ライフサイエンスコーパス: papilla

1 potentially adverse (hepatobiliary and renal papilla).

2 l ammonium facilitating its retention in the papilla.

3 ely epithelial matrix and mesenchymal dermal papilla.

4 the frequency range sensed by the amphibian papilla.

5 provide the major contribution to the dental papilla.

6 e, enclosing the cells of the forming dental papilla.

7 cceptable outcomes in terms of interproximal papilla.

8 ert with the epithelium to create the dental papilla.

9 ssed markers of the dermal sheath and dermal papilla.

10 loss of the interproximal height of bone and papilla.

11 ation of epithelial tubules to form a mature papilla.

12 y subdivision, the cochlear duct, or basilar papilla.

13 to the dorsal anterior tongue and fungiform papilla.

14 ontact area of the crowns on the interdental papilla.

15 ffusible IGF antagonist Igfbp3 in the dermal papilla.

16 t genes specifically expressed in the dermal papilla.

17 contact area to the tip of the interproximal papilla.

18 ed renal pelvis (hydronephrosis) and a small papilla.

19 n at the soft tissue margin, but not for the papilla.

20 cular marker, sonic hedgehog, is within each papilla.

21 ed a preparation of the bullfrog's amphibian papilla.

22 the deepithelialized portion of the original papilla.

23 Bcl-2, and becomes visible in the follicular papilla.

24 l new molecular landscapes within the dermal papilla.

25 DPCs have high resemblance to intact dermal papilla.

26 ct point to the bone and the presence of the papilla.

27 rom the frog sacculus and the turtle basilar papilla.

28 n of Fgf3 and Fgf10 expression in the dental papilla.

29 er of principal cells expressing PCNA in the papilla.

30 of ACh to hair cells in the chicken basilar papilla.

31 n (APC) applied circumferentially around the papilla.

32 r buds also show abnormalities in the dermal papilla.

33 the result of endoscopic intervention of the papilla.

34 illa: papilla, pit, spot, knob, and modified papilla.

35 rising from underneath the hood of the major papilla.

36 ingival index, papillary index (PPI) (0 = no papilla, 1 = less than half, 2 = more than half but not

37 s including the papillary index (PPI) (0, no papilla; 1, less than half; 2, more than half but not co

38 otein and mRNA were highly enriched in renal papilla, a proposed niche of kidney stem cells.

39 mTert mRNA levels increased in renal papilla after ischemia-reperfusion injury, but genetical

40 , whereas SFRP2 is maintained in the basilar papilla along with Fzd10 and Wnt7b.

41 ues, Cldn4 expression was substantial in the papilla and absent in the cortex.

42 e reciprocal relationship between the dermal papilla and adjacent HF epithelial cells.

43 f our five senses, genetic analyses of taste papilla and bud development are lacking.

44 t the bell stage, indicating that the dental papilla and dental follicle are still not defined popula

45 t to the tip of the bud form both the dental papilla and dental follicle.

46 of IP-associated genes in cultured HF dermal papilla and dermal sheath cup cells (DSCCs) compared wit

47 Troy(+) cells are present in the cortex and papilla and display an immature tubular phenotype.

48 e expression of Fgf3 and Fgf10 in the dental papilla and exhibited significant deficit in cell prolif

49 heir immediate progeny) migrate to the upper papilla and form a compartment of rapidly proliferating

50 the basal layer of the IFE and in the dermal papilla and hair bulb.

51 The results suggest that pit, papilla and knob sensilla act in contact chemosensation.

52 We classify three subtypes of papilla and pit sensilla, respectively, and two subtypes

53 ts highlight the difficulty of targeting the papilla and presumptive odontoblasts at early stages of

54 organs in anuran amphibians - the amphibian papilla and sacculus, both detectors of weak environment

55 pressed SUR1 and Kir6.2, whereas both dermal papilla and sheath exhibited SUR2B and Kir6.1.

56 or transit amplifying cells that support the papilla and specialized taste buds.

57 s maintained in signaling centers throughout papilla and taste bud development and differentiation.

58 -catenin signaling is critical for fungiform papilla and taste bud development.

