ライフサイエンスコーパス: biomineralization

1 hanisms of biological mineral morphogenesis (biomineralization).

2 characterization of enzymes responsible for biomineralization.

3 the previously proposed checkpoint model for biomineralization.

4 t is known about the mechanisms of magnetite biomineralization.

5 g to vascular remodeling and calcium-related biomineralization.

6 potential of engineered functional material biomineralization.

7 ce of the mycelium as a reactive network for biomineralization.

8 cedented insight into the earliest stages of biomineralization.

9 inding protein that plays a critical role in biomineralization.

10 ined for their properties of CaCO3 and SrCO3 biomineralization.

11 , including nucleation, crystallization, and biomineralization.

12 he protein-mineral interactions essential to biomineralization.

13 secreted proteins and is critical for proper biomineralization.

14 xpression of ZBTB16 and specific markers for biomineralization.

15 l to assessing the role of these proteins in biomineralization.

16 riginal connection between cell division and biomineralization.

17 sport to supply ACC in a vertebrate model of biomineralization.

18 lular substrates and play important roles in biomineralization.

19 tion include extracellular and intracellular biomineralization.

20 of cell types that can participate in valve biomineralization.

21 gen synthesis, hydroxyproline formation, and biomineralization.

22 ndicative for growth of bacteria involved in biomineralization.

23 rigin of magnetoreception based on magnetite biomineralization.

24 implications for patients with disorders of biomineralization.

25 without necessarily enhancing the extent of biomineralization.

26 s for understanding molecular recognition in biomineralization.

27 cts of different C termini on the process of biomineralization.

28 mpact the physiological processes that drive biomineralization.

29 ng 'moldable' nanoparticles in extracellular biomineralization.

30 roteins and also biological organisms during biomineralization.

31 FGF23 in disorders of phosphate handling and biomineralization.

32 of amelogenin-mineral interactions in enamel biomineralization.

33 tivation step for its biological function in biomineralization.

34 l applications of nanoparticle synthesis via biomineralization.

35 standing of the factors that regulate enamel biomineralization.

36 tion of glass ceramics, and the mechanism of biomineralization.

37 calcification is a highly regulated form of biomineralization.

38 solution this short peptide induces in vitro biomineralization.

39 amental mechanisms by which fluoride affects biomineralization.

40 ring low temperature inorganic synthesis and biomineralization.

41 nfluenced crystal growth--a process known as biomineralization.

42 es of metal transport in visual function and biomineralization.

43 lear evolutionary and societal importance of biomineralization.

44 the interaction mechanisms with CuNPs during biomineralization.

45 al acidification have deleterious effects on biomineralization.

46 tools toward understanding the mechanisms of biomineralization.

47 ving the origin of sponge spiculogenesis and biomineralization.

48 y, electrocatalysis, corrosion, to microbial biomineralization.

49 racterization of the enzymes responsible for biomineralization.

50 most remarkable examples of matrix-mediated biomineralization.

51 here iron ions accumulate prior to magnetite biomineralization.

52 ise difficult oxidation reaction, as well as biomineralization.

53 ts into the molecular mechanism of manganese biomineralization.

54 reservation rather than a product of in vivo biomineralization(4-7).

55 ing the cellular and molecular mechanisms of biomineralization, a process common to all branches of l

56 ause (i) it can enhance our understanding of biomineralization and (ii) it offers a straightforward r

57 ds to a significant enhancement of magnetite biomineralization and an increase in the cellular magnet

58 owledge is essential for understanding coral biomineralization and assessing the potential impacts of

59 ight provide new ideas for investigations of biomineralization and biomimetics.

60 ing shell is an excellent model for studying biomineralization and evolution.

61 tion approach are fundamentally important to biomineralization and general synthesis strategy for bio

62 the role of the animal in living stony coral biomineralization and how it evolved has profound implic

63 to the self-organization of nanoparticles in biomineralization and improve design strategies of bioma

64 aling activates hundreds of genes, including biomineralization and interestingly, vascularization gen

65 es also drove divergent pathways of Fe and S biomineralization and led to more As(V) and SO4 reductio

66 nderstanding of the fundamental chemistry in biomineralization and mineral-carbonation processes.

67 tially expressed miRNAs, mainly involving in biomineralization and pigmentation through functional en

68 sting model protein system for understanding biomineralization and protein assembly.

69 a hitherto unknown connection between tooth biomineralization and retinal function.

