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1 fecting the quality and/or quantity of tooth enamel.
2 ons that result in defective or absent tooth enamel.
3 eroendocrine cells, pineal gland, and dental enamel.
4 iety signaling, and the maturation of dental enamel.
5  portion of octacalcium phosphate, unlike WT enamel.
6 ral Wendat bone and tooth collagen and tooth enamel.
7 nsformed into apatite-like crystals in older enamel.
8 and endlessly generate ameloblasts, and thus enamel.
9 riation in amelogenins can lead to malformed enamel.
10 ing much less severely affected than coronal enamel.
11 rized by the demineralization of the tooth's enamel.
12  the prevention and restoration of defective enamel.
13  can be utilized toward future generation of enamel.
14 terozygous mice secreted structurally normal enamel.
15  produces lactic acid to degrade the tooth's enamel.
16 imetic approach to the regeneration of human enamel.
17 at were more consistent with wear types than enamel.
18  matrix and formation of properly structured enamel.
19 cts and reduced fracture toughness of dental enamel.
20 sses may affect the mechanical resilience of enamel.
21 indicate minimal impact of diagenesis on the enamel.
22 ormation occurred significantly faster in KI enamel.
23 usively showed that BPA facilitated in vitro enamel adhesion without detrimental effects of the aggre
24      The use of Ca isotope analysis in tooth enamel allows microsampling and offers an independent ap
25                                           KI enamel also exhibited hypoplasia and numerous surface de
26 eral crystals were observed in secretory HET enamel, although to a lesser extent than that seen in KO
27  due to the highly hierarchical structure of enamel and additional complexities arising from chemical
28                 In the in vivo caries model, enamel and dentin carious lesions were significantly red
29                 There were no differences in enamel and dentin densities between GACI and control tee
30 lization, gap progress could be seen on both enamel and dentin even after irradiation; furthermore, t
31 s, including supernumerary or missing teeth, enamel and dentin hypoplasia, or teeth crowding.
32                                  Mineralized enamel and dentin provide protection to the dental pulp,
33 or each posterior group) for 2 tissue types (enamel and dentine).
34 ere used to image daily growth increments in enamel and dentine.
35 ly destructive surface acid etching of tooth enamel and subsequent identification of sex chromosome-l
36 ology, the shape of the junction between the enamel and the dentine within a tooth, captures importan
37 pound occlusal surfaces, thick and prismatic enamel, and a novel enamel-to-bone tooth attachment.
38 the first mineral phase formed in developing enamel, and prevents apatitic crystal formation.
39 el rods, the hallmark component of mammalian enamel, and, unlike WT enamel, appears to be composed of
40  secreted enamel was abnormal, with cervical enamel appearing much less severely affected than corona
41 omponent of mammalian enamel, and, unlike WT enamel, appears to be composed of less organized arrays
42 itions are recorded in human deciduous tooth enamel as marked variations in Ca isotope ratios (delta(
43 e, and their incorporation in forming dental enamel at low concentrations promotes mineralization.
44 sis) and the functional properties of mature enamel, attempts to repair lesions in this material or t
45   In addition, these mice also had increased enamel attrition, accompanied by excessive deposition of
46 se that the protein variants cause malformed enamel because they bind excessively to HAP and disrupt
47  and stable carbon isotope analysis of human enamel bioapatite, from 137 well-dated ancient Mongolian
48 ablished, and by comparing caries lesions on enamel blocks cocultured with biofilms treated with sucr
49 ledonous plants - cause very minor damage to enamel but are themselves heavily abraded (worn) in the
50 shown that phytoliths are softer than dental enamel but still act as abrasive agents.
51             Among the main elements found in enamel, Ca(2+) is the most abundant ion, yet how amelobl
52                     Stable isotope data from enamel carbonates and dentin collagen (childhood diet) a
53 racteristic curve (AUC) for the diagnosis of enamel caries and dentin caries were calculated to quant
54     Functional impairment and loss of dental enamel, caused by developmental defects or tooth decay (
55                  Primary enamel cells and an enamel cell line (LS8) exposed to fluoride showed decrea
56                 Knockdown experiments in the enamel cell line LS8 suggested that ORAI2 and ORAI3 modu
57  molecular mechanism and function of Ambn in enamel cell-matrix interaction.
