ライフサイエンスコーパス: mineralization

1 on of ANKH mutants with different degrees in mineralization.

2 at iron oxidation is productively coupled to mineralization.

3 for temperature sensitivity (Q(10) ) of SOM mineralization.

4 al extracellular levels of PP(i), inhibiting mineralization.

5 markedly prevents osteoblast generation and mineralization.

6 scovery of polyP as phosphate source in bone mineralization.

7 ionate decrease in bone strength relative to mineralization.

8 membrane, which contains proteins regulating mineralization.

9 cture and dynamics as well as defective bone mineralization.

10 providing a broad overview of radular teeth mineralization.

11 mediate that is continually generated during mineralization.

12 domains affect collagen fibrillogenesis and mineralization.

13 eriosteal vascularization, ossification, and mineralization.

14 stablished mineral deposits failed to reduce mineralization.

15 -phosphate acts in paracrine to promote bone mineralization.

16 pyrophosphate, failed to reduce muzzle skin mineralization.

17 etween soil micro-food webs and soil C and N mineralization.

18 role in regulating skeletal and soft tissue mineralization.

19 nd for osteogenic differentiation and matrix mineralization.

20 lular matrix macromolecules control collagen mineralization.

21 e in trabecular rods, and EDX confirmed less mineralization.

22 ved structures that often arise in accretive mineralization.

23 ded to reduce microbial biomass and nitrogen mineralization.

24 teraction are responsible for intrafibrillar mineralization.

25 imbalanced metabolism, leading to defective mineralization.

26 for polyelectrolyte-directed intrafibrillar mineralization.

27 specific roles in the initiation of skeletal mineralization.

28 in extracellular matrix (ECM) formation and mineralization.

29 sm that causes defective skeletal and dental mineralization.

30 ensional model of extracellular matrix (ECM) mineralization.

31 ntrast with known patterns of post-mortem Fe mineralization.

32 the matrix vesicle membrane during skeletal mineralization.

33 rise calcification, silicification, and iron mineralization.

34 racellular inorganic pyrophosphate, increase mineralization.

35 of amelogenin was capable of guiding apatite mineralization.

36 dental enamel at low concentrations promotes mineralization.

37 ermine the role of matrix GAGs in control of mineralization.

38 opportunities for disorders of inappropriate mineralization.

39 crobial dynamics and in predicting pesticide mineralization.

40 than the increases in microbial necromass N mineralization.

41 ct in the proliferation, differentiation and mineralization abilities of patDp/+ osteoblasts while os

42 The structural and mineralization abnormality led to slight reduction in ap

43 s of injury, indicative of acute heterotopic mineralization along the cortical surface.

44 g a 7 year experiment that captured complete mineralization among 21 temperate tree species, we demon

45 ameloblasts and plays a major role in enamel mineralization and ameloblast differentiation.

46 ted a central role for these bacteria in the mineralization and biogeochemical transformation of sink

47 s loss was characterized by impaired osteoid mineralization and bone formation.

48 imaging shows significantly increased tissue mineralization and calcium deposition at the tissue-impl

49 able after 6 months although the kinetics of mineralization and cell-mineral interactions depended on

50 e for a role for cementocytes in perilacunar mineralization and cementum biology.

51 acellular inorganic pyrophosphate, increased mineralization and co-localised with LC3.

52 formation in vitro, as evidenced by reduced mineralization and decreased bone sialoprotein expressio

53 -cell conditioned medium impaired osteoblast mineralization and enhanced osteoclast-progenitor surviv

54 suppressed cementoblast differentiation and mineralization and exerted a proinflammatory effect on c

55 N(min) ), that is, the net balance between N mineralization and immobilization, which could severely

56 such functions on protein surfaces influence mineralization and in what ways specific alterations sub

57 normalities were suggestive of impaired bone mineralization and normalized at 6 months with correctio

58 al kinase (JNK) inhibition suppresses matrix mineralization and OCN expression but increases OPN expr

59 energy homeostasis of osteoblasts, impaired mineralization and reduced bone mass.

