ライフサイエンスコーパス: papillae

1 thogen detection where it accumulates within papillae.

2 Effects were selective, sparing nontaste papillae.

3 ip between nerve and taste buds in fungiform papillae.

4 ue lesion, which comprises swollen fungiform papillae.

5 modeling process that forms the adult rectal papillae.

6 tes the formation of ectopic teeth and taste papillae.

7 distinct cell wall characteristics including papillae.

8 to correctly locate and innervate fungiform papillae.

9 e cell types, but do not contribute to taste papillae.

10 ory cell differentiation in developing taste papillae.

11 th in guard/awl/auchene and in zigzag dermal papillae.

12 expression is confined to a subset of dermal papillae.

13 ential roles in the development of fungiform papillae.

14 DNF and NT4 disrupt innervation to fungiform papillae.

15 during the initial innervation of fungiform papillae.

16 ture taste cells, and low levels in filiform papillae.

17 taste filiform papillae instead of gustatory papillae.

18 he most likely member present in mouse taste papillae.

19 s secreted to the cell wall of the stigmatic papillae.

20 sory nerve fibers in the core of the lingual papillae.

21 ail to penetrate the epidermal cell wall and papillae.

22 se to denervation of taste buds in fungiform papillae.

23 a placodes and then to regions of developing papillae.

24 ializations in the form of gustatory (taste) papillae.

25 lized in the basement membrane region of the papillae.

26 localized within early tongue and developing papillae.

27 e that matched the distribution of fungiform papillae.

28 fibers in the dermal nerve plexus and dermal papillae.

29 he foliate, vallate, and posterior fungiform papillae.

30 n circumvallate, foliate and fungiform taste papillae.

31 ) induced by acidic stimuli in rat fungiform papillae.

32 -OE and NT4-OE mice innervated few fungiform papillae.

33 ed in taste buds of circumvallate or incisal papillae.

34 or right fungiform, or left or right foliate papillae.

35 quently arranged in clusters of two or three papillae.

36 ste cells with synapses in rat circumvallate papillae.

37 s examined in adult and developing rat taste papillae.

38 rs were seen in close association with taste papillae.

39 e, and Merkel endings on rete pegs in dermal papillae.

40 o IL-1 and TNF by injection into interdental papillae.

41 nasoincisor duct and epiglottis > fungiform papillae.

42 nnervation, ruling out neuronal induction of papillae.

43 r beta and gamma rENaC in taste cells of all papillae.

44 lf of the taste cells in foliate and vallate papillae.

45 on or development of taste buds within taste papillae.

46 solated taste cells from mouse circumvallate papillae.

47 nchors (37 of 44 images [84.1%]) were dermal papillae.

48 s such as teeth, salivary glands and lingual papillae.

49 rmalities, and telogen-like condensed dermal papillae.

50 ned effect on the existence of interproximal papillae.

51 occurs outside of the plasma membrane within papillae.

52 sites of pathogen detection for export into papillae.

53 ved cells is in close association with taste papillae.

54 ch as asexual propagules or secretory hairs (papillae) [10-12].

55 with periodontitis contributed 198 gingival papillae: 158 'diseased' (bleeding-on-probing, PD > 4 mm

56 he renal cortex, the medullary pyramids with papillae (2 vertical and 3 horizontal), and the renal pe

57 alized to regions including the oral sensory papillae, acetabular ducts, tegument, acetabular glands,

58 papilla number and size, and maintenance of papillae after morphogenesis is advanced.

59 (P < 0.01), but not L6-Fc, into rat gingival papillae after P. gingivalis infection resulted in signi

60 in taste buds, whereas 43% of the fungiform papillae also had additional labeled innervation to the

61 the embryonic relationship between placodes, papillae and adult taste buds has not been defined.

62 nication between pollen grains and stigmatic papillae and are fundamentally important, as they are th

63 (+) SP(-) fibers were numerous within dermal papillae and around hair shafts (n = 4).

64 ustered pattern between papillae, and within papillae and early taste buds.

