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1 a 3-way interaction profile within the white pulp.
2 sed by many cell types throughout the dental pulp.
3 cyanidin (m/z of 863) was observed in coffee pulp.
4 h fruits were higher than those found in the pulp.
5 nd for the nutritional enhancement of banana pulp.
6 try feed materials such as molasses and beet pulp.
7 ion of the oxidized procyanidins from coffee pulp.
8 ion, and antioxidant properties of araca-boi pulp.
9 sue with no drug action detected in the root pulp.
10 the maintenance of stem cell pools in dental pulps.
11 tonin, dopamine, histamine and tyramine than pulps.
12 decreased during the ripening process in the pulps.
13 ifferences between the raw and the fermented pulps.
14 blood vessels in physiological human dental pulps.
17 , and iNKT cells recruited outside the white pulp; 2) followed by long-lasting contacts (12 to 24 h)
18 male adults underwent two protocols: Avocado pulp (600 mg in capsule) and placebo (600 mg starch in c
19 entage bioavailability was from baobab fruit pulp (99.7% +/- 0.13 and 1.74 +/- 0.01 mg/100 g) respect
20 loss of white pulp and grossly expanded red pulp, a deficit of Peyer patches, and small lymph nodes
21 gest source of xylan found so far in a fruit pulp and could be suitable for applications in the indus
23 em cells (hDPSCs) reside in postnatal dental pulp and exhibit the potential to differentiate into odo
25 (+) cells, splenomegaly with a loss of white pulp and grossly expanded red pulp, a deficit of Peyer p
26 Considering the importance of acai-berry pulp and its perishability, the inactivation kinetics of
28 of Ddr2 in primary cell cultures from dental pulp and PDL inhibited differentiation of cells to odont
30 hin and epicatechin were the major ones from pulp and peel, whereas seed displayed caffeic acid, cate
32 survival of undifferentiated cells in dental pulp and promoted the formation of 2.3GFP(+) preodontobl
33 tioxidant activity in ethanolic extracts.The pulp and seeds were excellent sources of fiber (25.62%-4
34 lyphenol composition of L. tomentosa fruits (pulp and seeds) and measure antioxidant activity in etha
35 ed by lyophilization of whole fruits, seeds, pulp and skin from chilto (Solanum betaceum Cav) cultiva
36 ria chiotilla and Stenocereus queretaroensis pulp and skin pigments through a spray drying process wa
40 the colony exposed to pectin-rich sugar beet pulp and to xylan-rich wheat bran showed high pectinolyt
42 o extract proteins from "Musang King" durian pulps and subsequently proteins with different abundance
44 ates and in different fruit fractions (peel, pulp, and calyx of ripe fruits) were investigated by HPL
48 alatable to humans, and nonbitterness of the pulp apparently was a trait favoured early during domest
50 eatment, as indicated by the increase in red pulp area, the number of nucleated erythroblasts, and ex
51 solid content, titratable acidity, pH of the pulp as well as in sugar content and decreased starch de
52 d from unripe and ripe inaja palm tree fruit pulp, as well as co-products that were generated after o
54 total number of neurites present within the pulp at P7, with a significant accumulation of aberrant
56 d newly formed tertiary dentin at the dentin-pulp boundary in recombinant CPNE7-treated teeth when co
57 regulation of innervation of the mouse tooth pulp by dental pulpal afferent (DPA) neurons of the trig
58 emical profile of the pitomba fruit peel and pulp by electrospray ionization-Fourier transform-mass s
60 ted avocados after drying peeled or unpeeled pulps by convection oven, microwave or freeze-drying.
