ライフサイエンスコーパス: papillae

1 yet functional, and the electrocytes lacked papillae.

2 ned effect on the existence of interproximal papillae.

3 that SCCs are particularly numerous on these papillae.

4 occurs outside of the plasma membrane within papillae.

5 sites of pathogen detection for export into papillae.

6 ved cells is in close association with taste papillae.

7 ip between nerve and taste buds in fungiform papillae.

8 that are particularly numerous on cutaneous papillae.

9 modeling process that forms the adult rectal papillae.

10 tes the formation of ectopic teeth and taste papillae.

11 to correctly locate and innervate fungiform papillae.

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

13 ory cell differentiation in developing taste papillae.

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

15 s were not different among the four types of papillae.

16 expression is confined to a subset of dermal papillae.

17 ential roles in the development of fungiform papillae.

18 DNF and NT4 disrupt innervation to fungiform papillae.

19 tendency of pollen tubes to coil around the papillae.

20 during the initial innervation of fungiform papillae.

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

22 taste filiform papillae instead of gustatory papillae.

23 d cv Spence contained dense costal ridges of papillae.

24 he most likely member present in mouse taste papillae.

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

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

27 ail to penetrate the epidermal cell wall and papillae.

28 se to denervation of taste buds in fungiform papillae.

29 a placodes and then to regions of developing papillae.

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

31 lized in the basement membrane region of the papillae.

32 localized within early tongue and developing papillae.

33 e that matched the distribution of fungiform papillae.

34 fibers in the dermal nerve plexus and dermal papillae.

35 i nerve to innervate taste buds in fungiform papillae.

36 he foliate, vallate, and posterior fungiform papillae.

37 n circumvallate, foliate and fungiform taste papillae.

38 ching in highly resorptive Drosophila rectal papillae.

39 ) induced by acidic stimuli in rat fungiform papillae.

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

41 ed in taste buds of circumvallate or incisal papillae.

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

43 quently arranged in clusters of two or three papillae.

44 ste cells with synapses in rat circumvallate papillae.

45 s examined in adult and developing rat taste papillae.

46 rs were seen in close association with taste papillae.

47 sion compared with those in WT circumvallate papillae.

48 ivided based on the height of the anatomical papillae.

49 thogen detection where it accumulates within papillae.

50 Effects were selective, sparing nontaste papillae.

51 ue lesion, which comprises swollen fungiform papillae.

52 distinct cell wall characteristics including papillae.

53 solated taste cells from mouse circumvallate papillae.

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

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

56 rmalities, and telogen-like condensed dermal papillae.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 s have a central lumen connected to the tiny papillae and leading to the body cavity.

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

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

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

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

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

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

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

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

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

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

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

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

84 massive overproduction of enlarged fungiform papillae and taste buds.

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

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

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

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

89 d by the mechanical properties of the stigma papillae and the organization of structures called corti

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

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

92 e vesicles are furnished with numerous small papillae, and can be divided into a basal part and a dis

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

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

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

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

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

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

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

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

101 sults suggest that over six months fungiform papillae are anatomically stable, playing a greater role

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

103 Taste papillae are ectodermal specializations that serve to ho

104 Fungiform papillae are epithelial specializations that develop in

105 Whereas papillae are highly dependent on transcytosis of premade

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

107 vated by the trigeminal nerve, the gill pore papillae are innervated by branchial nerves, and the dor

108 ated by branchial nerves, and the dorsal fin papillae are innervated by spinal nerves.

109 riments demonstrated that the oral and nasal papillae are innervated by the trigeminal nerve, the gil

110 Ectopic papillae are innervated in the stabilizing beta-catenin

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

112 d on the jaw margin while TBs and other oral papillae are located on the tongue.

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

114 Fungiform papillae are repeated epithelial structures that house t

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

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

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

118 Nerve fibers extended into the gill pore papillae, as far as the SCCs and serotonergic fibers ext

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

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

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

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

123 biphasic EOD of 1.3 ms duration, shows small papillae (average area 136 mum(2) ).

124 accompanied by a small change in size of the papillae (average area 159 mum(2) ).

125 featured a prominent increase in size of the papillae (average area 402 mum(2) ).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

144 r taste perception correlates with fungiform papillae density (FPD).

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

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

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

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

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

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

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

152 ignaling is a crucial regulator of fungiform papillae development.

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

154 Fungiform papillae did not develop on pharyngeal or ventral tongue

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

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

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

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

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

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

161 Few SCCs were located on small nub-like papillae during the parasitic juvenile stage, but SCCs w

162 Papillae emerge more frequently in some strains than in

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

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

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

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

167 r1p/Psr2p complex (WPPC) plays a key role in papillae expansion.

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

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

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

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

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

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

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

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

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

177 We provide evidence that leaf papillae function as specialized structures for Na(+) se

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

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

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

181 Fungiform papillae house taste buds on the anterior dorsal tongue.

182 nses, which induced the formation of callose papillae, hydrogen peroxide accumulation and the Salicyl

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

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

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

186 Noggin substantially increases number of papillae in E14 cultures.

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

188 e stage, but SCCs were abundant on prominent papillae in migrating and in spawning adults.

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

190 Restoring papillae in the gingival embrasures of the esthetic zone

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

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

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

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

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

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

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

198 taste bud precursors directly, but enlarges papillae indirectly.

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

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

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

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

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

204 me but the stability of individual fungiform papillae is unclear.

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

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

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

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

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

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

211 preys (Petromyzon marinus L.) have cutaneous papillae located around the oral disk, nostril, gill por

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

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

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

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

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

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

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

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

220 hips of the taste cells in the circumvallate papillae of adult mice.

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

222 cells and their afferent fibers in amphibian papillae of either male or female bullfrogs.

223 ed that tongue intermolar eminence (IE) oral papillae of Follistatin (a BMP antagonist) mouse mutants

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

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

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

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

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

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

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

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

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

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

234 ratory system of many vertebrates, including papillae on lamprey gill pores.

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

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

237 filaments, which regularly extended into the papillae, only in the oldest specimen-probably serving a

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

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

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

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

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

243 NIPSA may represent a promising papillae preservation technique in the treatment of intr

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

245 derivative exosomes promoted tongue lingual papillae recovery and taste bud regeneration as evidence

246 the additional innervation in the fungiform papillae remained.

247 ere treated with reflection of interproximal papillae, root planing assisted with endoscope evaluatio

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

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

250 These papillae show the hallmarks of a mechanoreceptor, contai

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

252 We show that papillae specifically expand within the U cell subpopula

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

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

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

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

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

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

259 Of particular interest was the appearance of papillae, surface specializations of the uninnervated an

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

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

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

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

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

265 regulation and dynamics of the expansion of papillae that arise during colony aging, which consist o

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

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

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

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

270 In papillae, this centriole retention contributes to aneupl

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

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

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

274 racterized the response profile of gill pore papillae to some chemicals and showed that trout-derived

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

276 In circumvallate papillae, TRPV4 colocalized with a type IV cell and epit

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

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

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

280 thelium and aberrant innervation to filiform papillae was observed.

281 Gill pore papillae were absent and SCCs were sparse during the lar

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

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

284 This feature localized to sites where papillae were deposited.

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

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

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

288 Fungiform papillae were initially present on tongues of newborn BD

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

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

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

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

293 The cv HI10 papillae were shown to act as Na(+) sinks when plants we

294 The basilar papillae were studied by conventional transmission elect

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

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

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

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

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

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

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