65 y the M-phase-capable polyploid cells of the papillae and female germline can retain centrioles.

66 , we report that Shh expression in fungiform papillae and formation of normal mature fungiform papill

67 ophins, is expressed in developing gustatory papillae and is thought to be the neurotrophin that supp

68 In taste bud cells of vallate papillae and nasoincisor ducts, double-labeling experime

69 but is unexpectedly restricted to the dermal papillae and outer root sheath.

70 s bulge markers; the follicles induce dermal papillae and provide a niche for melanocytes, and they u

71 ns in the maintenance of fungiform gustatory papillae and raises the possibility for an earlier role

72 Characterization of the renal papillae and Randall's plaques in different types of sto

73 the tongue is covered with long filamentous papillae and resembles a brush or mop.

74 ing mesenchyme in one such system, the taste papillae and sensory taste buds of the mouse tongue.

75 nses of 120 taste cells of the rat fungiform papillae and soft palate maintained within the intact ep

76 enic lines had severe reduction in fungiform papillae and taste bud number, primarily in the dorsal m

77 Fungiform papillae and taste buds were reduced in number by about

78 s roles in forming and maintaining fungiform papillae and taste buds, most likely via stage-specific

79 important roles in the development of taste papillae and taste buds.

80 massive overproduction of enlarged fungiform papillae and taste buds.

81 natal and postnatal development of gustatory papillae and taste buds.

82 ue mesenchyme and epithelium including taste papillae and taste buds.

83 that is involved in the development of taste papillae and taste buds.

84 gate the fast oscillatory motion of the oral papillae and the exiting liquid jet that oscillates with

85 the interplay between the elasticity of oral papillae and the fast unsteady flow during squirting.

86 the abundance of axons innervating fungiform papillae and the normal numbers of geniculate ganglion n

87 Deletion of CCN2 in dermal papillae and the outer root sheath results in a shortene

88 n at high concentration to form and maintain papillae and, at low concentration, to activate between-

89 th normal-appearing follicle sheaths, dermal papillae, and barb ridges were induced.

90 d A. actinomycetemcomitans into the gingival papillae, and donor B cells from normal rats immunized w

91 nsively in the basal cells around developing papillae, and ErbB2 and c-kit immunoreactive neuronal fi

92 units in nearly all taste cells of fungiform papillae, and in about half of the taste cells in foliat

93 high levels in taste bud placodes, fungiform papillae, and mature taste cells, and low levels in fili

94 and Merkel endings around the base of dermal papillae, and Merkel endings on rete pegs in dermal papi

95 ntal probing depth, good preservation of the papillae, and no gingival recession.

96 nesis of oral organs, including teeth, taste papillae, and taste buds, and is essential for these pro

97 ystem, the biliary tree, the major and minor papillae, and the duodenum, will be described.

98 ck, PEN1 appears to be actively recruited to papillae, and there is a 2-h delay in papillae formation

99 and progress to a clustered pattern between papillae, and within papillae and early taste buds.

100 atmospheric conditions, kanamycin-resistant papillae appeared after only about 5-6 weeks of incubati

101 The papillae are due to mutations that allow the cells to ov

102 Taste papillae are ectodermal specializations that serve to ho

103 Fungiform papillae are epithelial specializations that develop in

104 Whereas papillae are highly dependent on transcytosis of premade

105 ads for a highly localized protein delivery, papillae are inhibited in the surround of BMP-soaked bea

106 Ectopic papillae are innervated in the stabilizing beta-catenin

107 es from gestational day 14 rat embryos, when papillae are just beginning to emerge on dorsal tongue,

108 Effects on papillae are not random but are more pronounced in speci

109 rthermore, on anterior tongue, the fungiform papillae are patterned in rows.

110 Fungiform papillae are repeated epithelial structures that house t

111 However, once papillae are well formed (E16-E18), Shh apparently does

112 orphological analyses implicate the filiform papillae as being particularly sensitive to trauma in K6

113 s in the oral mucosa, and implicate filiform papillae as being the major stress bearing structures in

114 Such aneuploidy is well tolerated in papillae, as it does not significantly impair cell viabi

115 nnervation and a reduced number of fungiform papillae at birth.