62 nal core of osteodentine instead of a hollow pulp cavity), but also one feature that has not been kno
64 ta-catenin in dentinogenesis, we used dental pulp cells from a panel of transgenic mice, in which flu
65 Insights into the role of mesenchymal dental pulp cells in attenuating dentin resorption in homeostas
66 ta-catenin signaling is highly restricted to pulp cells in the immediate location of the damage in th
68 ation, whereas early and limited exposure of pulp cells to FGF2 resulted in marked increases in odont
74 ridge after insult are necessary to seal the pulp chamber in an effort to maintain natural dentition
75 r pulp chamber roof predentin layer, thinner pulp chamber roof dentin, and thicker pulp chamber floor
76 L/+) and Dspp(P19L/P19L) mice had a narrower pulp chamber roof predentin layer, thinner pulp chamber
78 GI type III characterized by enlarged dental pulp chambers, while the teeth of older Dspp(P19L/+) and
80 gs controlled ripening, maintaining peel and pulp colors, firmness, soluble solids (SS), titratable a
81 moisture loss and maintained both flesh and pulp colour by inhibiting polyphenol oxidase (PPO) activ
83 erlying lycopene accumulation, red or orange pulp colour, and fruit size and shape are only just begi
86 ed during in vitro mineralization of primary pulp cultures and during reparative dentinogenesis follo
87 differentiation of remaining progenitors in pulp cultures into functional odontoblasts but prevented
89 ains, the serotonin and dopamine contents in pulp decreased until stage 5 and increased at stage 7.
90 est calcium content was found in the pumpkin pulp dehydrated in 50% xylitol and inulin solutions with
91 ce delta(18)O and fertilisation practices on pulp delta(15)N was demonstrated and must be considered
92 ement of up to 50% tomato pulp by strawberry pulp did not change the acidity, flavor, and overall acc
95 ells derived from bone marrow (BMSC), dental pulp (DPSC) and dental apical papilla (SCAP) to engineer
96 C) with stem cells derived from human dental pulp (DPSC), apical papilla (SCAP) and follicle (DFSC) d
98 ack of expression in odontoblasts and dental pulp during tooth development, the BSP-GFPtpz transgene
99 ration, which may be useful in future dentin-pulp engineering strategies that target fibroblast C5L2
102 ntents of FOS and CGA were maintained in the pulping, enzymatic maceration and microfiltration, leadi
103 n induction of experimental periodontitis or pulp exposure compared with those of the wild-type (WT)
104 all-molecule GSK-3 inhibitor drugs following pulp exposure in mouse molars results in reparative dent
105 rocesses 2 wk following tooth injury without pulp exposure, whereas EphB2 was expressed in the center
108 models able to distinguish olive leaves and pulp extracts among seven cultivars from several Spanish
115 are embedded in a reticular meshwork of red pulp fibroblasts characterized by the expression of the
117 Conditional deletion of Csf1 in WT1(+) red pulp fibroblasts, but not white pulp fibroblasts, drasti
118 n WT1(+) red pulp fibroblasts, but not white pulp fibroblasts, drastically altered the RPM network wi
122 buticaba, raspberry, caja and soursop frozen pulps (FPs) using a digestion model coupled with a simul
123 on process allowed the detoxification of the pulp from caffeine by 50%, while significantly reducing
125 the primary metabolome of Aglianicone grape pulp from two different vineyards and the observed metab
128 Increasing the concentration of blackberry pulp (from 0 to 40%, mass/mass of dry starch) in the fil
134 the bioactive compounds of Eugenia stipitata pulp have antimutagenic, anticarcinogenic and antigenoto
135 s fruit is very appreciated due to its sweet pulp (high sucrose content, 16.3%) and attractive taste.