60 C1-CTT into pkd1-morphant fish restores bone mineralization and reduces the severity of the curly tai

61 aning, the skeleton is restored to its prior mineralization and strength, but the factors that regula

62 GH accelerated growth and improved mineralization and the cortical bone, but it failed in n

63 summarize the pathological roles of ENPP1 in mineralization and these soft tissue disorders.

64 cts of red blood cells on smooth muscle cell mineralization and vascular calcification and the possib

65 This is initiated rapidly (primary mineralization), and continues slowly (secondary mineral

66 n, endothelial dysfunction, hemostasis, bone mineralization, and body composition.

67 eased extracellular inorganic pyrophosphate, mineralization, and ENPP1 activity.

68 labeled molecules to balance transformation, mineralization, and formation of nonextractable residues

69 ch included Ibsp and Phex, genes involved in mineralization, and Loxl4, which encodes a lysyl oxidase

70 ondrogenesis in OAC, it induced hypertrophy, mineralization, and MMP-13 in OA-MSC.

71 alent iron PRBs that competes with carbonate mineralization, and this process is important for unders

72 grassland on: (a) soil organic matter (SOM) mineralization; and (b) the importance of biotic factors

73 No known regulators of mineralization are modified in the brittle cortical bone

74 The pathomechanisms of ectopic mineralization are poorly understood.

75 mulation shows increased cell attachment and mineralization around microcracks and a higher expressio

76 ase-20 is a critical regulator of the enamel mineralization as only a recombinant analog of a MMP20-c

77 anting vegetation decreased the Q(10) of SOM mineralization as soil bulk density, the most important

78 Using in vitro mineralization assays we showed that both recombinant an

79 Enpp1 mutant mice, another model of ectopic mineralization associated with reduced inorganic pyropho

80 used by pathogenic variants in other ectopic mineralization-associated genes.

81 The SOC mineralization at elevated incubation temperature was 72

82 Induction of biomimetic mineralization at near physiological conditions reveals

83 t on a number of processes from dissolution, mineralization, biology, electrocatalysis, corrosion, to

84 quirements of osteoblast differentiation and mineralization, both essential for regular bone formatio

85 es commonly associated with ossification and mineralization but also genes important for general prot

86 emoval with trypsin also reduced the rate of mineralization, but to a lesser extent than GAG removal,

87 reactive Fe(III) phases suppress DOM and SOM mineralization by 35 and 47%, respectively.

88 rsely, adding (57)Fe(II) alone increases SOM mineralization by 8% following oxidation to (57)Fe(III).

89 -containing integrin, resulting in increased mineralization by and differentiation of osteoblasts.

90 rs c-Fos and JunB, but stimulated osteoblast mineralization by regulating bone morphogenetic protein

91 gesting that there are various ways by which mineralization can be directed in bioinspired approaches

92 emic factors regulating extracellular matrix mineralization can be possible therapeutic strategies to

93 future use for programmable, target-oriented mineralization control.

94 osteogenic differentiation attenuated matrix mineralization, cytoskeletal rearrangement, mitochondria

95 Theory and models posit that C mineralization declines under elevated moisture and asso

96 Rates of N mineralization, denitrification and N(2) O emission demo

97 ticum (PXE), a heritable multisystem ectopic mineralization disorder.

98 soon become available for heritable ectopic mineralization disorders with application to common calc

99 Recent studies on heritable ectopic mineralization disorders with defined gene defects have

100 calcification of infancy, heritable ectopic mineralization disorders without effective treatment.

101 n pseudoxanthoma elasticum and other ectopic mineralization disorders, as presented in the symposium,

102 icum (PXE), a prototype of heritable ectopic mineralization disorders, is caused by mutations in the

103 a prototype of heritable multisystem ectopic mineralization disorders, is caused by mutations in the

104 icum (PXE), a prototype of heritable ectopic mineralization disorders, is caused in most cases by ina

105 lasticum is a prototype of heritable ectopic mineralization disorders, with phenotypic overlap with g

106 raphy was used to measure the degree of bone mineralization (DMB), and Fourier transform infrared mic

107 Indeed, deleting Tbx1 triggers accelerated mineralization due to accelerated chondrocyte differenti

108 computational lines of evidence for HFPO-DA mineralization during electrochemical oxidation at a bor

109 l culture, and acted as nucleation point for mineralization during osteogenesis.

