ライフサイエンスコーパス: pulp

1 dry pulp) and anthocyanins (168.9mg/100g dry pulp).

2 tween the dry matter and oil contents in the pulp.

3 te pulp, merged with components of the white pulp.

4 p 3 were observed mainly in peel but not in pulp.

5 er rise of reducing and total sugar in guava pulp.

6 lisation of resident stem cells in the tooth pulp.

7 try feed materials such as molasses and beet pulp.

8 ide better microencapsulation of the jussara pulp.

9 in many orofacial tissues, including dental pulp.

10 e different parts of berries: skin, seed and pulp.

11 ost equally over the supernatant, pellet and pulp.

12 ion potentials similar to DPSCs from healthy pulp.

13 ere found below the LOQ in coconut water and pulp.

14 dant and antimutagenic activities of copaiba pulp.

15 avonoids, with higher content in relation to pulp.

16 ged blood vessels were observed in the tooth pulp.

17 hed wheat bran, sugar beet pectin and coffee pulp.

18 soquercitrin, were identified in the copaiba pulp.

19 meable channels, are present in human dental pulp.

20 d cellulose nanofibrils (CNF) made from wood pulp.

21 re adjacent to Tcf21(+) stromal cells in red pulp.

22 content of 332.00microg/g dw compared to the pulp.

23 f.w. in peel and 97.33-217.36mg/kg in quince pulp.

24 patatin and protease inhibitors from potato pulp.

25 s a 10-fold higher phenolic content than the pulp.

26 kali extract and 4.2% of the dry matter acai pulp.

27 s and adjacent teeth with vital and necrotic pulps.

28 a dentinogenic response in teeth with viable pulps.

29 traction procedures assessing acai and grape pulps.

30 es are also derived from lignin during kraft pulping.

31 The pulp adhered only partially to the seeds in 5 of the 6 a

32 verexpression of TNF-alpha in both the tooth pulp and bone to study oral pain that would result from

33 gest source of xylan found so far in a fruit pulp and could be suitable for applications in the indus

34 e models and a pathological reduction in red pulp and extramedullary hematopoiesis.

35 n of genes from the flavonoid pathway in the pulp and juice than those kept at 4 degrees C.

36 results showed that in many samples of beet pulp and molasses the content of "undesirable substances

37 materials makes it a target molecule of the pulp and paper industry's bleaching efforts.

38 ed to extensively map the proteome of orange pulp and peel and, via this fingerprinting, to detect it

39 hin and epicatechin were the major ones from pulp and peel, whereas seed displayed caffeic acid, cate

40 ed by lyophilization of whole fruits, seeds, pulp and skin from chilto (Solanum betaceum Cav) cultiva

41 The delta(13)C and delta(15)N of pulp and the delta(18)O of juice can be considered effec

42 These are first reports of AGII in papaya pulp and the first reports of an in vitro biological act

43 is the interface between the nonlymphoid red pulp and the lymphoid white pulp, merged with components

44 splenic neutrophils that localize in the red pulp and the marginal zone.

45 nate immunomodulatory activity in the dental pulp and their capability for pulp repair.

46 inked to the presence of nerve fibers in the pulp and to the healing mechanism by sprouting of the ne

47 otenoid profiles of different tissues (peel, pulp and whole fruit) of Spanish Sanguinos (red) and Ver

48 ting the changes in the proteomic profile of pulped and natural C. arabica grains dried in a yard or

49 s their bioaccessibilities were evaluated in pulps and compared to those in fresh juice.

50 Oranges (N and CC) pulps and juices presented higher bioaccessibilities tha

51 in both hydroxycinnamates (421.6mg/100g dry pulp) and anthocyanins (168.9mg/100g dry pulp).

52 in vitro gastrointestinal digestion of acai pulp, and a subsequent pH-controlled, anaerobic, batch-c

53 ates and in different fruit fractions (peel, pulp, and calyx of ripe fruits) were investigated by HPL

54 cells in irreversibly inflamed human dental pulp, and extracts of this tissue have significantly inc

55 applied to determine metal ions in the peel, pulp, and seed of Passiflora edulis f.

56 peel of kumquat were higher than those from pulp, and those extracted from immature kumquat were hig

57 nchymal tissues, the periodontium and dental pulp, are maintained by distinct pools of stem cells.

