and taste buds.
40 -/-) mice the abundance of axons innervating fungiform papillae and the normal numbers of geniculate
41   These results suggest that over six months fungiform papillae are anatomically stable, playing a gr
42                                              Fungiform papillae are epithelial specializations that d
43         Furthermore, on anterior tongue, the fungiform papillae are patterned in rows.
44                                              Fungiform papillae are repeated epithelial structures th
45 ustatory innervation and a reduced number of fungiform papillae at birth.
46 cells from mouse circumvallate, foliate, and fungiform papillae but not in a variety of other cells,
47 all taste buds disappeared in more posterior fungiform papillae by 15 days posttransection, the anter
48 -expressing cells per taste bud, whereas the fungiform papillae contained 3.06 and 0.23 cells per tas
49  to whether taste perception correlates with fungiform papillae density (FPD).
50 form papillae and formation of normal mature fungiform papillae depend on signaling through Wnt and b
51                                 In addition, fungiform papillae developed on posterior oral tongue, j
52                                 Furthermore, fungiform papillae developed on these tongues on a cultu
53 that FGF signaling is a crucial regulator of fungiform papillae development.
54  which is the main activation pathway during fungiform papillae development; however, this effect doe
55                                              Fungiform papillae did not develop on pharyngeal or vent
56                               Taste cells of fungiform papillae did not show immunoreactivity for pre
57  single circumvallate papilla, regions where fungiform papillae do not typically develop.
58  were sustained, TB were not restored in all fungiform papillae even with prolonged recovery for seve
59                                 In addition, fungiform papillae formed in the tongue cultures in the
60                In the rat, taste buds of the fungiform papillae had fewer gustducin-positive cells (3
61                            Most (57%) of the fungiform papillae had labeled innervation only in taste
62                                              Fungiform papillae house taste buds on the anterior dors
63 initial formation and early morphogenesis of fungiform papillae in a patterned array.
64 nor does the tongue retain competency to add fungiform papillae in atypical locations.
65                   The Shh protein was in all fungiform papillae in embryonic tongues, and tongue cult
66 erefore, robust, reproducible development of fungiform papillae in patterns is supported in rat tongu
67 ed tongue results in an increased density of fungiform papillae in the mutant tongues.
68  buds, and stratified squamous epithelium of fungiform papillae in the tongue, as well as in skeletal
69 al Wnt paths in regulating tongue growth and fungiform papillae is proposed in a model, through the R
70 es with time but the stability of individual fungiform papillae is unclear.
71                                              Fungiform papillae must contain long-lived, sustaining o
72 w it encompasses additional phenotypes (e.g. fungiform papillae number, bitterness of quinine) and em
73                                              Fungiform papillae of a SARS-CoV-2(+) patient exhibiting
74 lso expressed in the nail bed epithelium and fungiform papillae of dorsal tongue epithelium.
75 curs in vibrissae follicles, in filiform and fungiform papillae of oral mucosa.
76 erally and appear to originate in the dorsal fungiform papillae of the tongue epithelium.
77  map the spatial arrangement of filiform and fungiform papillae on a surface.
78 an irreversibly alter number and location of fungiform papillae on anterior tongue and elicit papilla
79 petence of dorsal lingual epithelium to form fungiform papillae on both anterior and posterior oral t
80 rmates and made quantitative analyses of all fungiform papillae on the anterior tongue, the single ci
81  colocalized within papilla placodes and the fungiform papillae per se, have opposing inhibitory and
82 ut most of the additional innervation in the fungiform papillae remained.
83 s chorda tympani fibers to distinguish their fungiform papillae targets from non-gustatory epithelium
84  continuity and cell turnover of a patient's fungiform papillae taste stem cell layer were disrupted
85                                       In all fungiform papillae that form under various culture condi
86 umbers of embryonic taste buds in developing fungiform papillae until birth are not correlated with t
87          In addition, the size and number of fungiform papillae were greatly reduced in Lef1 knockout
88                                              Fungiform papillae were initially present on tongues of
89                  No degenerative deficits of fungiform papillae were observed for the first 3 weeks o
90                                    Remaining fungiform papillae were selectively concentrated in the
91                     However, these remaining fungiform papillae were smaller in appearance and many d
92 ithelial targets of gustatory neurons (i.e., fungiform papillae) before their innervation, and BDNF o
93 ngs from isolated taste cells showed that in fungiform papillae, aldosterone increased the number of
94  three subunits in nearly all taste cells of fungiform papillae, and in about half of the taste cells
95 gue, with high levels in taste bud placodes, fungiform papillae, and mature taste cells, and low leve
96  60, there was 63% decrease in the number of fungiform papillae, and remaining papillae were smaller
97 ate neurons approach their target cells, the fungiform papillae, beginning on E13.5, at which time we
98 bute not only to maintenance of filiform and fungiform papillae, but also to taste buds.
