ライフサイエンスコーパス: papilla

1 vasculature on the optic disc (Bergmeister's papilla).

2 herapeutic ERCP and had naive major duodenal papilla.

3 rom the frog sacculus and the turtle basilar papilla.

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

5 er of principal cells expressing PCNA in the papilla.

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

7 n (APC) applied circumferentially around the papilla.

8 r buds also show abnormalities in the dermal papilla.

9 the result of endoscopic intervention of the papilla.

10 rising from underneath the hood of the major papilla.

11 l ammonium facilitating its retention in the papilla.

12 ely epithelial matrix and mesenchymal dermal papilla.

13 the frequency range sensed by the amphibian papilla.

14 provide the major contribution to the dental papilla.

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

16 cceptable outcomes in terms of interproximal papilla.

17 ert with the epithelium to create the dental papilla.

18 ssed markers of the dermal sheath and dermal papilla.

19 loss of the interproximal height of bone and papilla.

20 ation of epithelial tubules to form a mature papilla.

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

22 e difficult to cannulate compared to regular papilla.

23 to the dorsal anterior tongue and fungiform papilla.

24 ith greater SBC failure compared with Type 1 papilla.

25 thin the chicken auditory organ: the basilar papilla.

26 etic alopecia by interfering with the dermal papilla.

27 l new molecular landscapes within the dermal papilla.

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

29 ontact area of the crowns on the interdental papilla.

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

31 DPCs have high resemblance to intact dermal papilla.

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

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

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

35 afferent fiber synapse in bullfrog amphibian papilla adjust to a wide range of physiological temperat

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

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

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

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

40 Eligible patients (>=18 years) with native papilla and common bile duct stones (<=1.5 cm in size an

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

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

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

44 talloproteinase 1 was elevated in the dermal papilla and dermal sheath in situ.

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

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

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

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

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

50 ted by reduced proliferation of human dermal papilla and predominantly epithelial keratinocytes after

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

52 Small papilla and protruding or pendulous papilla are more dif

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

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

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

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

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

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

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

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

61 The failure rates of SBC with Type 3 papilla and Type 4 papilla were 11.11% and 6.25%, respec

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

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

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

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

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

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

68 Small papilla and protruding or pendulous papilla are more difficult to cannulate compared to regu

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

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

71 The distal papilla around tooth-bound implant-supported restoration

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

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

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

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

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

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

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

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

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

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

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

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

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

85 describe a unilateral case of Bergmeister's papilla (BP) in a young female patient suffering from ty

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

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

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

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

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

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

92 gma by ensuring mechanical anisotropy of the papilla cell wall.

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

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

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

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

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

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

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

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

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

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

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

104 d CMFs in aged Col-0 and katanin1-5 (ktn1-5) papilla cells is accompanied by a tendency of pollen tub

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

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

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

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

109 tubes first grow within the cell wall of the papilla cells, applying pressure to the cell.

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

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

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

113 ower recession of the tip of the interdental papilla compared with MIST (P < 0.001).

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

115 The dermal papilla comprises the specialised mesenchymal cells at t

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

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

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

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

120 -posterior Wnt2b signaling within the dermal papilla controls barbule cell fates with spatiotemporal

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

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

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

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

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

126 can be separated from that directing lingual papilla development.

127 through papilla placode appearance and taste papilla development.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

143 rget lung CSCs but not normal primary dermal papilla (DP) stem cells.

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

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

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

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

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

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

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

151 so had additional labeled innervation to the papilla epithelium.

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

153 Tumescence and papilla erection persist throughout tongue retraction, a

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

155 closure, we found that hair follicle dermal papilla fibroblasts could accelerate closure of in vitro

156 a cytokine array to determine how the dermal papilla fibroblasts were eliciting this effect and ident

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

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

159 Papilla formation at the site of attack is essential for

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

161 We suggest that papilla formation requires rapid reorganization of mater

162 pressed in both dental epithelium and dental papilla from E14.5 and persisted in both tissues at late

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

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

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

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

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

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

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

170 %, p = 0.020) compared to the other types of papilla However, papilla morphology was not a significan

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

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

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

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

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

176 % success in 56 procedures) or at the intact papilla in short-limb Roux-en-Y (80 % in 15 procedures)

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

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

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

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

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

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

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

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

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

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

187 The papilla indexes showed significant differences among the

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

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

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

191 rgical technique, that keeps the interdental papilla intact, seems promising to provide optimal bioma

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

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

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

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

196 Small papilla is associated with a higher rate of post-ERCP pa

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

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

199 , an apatite deposit at the tip of the renal papilla, is considered to at the origin of these stones.

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

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

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

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

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

205 The papilla material is subsequently presumed to be sorted i

206 e transport processes of stimuli through the papilla matrix to reach taste receptors, processes that

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

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

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

210 tected in the dental follicle/sac and dental papilla mesenchyme of developing teeth and in odontoblas

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

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

213 We investigated whether duodenal major papilla morphology could be a risk factor for failure of

214 pared to the other types of papilla However, papilla morphology was not a significant risk factor for

215 We used Haraldsson's classification for papilla morphology, as follows: Regular (Type 1), Small

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

217 >/= 3 mm), and, when available, a 'healthy' papilla (n = 69; no bleeding-on-probing, probing depth <

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

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

220 In the multivariate analysis, Type 2 papilla (odd ratio 7.18, p = 0.045) and Type 3 papilla (

221 pilla (odd ratio 7.18, p = 0.045) and Type 3 papilla (odd ratio 7.44, p = 0.016) were associated with

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

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

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

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

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

227 partment and androgen receptor in the dermal papilla of miniaturized hair.

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

229 , we described anatomic changes within renal papilla of Npr2 knockout (Npr2(-/-)) mice.

230 totic cells (cleaved caspase 3) in the renal papilla of Npr2(-/-) mice.

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

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

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

234 e expression of Wnt4 and Axin2 in the dental papilla of the presumptive root furcating region, where

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

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

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

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

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

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

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

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

243 ate the clinical applicability of the entire papilla preservation (EPP) technique in the regenerative

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

245 Papilla preservation flaps were raised, and defects were

246 Combination therapy of papilla preservation, connective tissue grafting, and co

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

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

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

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

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

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

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

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

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

256 n of enamel matrix derivative (EMD) added to papilla reflection/root preparation (PR/RP) could enhanc

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

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

259 to reprogram stem cells from a tooth apical papilla (SCAP) of a patient with OFCD, termed SCAP-O, in

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

261 (BMSC), dental pulp (DPSC) and dental apical papilla (SCAP) to engineer pericyte-supported vascular c

262 human mesenchymal stem cells from the apical papilla (SCAP) to reduce local inflammation and provide

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

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

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

266 Papilla scores increased significantly (P <0.001; Wilcox

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

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

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

270 epithelial stem cells that respond to dermal papilla signaling.

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

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

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

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

275 surgical technique (MIST) and a non-incised papilla surgical approach (NIPSA) in periodontal reconst

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

291 Type 2 papilla was correlated with a higher rate of post-ERCP p

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

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

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

295 rates of SBC with Type 3 papilla and Type 4 papilla were 11.11% and 6.25%, respectively.

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

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

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

299 nd placed under the intact defect-associated papilla with palatal positioning suture.

300 that time-concentration profiles within the papilla zone rise with significant delay that well match