110 fflux and accelerated differentiation to the mineralization end point.

111 Extracellular inorganic pyrophosphate, mineralization, ENPP1 activity expression of ENPP1, TNAP

112 unctate co-localisations with LC3, increased mineralization, ENPP1 and ENPP1 activity with an initial

113 rges from piezoelectric scaffolds can induce mineralization from surrounding media.

114 Close to the tendon mineralization front, calcium-rich deposits appear betwe

115 he candidate genes into the existing ectopic mineralization gene network expands the current knowledg

116 Microbe-mediated mineralization has important applications ranging from p

117 In many lineages of anurans, increased mineralization has led to hyperossified skulls, but the

118 tions on complementary mechanisms of ectopic mineralization have resulted in development of potential

119 should be the first step in correcting bone mineralization impairment before specific osteoporosis t

120 ro, and for long-term in vivo monitoring the mineralization in 3D scaffolds subcutaneously implanted

121 reased plasma PPi, and significantly reduced mineralization in Abcc6(-/-) mice.

122 y the SMAD3 mutation, consistent with higher mineralization in affected than in unaffected bone, but

123 e and function to the observed abnormal bone mineralization in AIS, which may shed light on etiopatho

124 nstitution of ABCC6 might counteract ectopic mineralization in an Abcc6(-/-) mouse model of pseudoxan

125 nt in the respired CO2, with higher fullerol mineralization in an organic, clay-rich soil versus a si

126 Acetate was a key intermediate for carbon mineralization in both zones.

127 of the molecular mechanisms of radular teeth mineralization in chitons.

128 ations for understanding control of collagen mineralization in connective tissues.

129 in elucidation of the mechanisms of ectopic mineralization in general.

130 f of the CO2 produced came from plant tissue mineralization in invasive and native communities; the r

131 ular stress and indeed 4PBA ameliorated bone mineralization in larvae and skeletal deformities in adu

132 chondrocytes, and cartilage growth and bone mineralization in medaka fish.

133 These results indicate that GAGs promote mineralization in mineralized dental tissues rather than

134 confirmed as a major determinant for ectopic mineralization in multiple tissues.

135 s used to locally stimulate osteogenesis and mineralization in order to produce integrated osteochond

136 uring bone formation and are used to monitor mineralization in osteological studies.

137 and chondrodysplasia, but showed unimpaired mineralization in primary and secondary enchondral ossif

138 that for the period 1970-2030, global carbon mineralization in reservoirs exceeds carbon fixation (P<

139 s of gene expression, matrix deposition, and mineralization in response to the two materials, with Ti

140 skeletal development and suggested decreased mineralization in Slc7a7Lbu/Lbu mice, respectively.

141 he network that, as a whole, governs ectopic mineralization in soft connective tissues.

142 showed defects in chondrocyte maturation and mineralization in the absence of Ddr2.

143 understand how alpha-CAs contribute to shell mineralization in the marine Mediterranean mussel (Mytil

144 ) double-mutant mice showed 52% reduction of mineralization in the muzzle skin compared with the Abcc

145 of plasma TNAP activity and 58% reduction of mineralization in the muzzle skin of Abcc6(-/-) mice.

146 consequently, significantly reduced ectopic mineralization in the skin of young mice.

147 duced PPi is a major determinant for ectopic mineralization in these conditions.

148 ratio is the cause of soft connective tissue mineralization in these disorders.

149 er to account for a large fraction of carbon mineralization in this system.

150 The Q(10) of SOM mineralization in topsoil was 14% higher than in subsoil

151 cementum protein 1-derived peptide regulates mineralization in vitro and promotes bone regeneration i

152 PTHrP1-17 promotes osteoblast migration and mineralization in vitro, and systemic administration of

153 ramolecular assemblies that regulate ordered mineralization in vitro, as observed in enamel rods.