116 s reach the basal lamina of developing taste papillae at E14 to densely innervate the papillary epith

117 report that Sox2 is expressed in all dermal papillae at E16.5, but from E18.5 onwards expression is

118 Ptc encircles the dense Shh immunoproduct in papillae at various stages.

119 in the form of cell wall thickenings called papillae, at site of wall penetration.

120 ongue tip become engorged with blood and the papillae become erect.

121 argets of gustatory neurons (i.e., fungiform papillae) before their innervation, and BDNF overexpress

122 s approach their target cells, the fungiform papillae, beginning on E13.5, at which time we found rob

123 the plant secretes cell wall appositions or papillae beneath the penetration peg of the fungus.

124 erythema and enlargement of the interdental papillae between the left maxillary canine, lateral inci

125 hypersensitive reaction or produce lignified papillae (both involving reactive oxygen species) to res

126 e organization and morphogenesis of filiform papillae but appears to be dispensable for embryonic hai

127 mouse circumvallate, foliate, and fungiform papillae but not in a variety of other cells, including

128 t, the trigeminal ganglion, which innervates papillae but not taste buds on the anterior tongue, is r

129 nly to maintenance of filiform and fungiform papillae, but also to taste buds.

130 n 4 (BMP4) are expressed in developing taste papillae, but the roles of these signaling molecules in

131 buds disappeared in more posterior fungiform papillae by 15 days posttransection, the anterior tip of

132 ults indicate that CCN2 expression by dermal papillae cells is a physiologically relevant suppressor

133 In vallate papillae, cells expressed either A or Lewis(b), but not

134 yperplasia, and elongation of lamina propria papillae, characteristic of chronic reflux esophagitis.

135 alatal tissue involving marginal gingiva and papillae) compared with conventional palatal grafts.

136 The lingual taste organs are papillae, composed of an epithelium that includes specia

137 ndings indicate that human follicular dermal papillae contain K(ATP) channels that can respond to min

138 g cells per taste bud, whereas the fungiform papillae contained 3.06 and 0.23 cells per taste bud, re

139 junction (DEJ); nonhomogenously distributed papillae; continuous (lentiginous) proliferation of cell

140 in CD36, which is expressed by circumvallate papillae (CVP) of the mouse tongue, has been implicated

141 lae and formation of normal mature fungiform papillae depend on signaling through Wnt and beta-cateni

142 lved in the transcription of genes promoting papillae deposition in trichomes.

143 nscription of a subset of genes that promote papillae deposition in trichomes.

144 rstand the molecular processes important for papillae deposition on the cell wall surface, we identif

145 s (E)12-E18] were used, in which tongues and papillae develop with native spatial, temporal, and mole

146 In addition, fungiform papillae developed on posterior oral tongue, just in fro

147 ported to regulate certain aspects of floral papillae development, did not complement the glabrous 1

148 tumor 1 protein (WT1) in circumvallate (CV) papillae development.

149 ignaling is a crucial regulator of fungiform papillae development.

150 the main activation pathway during fungiform papillae development; however, this effect does not occu

151 Fungiform papillae did not develop on pharyngeal or ventral tongue

152 Taste cells of fungiform papillae did not show immunoreactivity for presynaptic p

153 r than to the compression of the interdental papillae (direct effect).

154 Cells isolated from papillae display two distinct gross phenotypes (group A

155 rcumvallate papilla, regions where fungiform papillae do not typically develop.

156 ells (SCs) and underlying mesenchymal dermal papillae (DP) generates sufficient activating cues to ov

157 mponents of the feather follicle: the dermal papillae (DP) which controls feather regeneration and ax

158 During hair follicle morphogenesis, dermal papillae (DPs) function as mesenchymal signaling centers

159 he larva has groups of neurons in its apical papillae, epidermal neurons in the rostral and apical tr

160 al fibers were often seen entering the taste papillae epithelium, where new taste buds form, and by p

161 s significantly lower than that of fungiform papillae, especially for beta and gamma subunits.