70 h in understanding the processes involved in biomineralization and revealing information that is impo

71 s for understanding multiscale complexity of biomineralization and show a prospect for material scien

72 Implications of RLS growth on biomineralization and spherulitic crystal growth are not

73 raction of multiple biomolecules to catalyze biomineralization and template growth.

74 n environmental trigger for the evolution of biomineralization and the 'Cambrian explosion' of ecolog

75 anding of the regulatory networks that drive biomineralization and their evolution is far from clear.

76 ions regarding both their extent of original biomineralization and their phylogenetic affinity.

77 m to investigate the processes implicated in biomineralization and to unravel the complex roles of pr

78 vided novel insights into microbial-mediated biomineralization and, therefore, provides a powerful me

79 nding the role of calcium in bone formation, biomineralization, and bone diseases like osteoporosis.

80 s critical in areas such as pharmaceuticals, biomineralization, and catalysis.

81 offers a new approach to study mechanisms of biomineralization, and perhaps ultimately new techniques

82 ant in material synthesis, climate modeling, biomineralization, and pharmaceutical formulation.

83 luble molecules for sensing applications, or biomineralization approaches for the controlled formatio

84 Here we report on new biomineralization architectures of previously unsuspecte

85 nesis, magnetosome protein localization, and biomineralization are placed under discrete genetic cont

86 nexpected temporal compensatory responses in biomineralization as a mechanism for resistance to alter

87 r qualitative and quantitative trade-offs in biomineralization as compensatory responses to altered e

88 best model organisms for studying magnetite biomineralization, as their genomes are sequenced and to

89 rthropods are ideal model organisms to study biomineralization because they regularly molt their exos

90 believed to play an essential role in enamel biomineralization, because defects in KLK4 cause hypomat

91 interactions also play an important role in biomineralization, biomedicine, and in assembling the bu

92 reduced miR-204 expression promotes vascular biomineralization by augmenting the expression of the tr

93 ngs indicate that intracellular Ca-carbonate biomineralization by cyanobacteria has been overlooked b

94 ory of intra- and extracellular Ca-carbonate biomineralization by cyanobacteria.

95 Biomineralization by marine phytoplankton, such as the s

96 structural information for understanding Mn biomineralization by such unexplored enzymes.Significant

97 synthesis in the absence of the other major biomineralization candidates.

98 calcite--which is of tremendous relevance to biomineralization, carbon sequestration, paleogeochemist

99 stigate biologically induced metal carbonate biomineralization, CdCl2 was contacted with supernatants

100 nt materials and processes, including marine biomineralization, cement hydration, corrosion inhibitio

101 Furthermore, biomineralization changes in mollusk shells can be used

102 verse areas of inquiry, such as nanoconfined biomineralization, CO2 sequestration in porous aquifers,

103 luding predation and most of its variations, biomineralization, colonial or clonal growth, bioerosion

104 This biomineralization concept is postulated to act as an arc

105 s an important advance in the translation of biomineralization concepts into regimes for in-situ remi

106 The transformation sequence observed in biomineralization could be mainly energetically driven;

107 genetic requirements for proteolysis causes biomineralization defects, showing that proper regulatio

108 This also indicated species specificity in biomineralization depending on nutrition and physiology.

109 ystalline surfaces play an important role in biomineralization, determine survival of some organisms

110 Cs, but most likely are directly involved in biomineralization during sea urchin embryonic developmen

111 ralized tissues suggest distinct pathways of biomineralization, e.g., the nature of the equilibrium b

112 side chains and resulting metallocluster for biomineralization emerges from the lower iron oxidation

113 activation of MamE-dependent proteolysis of biomineralization factors and direct binding to transiti

114 oteolytic processing of itself and two other biomineralization factors in vivo Here, we have analyzed

115 blastic cultures occurs within extracellular biomineralization foci (BMF) within 12 h after addition

116 r surface of HAp material after hydrothermal biomineralization for 5 days has considerable capability

117 re used to mimic nondestructive detection of biomineralization for intact real-size 3D tissue enginee

118 of vertebrates evolved, but reading this pre-biomineralization fossil record is fraught with difficul

119 Biomineralization frequently occurs via transient amorph

120 These MOFs were able to induce in vitro biomineralization from pre-osteoblastic MC3T3 cells and

121 predicted by the GRN and show that candidate biomineralization genes from different shell layers, and

122 Here, we identify and characterize two new biomineralization genes, p58-a and p58-b.

123 discovery may have important implications in biomineralization, geology, and industrial processes bas

124 monas stutzeri strain DCP-Ps1 to drive CaCO3 biomineralization has been investigated in a microfluidi