59 of how Shh transduced signals act in tongue, papilla and taste bud formation and maintenance, it is n

60 ts used in cancer treatments, disrupts taste papilla and taste bud integrity and can eliminate respon

61 d maintenance of taste organs, the fungiform papilla and taste bud, and surrounding lingual cells.

62 ult kidney, Troy(+) cells are present in the papilla and these cells continue to contribute to collec

63 sues, ZAC1 expression was substantial in the papilla and was absent in the cortex.

64 ues, MUPP1 expression was substantial in the papilla and was absent in the cortex.

65 ss population), SCAP (stem cells from apical papilla), and SHED (stem cells from human-exfoliated dec

66 uria, decreased ammonium accumulation in the papilla, and chronic hyperchloremic metabolic acidosis.

67 eled by any GAL4 driver, neurons of the pit, papilla, and knob type are labeled by partially overlapp

68 g's epithelial root sheath (HERS) and apical papilla (AP) is crucial for proper tooth root developmen

69 The follicle dermal papilla appears to be the site of androgen action; howev

70 tudy, quantitative parameters of interdental papilla are investigated in patients with chronic period

71 cyte stem cells more distant from the dermal papilla are unscathed, thereby preventing hair greying t

72 Flanking the basilar papilla are Wnt7a, Wnt9a, Wnt11, and SFRP2 on the neural

73 0A4 expression was many -fold greater in the papilla as compared with the cortex and increased furthe

74 ed expression of Msx1 and Bmp4 in the dental papilla as well as expression of Bmp4, p21, and Shh in t

75 Some cells in the presumptive dental papilla at the cap stage contribute to the follicle at t

76 t that the transplantation of a human apical papilla at the lesion site improves gait in spinally inj

77 ell homeostasis beneath the stem cell-dermal papilla-based epithelial-mesenchymal interaction layer a

78 gesting that the cells migrated to the upper papilla before entering the cell cycle.

79 e width on the presence of the interproximal papilla between adjacent implants in esthetic areas of t

80 ave an effect on the incidence and height of papilla between adjacent implants in esthetic areas, and

81 The papilla between the teeth with recession was coronally a

82 rproximal contact to the tip of the gingival papilla (black space), distance from the base of the int

83 he modified Quigley-Hein plaque index (QHI), papilla bleeding index (PBI), and gingival index (GI) we

84 clinical attachment level, plaque index, and papilla bleeding index were recorded.

85 Plaque index, papilla bleeding index, recession depth (RD), recession

86 Probing depth and plaque, papilla bleeding, and hyperplastic index scores were rec

87 veloping tonotopic axis of the chick basilar papilla (BP) identified a gradient of Bmp7.

88 s of cell orientation in the chicken basilar papilla (BP), Vangl2 is present at supporting cell junct

89 es (Esrrg(-/-)) showed agenesis of the renal papilla but normal development of the cortex and remaini

90 thways among supporting cells in the basilar papilla but not in the utricular macula.

91 S100A4 was also observed in the medulla and papilla, but not the cortex of a human kidney.

92 ductal expression becomes localized to renal papilla by 18.5 dpc.

93 ed in the key follicle regulator, the dermal papilla, by analyzing individual follicular structures a

94 dge of the avian auditory organ, the basilar papilla, by embryonic day 5 (E5).

95 Normally, pollen tubes travel down the papilla cell and into the style.

96 ession stigma made numerous turns around the papilla cell before growing toward the style.

97 lated in both frontal scalp and beard dermal papilla cell cultures by dexamethasone.

98 fects of recombinant amelogenins on pulp and papilla cell proliferation were measured by Brd U immuno

99 Dermal papilla cells (DPCs) located in the hair bulb are the ma

100 Dermal papilla cells (DPCs) taken from male androgenetic alopec

101 ultured with either human dental mesenchymal/papilla cells (FDPCs) or human dental pulp cells (ADPCs)

102 occipital and frontal scalp and beard dermal papilla cells (n = 10) were established.

103 viously unrecognised heterogeneity in dermal papilla cells and shown that Sox2-positive cells specify

104 Communication between dermal papilla cells and the overlying epithelium is essential

105 d/or aromatase expression in cultured dermal papilla cells derived from human hair follicles.