58                                      Primary enamel cells and an enamel cell line (LS8) exposed to fl
59  important role of ORAI1 in Ca(2+) influx in enamel cells and establish a link between SOCE, mitochon
60 analyzed the effects of fluoride exposure in enamel cells to assess its impact on Ca(2+) signaling.
61           In an enamel protein intake assay, enamel cells transfected with miR-153 show a decreased a
62                                           In enamel cells, fluoride exposure affected the functioning
63  enamel despite having increased SOCE in the enamel cells.
64  enamel defects and reduced SOCE in isolated enamel cells.
65 ng an intraoral stent containing retrievable enamel chips.
66 which are the fundamental building blocks of enamel, comprise two nanometric layers enriched in magne
67                                       Dental enamel comprises interwoven arrays of extremely long and
68        Raman results indicated that Mmp20-KO enamel contains a significant portion of octacalcium pho
69                          Tooth is made of an enamel-covered crown and a cementum-covered root.
70 f this study was to nondestructively analyze enamel crack behavior on different areas of teeth using
71  use in clinical studies for the analysis of enamel crack behavior.
72 each arch ( n = 80 teeth) were inspected for enamel crack patterns on functional, contact and nonfunc
73 a role in the biomineralization of the thick enamel crowns that characterize the large molars in Giga
74 s in regulating ACP-phase transformation and enamel crystal growth, and in maintaining ameloblast int
75 d fluorapatite (FA) crystals, which resemble enamel crystals and are bioactive.
76                                              Enamel crystals form de novo in a rich extracellular env
77                           The orientation of enamel crystals, however, is poorly understood.
78 hat MMP-20 prevents protein occlusion inside enamel crystals, we hypothesized that addition of MMP-20
79 egulate the shape and orientation of growing enamel crystals.
80    However, it is frequently associated with enamel damage that include chipping, demineralisation, a
81 d greater adhesive remnants with evidence of enamel damage.
82    Furthermore, the BPA etchant caused lower enamel decalcification with extensive calcium-phosphate
83                                The glass and enameled decorations of bottles of alcoholic beverages s
84         ORAI1-deficient patients have dental enamel defects and anhidrosis, representing a new form o
85 ed deletion of the Orai1 gene in mice showed enamel defects and reduced SOCE in isolated enamel cells
86 le of ORAI proteins in enamel, we identified enamel defects in a patient with an ORAI1 null mutation.
87 uses dental fluorosis, visually recognizable enamel defects that can increase the risk of caries.
88 tion to the characteristic hypocalcification enamel defects, which have never been well documented.
89 ciency, anhidrotic ectodermal dysplasia, and enamel defects.
90 growth retardation, corneal edema, and tooth enamel defects.
91 (WD) in terrestrial environments using tooth enamel delta(18)O values, and use this approach to addre
92                                     Distinct enamel delta(66)Zn values of the fossil taxa (delta(66)Z
93 for clinical performance are unable to limit enamel demineralisation, adhesive remnants and damage ca
94                                              Enamel density was unaffected, though enamel volume was
95 ELY (amelogenin isoform Y) is present in the enamel dental tissue of male individuals only, while AME
96 rogel extraction LC-MS/MS, peptides from the enamel, dentin, periodontal ligament, alveolar bone, pul
97     For proximal lesions extending up to the enamel-dentin junction, 48% (95% CI, 40%-56%) of dentist
98 ns: those confined to enamel or reaching the enamel-dentin junction.
99                                              Enamel-dentine junction (EDJ) morphology, the shape of t
100 e mandibular premolars of the species at the enamel-dentine junction (EDJ).
101                                        Using enamel-dentine junction morphology, enamel thickness and
102 -lines to reconstruct tooth growth along the enamel/dentine and then cementum/dentine boundaries.
103       However, Orai2(-/-) mice showed normal enamel despite having increased SOCE in the enamel cells
104 cluding hardness, are comparable to those of enamel despite the nanocomposites having a smaller hard-
105 itive odontopathogen that contributes to the enamel-destructive disease dental caries, lacks the capa
106 8 (PN8) induced AI-like pathologies when the enamel development reached maturity (PN12).