125 This Zn silicate biomineralization has relevant implications for phytorem

126 natural peptides with the ability to promote biomineralization have the potential to be utilized in h

127 Studies in biomineralization, however, are largely limited to atomi

128 the known functions of amelogenin in enamel biomineralization, i.e., self-assembly, associations wit

129 mics two main strategies of morphogenesis in biomineralization, i.e., spatial and morphological contr

130 tence of at least two distinct mechanisms of biomineralization: (i) one with Ca-carbonate inclusions

131 We have created a model system of biomineralization in a cellular environment by expressin

132 We describe physiological biomineralization in collagenous matrices as well as a m

133 ere, we investigate the process of magnetite biomineralization in Desulfovibrio magneticus sp. RS-1,

134 e contributes to the very different forms of biomineralization in diatoms and coccolithophores.

135 The VEGF pathway is essential for biomineralization in echinoderms, while in many other ph

136 rst step toward in vivo studies of magnetite biomineralization in magnetotactic bacteria.

137 ications for reconstructing the evolution of biomineralization in metazoans.

138 rnal Mg-banding is an intrinsic component of biomineralization in planktic foraminifera.

139 Biomineralization in sea urchin embryos is a crystal gro

140 insight into the phylogeny and evolution of biomineralization in the Demosopongiae.

141 vascularization and specifically coopted for biomineralization in the echinoderm phylum.

142 nd demonstrates a central role for bacterial biomineralization in the formation of highly pure Au in

143 e a cellular biology perspective, we studied biomineralization in the Soas-2 osteosarcoma cell line.

144 erize and spatially resolve the mechanism of biomineralization in those microorganisms.

145 many genes with proven or predicted roles in biomineralization in vegf3 morphants.

146 ing and show that it is required to initiate biomineralization in vivo.

147 these factors play a minor role in magnetite biomineralization in vivo.

148 rarchical levels of control found in natural biomineralization, including genetic, chemical, spatial,

149 bstrates suggest roles for the kinase beyond biomineralization, including lipid homeostasis, wound he

150 and several secreted proteins implicated in biomineralization, including the small integrin-binding

151 keleton and appear to have evolved carbonate biomineralization independently millions of years after

152 In biomineralization, inorganic materials are formed with r

153 Biomineralization is a widely dispersed and highly regul

154 Biomineralization is believed to have evolved rapidly an

155 nderstanding the biological control of coral biomineralization is critical to informing future models

156 understanding of other key events in enamel biomineralization is limited.

157 Biomineralization is mediated by specialized proteins th

158 pposed to the complete loss of mamE where no biomineralization is observed, the protease-deficient va

159 A new strategy based on biomineralization is presented to rationally tune the em

160 Biomineralization is regulated by inorganic pyrophosphat

161 Biomineralization is the process by which living organis

162 Biomineralization is the process where biological system

163 nterplay between noncollagenous proteins and biomineralization is widely accepted, yet the contributi

164 lected for this study due to its key role in biomineralization, is expressed in many species and tiss

165 ves to control crystallization, as occurs in biomineralization, is rarely investigated due to the vas

166 re presumed to play a role in the process of biomineralization, key questions regarding the nature of

167 in all populations and occurred in genes for biomineralization, lipid metabolism, and ion homeostasis

168 luded accumulation of the acidotropic silica biomineralization marker PDMPO.

169 Fe biomineralization may have protected oxygenic photosynth

170 c mutants further demonstrate increased iron biomineralization measured by a novel fluorescent geneti

171 Here, we show that bivalves modify the main biomineralization mechanism during the event to continue

172 mosponges, called spicules, follows a unique biomineralization mechanism in which polycondensation of

173 t biological processes play key roles in the biomineralization mechanism.

174 ructures, which requires a highly controlled biomineralization mechanism; this capability dates back

175 Two main lead biomineralization mechanisms were therefore distinguishe

176 The first step of iron biomineralization mediated by ferritin is the oxidation

177 ar mechanisms of mineral growth that control biomineralization, mineral scaling and industrial materi

178 We characterized two biomineralization modules of the GRN and hypothesize tha

179 croenvironment, including its protein-guided biomineralization, nanostructure, vasculature, innervati

180 One fascinating example of silicon biomineralization occurs in the diatoms, unicellular alg

181 of the cyanobacteria in which intracellular biomineralization occurs remain unknown.

182 likely representing an organic template for biomineralization of aragonite on the calcite layer.

183 Biomineralization of Au occurred in the presence of viab

184 olutionary conserved function related to the biomineralization of bones.