137 d the complex histologic structure of native pulp in situ with highly organized physiologic patterns
138 sed to characterize raw and fermented coffee pulps in terms of their phenolic composition and caffein
140 ifferent cookies formulated with 10.5% peach pulp incorporation and 50% fat or added-sucrose reductio
142 down-regulation of proteins in frozen durian pulps indicated that frozen storage has affected protein
143 susceptible to damage as a result of caries, pulp infection and inflammation all of which are major p
144 ld assist in uncovering mechanisms for tooth pulp inflammatory pain and other forms of trigeminal pai
148 genesis, the timing and patterning of dental pulp innervation require both chemoattractive and chemor
150 aims to evaluate the effect of acute avocado pulp intake on cardiovascular and autonomic recovery sub
156 ke, rapeseed press cake, sea buckthorn spent pulp, leek leaves, parsley waste, pumpkin kernel cake, a
157 decreased adipogenic potential, form dentin pulp-like complexes, and are resistant to oncogenic tran
158 gineer pre-vascularized, cell-laden hydrogel pulp-like tissue constructs in full-length root canals f
159 RSs, and less cellularized host cell-derived pulp-like tissue was observed in the G2 acellular GelMA
160 lyses of harvested samples found that robust pulp-like tissues formed in G1, GelMA encapsulated hDPSC
162 s revealed dramatic up-regulation of the red-pulp macrophage lineage-defining transcription factor Sp
164 Located within red pulp cords, splenic red pulp macrophages (RPMs) are constantly exposed to the bl
167 agocytes (iHPCs), which resemble splenic red pulp macrophages but are a distinct population derived f
170 ol and acetone extracts from quince peel and pulp, namely 3-O-caffeoylquinic acid (3-CQA), 4-p-coumar
171 ify chemical changes in the green beans from pulped natural coffee stored in different packaging mate
172 ory quality of coffee beans, for natural and pulped natural coffee stored in different packaging.
175 es suffer from dental infections, leading to pulp necrosis, arrested tooth-root development and tooth
176 unctional mechanism linking C5aR and C5L2 in pulp nerve regeneration, which may be useful in future d
180 yl esters (FAMEs) profiles of fruit peel and pulp of 4 Spanish cultivars of Ziziphus jujuba were stud
181 ltrasound study identified spaces within the pulp of distal phalanx of the fingers and toes that halv
184 pt levels of PYP1, 2 and 6 genes in peel and pulp of sweet orange were accompanied by the accumulatio
185 bioactive phenolic compounds in the peel and pulp of the mango fruit (Mangifera indica L.) cultivated
187 f bioactive compounds and AAC were higher in pulps of both oranges and mandarin than in their corresp
188 influence of the incorporation of blackberry pulp on properties of arrowroot starch films has been st
190 sumptive root furcating region, where dental pulp overgrowth occurred, was increased in K14-Cre;Wnt10
192 lations, and results highlighted that dental pulp pericytes are already precommitted to an odontoblas
197 critical steps of dentin-pulp regeneration: pulp progenitor's recruitment and pulp nerve sprouting.
199 ft untreated threaten exposure of the dental pulp, providing facile access for bacteria to cause seve
200 were made using different tomato/strawberry pulp ratios (100:0; 75:25; 50:50; 25:75; 0:100) and char
202 ffect of residual bacteria on the outcome of pulp regeneration mediated by a tissue-engineered constr
206 ent breakthroughs in pulp stem cell-mediated pulp regeneration, emphasizing the crucial achievement o
210 n participates in 2 critical steps of dentin-pulp regeneration: pulp progenitor's recruitment and pul
211 se changes to the lipid composition in white pulp regions of the spleen, as anticipated, based on pat
214 naringin and limonene from kinnow pomace and pulp residue and showed high acceptability for food prod
215 of by-products like kinnow pomace and kinnow pulp residue by using various food grade mild chemical m
217 Differential protein analyses of the durian pulp revealed that 15 proteins were down-regulated and t
220 drug-induced Wnt-activity within the dental pulp, RNA of short-term induced (24-h) molars is extract
221 e redissolution of the powders from skin and pulp samples do not present significant differences; the
222 In conclusion whole CLARITY-cleared dental pulp samples revealed 3D-morphological neurovascular int