58 solid content, titratable acidity, pH of the pulp as well as in sugar content and decreased starch de

59 acid to pretreat a kraft bleached Eucalyptus pulp (BEP) fibers to facilitate mechanical fibrillation

60 Highly relevant for pulp bleaching are the findings on intermediates of the

61 mills across Canada, representing the major pulping, bleaching, and effluent treatment technologies.

62 Potato pulp by-product rich in galactan-rich rhamnogalacturonan

63 s the most abundant polysaccharide in potato pulp by-product.

64 volatile fraction composition of these fruit pulps by increasing substantially the number of compound

65 Jucara pulp can modulate the intestinal microbiota in vitro, pr

66 Direct pulp capping involves the placement of dental materials

67 Although numerous direct pulp capping materials are available, the use of small b

68 er study for their potential clinical use as pulp capping materials.

69 hat can serve as biocompatible and bioactive pulp-capping materials, driving dentin bridge formation

70 Furthermore, transplantation and pulp-capping procedures revealed that this DSP domain in

71 genic/osteogenic differentiation from dental pulp cells (DPCs) in vitro.

72 Human dental pulp cells (DPCs), adherent cells derived from dental pu

73 C90028, the cytotoxicity toward human dental pulp cells (HDPCs), and the mechanical properties of a s

74 are able to identify the formation of tooth pulp cells and odontoblasts in bioengineered teeth.

75 i1, Numb, and Notch expression in the dental pulp cells and odontoblasts of DSPP-null mice when compa

76 drogels were seeded either with human dental pulp cells from patients with characterized PHEX mutatio

77 Insights into the role of mesenchymal dental pulp cells in attenuating dentin resorption in homeostas

78 In conclusion, data indicate that culture of pulp cells in the presence of ECM better replicates the

79 are unable to contribute to the formation of pulp cells or odontoblasts, and at ratios of 1:1, they i

80 C/HUVEC-encapsulated GelMA constructs formed pulp cells that attached to the inner dentin surface of

81 Continuous exposure of pulp cells to FGF2 inhibited odontoblast differentiation

82 ation, whereas early and limited exposure of pulp cells to FGF2 resulted in marked increases in odont

83 iation could be achieved by culturing dental pulp cells with their associated ECM.

84 orcine dental epithelial cells, human dental pulp cells, and human umbilical vein endothelial cells (

85 Postnatal pulp cells, however, lose all tooth-inducing and tooth-f

86 cts of FGF signaling on the proliferation of pulp cells, there are conflicting results regarding its

87 ic cells and populations of postnatal dental pulp cells; however, these cells are unable to contribut

88 an clinically evident and rarely invaded the pulp chamber.

89 wing a high incidence of taurodontism: large pulp chambers lacking or showing delayed bifurcation or

90 ion of the carrot juice with peel (CJPL) and pulp (CJPP) extracts.

91 rent genotypes of mamey sapote with distinct pulp colors are consumed in countries from Central to So

92 moisture loss and maintained both flesh and pulp colour by inhibiting polyphenol oxidase (PPO) activ

93 The pulp colour was highly correlated with total phenolic co

94 may serve as a therapeutic agent for dentin-pulp complex regeneration in dental caries.

95 t of the calvaria, alveolar bone, and dentin-pulp complex.

96 y for engineering of pre-vascularized dental pulp constructs offering potentially beneficial translat

97 influence of ultrasound processing on tomato pulp containing no sunflower oil, or increasing amounts

98 Mango pulp contains antioxidant, such as mangiferin, that can

99 Coffee cherry pulp contains considerable amounts of phenolic compounds

100 mples from a Swedish chemi-thermo-mechanical pulp (CTMP) mill collected at different purification sta

101 neralization phase of the in vitro growth of pulp cultures derived from a series of green fluorescent

102 differentiation of remaining progenitors in pulp cultures into functional odontoblasts but prevented

103 er; delta(15)N and delta(13)C content of the pulp, (D/H)I and (D/H)II in ethanol and the concentratio

104 ce delta(18)O and fertilisation practices on pulp delta(15)N was demonstrated and must be considered

105 ns in internal resorption in the root canal, pulp/dentin regeneration, and root resorption in orthodo

106 cells (DPSCs) can be isolated from inflamed pulp derived from carious teeth with symptomatic irrever

107 suggest that LNGFR(Low+)THY-1(High+) dental pulp-derived cells provide an excellent source of materi

108 Prospectively isolated, dental pulp-derived LNGFR(Low+)THY-1(High+) cells represent a h

109 ispersions, composed of suspended particles (pulp) dispersed in a colloidal liquid medium (serum).