106 at Blimp1 is dynamically regulated in dermal papilla cells during hair follicle (HF) morphogenesis an

107 eonatal foreskins and cultured murine dermal papilla cells from adult GFP transgenic mice and grafted

108 ature can be partially restored by growth of papilla cells in 3D spheroid cultures.

109 bal gene expression analysis of human dermal papilla cells in culture and discovered very rapid and p

110 te this process in humans using human dermal papilla cells in human skin have failed, suggesting that

111 to enrich for hair follicle-inducing dermal papilla cells in the dermal preparation.

112 d and androgen-treated cultured human dermal papilla cells isolated from beard (androgen-sensitive) a

113 in have failed, suggesting that human dermal papilla cells lose key inductive properties upon culture

114 on, this study supports that cultured dermal papilla cells provide a cell-based model system that is

115 ese genes in cultured beard and scalp dermal papilla cells reflected similar differences in microdiss

116 ignificantly upregulated in DSCCs and dermal papilla cells relative to FBs.

117 keratinocytes and fibroblasts without dermal papilla cells served as positive and negative controls r

118 nd-expressing cells, from placode and apical papilla cells to taste bud cells only, a surrounding pop

119 Proliferation of papilla cells was enhanced by recombinant human amelogen

120 ve capability, and we show that human dermal papilla cells, when grown as spheroids, are capable of i

121 d them with Sox2(-) (GFP(-)) CD133(+) dermal papilla cells.

122 tentially novel signaling pathways in dermal papilla cells.

123 1d, was slightly upregulated in beard dermal papilla cells.

124 significantly higher levels in beard dermal papilla cells.

125 Cs in hair-related studies often lack dermal papilla characteristics.

126 The BCR repertoires of the duodenal papilla comprised the same dominant IgG4+ clones as the

127 The dermal papilla comprises the specialised mesenchymal cells at t

128 tested, even in non-TM species whose basilar papilla contained as few as 50-60 hair cells.

129 The kidney papilla contains a population of cells with several char

130 Because the renal papilla contains DNA label-retaining cells and has been

131 G expression in late bell-stage human dental papilla contributes to the inductive potential of dental

132 er, innervation, which was maintained in the papilla core throughout treatment, was not sufficient to

133 oposed measuring methodology, four different papilla-deficit situations around ceramic implants could

134 terestingly, hair cells in the avian basilar papilla demonstrate both electrical resonance and force-

135 The presence of interproximal papilla depends on the distance between the contact poin

136 oncanonical Wnt pathways in tongue and taste papilla development have not been explored.

137 hibitory and activating or inducing roles in papilla development in linear patterns.

138 can be separated from that directing lingual papilla development.

139 through papilla placode appearance and taste papilla development.

140 Although label-retaining cells in the renal papilla diminished with time after ischemia-reperfusion

141 The presence or absence of the gingival papilla, distance from the base of the interproximal con

142 In neonatal mouse skin, two types of dermal papilla (DP) are distinguished by Sox2 expression: CD133

143 ly strategies for the interactions of dermal papilla (DP) cells with adipose-derived stem cells (ASCs

144 ive cues from specialized mesenchymal dermal papilla (DP) cells.

145 The hair follicle dermal papilla (DP) expresses androgen receptors (AR) and plays

146 Dermal papilla (DP) from laminin-511 mutants showed development

147 How dermal papilla (DP) niche cells regulate hair follicle progenit

148 ption factor Sox2 is expressed in the dermal papilla (DP) of guard/awl/auchene hair follicles and by

149 1) is expressed by fibroblasts in the dermal papilla (DP) of the hair follicle (HF).

150 in of function of beta-catenin in the dermal papilla (DP) of the hair follicle results in yellow and

151 ption factor Tbx18 specifically marks dermal papilla (DP) precursor cells during embryonic hair folli

152 The dermal papilla (DP) provide instructive signals required to act

153 Functional testing of dermal papilla (DP) signaling inputs into hair follicle (HF) mo

154 tic ablation of previously identified dermal papilla (DP) signature genes in embryonic DP precursors

155 ecialized mesenchymal population, the dermal papilla (DP), that is embedded in the hair bulb.