107 relieve ER stress or modulate the UPR during enamel development to ameliorate the clinical phenotype.
108 erwent progressive cell pathology throughout enamel development.
109 irectly links ADAM10 to an important role in enamel development.
110 lds for regulating mineral morphology during enamel development.
111 rrier proteins are critical steps for proper enamel development.
112                    For occlusal lesions with enamel discoloration/cavitation but no clinical/radiogra
113 fect the diffusivity of peroxide through the enamel discs.
114 merous surface defects, whereas heterozygous enamel displayed highly variable mosaic structures with
115           Humans cannot repair or regenerate enamel, due to early loss of tooth epithelial SCs.
116 haracterized by abnormal formation of dental enamel, either in isolation or as part of a syndrome.
117 that Lanzhousaurus had a rapid rate of tooth enamel elongation or amelogenesis at 0.24 mm/day with de
118 logenesis to proceed, the cells of the inner enamel epithelium (IEE) must first proliferate and then
119   AmeloD was uniquely expressed in the inner enamel epithelium (IEE), but its expression was suppress
120 anonical Wnt signaling activity in the inner enamel epithelium and the underlying mesenchyme at the e
121      Its capacity to protect against initial enamel erosion was also tested in vitro via changes in s
122 n of the three solutions against citric acid enamel erosion, enamel specimens were immersed in the co
123 tal products might confer protection against enamel erosion.
124             This study reports a novel "safe enamel etch" clinically viable procedure that was accomp
125                                     Although enamel etched with clinically used PA gel yielded higher
126 Characteristic rod structures observed in WT enamel exhibited amorphous features in newly deposited e
127  local, given that the isotopic ratio of the enamel falls within the local range and is comparable wi
128 de has seen progress in our understanding of enamel formation (amelogenesis) and the functional prope
129 atrix protein and plays an essential role in enamel formation (amelogenesis).
130 serve a critical physiologic function during enamel formation and suggested a neomorphic mutation mec
131 tant mice we recently generated, we analyzed enamel formation in the mouse incisor.
132 , transit-amplifying cell proliferation, and enamel formation in the mouse incisor.
133  dental abnormalities, including hypomorphic enamel formation, has been reported in patients with EvC
134  our understanding of the natural process of enamel formation, templated crystal growth was achieved
135 eostasis, which further leads to hypomorphic enamel formation.
136 ding of molecular genetic pathology of tooth enamel formation.
137               Amelogenesis is the process of enamel formation.
138 no measurable variation in delta(44/42)Ca of enamel formed during this time.
139 chromosome-linked isoforms of amelogenin, an enamel-forming protein, by nanoflow liquid chromatograph
140 ene epoch(7-9), using the proteome of dental enamel from a Stephanorhinus tooth that is approximately
141 ted the evolution of (44)Ca/(42)Ca ratios in enamel from in utero development to first months of post
142 he diet-related delta(66)Zn values in fossil enamel from THM cave suggest an excellent long-term pres
143 er, maximum concentrations that leached from enameled glass fragments according to a standard test th
144  a sequential microsampling method along the enamel growth axis, we collected more than 150 enamel mi
145  we report the onset of weaning and rates of enamel growth using an unprecedented sample set of three
146                                       Higher enamel hardness decrease and higher enamel roughness wer
147                                  Our abiotic enamels have viscoelastic figures of merit (VFOM) and we
148 ovel genetic locus for corneal dystrophy and enamel hypomineralization without acidemia.
149 or omadacycline include tooth discoloration; enamel hypoplasia; inhibition of bone growth following u
150 exhibit acidemia, corneal edema, weak dental enamel, impacted colons, nutritional defects, and a gene
151 ich resemble, respectively, human dentin and enamel in hardness, stiffness, and strength and exhibit
152                                              Enamel includes morphologically aligned, parallel, ~50 n
153 ough to a lesser extent than that seen in KO enamel, indicating that the level of MMP20 expression ha
154     Here we performed ex vivo replication of enamel-inspired columnar nanocomposites by sequential gr
155  and the initiation of new cracks within the enamel (internal cracks) were observed as bright areas.
