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1 r population and not multipotent MSCs in the dental pulp.
2 sitive nociceptors in trigeminal ganglia and dental pulp.
3 ve nociceptors in the trigeminal ganglia and dental pulp.
4 involved in inflammatory hyperalgesia in the dental pulp.
5 erentiation, thus maintaining homeostasis in dental pulp.
6 rom peptidergic afferents innervating bovine dental pulp.
7 e neurons via in vitro superfusion of bovine dental pulp.
8 g trigeminal nerve fibers that innervate the dental pulp.
9 expression by cells derived from the porcine dental pulp.
10 erative population of cells from adult human dental pulp.
11 4 [IL-4], and IL-10) were detected in human dental pulp.
12 rvival function for Msx1 in odontoblasts and dental pulp.
13 ut not by odontoblasts or other cells in the dental pulp.
14 both metabolic and transductive processes in dental pulp.
15 s found in many orofacial tissues, including dental pulp.
16 ATP-permeable channels, are present in human dental pulp.
17 ohydrolases (NTPDases), are present in human dental pulp.
18 f selective cytokines in the regeneration of dental pulp.
19 2) on the revascularization of severed human dental pulps.
20 the hypothesis that EAA receptors in bovine dental pulp activate a population of peptidergic sensory
21 produced by PDL (periodontal ligament), DPA (dental pulp adult), and GF (gingival fibroblast) cells.
23 of versican and link protein coincide in the dental pulp and are enriched in the peripheral area of t
24 sor population isolated from postnatal human dental pulp and have the ability to regenerate a reparat
25 resorption occurs following infection of the dental pulp and is mediated mainly by IL-1alpha in the m
26 on of the local complement system within the dental pulp and its role in initiating the regeneration
27 nated and unmyelinated nerve fibers in human dental pulp and may play a role in dental pain mechanism
28 red for ATP release and degradation in human dental pulp and that pannexin channels are involved in e
30 munohistochemical staining of infected human dental pulp and tissue from experimental dental pulpitis
31 enhanced neovascularization of severed human dental pulps and suggest that topical application of an
32 immune cells in irreversibly inflamed human dental pulp, and extracts of this tissue have significan
33 and distribution of P2X3 receptors in human dental pulp, and their co-localization with other neural
34 y of capsaicin-sensitive neurons innervating dental pulp, and these factors may be significant clinic
38 nt mesenchymal tissues, the periodontium and dental pulp, are maintained by distinct pools of stem ce
40 (TNF-alpha) could be a mediator involved in dental pulp cell differentiation toward an odontoblastic
41 l mesenchymal/papilla cells (FDPCs) or human dental pulp cells (ADPCs) under 2-dimensional or 3-dimen
43 imensional (3D) tissues were engineered from dental pulp cells (DPCs) and assessed as a device for pu
44 e-aspartic acid (RGD) peptides, will bind to dental pulp cells (DPCs) and modulate their differentiat
45 ential for osseointegration engineering with dental pulp cells (DPCs) by testing a hypothesis that DP
50 n vitro, Wnt5a was increased 8-fold in human dental pulp cells (HDPCs) after TNF-alpha stimulation co
51 ans ATCC90028, the cytotoxicity toward human dental pulp cells (HDPCs), and the mechanical properties
52 nt cells from donor-matched rat dental pulp (dental pulp cells [DPCs]) and alveolar bone (alveolar bo
55 nx2, Gli1, Numb, and Notch expression in the dental pulp cells and odontoblasts of DSPP-null mice whe
56 ficantly ameliorated its cytotoxicity to the dental pulp cells and restored their odontoblast-like ce
60 ginate hydrogel with pulp ECM components and dental pulp cells followed by differentiation induction
61 agen hydrogels were seeded either with human dental pulp cells from patients with characterized PHEX
67 tudy was that LTA induces VEGF expression in dental pulp cells through TLR2 and PI3k/Akt signaling.
68 amined the effects of continuous exposure of dental pulp cells to FGF2 and showed that the effects of
69 that TNF-alpha stimulates differentiation of dental pulp cells toward an odontoblastic phenotype via
75 with porcine dental epithelial cells, human dental pulp cells, and human umbilical vein endothelial
79 embryonic cells and populations of postnatal dental pulp cells; however, these cells are unable to co
81 tus for ATP release and degradation in human dental pulp, consistent with the involvement of ATP sign
82 strategy for engineering of pre-vascularized dental pulp constructs offering potentially beneficial t
85 ed and adherent cells from donor-matched rat dental pulp (dental pulp cells [DPCs]) and alveolar bone
86 domain peptide (MDP) hydrogel scaffolds with dental pulp-derived cells but were limited in their abil
87 indings suggest that LNGFR(Low+)THY-1(High+) dental pulp-derived cells provide an excellent source of
89 , indicating a functional bioactivity of the dental pulp-derived neurotrophic factors in vivo by resc
90 Based on these findings, we propose that dental pulp-derived neurotrophic factors play an importa
92 ls (BMSC) with stem cells derived from human dental pulp (DPSC), apical papilla (SCAP) and follicle (
95 cretion is evoked from isolated terminals of dental pulp fibers via the bradykinin B2 receptor-depend
96 n in dental pulp stem cells (DPSC) and human dental pulp fibroblasts (HDPF) through mitogen-activated
97 e C5a receptor (C5aR), here we show that all dental pulp fibroblasts, localized beneath the carious i
112 heroids can successfully regenerate vascular dental pulp-like tissue and also highlight the significa
113 en fabricated pre-vascularized, full-length, dental pulp-like tissue constructs by dispensing OD21 ce
114 PC engineered tissues can regenerate a vital dental pulp-like tissue in a tooth root canal system and
115 activation of AMPA and kainate receptors in dental pulp may contribute to peripheral release of vaso
116 Up-regulation of VEGF expression in the dental pulp may result in increased intra-pulpal pressur
117 aled that this DSP domain induces endogenous dental pulp mesenchymal cell proliferation, differentiat
121 nhanced TRPA1 expression was also evident in dental pulp of carious compared with noncarious teeth.