185 s Neurospora crassa was investigated for the biomineralization of calcium carbonate and its potential

186 The microbial induced biomineralization of calcium carbonate using the ureolyt

187 In the ectopic biomineralization of calcium oxalate kidney stones, the

188 Employment of cyanobacteria in biomineralization of carbon dioxide by calcium carbonate

189 ulting in challenges to study the growth and biomineralization of complex hard mineralized tissues.

190 rea and calcium-containing medium, extensive biomineralization of fungal filaments was observed.

191 led to an increased level of interest in the biomineralization of gold.

192 ix proteins can have profound effects on the biomineralization of hard tissues.

193 ivorans bacterial cells served as nuclei for biomineralization of initially spherical vaterite precip

194 On Earth, magnetotactic bacteria perform biomineralization of intracellular magnetite nanoparticl

195 Biomineralization of iron granules occurs in the iron de

196 ely transformed into aragonite or calcite in biomineralization of marine invertebrate shells or avian

197 sly showed that this mobilization was due to biomineralization of metallic Cu nanoparticles associate

198 the transformation and biologically induced biomineralization of metals by microorganisms is not wel

199 Pyromorphite formation represents biomineralization of mobile lead species into a very sta

200 This is the first report of biomineralization of olekminskite and coprecipitation of

201 We investigated shell biomineralization of selectively bred and wild-type fami

202 tion of their bivalved bauplan preceding the biomineralization of shell valves in crown brachiopods.

203 lled magnetosomes, which are tasked with the biomineralization of small crystals of the iron oxide ma

204 Here, we monitored the biomineralization of the mantis shrimp dactyl club-a mod

205 erved in enamel proteomes, had a role in the biomineralization of the thick enamel crowns that charac

206 g dental enamel, plays a crucial role in the biomineralization of this tissue.

207 biological formation of inorganic materials (biomineralization) often occurs in specialized intracell

208 to the evolution and environmental impact of biomineralization on Earth, especially if their biologic

209 in biogeochemistry models, which often base biomineralization only on SI (caused by biotic or abioti

210 the lack of a mutual biochemical toolkit for biomineralization or evidence of homology, shells from d

211 k more efficiently, via increased cell size, biomineralization or increased CN of eukaryotic phytopla

212 as now emerged as a highly regulated form of biomineralization organized by collagenous and elastin e

213 n hemozoin formation and underscore the heme biomineralization pathway as an attractive target for th

214 sclerites which provides information on the biomineralization pathway in C. rubrum.

215 eton interface, skeletal organic matrix, and biomineralization pathways.

216 es, but has maintained its distinct skeletal biomineralization pattern for at least 40 My: Well-prese

217 des, and instead suggest a semiintracellular biomineralization pattern known from other unicellular c

218 These findings support biomineralization plasticity as a potentially advantageo

219 s in secondary Au formation, we assessed the biomineralization potential of biofilms growing in quart

220 rgins of the colony and represents a type of biomineralization previously unknown in cheilostome bryo

221 ials have been synthesized using a fungal Mn biomineralization process based on urease-mediated Mn ca

222 Its formation involves the fastest known biomineralization process in vertebrates.

223 simultaneously alongside the opposite redox biomineralization process of mycogenic Mn(II) oxidation

224 characterization of organic matrices in the biomineralization process of this species was studied to

225 Further insight into the biomineralization process over time was provided by a co

226 The mechanisms underlying this biomineralization process remain enigmatic.

227 deposits at the surface of the Earth using a biomineralization process that has been almost systemati

228 ormed by the evolutionarily highly conserved biomineralization process that is controlled by extracel

229 ombined this hydrogel network with a calcite biomineralization process to stabilize soil.

230 thesis of electrode materials using a fungal biomineralization process, thus providing a novel strate

231 nature of bone and provide insights into the biomineralization process.

232 how protein variants can affect steps of the biomineralization process.

233 ith minerals are essential for understanding biomineralization processes and the function of intrinsi

234 Biomineralization processes are of key importance in the

235 cular processes ruling mineral evolution and biomineralization processes has been gained.

236 Intricate biomineralization processes in molluscs engineer hierarc

237 An elegant example of such biomineralization processes is the production of nano-sc

238 In these biomineralization processes the organisms use a twofold

239 , where these are widely used as a model for biomineralization processes.