110 C) with stem cells derived from human dental pulp (DPSC), apical papilla (SCAP) and follicle (DFSC) d

111 ected T cells were numerous within the white pulp during acute infection, but were rarely observed th

112 c acid and carotenoid degradation in acerola pulp during ohmic heating was evaluated.

113 ration, which may be useful in future dentin-pulp engineering strategies that target fibroblast C5L2

114 ntents of FOS and CGA were maintained in the pulping, enzymatic maceration and microfiltration, leadi

115 mice produced greater splenomegaly with red pulp expansion and obscured architecture.

116 Using an experimental pulp exposure model in molars to induce reparative denti

117 In a model of tooth injury with pulp exposure, ephrinB1 was strongly expressed in odonto

118 rocesses 2 wk following tooth injury without pulp exposure, whereas EphB2 was expressed in the center

119 During caries, dental pulp expresses a range of pro-inflammatory cytokines in

120 old that mimics the complexity of the dental pulp extracellular matrix (ECM).

121 in PCa cells could be inhibited by Graviola pulp extract (GPE) that contains unique acetogenins with

122 Jackfruit pulp extract was sequentially fractionated by chromatogr

123 loited commercially by local farmers for the pulp extracted from its fruits.

124 detected mainly in the peel but also in the pulp extracts.

125 ss by linking the neurite outgrowth to human pulp fibroblast through complement system activation.

126 e C5a active receptor (C5aR/CD88) by injured pulp fibroblasts controls the direction of neurite outgr

127 While few pulp fibroblasts in intact teeth and in untreated fibrob

128 tooth sections in vivo and on primary human pulp fibroblasts in vitro, the authors reveal that C5L2

129 he dentin-pulp regeneration process, linking pulp fibroblasts to the nerve sprouting through the comp

130 as a negative regulator of BDNF secretion by pulp fibroblasts under carious teeth.

131 eveal that C5L2 and C5aR are co-expressed by pulp fibroblasts under lipoteichoic acid (LTA) stimulati

132 rve regeneration in the secretion of BDNF by pulp fibroblasts under sites of carious injury.

133 eceptor (C5aR), here we show that all dental pulp fibroblasts, localized beneath the carious injury s

134 The NGF secretion by LTA-stimulated pulp fibroblasts, which is negatively regulated by C5aR

135 ter complement synthesis and activation from pulp fibroblasts, with the C5aR of these cells mediated

136 brain-derived neurotrophic factor (BDNF) by pulp fibroblasts.

137 odulation of NGF secretion by LTA-stimulated pulp fibroblasts.

138 sion of C5aR in lipoteichoic acid-stimulated pulp fibroblasts.

139 y increases BDNF secretion by LTA-stimulated pulp fibroblasts.

140 dry matter (DM), titratable acidity (TA) and pulp firmness (PF).

141 Irradiation caused immediate reductions in pulp firmness, vitamin E, individual sugars and caroteno

142 - and red-grape peels and red-beet peels and pulp) for the purpose of increasing the wastes' value.

143 ds were extracted from seed mucilage and the pulp fractions from red tamarillo (Solanum betaceum Cav.

144 ic failure, while also protecting the dental pulp from bacterial attack.

145 d phenolic compounds in lyophilized peel and pulp from fresh fruit.

146 Thus, this study reports that human dental pulp from healthy extracted teeth can be successfully de

147 Buriti pulp from the Cerrado presented higher phenolic levels (

148 ivity, and sensorial acceptance of six fruit pulps from the Brazilian Cerrado.

149 a. 124 mug retinol-activity-equivalents/100g pulp, FW).

150 from araticum fruit followed the order peel>pulp>seed.