162 ained, TB were not restored in all fungiform papillae even with prolonged recovery for several months

163 plasma membrane maintenance during stigmatic papillae expansion and pollen development, respectively.

164 Fungiform taste papillae form a regular array on the dorsal tongue.

165 gnaling in cultured tongue explants enhanced papillae formation and was accompanied by an up-regulati

166 ted to papillae, and there is a 2-h delay in papillae formation in the pen1-1 mutant.

167 ted results show that MED25 is necessary for papillae formation on the cell wall surface of leaf tric

168 AGE: Glassy Hair 1 (GLH1) gene that promotes papillae formation on trichome cell walls was identified

169 Y HAIR 1 (GLH1) gene, which is necessary for papillae formation.

170 buds, which are housed in specialized taste papillae found in a stereotyped pattern on the surface o

171 ere observed in the developing circumvallate papillae from 15.5 days of gestation until birth.

172 ts noggin and follistatin, in development of papillae from a stage before morphological initiation (E

173 glia that innervate taste buds and gustatory papillae (geniculate and petrosal) are reduced in volume

174 -gustducin in the order: foliate and vallate papillae > nasoincisor duct and epiglottis > fungiform p

175 Most (57%) of the fungiform papillae had labeled innervation only in taste buds, whe

176 Only egfr(-/-) fungiform taste papillae had robust gustatory innervation, markedly redu

177 vestigated in cultured human fungiform taste papillae (HBO) cells with five arginyl dipeptides: Ala-A

178 Preserved number of papillae in a shortened tongue results in an increased d

179 control fusion protein (L6-Fc) into gingival papillae in addition to P. gingivalis infection.

180 he tongue retain competency to add fungiform papillae in atypical locations.

181 Noggin substantially increases number of papillae in E14 cultures.

182 The Shh protein was in all fungiform papillae in embryonic tongues, and tongue cultures with

183 n-expressing cells at the tips of the dermal papillae in epidermis from several body sites, whereas a

184 l as the time course of innervation of taste papillae in mouse embryos from embryonic day 12 (E12) to

185 pathology of Randall's plaques and the renal papillae in patients with nephrolithiasis, detailing gen

186 utator phenotype by the large number of blue papillae in the full-size colonies.

187 Restoring papillae in the gingival embrasures of the esthetic zone

188 egatively regulates the development of taste papillae in the lingual epithelium: in Fst(-/-) tongue,

189 results in an increased density of fungiform papillae in the mutant tongues.

190 ted that sour taste cells from circumvallate papillae in the posterior tongue express a proton curren

191 stratified squamous epithelium of fungiform papillae in the tongue, as well as in skeletal muscle ce

192 A total of 259 papillae, in 60 patients, were examined.

193 noggin induce increased numbers of fungiform papillae, in a concentration-dependent manner, compared

194 uds (TB) in both fungiform and circumvallate papillae, including disruption of TB progenitor-cell pro

195 taste bud precursors directly, but enlarges papillae indirectly.

196 Whereas gustatory ganglia and the taste papillae initially form independently, our results sugge

197 attracted to and invaded non-taste filiform papillae instead of gustatory papillae.

198 Deposition of cell wall-reinforcing papillae is an integral component of the plant immune re

199 rn of Shh expression within developing taste papillae is established prior to innervation, ruling out

200 initiation of the morphogenesis of gustatory papillae is independent of innervation.

201 However, the BMP inhibitory effect on papillae is not prevented by disrupting sonic hedgehog s

202 hs in regulating tongue growth and fungiform papillae is proposed in a model, through the Ror2 recept

203 onferred by localized cell wall appositions (papillae), is one of the best-studied processes in plant

204 nd nectar, trapped between the rows of erect papillae, is carried into the mouth.

205 e papillation pattern: a predominant ring of papillae just inside the edge of the colony, implying th

206 mplex MED25 gene is responsible for the near papillae-less phenotype of the glh1 mutant.