154 chymal stem cell proliferation or osteoblast mineralization in vitro, nor was there evidence of cytot

155 ed odontogenic gene expression and increased mineralization in vitro.

156 Proteins controlling mineralization in vivo are diverse, suggesting that ther

157 wed enhanced odontogenic differentiation and mineralization in vivo.

158 Temperature sensitivity of anaerobic carbon mineralization in wetlands remains poorly represented in

159 oskeletal development and for rib growth and mineralization in zebrafish.

160 ose a comprehensive role for EVs in eggshell mineralization, in which annexins transfer calcium into

161 autophagy, inflammation, apoptosis, loss of mineralization inhibition, impaired mineral resorption,

162 such as crystalline structure, initiation of mineralization, inhibition, and biological/environmental

163 teeth, liver, and kidney that hydrolyzes the mineralization inhibitor inorganic pyrophosphate.

164 irculating levels of pyrophosphate, a potent mineralization inhibitor.

165 ion and subsequent gene up-regulation of the mineralization inhibitors matrix Gla protein and osteopo

166 We conclude that secondary mineralization involves EphrinB2-RhoA-limited autophagy

167 Ectopic mineralization is a global problem and leading cause of

168 Mineralization is a key process in the formation of bone

169 While osteoid mineralization is initiated at normal rate, mineral accr

170 Skeletal mineralization is initiated in utero and continues throu

171 ral protein template that could guide enamel mineralization is limited at this date.

172 Microbe-mediated mineralization is ubiquitous in nature, involving bacter

173 rbance under WP-CT and WF-CT accelerated SOC mineralization leading to soil C loss.

174 CD63, AnX2 (sEV markers) and ALP expression (mineralization marker) in the arterial media.

175 Moreover, the mineralization mechanism allows a simple one-step route

176 The mineralization mechanism by which cellulosic, keratinous

177 fundamental for an improved understanding of mineralization mechanisms in vertebrate tissues.

178 specific brain injury, cortical volume loss, mineralization, microangiopathy and neurocognitive impai

179 C and N (SMBC and SMBN), cumulative CO(2)-C mineralization (MINC) following conversion of P. austral

180 ng from microbial immobilization to enhanced mineralization, nitrification and denitrification in ter

181 rkers in the oviduct segments where eggshell mineralization occurs.

182 A maximum comparative mineralization of 95% was obtained for the PLA foam with

183 allel factor analysis demonstrated the large mineralization of all wastewater components at 6 h, whic

184 Advanced mineralization of amniote eggshell (>=150 um in thicknes

185 is is the first study to report the complete mineralization of ATO by soil microorganisms, expanding

186 ZOL-GO nanostructures can facilitate the mineralization of BM-MSC cells, demonstrated by the form

187 cells, as well as the effect of the drugs on mineralization of BM-MSCs are investigated using a varie

188 n to immune responses and the protein-driven mineralization of bone.

189 Mineralization of bones and teeth is tightly regulated b

190 red how these components are involved in the mineralization of calcium carbonate crystals and environ

191 key components for structural formation and mineralization of calcium carbonate crystals.

192 es governing the fixation, partitioning, and mineralization of carbon in soils are under increasing s

193 it has been hypothesized that these inhibit mineralization of collagen in this tissue.

194 preferentially reduced, increasing anaerobic mineralization of DOM and SOM by 74% and 32-41%, respect

195 served highly efficient (>80%) photochemical mineralization of DOM within hours in a solar simulator

196 timescale, providing opportunities to track mineralization of entire tissues.

197 d from Phlpp1-deficient osteoclasts enhanced mineralization of ex vivo osteoblast cultures, an effect

198 , but not intact human erythrocytes promoted mineralization of human arterial smooth muscle cells in

199 This type of asymmetric mineralization of lateral walls results from the vertica

200 Selective microbial mineralization of litter components and the accumulation

201 roliferation, osteogenic differentiation and mineralization of MC3T3-E1 mouse preosteoblasts in vitro

202 abolic interaction to accomplish cooperative mineralization of organic compounds to CH4 and CO2 .

203 ration necessary for the differentiation and mineralization of osteoblasts.