156 s of precursors for the hair follicle dermal papilla (DP).

157 he base of the follicle, known as the dermal papilla (DP).

158 a specialized mesenchymal niche, the dermal papilla (DP).

159 the Wnt3a gradient is dictated by the dermal papilla (DP).

160 either divided nor migrated out of the renal papilla during kidney repair.

161 Finally, in contrast to the chick basilar papilla, ectopic activation of Notch signaling did not i

162 is unique sensory organ includes taste buds, papilla epithelium and lateral walls that extend into un

163 Taste buds arise from papilla epithelium and, unusually for epithelial derivat

164 so had additional labeled innervation to the papilla epithelium.

165 rily responsible for tip elongation, whereas papilla erection is a hydraulic process driven by blood

166 Tumescence and papilla erection persist throughout tongue retraction, a

167 ing melanocytes located above the follicular papilla expresses Fas, TUNEL, and is likely to undergo a

168 etry of proteins pulled down from rat kidney papilla extract using a GST-AQP2 C-terminal fusion prote

169 -1) (gnom(B)(/E)) mutant revealed a delay in papilla formation and reduced penetration resistance.

170 tures, exogenous Wnt5a profoundly suppresses papilla formation and simultaneously decreases canonical

171 Papilla formation at the site of attack is essential for

172 We observed that during fungiform papilla formation in mice, Shh and components of the Wnt

173 in culture medium or by bead, does not alter papilla formation or number.

174 We suggest that papilla formation requires rapid reorganization of mater

175 owever, exogenous BMP2, 4 or 7 each inhibits papilla formation so that there is a decrease in papilla

176 Follicular papilla (FP) cells, but not their closely related dermal

177 In addition to the 'core' dermal papilla gene signature, each subpopulation expressed dis

178 p-Hh signaling pathway is crucial for apical papilla growth and proper root formation.

179 pacitance measurements of bullfrog amphibian papilla hair cells dialyzed with high concentrations of

180 ion in the mesenchymal component, the dermal papilla, has hampered progress towards understanding the

181 factors affect the central maxillary incisor papilla height (PH) and central clinically observable PH

182 le measurements including the papilla index, papilla height (PH), and gingival level (GL) were assess

183 cluded probing depth, buccal flap thickness, papilla height, and bleeding on probing.

184 tachment loss [AL] > or =3 mm) and a healthy papilla, if available (no BOP, PD < or =4 mm, and AL < o

185 ERCP at the level of the intact papilla in long limb Roux-en-Y is less successful as com

186 in 15 procedures) as compared to the intact papilla in long-limb (58 % in 24 procedures; P = 0.040).

187 rs, but confined to the hair follicle dermal papilla in normal postnatal skin.

188 s and quantitative parameters of interdental papilla in patients with CP.

189 % success in 56 procedures) or at the intact papilla in short-limb Roux-en-Y (80 % in 15 procedures)

190 ithin the apical half of the chicken basilar papilla in vivo and found broadly-tuned travelling waves

191 s connecting supporting cells of the basilar papilla, in which its immunofluorescence colocalized wit

192 vivo and found that some cells in the kidney papilla, including LRCs, migrated toward other parts of

193 At the 10-year follow-up visit, the papilla index and the apico-coronal location of mid-bucc

194 the two groups in the amount of bone gain or papilla index change during 2 years.

195 The papilla index decreased from baseline to 1 year in both

196 erence of mid-buccal gingival level (WDBGL), papilla index score (WDPIS), and width of keratinized gi

197 ft tissue profile measurements including the papilla index, papilla height (PH), and gingival level (

198 Other clinical parameters (papilla index, PH, GL, PI, and GI) showed no significant

199 ngiva [WKG], facial soft tissue level [FST], papilla index, plaque index, and bleeding on probing) we

200 Measurements of implant stability, papilla index, plaque, peri-implant mucosa, and marginal

201 The papilla indexes showed significant differences among the

202 cal Wnt signaling is known to regulate taste papilla induction and numbers, roles for noncanonical Wn

203 ional role of Blimp1 in promoting the dermal papilla inductive signaling cascade that initiates HF gr

204 s both a target and a mediator of key dermal papilla inductive signaling pathways including transform

205 aining showed the preservation of the apical papilla integrity and the presence of numerous human cel

206 lk analyses, after transplantation of apical papilla into the injured spinal cord wound, whereas the

207 The adult fungiform taste papilla is a complex of specialized cell types residing

208 roughout the kidney and found that the upper papilla is a site of enhanced cell cycling.

