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1 er scaffold (19 +/- 8% osteoid and 10 +/- 2% mineralized tissue).
2 ted to the ability of these cells to augment mineralized tissue.
3 ressed where osteoblasts attempted to repair mineralized tissue.
4 stylus of Cryptochiton stelleri is in fact a mineralized tissue.
5 ysical and chemical properties of the mature mineralized tissue.
6  of remaining bone grafting material and non-mineralized tissue.
7 ft material, and 39.6% connective tissue/non-mineralized tissue.
8 rent organization of the mineralized and non-mineralized tissues.
9 onal cleavage fragments found in extracts of mineralized tissues.
10 ls, we demonstrate that Dmp1 is specific for mineralized tissues.
11 formation, is largely restricted to cells in mineralized tissues.
12 al cavity and which control the formation of mineralized tissues.
13 hromosome 5 near other genes associated with mineralized tissues.
14 on is the process by which organisms produce mineralized tissues.
15 te ([Ca(5)(PO(4))(3)OH]), a key component of mineralized tissues.
16 surface environments or targeted delivery in mineralized tissues.
17 growth and biomineralization of complex hard mineralized tissues.
18 egies for the regeneration of bone and other mineralized tissues.
19 t in the extracellular function of FAM20C in mineralized tissues.
20 narily reserved molecule highly expressed in mineralized tissues.
21 r role in the ability of organisms to create mineralized tissues.
22 mouse dentoalveolar phenotype, including all mineralized tissues.
23 and overall hypomineralization in the dental mineralized tissues.
24 s proteolytically processed fragments in the mineralized tissues.
25 y to control the structure and properties of mineralized tissues.
26 re unique to cells responsible for producing mineralized tissues.
27 ave not been isolated or confirmed in mature mineralized tissues.
28 provide clues to the evolutionary origins of mineralized tissues.
29 portant role in the embryonic development of mineralized tissues.
30 ing evolution, particularly the evolution of mineralized tissues.
31 stomorphometric analysis of the newly formed mineralized tissues.
32 otal tissue area; mean +/- SD; p < 0.05) and mineralized tissue (14 +/- 2%; P < 0.05) within a rat cr
33 te significantly increased the generation of mineralized tissue (19 +/- 4%; P < 0.05) compared with m
34 ologically, flapless ARP revealed more vital mineralized tissue (44 +/- 10%) compared to the flap gro
35  tooth, which consists of two characteristic mineralized tissues, a highly mineralized surface layer
36 and Von Kossa) were performed on the ex-vivo mineralized tissue after 60 days of implantation in vivo
37 2-deficient osteoclasts are unable to resorb mineralized tissue and cannot form an acidified, extrace
38 reased interfacial strength between cultured mineralized tissue and titanium, but did not alter the i
39 lls from long-standing IDDM patients to form mineralized tissue and to determine whether these cells
40 tics may be altered in their ability to form mineralized tissue and to respond to growth factors, fun
41 ctions as an extracellular matrix protein in mineralized tissues and a cytokine that is active in cel
42 ple and distinct roles in the development of mineralized tissues and that the influence of ENPP1 on o
43 . the osteonal structures in which layers of mineralized tissue are organized in lamellae around a ce
44                                    The major mineralized tissues are bone and teeth, which share seve
45                                              Mineralized tissues are uniquely challenging as extensiv
46                                   Vertebrate mineralized tissues are vital to the adaptive evolution
47              However, genes more specific to mineralized tissues arose subsequent to the genome dupli
48  in the scaffold-treated defects, and entire mineralized tissue, as well as newly formed bone, was si
49 gnized that this protein is expressed in non-mineralized tissues, as well as in cancerous lesions.
50  inhibited the proliferation, migration, and mineralized tissue-associated gene expression of OCCM-30
51 0) in terms of proliferation, migration, and mineralized tissue-associated gene expression.