207 By 12 weeks, the changes in plaque, papillae level, and probing depths were significantly gr

208 re measured for plaque, relative interdental papillae level, Eastman interdental bleeding index, prob

209 Moreover, both midfacial tissue and the papillae maintained the early increase recorded before t

210 In mice vallate papillae, many, but not all, bitter-responsive cells exp

211 ng more coronally to terminate apical to the papillae mesial and distal to the teeth exhibiting the d

212 In circumvallate and foliate papillae, most T1r3-expressing cells also express a gene

213 RSL1 function do not develop rhizoids, slime papillae, mucilage papillae, or gemmae.

214 Fungiform papillae must contain long-lived, sustaining or stem cel

215 contributing with >/= 2 'diseased' gingival papillae (n = 241; with bleeding-on-probing, probing dep

216 passes additional phenotypes (e.g. fungiform papillae number, bitterness of quinine) and emerging rec

217 sed in the nail bed epithelium and fungiform papillae of dorsal tongue epithelium.

218 l skin, Sox2 is only expressed in the dermal papillae of guard/awl/auchene follicles, whereas CD133 i

219 brissae follicles, in filiform and fungiform papillae of oral mucosa.

220 and neuropeptide Y (NPY) from circumvallate papillae of Tas1r3(+/+), Tas1r3(+/-) and Tas1r3 (-/-) mi

221 in the base of glands from BE tissue, in the papillae of the basal layer of the esophageal squamous e

222 ied tips of the filiform (but not fungiform) papillae of the dorsal tongue and in the superficial squ

223 to measure the distribution of PO2 in dermal papillae of the finger nail folds of healthy human subje

224 sts of two distinct zones, one overlying the papillae of the supporting connective tissue (PBL) and t

225 appear to originate in the dorsal fungiform papillae of the tongue epithelium.

226 o the specialized secretory epidermal cells (papillae) of the stigma, which receive and discriminate

227 ransposition events by the formation of blue papillae on a colony.

228 sibly alter number and location of fungiform papillae on anterior tongue and elicit papilla formation

229 dorsal lingual epithelium to form fungiform papillae on both anterior and posterior oral tongue is r

230 umber and spatial pattern of fungiform taste papillae on embryonic rat tongue, during a specific peri

231 made quantitative analyses of all fungiform papillae on the anterior tongue, the single circumvallat

232 revealed a hitherto unappreciated pattern of papillae on the dorsal surface of the tongue that depend

233 ulticellular taste buds located within taste papillae on the tongue.

234 t develop rhizoids, slime papillae, mucilage papillae, or gemmae.

235 erm of ascidian larvae contains the adhesive papillae, or palps, which play an important role in trig

236 ndocycles in precursors of Drosophila rectal papillae (papillar cells).

237 l modeling, we show how aberrations in taste papillae patterning in Fst(-/-) mice could result from d

238 ed within papilla placodes and the fungiform papillae per se, have opposing inhibitory and activating

239 hile it has been generally believed that the papillae provide a structural barrier to slow fungal pen

240 the additional innervation in the fungiform papillae remained.

241 a derive BDNF support from target organs and papillae require sensory innervation for morphogenesis.

242 buds and strips of lingual tissue from taste papillae secrete ATP upon taste stimulation.

243 Interestingly, the dermal papillae shape varies and their sizes increase in circum

244 These papillae show the hallmarks of a mechanoreceptor, contai

245 In taste buds of the circumvallate papillae, some taste receptor cells (TRCs) express YRs l

246 ced growth rate, reduced number of fungiform papillae, spinal abnormalities, and sensory and sympathe

247 and they failed to evolve into hair follicle papillae, suggesting that the adjacent mesenchyme is a c

248 es accumulate in the encasement, but not the papillae, suggesting that two independent pathways form

249 Appearance of membrane material in papillae suggests secretion of exosomes.

250 , the precise expression of SSP in stigmatic papillae suggests that it may have a more general functi

251 dult taste buds and in and around developing papillae suggests that these receptors may play a role i

252 Similarly, in cultured chicken basilar papillae, supporting cell proliferation in response to h

253 organ, which contains connective tissue and papillae suspended in a gel-like matrix.