224 loping a biocompatible decellularised dental pulp scaffold, which is able to support dental pulp stem
225 istochemistry performed on human third molar pulp sections showed a perivascular co-localization of t
227 Upon release from arterioles into the red pulp sinuses, T cells latched onto perivascular stromal
228 , flavonoid and lycopene content from tomato pulp (Solanum lycopersicum) by using response surface me
229 how that macrophages are required for dental pulp stem cell activation and appropriate reparative den
230 /Yb/Tm and HAp:Gd/Eu powders in human dental pulp stem cell cultures indicated their good biocompatib
233 ing to current pulp regeneration strategies, pulp stem cell-mediated approaches to regeneration have
234 review, we summarize recent breakthroughs in pulp stem cell-mediated pulp regeneration, emphasizing t
235 beta-d-glucoside (THSG)-treated human dental pulp stem cells (DPSC) on the healing of experimental pe
238 to chitosan scaffolds and tested with Dental Pulp Stem Cells (DPSCs) to check their regenerative pote
240 hymal stem cells, including postnatal dental pulp stem cells (from permanent teeth) and stem cells fr
241 from both mineralizing primary human dental pulp stem cells (hDPSCs) and an immortalized murine odon
243 of C5L2 is highly modulated in human dental pulp stem cells (hDPSCs) undergoing odontoblastic differ
244 g reparative dentine formation by activating pulp stem cells and promoting an anti-inflammatory macro
245 kin-6 [IL-6]) promote self-renewal of dental pulp stem cells cultured in low-attachment conditions.
248 f this study is to investigate if the dental pulp stem cells express C5L2 and if this receptor partic
251 ved IL-6 enhances the self-renewal of dental pulp stem cells via STAT3 signaling and induction of Bmi
252 ding odontoblastic differentiation of dental pulp stem cells, and may be useful in future dentin-pulp
253 l and triple antibiotic paste, ferret dental pulp stem cells, encapsulated in a hydrogel scaffold, we
258 that the NPSCs primarily localize in the red pulp, suggesting that the observed changes in lipid comp
260 cruiting endogenous stem cells of the dental pulp, through an easy-to-handle delivery vehicle which a
261 he feasibility of decellularising rat dental pulp tissue and evaluate the ability of such scaffold to
262 The presence of stem cells within the dental-pulp tissue as well as their differentiation into a new
263 n of the spatial relationships of the dental pulp tissue at the whole-organ has remained challenging.
265 ediate location of the damage in the coronal pulp tissue with no drug action detected in the root pul
266 activity was highest (p <= 0.05) in peel and pulp tissues (85% alpha-glucosidase and 8% alpha-amylase
270 a dental pulp injury model that exposes the pulp to the outside environment, a procedure we have pre
272 , we detected ecto-AMPase activity in dental pulp, trigeminal ganglia (TG) neurons, and their nerve f
273 partments accountable for distending digital pulp under normal circumstances and skin wrinkling after
274 he stability of bioactive compounds in butia pulp upon pasteurization, during 12months of frozen stor
276 d and carotenoid ester composition of lucuma pulps (var. Molina and Beltran) and assess their bioacce
278 keratinized tissue, percussion sensitivity, pulp vitality tests, radiographic pathology, and root-cr
282 rages against the sedimentation of the fruit pulp was clearly affected by the increase of temperature
283 mical and sensory parameters, pasta with 30% pulp was found to be most acceptable with the overall ac
284 celerated oxidative degradation of wolfberry pulp was kinetically monitored using model-free and mode
286 Zn), iron (Fe), and copper (Cu) in the fruit pulp was similar with all three fertilizers, but the cal
288 lly, the dielectric properties of acai-berry pulp were evaluated at 915 and 2,450 MHz for temperature
289 ze, and mineral composition of passion fruit pulp were evaluated when treated with a mineral fertiliz
290 , and the oils from microwave dried unpeeled pulp were those that presented the best performance.
294 and dentin provide protection to the dental pulp, which is vital tissue rich with cells, vasculature
296 iated with different color hues of the fruit pulp, while the widely variable carotenoid content (3.7-
297 ntioxidant capacity in relation to untreated pulp, while ultrasound at 5000 J g(-1) increased the rel
298 used CLARITY to study the whole human dental pulp with emphasis on the neurovascular components.