151 Watermelon pulp had 59.95mglycopene/100g on fresh weight basis.

152 AA and TPC, while FM with added sweet potato pulp had the best sensory acceptance.

153 For export, the pulp has to be separated from the skin which is usually

154 ing the potential prebiotic effect of jucara pulp; however, human studies are necessary to prove its

155 This enabled the pulp hydrocolloid to entrap more bile acids (35-38% at a

156 The pulp hydrocolloid, however, possessed high oil-holding a

157 good foaming capacity (32-36%), whereas the pulp hydrocolloids that were extracted, using 72% ethano

158 66 to <0.01M and the moisture content of the pulp increased from 93% to 97% (wet basis), showing the

159 Carob pulp increased the concentration of polyunsaturated fatt

160 nfected, which primarily occurred in the red pulp independent of T cells.

161 The composition of fruit pulps indicated the potential there for the development

162 Here, we use a nonexposed pulp injury model to investigate the mechanisms of react

163 aling is pivotal for tooth repair in exposed pulp injury, and the pathway can be activated by small-m

164 tegies that target fibroblast C5L2 to induce pulp innervation.

165 as permanent filling materials at the dentin-pulp interface in direct contact with irreversibly injur

166 rmented milks (FM) with/without sweet potato pulp (Ipomoea batatas).

167 Coffee cherry pulp is a by-product obtained during coffee production.

168 Industrially the avocado pulp is exploited principally as oil and paste, generati

169 ratively exposed dentine in teeth with vital pulps is concerned.

170 emical and proteomics analysis of the fruit, pulp juice and seeds of these three species.

171 ion analysis and protein profiling of fruit (pulp juice and seeds).

172 f sugar, organic acid, and phenol content in pulp juice revealed equivalence among the three species,

173 Proteins were extracted from seeds and pulp juice, resolved by two dimensional electrophoresis

174 residue comprising mainly peels, seeds, and pulp, known as apple pomace.

175 icated pre-vascularized, full-length, dental pulp-like tissue constructs by dispensing OD21 cell-lade

176 gineer pre-vascularized, cell-laden hydrogel pulp-like tissue constructs in full-length root canals f

177 RSs, and less cellularized host cell-derived pulp-like tissue was observed in the G2 acellular GelMA

178 lyses of harvested samples found that robust pulp-like tissues formed in G1, GelMA encapsulated hDPSC

179 was to define reliable methods to regenerate pulp-like tissues in tooth root segments (RSs).

180 Additionally, red pulp macrophages, a discrete subset of yolk sac-derived

181 tal caries that has not penetrated the tooth pulp, maintenance of as much unaffected dentine as possi

182 showed that herbal extracts and sweet potato pulp may be used to develop new dairy foods with potenti

183 nonlymphoid red pulp and the lymphoid white pulp, merged with components of the white pulp.

184 at this DSP domain induces endogenous dental pulp mesenchymal cell proliferation, differentiation and

185 cost-effective solutions for the effects of pulp mill effluents on fish reproduction.

186 For Kraft and mechanical pulp mills, effluents containing less than 20 mg/L BOD5

187 ol and acetone extracts from quince peel and pulp, namely 3-O-caffeoylquinic acid (3-CQA), 4-p-coumar

188 es suffer from dental infections, leading to pulp necrosis, arrested tooth-root development and tooth

189 urrent study sheds light on the mechanism of pulp nerve regeneration by identifying C5L2 as a negativ

190 work aims to investigate the role of C5L2 in pulp nerve regeneration in the secretion of BDNF by pulp

191 unctional mechanism linking C5aR and C5L2 in pulp nerve regeneration, which may be useful in future d

192 C5a could be an initial signal orchestrating pulp nerve sprouting beneath carious injury, a critical

193 whereas EphB2 was expressed in the center of pulp niches but not odontoblasts.

194 almitate were the most abundant in peels and pulp of all samples.

195 trogenous compounds, especially GABA, in the pulp of Cabernet Sauvignon grapes suggests changes in st

196 The fruit pulp of Eugenia jambolana (jamun) is a rich source of an

197 mpounds and total flavonoids contents in the pulp of mamey apple fruits.

198 ocyanin biosynthesis and accumulation in the pulp of Moro blood and Pera blond oranges (Citrus sinens

199 nd bioactive compounds content of the edible pulp of six Mammea americana accessions.

200 accumulated at the T/B borders in the white pulp of the spleen and that OX40-dependent signals direc

201 and all three materials were seen in the red pulp of the spleen.