52  significant difference in the expression of mineralized tissue-associated genes, including BSP and R
53                            The expression of mineralized tissue-associated genes, including Type I co
54                       The mRNA expression of mineralized tissue-associated markers of bone sialoprote
55       After 90 days, the mean percentages of mineralized tissue at the interface in the test and cont
56 o examine adhesion molecules associated with mineralized tissues, bone sialoprotein (BSP) and osteopo
57  of amorphous precursors that transform into mineralized tissues, but the templating mechanism remain
58  the concept that Msx2 controls formation of mineralized tissues by inhibition of the Wnt/beta-cateni
59 r directly into the outer layer of adjoining mineralized tissues (cementum and bone).
60           The periodontal complex includes 2 mineralized tissues, cementum and alveolar bone (AB), bo
61 oval reduced the rate of remineralization in mineralized tissues compared to the untreated control, w
62  +/- 13.4% of the interface area filled with mineralized tissue, compared to 17.14% +/- 8.6% in the c
63 ic matrix proteins of dentin and enamel, the mineralized tissues comprising a tooth crown.
64                 Despite the recognition that mineralized tissues contain proteins that are unusually
65                    These tissues thus form a mineralized-tissue continuum.
66                         Cellular cementum, a mineralized tissue covering apical tooth roots, grows by
67                                Cementum is a mineralized tissue covering the tooth root that function
68 ized structures (connective tissue/other non-mineralized tissue [CT]).
69  bone may be significant contributors to the mineralized tissue defects in human patients and animals
70 t development without inflammation and newly mineralized tissue deposited in the root canal system, w
71 eded in these scaffold systems, and distinct mineralized tissue differentiation were noted within the
72  a unique biological process by which highly mineralized tissues emerge into the outer world, and it
73 tomesenchyme culminating in the formation of mineralized tissues, enamel, and dentin.
74                           Teeth consist of 3 mineralized tissues: enamel, dentin, and cementum.
75 hile the hardness and elastic modulus of the mineralized tissue, evaluated by nano-indentation, were
76 t difference between both groups in terms of mineralized tissue formation (Group A = 27.0% +/- 22.1%
77 t difference between both groups in terms of mineralized tissue formation (Group A = 27.0% 22.1% vers
78  evidence supports BSP as a key regulator of mineralized tissue formation via evolutionarily conserve
79 anted into nude mice, DPSC/CTL cells induced mineralized tissue formation with significant increases
80 ides one well accepted paradigm for studying mineralized tissue formation.
81 ibitors, like PPi, play in the regulation of mineralized tissue formation.
82        In situ hybridization showed that the mineralized tissue formed by cementoblasts gave strong s
83              The amount of dentin-associated mineralized tissue formed in teeth with residual bacteri
84 es from cholesteric phase fibre bundles, and mineralized tissues from hierarchically organized fibres
85 ting that increased vascularization enhances mineralized tissue generation, but not necessarily osteo
86 n to be essential for transcription of other mineralized tissue genes, is also required for ameloblas
87      Biomineralization, the process by which mineralized tissues grow and harden via biogenic mineral
88 ng factors which facilitate the formation of mineralized tissue has significant clinical ramification
89 cture and composition, or microstructure, of mineralized tissues has an important role to play in det
90 h for designing new therapies for preserving mineralized tissue health.
91 olved in many molecular pathways controlling mineralized tissue homeostasis such as Wnt/sclerostin pa
92                       Cementum is a critical mineralized tissue; however, control of its formation re
93                          Also, while areolar mineralized tissue in elasmobranchs is generally conside
94            It is the only epithelial-derived mineralized tissue in mammals and has a distinct micro-
95 f the tooth crown, dental enamel is the most mineralized tissue in mammals, consisting of hydroxyapat
96 The role of mitochondria in enamel, the most mineralized tissue in the body, is poorly defined.
97    Enamel formation produces the most highly mineralized tissue in the human body.
98 se the production of collagenous protein and mineralized tissue in vitro, as compared to unsupplement
99 he required biochemical machinery to produce mineralized tissue in vitro, has been generated.
100 utions of bones, residual particles, and non-mineralized tissues in augmented masses between groups w
101 basis for a novel genetic system for various mineralized tissues in skeleton and teeth.