209 Since the follicular dermal papilla is known to control hair growth, and steroid hor

210 uency tuning within the apical avian basilar papilla is not mechanical, and likely derives from hair

211 show that JAK/STAT5 signaling in the dermal papilla is required for anagen onset in the murine hair

212 similar differences in microdissected dermal papilla isolated from intact beard and scalp follicles.

213 Although the bullfrog's amphibian papilla lacks the flexible basilar membrane that effects

214 ompartments (matrix keratinocytes and dermal papilla) leads to dynamic instabilities in the populatio

215 proteins become progressively restricted to papilla locations during tongue development.

216 tages, carries a risk of gingival recession, papilla loss, collapse of ridge contour, and other esthe

217 in fungiform papilla, taste bud and filiform papilla maintenance was shown by Gli2 constitutive activ

218 ation are preserved, as is expression of the papilla marker, Shh.

219 The papilla material is subsequently presumed to be sorted i

220 pp and Dmp1 gene expressions in mouse dental papilla mesenchymal cells.

221 nd enhance mineral formation of mouse dental papilla mesenchymal cells.

222 of mouse tooth development and mouse dental papilla mesenchymal cells.

223 beta-catenin within Shh(+) precursors during papilla morphogenesis also expands taste bud precursors

224 r taste placode formation, followed by taste papilla morphogenesis and taste bud differentiation, but

225 kkopf1 (Dkk1) blocks initiation of fungiform papilla morphogenesis.

226 However, fungiform papilla morphology, number and innervation are preserved

227 >/= 3 mm), and, when available, a 'healthy' papilla (n = 69; no bleeding-on-probing, probing depth <

228 r growth independently of mesenchymal dermal papilla niche signals normally required for hair regener

229 tagonizes canonical Wnt signaling to dictate papilla number and spacing.

230 lla formation so that there is a decrease in papilla number.

231 It is expressed in the dermal papilla of all pelage hair follicle types from the earli

232 of the sonic hedgehog pathway in the dermal papilla of developing hair follicles.

233 n4 expression significantly increased in the papilla of mice after 36 h of thirsting.

234 sion of Nup88 increased 410.4 +/- 22% in the papilla of mice after 36 h of thirsting.

235 C1 expression significantly increased in the papilla of mice following 36 h of fluid restriction and

236 Frequency tuning within the auditory papilla of most non-mammalian species is electrical, der

237 expressed in anthers of flower buds, stigma papilla of open flowers, and embryo and endosperm during

238 to regulate epithelial cell survival in the papilla of the developing kidney, allowing for the elong

239 th interstitial deposition of calcium in the papilla of the kidney.

240 o inability to reach or cannulate the intact papilla or bilioenteric anastomosis.

241 In the chicken cochlea (the basilar papilla or BP), dying hair cells are extruded from the e

242 uring normal homeostasis, LRCs of the kidney papilla (or their immediate progeny) migrate to the uppe

243 did not influence the incidence of gingival papilla (P >/=0.41) and black space (P >/=0.15).

244 ve roles for Wnt5a in tongue size, fungiform papilla patterning and development are shown and a neces

245 y may underlie evolutionary changes in taste papilla patterning.

246 presence of five external types of sensilla: papilla, pit, spot, knob, and modified papilla.

247 the initiation of tongue formation, through papilla placode appearance and taste papilla development

248 that the BMPs and noggin, colocalized within papilla placodes and the fungiform papillae per se, have

249 itiation (E13) or from a stage after the pre-papilla placodes have formed (E14).