156                                       Dental enamel is a principal component of teeth(1), and has evo
157           Biomimetic synthesis of artificial enamel is a promising strategy for the prevention and re
158 mum tissue hardness, most organic content in enamel is digested and removed at the maturation stage,
159 t, little is known regarding how hypomorphic enamel is formed in patients with EvC.
160                                The defective enamel is normal in thickness, severely hypomineralized,
161                                       Dental enamel is one of the most remarkable examples of matrix-
162                                              Enamel is secreted by ameloblasts derived from tooth epi
163                                              Enamel is the hardest and most resilient tissue in the h
164                            Fully mineralized enamel is the hardest tissue found in vertebrates owing
165 e outermost layer of the tooth crown, dental enamel is the most mineralized tissue in mammals, consis
166  distance between the bone crest and cemento-enamel junction (CEJ).
167      ABL was calculated by measuring cemento-enamel junction and alveolar crest distance.
168           Cracks originating from the dental-enamel junction and enamel tufts, crack deflections, and
169 %-28% 3D RSA bone loss apical to the cemento-enamel junction corresponded to a CRR of 1:1, relating t
170                                              Enamel Knoop microhardness and roughness were evaluated.
171 cervical loops and basal constriction around enamel knot at the center of the cap.
172 o signaling centers: the initiation knot and enamel knot.
173 t in the absence of phosphorylated AMELX, KI enamel lacks enamel rods, the hallmark component of mamm
174 o infiltrate through the entire depth of the enamel layer (~1 mm), which is significantly enhanced pe
175 rmation of these plate-like crystals, the KO enamel layer stopped growing in thickness, unlike WT and
176 nted in interrod crystals across most of the enamel layer thickness.
177 s appeared randomly within the developing KO enamel layer.
178 pped growing in thickness, unlike WT and HET enamel layers that continued to grow at the same rate.
179 uped as caries free (CF), caries active with enamel lesions (CAE), and caries active with dentin cari
180 ful in arresting caries progression in inner enamel lesions (E2) and 64% in outer dentin lesions (D1)
181         Generalized linear model showed that enamel lesions were significantly more likely to become
182 articularly in mammals with relatively thick enamel like hominids.
183  full-length amelogenin during the growth of enamel-like crystals on an etched enamel surface.
184 gnificant production of organized dentin and enamel-like tissues was observed in dTB-recell and nTB i
185 einaceous microenvironments depending on the enamel location.
186 operties of enamel resulting in irreversible enamel loss.
187                                       Dental enamel malformations, or amelogenesis imperfecta (AI), c
188  exon usage during RNA splicing, causing the enamel malformations.
189 olars revealed reductions in early expressed enamel matrix components (Odontogenic ameloblast-associa
190 rafts (ADMG) + CAF and SCTG + CAF or between enamel matrix derivative (EMD) + CAF and SCTG + CAF.
191 clinical trial was that local application of enamel matrix derivative (EMD) added to papilla reflecti
192            Connective tissue graft (CTG) and enamel matrix derivative (EMD) approaches provided super
193        In this study, the effect of using an enamel matrix derivative (EMD) as an adjunct to non-surg
194 sidering xenogeneic collagen matrix (CM) and enamel matrix derivative (EMD) characteristics, it is su
195 ally, the use of collagen matrix (CM) and/or enamel matrix derivative (EMD) for the treatment of dehi
196                                     Although enamel matrix derivative (EMD) has been used to promote
197 ith a xenogenous collagen matrix (CM) and/or enamel matrix derivative (EMD) in combination with a cor
198 nnective tissue graft (CTG) with and without enamel matrix derivative (EMD) in the treatment of multi
199 radiographic and patient-centered results of enamel matrix derivative (EMD) therapy in intrabony defe
200                                       Use of enamel matrix derivative (EMD) when dealing with non-con
201 modality as compared with the association of enamel matrix derivative (EMD) with ABG in the managemen
202 ogics in root coverage procedures, including enamel matrix derivative, platelet-derived growth factor
203 nin (AMELX) is the predominant extracellular enamel matrix protein and plays an essential role in ena
204                 Supramolecular assemblies of enamel matrix proteins (EMPs) play a key role as the str
205 , we found that proteolysis of extracellular enamel matrix proteins by MMP20 is not required for the
206 ghly conserved AH motif is absent from other enamel matrix proteins, including amelogenin, enamelin,
207 ns as the structural scaffolds in developing enamel matrix.