99 apillae was significantly lower than that of fungiform papillae, especially for beta and gamma subuni
100 s BMPs or noggin induce increased numbers of fungiform papillae, in a concentration-dependent manner,
101 uding reduced growth rate, reduced number of fungiform papillae, spinal abnormalities, and sensory an
102 mice, in which taste neurons innervated only fungiform papillae, taste neurons in BDNF-OE and NT4-OE
103                                     In early fungiform papillae, tenascin immunoreactivity is very we
104  To explain the loss of nerve innervation to fungiform papillae, the facial nerve of developing anima
105     In mice, individual taste buds reside in fungiform papillae, which develop at mid-gestation as ep
106 rda tympani nerve to innervate taste buds in fungiform papillae.
107 (Ca(2+)(I)) induced by acidic stimuli in rat fungiform papillae.
108 ns in BDNF-OE and NT4-OE mice innervated few fungiform papillae.
109 nique tongue lesion, which comprises swollen fungiform papillae.
110 papillae > nasoincisor duct and epiglottis > fungiform papillae.
111 epidermis and at times in close proximity to fungiform papillae.
112 relationship between nerve and taste buds in fungiform papillae.
113 tory axons to correctly locate and innervate fungiform papillae.
114 s play essential roles in the development of fungiform papillae.
115 ssion of BDNF and NT4 disrupt innervation to fungiform papillae.
116  before or during the initial innervation of fungiform papillae.
117 yte response to denervation of taste buds in fungiform papillae.
118  the tongue that matched the distribution of fungiform papillae.
119 ing from the foliate, vallate, and posterior fungiform papillae.
120  the cornified tips of the filiform (but not fungiform) papillae of the dorsal tongue and in the supe
121 e of Shh, we used an in vitro model of mouse fungiform papillary development to determine the effects
122 y restricted to developing circumvallate and fungiform papillary epithelia.
123 catenin signaling is activated in developing fungiform placodes and taste bud cells.
124                                              Fungiform taste bud degeneration after chorda tympani ne
125  spatiotemporal functions of beta-catenin in fungiform taste bud development.
126 mutant mice had a higher frequency of failed fungiform taste bud differentiation.
127                   The current study examines fungiform taste bud distribution and structure in adult
128                                      A mouse fungiform taste bud is innervated by only four to five g
129            To clarify age-related changes in fungiform taste bud volume, the current study investigat
130 ta are the first to characterize adult mouse fungiform taste buds and subsequent degeneration after u
131 ce to implement a slice preparation in which fungiform taste buds are in a relatively intact tissue e
132                                          Rat fungiform taste buds are more responsive to salts than t
133                         In contrast, hamster fungiform taste buds are more sensitive to sweet-tasting
134                                      Hamster fungiform taste buds contained twice as many gustducin-e
135                                         Most fungiform taste buds fail to become innervated when BDNF
136 the postnatal development and maintenance of fungiform taste buds in mice carrying a deletion of NT4/
137   There was a modest but significant loss of fungiform taste buds in Phox2b-Cre; p75(fx/fx) mice, alt
138 culate ganglion cells that innervated single fungiform taste buds were quantified in the tip- and mid
139                                 Degenerating fungiform taste buds were smaller due to a loss of taste
140                                              Fungiform taste buds were visualized and measured with t
141                          By injecting single fungiform taste buds with lipophilic retrograde neuroana
142 CT and IX-CT rats, there was regeneration of fungiform taste buds, although in both groups there were
143        We counted the number and diameter of fungiform taste buds, the prevalence of poorly different
144 of the nerve to regenerate and a loss of all fungiform taste buds.
145 of chemosensory innervation of the remaining fungiform taste buds.
146 ally undetectable by immunohistochemistry in fungiform taste buds.
147 e obtained whole-cell recordings from single fungiform taste cells of rat pups to examine the develop
148 ly 20% of the total outward current of mouse fungiform taste cells was composed of K(ATP) channels.
149                                    The adult fungiform taste papilla is a complex of specialized cell
150 responses was investigated in cultured human fungiform taste papillae (HBO) cells with five arginyl d
151                                              Fungiform taste papillae form a regular array on the dor
152                               Only egfr(-/-) fungiform taste papillae had robust gustatory innervatio
153 regulating the number and spatial pattern of fungiform taste papillae on embryonic rat tongue, during
154 c anterograde pseudorabies virus labeling of fungiform taste papillae to infect single or small numbe
155                                              Fungiform taste papillae were examined for allele-specif
156                The anterior tongue had fewer fungiform taste papillae, and the circumvallate papillae
157 of taste cells in circumvallate, foliate and fungiform taste papillae.
158 emoved, stained with methylene blue, and the fungiform taste pores counted on both sides.
159 nilateral apical Na+ fluxes in polarized rat fungiform taste receptor cells and by chorda tympani tas
160 ntigen, are expressed by significantly fewer fungiform than vallate taste cells in the rat.

 
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