204 The degree of mineralization of permanent tooth germs in dental age as

205 film formation and dramatically enhanced the mineralization of phenanthrene, up to 30 times greater t

206 c concentrations induced differentiation and mineralization of preosteoblastic MC3T3-E1 cells and pre

207 FPtpz transgene was detected during in vitro mineralization of primary pulp cultures and during repar

208 Sulfides could be produced through mineralization of reduced sulfur compounds or reduction

209 on use of infrared (IR) assisted heating for mineralization of soybean derived samples has been devel

210 n) oxide, and their impact on the subsequent mineralization of target compounds using H(2)O(2) or S(2

211 break the ether bond, but leads to stepwise mineralization of the acidic side chain.

212 trolling palatal shelf elevation, as well as mineralization of the bones of the secondary palate.

213 (GACI), characterized by severe, early-onset mineralization of the cardiovascular system, often with

214 uggested to be involved in calcium phosphate mineralization of the club, as indicated by in vitro stu

215 roliferation, proteoglycan distribution, and mineralization of the MCC.

216 tant biochrome coupled with early diagenetic mineralization of the ommatidial lenses.

217 on of the ring followed by ring cleavage and mineralization of the resulting products-does not accoun

218 at synthesize bone matrix and coordinate the mineralization of the skeleton.

219 rickets, lower limb deformities, pain, poor mineralization of the teeth and disproportionate short s

220 endothelial cells (HUVEC) and on osteoblast mineralization of vascular smooth muscle cells (VSMC).

221 Mineralization of WT bone marrow stromal cells cultured

222 cient circulating phosphate availability for mineralization or also by a direct, local intrinsic effe

223 y due to accelerated rates of organic matter mineralization or iron reduction beneath suboxic, stagna

224 Biota accelerated CO(2) mineralization over abiotic controls as ecosystem comple

225 ance with this approach, both for predicting mineralization parameters and for selecting effective co

226 ess regression model to predict the Gompertz mineralization parameters of the co-cultures of two and

227 out the potential of cluster/particle-driven mineralization pathways to intrinsically tailor the prop

228 Based on a dataset of mineralization performance for all pairs of 13 bacterial

229 ns would lead to amelioration of the ectopic mineralization phenotype in the Abcc6(-/-) mouse model o

230 le in Abcc6 yet with highly variable ectopic mineralization phenotypes of pseudoxanthoma elasticum.

231 t could influence the organ-specific ectopic mineralization phenotypes.

232 ment with Phen was sufficient to enhance the mineralization potential of DPSCs in vitro.

233 s; the rest of the CO2 was produced from SOM mineralization (priming).

234 Mineralization proceeds inwards by mineral deposition fr

235 Inspired by the mineralization process of bone, a material system that a

236 lagen, and mineral suggest a concept for the mineralization process, where ions and/or mineral precur

237 can be prevented by inhibiting the activated mineralization process.

238 he jawbone through an exquisitely controlled mineralization process: unmineralized collagen fibers of

239 These mineralization processes comprise calcification, silicif

240 xtinct lamniform sharks to examine the tooth mineralization processes in this group.

241 eomic data, we identified and sequenced Club Mineralization Protein 1 (CMP-1), an abundant mildly pho

242 able differentiation of different degrees of mineralization (R(2) = 0.92 compared with CT).

243 below this threshold, the areal hypolimnetic mineralization rate (AHM) decreased in proportion to APS

244 Moreover, an increased endocortical osteoid mineralization rate and higher trabecular and cortical b

245 The SOM mineralization rate decreased with grassland degradation

246 racing model to calculate the production and mineralization rates of necromass N.

247 Grazing reduced soil C and N mineralization rates via changes in plant biomass, soil

248 ees C and 30 degrees C for 10 weeks, and SOC mineralization rates were estimated using the first orde

249 biomass, and increasing FGR strongly reduced mineralization rates, because of lower root N concentrat

250 sed soil microbial biomass N and increased N mineralization rates, both in the presence and absence o

251 bacterial and fungal necromass N had similar mineralization rates, despite their contrasting chemistr

252 plant nitrogen (N) demand versus increased N mineralization rates.