202 Total carotenoid concentrations in the pulp of yellow- and red-peeled cashew apples were low (0

203 Their presence was investigated in fruit pulps of Annona squamosa from different locations.

204 f bioactive compounds and AAC were higher in pulps of both oranges and mandarin than in their corresp

205 Thus, pulps of oranges and mandarins displayed higher hesperid

206 includes either tamarind (Tamarindus indica) pulp or dried slices of Garcinia atroviridis fruit in th

207 0 million ha globally) for the production of pulp, paper, bioenergy, and other lignocellulosic produc

208 Pulp pasteurization resulted in a reduction in phenolic,

209 ylated and insoluble-bound forms of araticum pulp, peel and seed were for the first time characterize

210 he present study the antioxidant activity of pulp, peel and seeds of four cultivars from A. cherimola

211 e differences in the composition of the pear pulp, peel, leaves and seeds.

212 mediate vascularization of engineered dental pulp poses a major hurdle towards successful implementat

213 ons with faecal inoculate, the digested acai pulp precipitated reductions in the numbers of both the

214 st-like cell differentiation of human dental pulp progenitor cells (DPSCs).

215 n of the active Complement C5a fragment with pulp progenitor cells.

216 ely practiced, clinical protocols to improve pulp protection and dentine regeneration are not current

217 rrelated to seed weight (r=0.89) and seed-to-pulp ratio (r=0.73).

218 hurdle towards successful implementation of pulp regeneration as an effective therapeutic strategy f

219 Dentin-pulp regeneration is closely linked to the presence of n

220 ffect of residual bacteria on the outcome of pulp regeneration mediated by a tissue-engineered constr

221 infection may interfere with the success of pulp regeneration procedures.

222 incipient interventions targeting the dentin-pulp regeneration process by linking the neurite outgrow

223 sm in one of the initial steps of the dentin-pulp regeneration process, linking pulp fibroblasts to t

224 l in targeting the fibroblasts in the dentin-pulp regeneration process.

225 teeth and plays an important role in dental-pulp regeneration via interaction of the active Compleme

226 th carious injury, a critical step in dentin-pulp regeneration.

227 ssive functions of IP-DPSCs to enable dentin/pulp regeneration.

228 intact IP-DPSCs may be inadequate for dentin/pulp regeneration.

229 Cs) are considered to be suitable for dentin/pulp regeneration.

230 tructs in full-length root canals for dental pulp regeneration.

231 in the dental pulp and their capability for pulp repair.

232 The pulp represented between 50 and 70% of the weight of the

233 Pulp response of 0.1, 0.2 and 0.3 MPa groups showed only

234 the mechanism for caries resistance and the pulp responses in vital teeth following the use of the a

235 Pulp responses of vital dog's teeth to the augmented-pre

236 Fermentation of jucara pulp resulted in a significant increase in numbers of bi

237 Aqueous extraction of coffee pulps revealed a content of total polyphenols between 4.

238 ecific CD8(+) T cells within the splenic red pulp (RP) had higher two-dimensional (2D) effective affi

239 f other splenic compartments such as the red pulp (RP) largely unexplored despite asplenic patients s

240 Six dried coffee pulp samples and a beverage called Cascara produced in S

241 of phenolic compounds and carotenoids in the pulp, seed, and peel extracts of B. setosa fruits and th

242 ontent and antioxidant activity in the skin, pulp, seed, cane and leaf of one international (Muscat)

243 Fructose was the major sugar in pulp, seeds and peel (227.46, 45.36 and 67.49 g/kg dry m

244 I-MS(n) measurements in the fruits' peel and pulp showed that isorhamnetin 3-O-rutinoside was determi

245 l sulphate (SDS) enhanced PPO activity, with pulp showing a stronger increase than skin.

246 ca papaya L.) is a fleshy fruit with a rapid pulp softening during ripening.

247 ion behavior of a population of human dental pulp stem cell (hDPSC) on 64 combinations of nanopattern

248 Dental pulp stem cells (DPSC) are a relatively new alternative

249 Human dental pulp stem cells (DPSCs) can be isolated from inflamed pu

250 c MC3T3-E1 cells and preodontoblastic dental pulp stem cells (DPSCs) in a dose-dependent manner.

251 r autologous transplantation of human dental pulp stem cells (DPSCs) in endodontic treatment.