102    Requisites for development of this highly mineralized tissue include cell differentiation; product
103 ng the material properties of bone and other mineralized tissues, including mineralization, crystalli
104 t time that the signal in (31)P MR images of mineralized tissue is enhanced by a (1)H-(31)P nuclear O
105                                              Mineralized tissue is vital to many characteristic adapt
106 ral spacing of the collagen molecules in wet mineralized tissues is exactly proportional to the inver
107                             The formation of mineralized tissues is governed by extracellular matrix
108 P-1-Tolloid-like proteinases in formation of mineralized tissues is indicated, via proteolytic proces
109 thin this diversity, a common feature of all mineralized tissues is their high stiffness, implying th
110                            BSP expression in mineralized tissues is upregulated at onset of mineraliz
111 not unique to dentin but is present in other mineralized tissues like long bone, calvaria, and amelob
112                                  Cementum, a mineralized tissue lining the tooth root surface, is des
113              Proper formation of cementum, a mineralized tissue lining the tooth root surface, is req
114 ased fluorochrome labeling and expression of mineralized tissue markers, dentin matrix protein 1 (Dmp
115          Dentin matrix protein-1 (DMP1) is a mineralized tissue matrix protein synthesized by osteobl
116                                 Unlike other mineralized tissues, mature dental enamel is primarily (
117  that other signaling pathways important for mineralized tissue morphogenesis such as the Smad pathwa
118       Since there are 3 fragments within the mineralized tissues [N-terminal, C-terminal (57K), and a
119  is an extracellular matrix protein found in mineralized tissues of the skeleton and dentition.
120 entified dental pulp stem cells can generate mineralized tissue on titanium via the osteoblastic phen
121 ) by testing a hypothesis that DPCs generate mineralized tissue on titanium.
122 n, teeth, and otoconia are normally the only mineralized tissues or organs in the human body.
123 ellular matrix (ECM) protein associated with mineralized tissues, particularly bone and cementum.
124 ity (FAM) 20 gene family are associated with mineralized tissue phenotypes in humans.
125  study is to enrich the current knowledge of mineralized tissue phosphorylation events by analyzing t
126 ile acidic phosphoproteins, localized in the mineralized tissues, play key roles in control of minera
127        In the calvarial osseous defects, the mineralized tissue ratio was promoted with AMC spheroids
128 of bio-inspired nanostructured materials for mineralized tissue repair and regeneration.
129 al for developing bio-inspired approaches to mineralized tissue repair and regeneration.
130 reated defects were filled with trabeculated mineralized tissue similar to, but more mature, than tha
131 ration and stemness and the MSC-specific and mineralized tissue-specific gene expression of P-MSCs an
132 have been reported to induce expression of a mineralized tissue-specific marker, bone sialoprotein (B
133                                              Mineralized tissues such as dentin and bone assemble ext
134                                              Mineralized tissues, such as bones or teeth, are essenti
135                   Such contrasts between two mineralized tissues suggest distinct pathways of biomine
136  did not alter the intrinsic strength of the mineralized tissue, suggesting a role for proteoglycan/g
137 tion of CTR-positive cells to the surface of mineralized tissues suggests that bone and/or calcified
138 he outermost layer of teeth, is an acellular mineralized tissue that cannot regenerate; the mature ti
139                          Healthy dentin, the mineralized tissue that makes up the bulk of the tooth,
140 whale Mesoplodon densirostris are two highly mineralized tissues that contain over 95 wt.% mineral, i
141 genous tissue and is thus an exception among mineralized tissues that derive from the mesenchyme.
142 cant role in maintenance and regeneration of mineralized tissue, the success of procedures, such as g
143                       To efficiently degrade mineralized tissue, these multinucleated giant cells sec
144 noglycans were immunochemically localized at mineralized tissue-titanium interfaces.
145              Although a higher proportion of mineralized tissue was associated with the use of FDBA+R
146              Although a higher proportion of mineralized tissue was associated with the use of FDBA+R
147               Neither acute inflammation nor mineralized tissue was noted in any of the subcutaneous
148  a higher percentage of the area filled with mineralized tissue was seen at 90 days compared to 30 da
149 e spiked with calcium threonate, the area of mineralized tissue was significantly greater than in asc
150 efects treated with carrier + cementoblasts, mineralized tissues were noted at the healing site with
151 se 'hit' combinations directed hMSCs to form mineralized tissue when conditions were translated to 3D

 
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