253 Smad4 is necessary for the activation of the mineralization-related genes, it is dispensable for BMP2

254 onse functions for soil microbial carbon (C) mineralization remain a critical uncertainty for predict

255 and the mechanisms by which collagen directs mineralization remain unclear.

256 genous), and postmortem decay and taphonomic mineralization resulted in the formation of aragonite an

257 emplates create a confined space and control mineralization separated from seawater.

258 soil fauna, microbial biomass, and nitrogen mineralization shifted from neutral to negative with inc

259 ontaining amorphous calcium carbonate to the mineralization site.

260 e as guidance molecules to target EVs to the mineralization site.

261 e anthropogenic changes may alter net soil N mineralization (soil net N(min) ), that is, the net bala

262 e confirmed the presence of major vesicular, mineralization-specific and eggshell matrix proteins in

263 in and enamel was largely symmetrical at the mineralization stage, highlighting the difference betwee

264 lankton development, physiology and skeletal mineralization status, potentially reducing their defens

265 MMP20 enzyme degradation and HAP mineralization studies showed that the amino acid varian

266 From in vitro mineralization studies with HAp, CaCO(3) and gamma-FeOOH

267 ive to PTH stimulation and capable of matrix mineralization, subclones 14 and 24 do not faithfully re

268 s overexpressed in tissues in which eggshell mineralization takes place and that this overexpression

269 ACC in chicken uterine fluid where eggshell mineralization takes place.

270 Because complete wood mineralization takes years, most experiments focus on ho

271 mation from fields as diverse as bioinspired mineralization, templating, pharmaceuticals, colloidal c

272 ed higher cell attachment, proliferation and mineralization than the HCCS group in vitro.

273 n variable alterations of bone formation and mineralization that are caused by mutations in the ALPL

274 r CO(2) injection revealed nascent carbonate mineralization that was qualitatively consistent with ex

275 When calibrating against data on pesticide mineralization, the gene-centric and biomass-based model

276 alized tissues, play key roles in control of mineralization, the role of glycosaminoglycans (GAGs) is

277 to feedbacks of leaf traits on soil nitrogen mineralization through litter quality.

278 ults in menopausal symptoms and affects bone mineralization, thus limiting treatment duration or dema

279 ted molecules were observed as a function of mineralization time and matrix.

280 shift of glyphosate transformation from full mineralization to AMPA formation.

281 cific Northwest (IPNW), USA, and measure SOC mineralization under ambient and elevated incubation tem

282 consistent effects on soil carbon (C) and N mineralization under elevated temperature.

283 ralization), and continues slowly (secondary mineralization) until bone is remodeled.

284 ochthonous organic matter and its subsequent mineralization upon back-flooding-a common feature of ne

285 l x((13)C)DIC allowing to quantify microbial mineralization using mass-balance calculations.

286 ve, and simple approach to monitor microbial mineralization using reverse stable isotope labeling ana

287 todes) and ecosystem functions (soil C and N mineralization), using paired grazed and ungrazed plots

288 Resorcinol mineralization was >68% in the presence and absence of N

289 Mineralization was conducted in mineral matrixes commonl

290 However, when mineralization was induced via oxidative stress, DRP1 in

291 We confirmed that the mineralization was initially induced by (*)OH formed fro

292 The Q(10) of N mineralization was similar among intact, degraded and re

293 ionic electrolyte is used to direct collagen mineralization, we argue that additional types of long-r

294 ation- and polyanion-directed intrafibrillar mineralization, we challenge the popular paradigm that e

295 15 and 25 degrees C, and Q(10) values of SOM mineralization were determined.

296 asma levels of PPi and the degree of ectopic mineralization were determined.

297 Conversely, osteoblast differentiation and mineralization were inhibited when osteogenesis of affec

298 Osteoblast differentiation and mineralization were stimulated by the SMAD3 mutation, co

299 from Tg mice had reduced differentiation and mineralization with reduced Alpl and Runx2 transcripts.

300 0% of the injected CO(2) was sequestered via mineralization within two years, with the resulting carb