208 amel growth axis, we collected more than 150 enamel microsamples from 51 deciduous teeth of 12 differ
209 ) in regulating the initial formation of the enamel mineral structure during the secretory stage of a
210 ors in ameloblasts and plays a major role in enamel mineralization and ameloblast differentiation.
211 proteinase-20 is a critical regulator of the enamel mineralization as only a recombinant analog of a
212 structural protein template that could guide enamel mineralization is limited at this date.
213  delivering both anions and cations into the enamel nanopores.
214 ere able to extract proteins from the dental enamel of both individuals (~1600 years old) and to conf
215                            Here, we analyzed enamel of fossil teeth from the Late Pleistocene (38.4-1
216 etals, the pervasive use of Pb and Cd in the enamels of consumer bottles is brought into question.
217 ntrations and mobilities of Pb and Cd in the enamels of many bottles.
218 and TEM analyses indicated no differences in enamel or dentin Ddr1(-/-) versus WT molars.
219  demonstrating caries penetrating into inner enamel or outer dentin were included in the analyses.
220 f "early" carious lesions: those confined to enamel or reaching the enamel-dentin junction.
221 n, the early asymmetrical development of the enamel organ seems to be a plesiomorphic character for a
222 oss from nonrenal sites (such as the eye and enamel organ) and therefore require separate therapy.
223 ponent of pharyngeal teeth in zebrafish (the enamel organ) is derived from medial endoderm, as hither
224 ance a new model for Ca(2+) transport by the enamel organ.
225 t of cell types which combined represent the enamel organ.
226  self-assembly causes disorganization of the enamel organic matrix and yields enamel with disordered
227 , 9, 10, 15, 17, 19) were expressed in mouse enamel organs.
228 ing the proteome of Early Pleistocene dental enamel overcomes the limitations of phylogenetic inferen
229 is group of inherited disorders resulting in enamel pathologies.
230 m natural saliva on tooth surfaces, acquired enamel pellicle (AEP), protects against erosive wear.
231                                 The acquired enamel pellicle is an oral, fluid-derived protein layer
232    The functional properties of the acquired enamel pellicle will therefore be mostly dictated by the
233 rk has disclosed the critical role played by enamel peptides in sex classification of old skeletal re
234    Stim1 cKO mice showed a severely defected enamel phenotype, including reduced structural integrity
235 genin protein can lead to drastic changes in enamel phenotype, resulting in amelogenesis imperfecta,
236  analyses that perfectly segregated with the enamel phenotype.
237 ected to a significant degree the underlying enamel prism pattern.
238 umber anomalies, reduced tooth size, altered enamel prism patterning, and spontaneous age-induced per
239 ely cycling epithelial progenitors generates enamel-producing ameloblasts and adjacent layers of non-
240  proliferate and then differentiate into the enamel-producing ameloblasts.
241 nity, muscle hypotonia and defects in dental enamel production and sweat gland function.
242                                        In an enamel protein intake assay, enamel cells transfected wi
243                     In vertebrates, bone and enamel proteins are major Fam20C substrates.
244 R-153 show a decreased ability to endocytose enamel proteins.
245  The survival of an Early Pleistocene dental enamel proteome in the subtropics further expands the sc
246  and H. erectus fossils preserve evidence of enamel proteome phosphorylation and proteolytic digestio
247                          We retrieved dental enamel proteome sequences from a 1.9-million-year-old G.
248                   Here we present the dental enamel proteomes of H. antecessor from Atapuerca (Spain)
249 s, and pave the way for future studies using enamel proteomes to investigate hominin biology across t
250 n, which has not been previously observed in enamel proteomes, had a role in the biomineralization of
251 phate (PPi) to control the onset and rate of enamel regeneration and the use of leucine-rich amelogen
252 em function and to facilitate the biomimetic enamel regrowth, matrix metalloproteinase-20 (MMP-20) wa
253 As the hardest tissue formed by vertebrates, enamel represents nature's engineering masterpiece with
254 wear undermines the structural properties of enamel resulting in irreversible enamel loss.