240 S(0) is frequently invoked as a biomineralization product generated by enzymatic oxidati

241 an alter their mechanisms of calcite crystal biomineralization, promoting resilience to acidification

242 Fungi possess various biomineralization properties, as well as a filamentous m

243 These results define a new biomineralization protein and lay down the foundation fo

244 mpse toward the long-suspected mechanism for biomineralization protein control over mineral microstru

245 s study of a ten member polyanionic sequence biomineralization protein family, Asprich, and the exper

246 within the mineral-recognition domain of the biomineralization protein salivary statherin adsorbed on

247 droxyapatite (HAP) recognition domain of the biomineralization protein statherin, interacts with HAP,

248 at proteins) together with five known silica biomineralization proteins (four cingulins and one silaf

249 In many cases, the active regions of these biomineralization proteins are intrinsically disordered.

250 Although many candidate biomineralization proteins have been identified, functio

251 The phosphate moieties on biomineralization proteins play an essential role in min

252 Extracellular biomineralization proteins such as salivary statherin co

253 d three-dimensional (3D) structures occur in biomineralization proteins, the design of synthetic, sol

254 oparticles through the action of several key biomineralization proteins.

255 dy solution- and adsorbed-state ensembles of biomineralization proteins.

256 aining exon4 cause a specific enhancement of biomineralization related to stabilization of early-form

257 ndings suggest a molecular mechanism for how biomineralization-related enantiomers might exert hierar

258 nts a unique extensive proteomic analysis of biomineralization-related proteins in corals from which

259 c acids [4-6], the role of these proteins in biomineralization remains elusive [5, 6].

260 ern and fossil cells in order to investigate biomineralization response of ancient coccolithophores t

261 re distinct during various stages of silicon biomineralization responses.

262 etically heterogeneous group of disorders of biomineralization resulting from failure of normal ename

263 Enamel biomineralization results in a release of protons into t

264 and Al extracted by soil minerals to build a biomineralization rim, which can capture Zn.

265 s that carry out and regulate cynaobacterial biomineralization should put us in a position where we c

266 Biomineralization strategies include the use of hydrogel

267 Nature has evolved several unique biomineralization strategies to direct the synthesis and

268 lead geomycology and organic phosphates as a biomineralization substrate, and are also relevant to me

269 and phosphate mineralization demonstrates a biomineralization system that provides a versatile route

270 (ACC), an important precursor phase in many biomineralization systems.

271 ted a computational method to design protein-biomineralization systems.

272 e calcifying tissue-skeleton interface where biomineralization takes place.

273 nd the ensuing assembly process, inspired by biomineralization templates capable of surface reconfigu

274 ein, the different types of microbe-mediated biomineralization that occur in nature, their mechanisms

275 suspected to participate in buildings blocks biomineralization that self-assembles in a process that

276 Biomineralization, the process by which mineralized tiss

277 almost universally employed measure of coral biomineralization, the rate of linear extension, might n

278 of great importance, including frost heave, biomineralization, the synthesis of nanomaterials, and s

279 In many marine organisms, biomineralization-the crystallization of calcium-based i

280 escribe a simplistic method of intracellular biomineralization to produce plasmonic gold nanoparticle

281 From biomineralization to synthesis, organic additives provid

282 ing to its relevance in fields spanning from biomineralization to the rational design of functional n

283 This is the only description of the whole "biomineralization toolkit" of the matrices that, at leas

284 proteins in corals from which we identify a biomineralization "toolkit," an organic scaffold upon wh

285 we examine large-scale spatial variations in biomineralization under heterogeneous environmental grad

286 rom this work have demonstrated that modular biomineralization units can be effective at processing c

287 of culture that is associated with decreased biomineralization, up-regulate expression of cyclin D3 a

288 gene regulatory network (GRN) for molluscan biomineralization using Antarctic clam (Laternula ellipt

289 Biomineralization using protein cavities is an important

290 ent soft collagenous tissue was co-opted for biomineralization using redundant genes resulting from w

291 s were attenuated, but dexamethasone-induced biomineralization was accelerated.

292 of a previously unrecognized 'checkpoint' in biomineralization where MamE moderates the completion of

293 ality is ubiquitous in biology, including in biomineralization, where it is found in many hardened st

294 tion, tetrahedrally coordinated systems, and biomineralization, where single or multiple precursors t

295 bonate are believed to be central species of biomineralization, which serves as an important inspirat

296 en at the mat surface promotes Fe(III)-oxide biomineralization, which was supported using molecular a

297 he effects of abrupt climate change on shell biomineralization, while also offering an alternative vi

298 are consistent with in vivo intracellular Fe biomineralization, with subsequent in situ recrystalliza

299 target for antimalarial drugs has been heme biomineralization within the malarial parasite digestive

300 r metals present were removed via controlled biomineralization: zinc as ZnS in a sulfidogenic bioreac