254 ympani fibers to distinguish their fungiform papillae targets from non-gustatory epithelium.

255 ntial regulator that maintains lingual taste papillae, taste bud and progenitor cell proliferation an

256 hich taste neurons innervated only fungiform papillae, taste neurons in BDNF-OE and NT4-OE mice inner

257 genes in papillary patterns but develop more papillae that are larger and closer together than in con

258 In all fungiform papillae that form under various culture conditions, the

259 In addition, some papillae that formed in transgenic mice had two taste bu

260 earing widely spaced, hollow, broad, conical papillae that terminate in a single bifurcation producin

261 le for patterning and morphogenesis of taste papillae, the authors examined the time course and distr

262 n the loss of nerve innervation to fungiform papillae, the facial nerve of developing animals was lab

263 In papillae, this centriole retention contributes to aneupl

264 ells isolated from mouse vallate and foliate papillae to characterize voltage-gated currents in the t

265 Glossophaga soricina, uses dynamic erectile papillae to collect nectar.

266 eudorabies virus labeling of fungiform taste papillae to infect single or small numbers of geniculate

267 Giant papillae tongue disorder (GPTD) is a newly discovered, l

268 as highly expressed at the bottom of foliate papillae trenches.

269 g, and eliminating previously stented or cut papillae, two multilevel fixed effect multivariate model

270 embryonic taste buds in developing fungiform papillae until birth are not correlated with the neural

271 The incidence of papillae was analyzed using chi(2) for linear trend anal

272 Innervation of taste papillae was examined by using the panneuronal antibody

273 thelium and aberrant innervation to filiform papillae was observed.

274 he intensity of labeling in cells of vallate papillae was significantly lower than that of fungiform

275 hen 500 microm slices of foliate and vallate papillae were briefly exposed to 1 mM glutamate in the p

276 In addition, floral papillae were converted to multicellular trichomes.

277 yer as well as the characteristics of dermal papillae were defined from the grabbed images.

278 This feature localized to sites where papillae were deposited.

279 Fungiform taste papillae were examined for allele-specific TAS2R38 expre

280 n addition, the size and number of fungiform papillae were greatly reduced in Lef1 knockout mice.

281 Gingival papillae were grouped by the depth of the adjacent gingi

282 Fungiform papillae were initially present on tongues of newborn BD

283 Taste cells of rat foliate papillae were loaded with calcium green dextran (CaGD).

284 No degenerative deficits of fungiform papillae were observed for the first 3 weeks of postnata

285 At this stage, hair-follicle dermal papillae were observed to evaginate, forming highly unus

286 Gingival papillae were obtained from individuals (56 males and 62

287 Also, papillae were present in 78.5% of cases when the horizon

288 Interdental papillae were present in 85.7% of the cases when the ver

289 Remaining fungiform papillae were selectively concentrated in the tongue tip

290 However, these remaining fungiform papillae were smaller in appearance and many did not con

291 The basilar papillae were studied by conventional transmission elect

292 as coloration, length, and number of aboral papillae, which are highly variable and can be affected

293 Lingual taste buds form within taste papillae, which are specialized structures that develop

294 h within epithelial appendages, termed taste papillae, which arise at mid-gestation as epithelial thi

295 (PEN)1 is required for timely appearance of papillae, which contain callose and extracellular membra

296 e, individual taste buds reside in fungiform papillae, which develop at mid-gestation as epithelial p

297 nsely spaced, long, hollow, slender, conical papillae with multiple sharply pointed, strongly diverge

298 study analyzes the existence of interdental papillae with regard to the vertical dimensions between

299 tributed at least two diseased interproximal papillae (with bleeding on probing [BOP], probing depth

300 the anterior aspect of the hard palate, long papillae within the lamina propria and thick dense colla