255  required for the initial development of the enamel rod structure during the early secretory stage of
256  dominant and obscured the appearance of the enamel rod structure.
257 s' processes, consistent with the absence of enamel rods, and underwent progressive cell pathology th
258 nce of phosphorylated AMELX, KI enamel lacks enamel rods, the hallmark component of mammalian enamel,
259 ndicular or parallel to the direction of the enamel rods, were exposed to a PPi-stabilized supersatur
260  surfaces that were cut perpendicular to the enamel rods.
261 ered mineralization in vitro, as observed in enamel rods.
262 crystals of carbonated hydroxyapatite called enamel rods.
263   Higher enamel hardness decrease and higher enamel roughness were caused by the carbamide peroxide (
264  of known dietary histories, as well as nine enamel samples from permanent third molars.
265                                     However, enamel secreted thereafter was structurally abnormal; pr
266 olutions against citric acid enamel erosion, enamel specimens were immersed in the corresponding solu
267                              Here, we report enamel stable calcium isotope (delta(44/42)Ca) values ag
268  development of a new approach to regenerate enamel structure and properties.
269  conserved in invertebrates lacking bone and enamel, suggesting other ancestral functions.
270 valuate the bleaching ability, the effect on enamel surface and cytotoxicity of novel tooth-whitening
271 ies have shown that many traits of the outer enamel surface evolve neutrally and can be used to infer
272                                   Generally, enamel surface roughness increased with higher forage ph
273 rounding seeds are thought to induce complex enamel surface textures characterized by heavy pitting,
274  growth of enamel-like crystals on an etched enamel surface.
275 ition was reversed by the presence of etched enamel surfaces and led to the formation of large, rando
276 lant tissues do not regularly create pits on enamel surfaces despite high forces clearly being associ
277                                  Acid-etched enamel surfaces of extracted human molars, cut perpendic
278 xperimental etchants resulted in unblemished enamel surfaces with zero or minimal adhesive residue an
279 ibes a group of inherited diseases of dental enamel that have major clinical impact.
280 otype, resulting in amelogenesis imperfecta, enamel that is defective and easily damaged.
281    Using enamel-dentine junction morphology, enamel thickness and comparative morphology, we show tha
282      Cumulative growth curves for increasing enamel thickness and tooth height and age-of-attainment
283 tening gels were prepared and applied on the enamel three times per day once a week, for 4 weeks.
284 n assays we showed that both recombinant and enamel-tissue-based amelogenin nanoribbons are capable o
285 ces, thick and prismatic enamel, and a novel enamel-to-bone tooth attachment.
286 ginating from the dental-enamel junction and enamel tufts, crack deflections, and the initiation of n
287                              Secretory-stage enamel ultrastructures from each genotype as a function
288        Enamel density was unaffected, though enamel volume was significantly reduced in Hyp mice.
289   The architecture of the initially secreted enamel was abnormal, with cervical enamel appearing much
290   The ability of CaneCPI-5 to bind to dental enamel was evaluated using atomic force microscopy.
291 urprisingly, initial mineral formation in KO enamel was found to proceed in the same manner as in the
292 ssues revealed that deposition of dentin and enamel was largely symmetrical at the mineralization sta
293 drogen peroxide through 1-mm discs of bovine enamel was measured at steady-state conditions, and the
294                                        LAMB3 enamel was well mineralized but pitted.
295 nvestigation of the role of ORAI proteins in enamel, we identified enamel defects in a patient with a
296 r to, or higher than, those of natural tooth enamels-we achieve values that exceed the traditional ma
297 nism contributes to the unique resilience of enamel, which lasts a lifetime under extreme physical an
298 ibited amorphous features in newly deposited enamel, which subsequently transformed into apatite-like
299 at proteomic investigation of ancient dental enamel-which is the hardest tissue in vertebrates(11), a
300 tion of the enamel organic matrix and yields enamel with disordered hydroxyapatite crystallites.

 
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