250 rate that hair cells of the chicken auditory papilla possess an electromechanical force generator in

251 erivative (EMD) associated with a simplified papilla preservation flap (SPPF) technique to SPPF alone

252 Papilla preservation flaps were raised, and defects were

253 ultured and expanded fibroblasts following a papilla priming procedure suggests that the treatment is

254 st injections following a minimally invasive papilla priming procedure to augment open interproximal

255 bo injections beginning 1 week following the papilla priming procedure; two additional injections wer

256 histone 2B, we observed that the LRCs of the papilla proliferated only in its upper part, where they

257 crease or ameliorate the severity of central papilla recession by restorative/prosthetic or orthodont

258 Among all study patients, papilla recession status and PT-CP were significant inde

259 Age, papilla recession status, PT-CP, and BC-pCEJ were signif

260 Among patients with papilla recession, CW and PT-CP independently predicted

261 cantly associated with COPH in patients with papilla recession, especially IW, PTW, PT-CP, and BC-pCE

262 ith PH and COPH in patients with and without papilla recession.

263 sensory organ (the lagena macula and basilar papilla, respectively), which each have a distinct struc

264 erived from human dental pulp (DPSC), apical papilla (SCAP) and follicle (DFSC) during this study.

265 Stem cells of the apical papilla (SCAP) represent great promise regarding treatme

266 stem cells (PDLSCs), stem cells from apical papilla (SCAP), and dental follicle progenitor cells (DF

267 em cells, including stem cells of the apical papilla (SCAP), into the root canal system.

268 Stem cells from the apical papilla (SCAPs) are important for the formation and rege

269 Papilla scores increased significantly (P <0.001; Wilcox

270 ursors of adult HF stem cells and the dermal papilla/sheath niche, along with lineage-related keratin

271 Both the follicular epithelium and dermal papilla showed markedly decreased Wnt/beta-catenin signa

272 thermore, we pinpoint KIT-ligand as a dermal papilla signal promoting melanocyte stem cell differenti

273 epithelial stem cells that respond to dermal papilla signaling.

274 and BAN retained high proportions of dermal papilla signature gene and versican protein expression.

275 enes, sfrp-2 has been identified as a dermal papilla signature gene in mouse pelage follicles.

276 accelerates Type I cell differentiation, but papilla size is no longer enhanced.

277 follicle are still competent to form dental papilla specific cell types, such as odontoblasts, and p

278 xpression is required until the early dermal papilla stage for guard hair germs to make follicles, bu

279 rement for normal Shh signaling in fungiform papilla, taste bud and filiform papilla maintenance was

280 potent cell types from the hair follicle and papilla that can produce various sets of lineages.

281 forms the upper dermis, including the dermal papilla that regulates hair growth and the arrector pili

282 At the core is the dermal papilla, the organizing center, and the epithelial stem

283 o endogenous EDN3 upregulation in the dermal papilla, the secondary hair germ cells, and the epidermi

284 BC) to CP (BC-CP), BC to pCEJ (BC-pCEJ), and papilla tip (PT) to CP (PT-CP) and the interdental width

285 t is, by transplantation of the human apical papilla tissue itself into the lesion.

286 d from human and rodent epidermis and dermal papilla to reconstitute hair-follicle mini-organs.

287 We demonstrate that the intact dermal papilla transcriptional signature can be partially resto

288 Notably, the apical papilla transplant group presented with reduced Iba-1 ex

289 Eligible patients with native papilla undergoing ERCP were randomly assigned in a 1:1

290 expression increased 253% (P < 0.01) in the papilla upon 36 h of thirsting.

291 with the cortex and increased further in the papilla upon 36 h of thirsting.

292 We conclude that hair cells of the amphibian papilla use synaptic tuning as an additional mechanism f

293 The papilla was always present when vertical distance was </

294 e bone crest at the implant was </=5 mm, the papilla was completely present in 100% of cases.

295 In the x-ray image, the tip of the papilla was marked with a radiodense mixture of tungsten

296 When this distance was 10 mm, the papilla was still present in 67% of the cases, without a

297 The central papilla was visually assessed in 450 adults using standa

298 al follicle, and also the apical part of the papilla, where the roots will ultimately develop.

299 ney, Nup88 expression was substantial in the papilla, whereas it was nearly absent in the cortex.

300 hese mice exhibit a dysplastic circumvallate papilla with disrupted Shh expression.