122 mixed anaerobic infection, we inoculated the dental pulp of mice with six anaerobic pathogens contain
124 hronic interstitial polymicrobial infection, dental pulps of MCP-1(-/-) mice and controls were inocul
126 ain insight into the potential population in dental pulps of unerupted and erupted incisors that give
127 ntation with mesenchymal stem cells from the dental pulp on poly-l-lactic acid scaffolds in nude mice
128 for immediate vascularization of engineered dental pulp poses a major hurdle towards successful impl
132 carious teeth and plays an important role in dental-pulp regeneration via interaction of the active C
133 emperature and pH of isolated superfused rat dental pulp regulate capsaicin-induced release of calcit
136 that activation of beta(2)-adrenoceptors in dental pulp significantly reduces exocytosis of neuropep
137 re increased and deposited abnormally in the dental pulp, similar to the hereditary human tooth disor
138 om MEPE (Dentonin or AC-100) could stimulate dental pulp stem cell (DPSC) proliferation and/or differ
139 e adhesion behavior of a population of human dental pulp stem cell (hDPSC) on 64 combinations of nano
140 dothelial growth factor (VEGF) expression in dental pulp stem cells (DPSC) and human dental pulp fibr
145 oblastic MC3T3-E1 cells and preodontoblastic dental pulp stem cells (DPSCs) in a dose-dependent manne
146 tial for autologous transplantation of human dental pulp stem cells (DPSCs) in endodontic treatment.
147 differentiation and mineralization of human dental pulp stem cells (DPSCs) in two-dimensional cell c
149 se of scaffold-free microtissue spheroids of dental pulp stem cells (DPSCs) prevascularized by human
151 cells have been isolated and characterized: dental pulp stem cells (DPSCs), stem cells from exfoliat
152 terials that can support native functions of dental pulp stem cells (DPSCs), which are capable of reg
158 on the viability and proliferation of human dental pulp stem cells (hDPSCs) by comparing the cellula
161 characteristics of the previously identified dental pulp stem cells can generate mineralized tissue o
162 also observed in T4-4 preodontoblast cells, dental pulp stem cells, and primary preodontoblasts.
163 5% NaOCl and triple antibiotic paste, ferret dental pulp stem cells, encapsulated in a hydrogel scaff
170 This work is based on a hypothesis that dental pulp stem/progenitor cells can be induced to migr
172 useful indication of tissue distress in the dental pulp that could be used to investigate the early
173 populations in the rodent incisor apex, the dental pulp, the alveolar bone, the periodontal ligament
174 adult stem cells have been isolated from the dental pulp, the deciduous tooth, and the periodontium.
176 ered centrally and peripherally within whole dental pulp tissue are shown to be biocompatible, preser
179 veloping dental mesenchyme and whether adult dental pulp tissue maintains its inductive capability re
182 lp cells (DPCs), adherent cells derived from dental pulp tissues, are potential tools for cell transp
184 ated 3 methods of decellularization of human dental pulp to be used as a potential autograft scaffold
185 e present study used isolated superfused rat dental pulp to test the hypothesis that capsaicin recept
187 emistry, we detected ecto-AMPase activity in dental pulp, trigeminal ganglia (TG) neurons, and their
188 We further tested if ATP is released from dental pulp upon dentin mechanical or thermal stimulatio
189 rity and extracellular matrix composition of dental pulp varies considerably during tooth development
190 ction, we used an in vivo model in which the dental pulp was inoculated with six anaerobic pathogens,
193 trigeminal ganglia and by 26% (p < 0.05) in dental pulp when tissues were pre-treated with [Leu(31),
194 ude that BK evokes iCGRP release from bovine dental pulp which is enhanced by a positive interaction
195 present a unique precursor population in the dental pulp, which has multipotential and can regenerate
197 s study, the effect of mono-infection of the dental pulp with T. denticola and with polymicrobial "re
198 enchymal stromal cells, extracted from human dental pulp, with no adverse effects on cell viability,
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