252 that can support native functions of dental pulp stem cells (DPSCs), which are capable of regenerati

253 gulatory functions of disease-derived dental pulp stem cells (DPSCs).

254 G1 RSs were injected with human dental pulp stem cells (hDPSCs) and human umbilical vein endoth

255 l and triple antibiotic paste, ferret dental pulp stem cells, encapsulated in a hydrogel scaffold, we

256 ing in endothelial differentiation of dental pulp stem cells.

257 induce endothelial differentiation of dental pulp stem cells.

258 entiation and mineralization of human dental pulp stem cells.

259 Human dental pulp stem/progenitor cells (hDPSCs) are attractive candi

260 pha(glo) mice show inflammation in the tooth pulp that resembles pulpitis while also displaying perio

261 tions in the rodent incisor apex, the dental pulp, the alveolar bone, the periodontal ligament, the c

262 tial of targeting ephrinB1 as a regenerative pulp therapy.

263 and enamel; they show a lack of signal from pulp tissue and reduced signal from de-mineralized cario

264 a promising therapeutic strategy for dentin/pulp tissue engineering in future endodontic treatment.

265 romising new therapeutic strategy for dentin/pulp tissue engineering in future endodontic treatment.

266 lpitis is treated by the complete removal of pulp tissue followed by replacement with artificial mate

267 Here, we identified a dental pulp tissue-specific cell population based on the expres

268 ogical seal" between these materials and the pulp tissue.

269 in direct contact with irreversibly injured pulp tissue.

270 ment of dental materials directly onto vital pulp tissues after deep caries removal to stimulate the

271 s (DPCs), adherent cells derived from dental pulp tissues, are potential tools for cell transplantati

272 mesenchymal stromal cells in inflamed human pulp tissues.

273 ization treatment to regenerate human dental pulp tissues.

274 l fluorescence intensity was achieved with a pulp to AO/LDH ratio of 1:5 which can be used to detect

275 methods of decellularization of human dental pulp to be used as a potential autograft scaffold.

276 , we detected ecto-AMPase activity in dental pulp, trigeminal ganglia (TG) neurons, and their nerve f

277 he stability of bioactive compounds in butia pulp upon pasteurization, during 12months of frozen stor

278 total anthocyanin and total phenolic in acai pulp using a 3-step optimization approach.

279 ation of ten pesticides in coconut water and pulp using QuEChERS and LC-MS/MS.

280 ene extraction was optimized from watermelon pulp using response surface methodology using independen

281 ork was to study the spray drying of jussara pulp using ternary mixtures of gum Arabic (GA) and modif

282 potential fermentation properties of jucara pulp, using pH-controlled anaerobic batch cultures refle

283 nolics (121-9889 mg GAE 100 g(-1) dry weight pulp), vitamin C (31-1532 mg AA 100 mL(-1) juice) and an

284 The fresh pulp was acidic, sweet, succulent and crunchy.

285 spinning (HR-MAS) NMR spectroscopy of apple pulp was performed before and after two time points of c

286 Zn), iron (Fe), and copper (Cu) in the fruit pulp was similar with all three fertilizers, but the cal

287 tion with chlorophyll derivatives in spinach pulp was studied by adding 300ppm Zn(2+) for production

288 ze, and mineral composition of passion fruit pulp were evaluated when treated with a mineral fertiliz

289 that podoplanin(+) stromal cells in the red pulp were the primary producers of CXCL12 after P. yoeli

290 The pulps were extracted, grated and dried using solar dryer

291 Dried pulps were milled into flour with attrition milling mach

292 upernatant, green-protein pellet and fibrous pulp) were characterised in terms of composition, physic

293 iated with different color hues of the fruit pulp, while the widely variable carotenoid content (3.7-

294 agro-industrial wastes (apple peels, carrot pulp, white- and red-grape peels and red-beet peels and

295 Aqueous extracts of orange peel and pulp with high total phenolic contents (TPC) (25.94 and

296 l stromal cells, extracted from human dental pulp, with no adverse effects on cell viability, or on t

297 ble among the three species in both seed and pulp, with qualitative and quantitative differences in s

298 equivalent capacity (TEAC) of grape and acai pulps, with savings of time and reagents, moreover, avoi

299 fective affinity than those within the white pulp (WP).

300 ypes were evaluated for yield, fruit number, pulp yield, bioactive content (including phenolic compou