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1 hanisms of biological mineral morphogenesis (biomineralization).
2 racterization of the enzymes responsible for biomineralization.
3 ise difficult oxidation reaction, as well as biomineralization.
4 lular substrates and play important roles in biomineralization.
5 of cell types that can participate in valve biomineralization.
6 ts into the molecular mechanism of manganese biomineralization.
7 gen synthesis, hydroxyproline formation, and biomineralization.
8 ndicative for growth of bacteria involved in biomineralization.
9 implications for patients with disorders of biomineralization.
10 without necessarily enhancing the extent of biomineralization.
11 s for understanding molecular recognition in biomineralization.
12 cts of different C termini on the process of biomineralization.
13 mpact the physiological processes that drive biomineralization.
14 roteins and also biological organisms during biomineralization.
15 FGF23 in disorders of phosphate handling and biomineralization.
16 of amelogenin-mineral interactions in enamel biomineralization.
17 tivation step for its biological function in biomineralization.
18 standing of the factors that regulate enamel biomineralization.
19 characterization of enzymes responsible for biomineralization.
20 tion of glass ceramics, and the mechanism of biomineralization.
21 calcification is a highly regulated form of biomineralization.
22 solution this short peptide induces in vitro biomineralization.
23 amental mechanisms by which fluoride affects biomineralization.
24 ring low temperature inorganic synthesis and biomineralization.
25 nfluenced crystal growth--a process known as biomineralization.
26 most remarkable examples of matrix-mediated biomineralization.
27 es of metal transport in visual function and biomineralization.
28 ents that occur simultaneously during enamel biomineralization.
29 key epigenetic factor in controlling otolith biomineralization.
30 d in these studies may participate in normal biomineralization.
31 nisms of magnetosome formation and magnetite biomineralization.
32 produce an enamel matrix competent to direct biomineralization.
33 de nanocrystals, an example of extracellular biomineralization.
34 the previously proposed checkpoint model for biomineralization.
35 ns in amelogenin suggest their importance to biomineralization.
36 s of a shared genetic "toolkit" to carry out biomineralization.
37 tus purpuratus for gene products involved in biomineralization.
38 onated apatite crystals during dental enamel biomineralization.
39 ant for its function as a mediator of dentin biomineralization.
40 to a specific "effector" protein involved in biomineralization.
41 s to drive efforts to characterize manganese biomineralization.
42 for general physiochemical investigations of biomineralization.
43 ocluster precursors may play a major role in biomineralization.
44 illustrate features potentially important to biomineralization.
45 le order in a process that closely resembles biomineralization.
46 iation beyond the hypothesized role of PP in biomineralization.
47 h as a signaling molecule and a regulator of biomineralization.
48 echanism of mineral nucleation during enamel biomineralization.
49 ed for epithelial-mesenchymal transition and biomineralization.
50 has led to a growing interest in the area of biomineralization.
51 here iron ions accumulate prior to magnetite biomineralization.
52 t is known about the mechanisms of magnetite biomineralization.
53 g to vascular remodeling and calcium-related biomineralization.
54 potential of engineered functional material biomineralization.
55 ce of the mycelium as a reactive network for biomineralization.
56 cedented insight into the earliest stages of biomineralization.
57 inding protein that plays a critical role in biomineralization.
58 ined for their properties of CaCO3 and SrCO3 biomineralization.
59 , including nucleation, crystallization, and biomineralization.
60 he protein-mineral interactions essential to biomineralization.
61 secreted proteins and is critical for proper biomineralization.
62 xpression of ZBTB16 and specific markers for biomineralization.
63 l to assessing the role of these proteins in biomineralization.
64 riginal connection between cell division and biomineralization.
65 ing the cellular and molecular mechanisms of biomineralization, a process common to all branches of l
66 ds to a significant enhancement of magnetite biomineralization and an increase in the cellular magnet
67 s play key roles as structural components in biomineralization and as a second messenger in signaling
69 owledge is essential for understanding coral biomineralization and assessing the potential impacts of
71 magnetosome precisely coordinates magnetite biomineralization and can serve as a model system for th
73 improved understanding of diverse systems of biomineralization and design of new synthetic growth mod
74 protein to membrane interactions critical to biomineralization and enamel architecture while suggesti
76 tion approach are fundamentally important to biomineralization and general synthesis strategy for bio
77 es also drove divergent pathways of Fe and S biomineralization and led to more As(V) and SO4 reductio
78 nderstanding of the fundamental chemistry in biomineralization and mineral-carbonation processes.
81 acellular matrix proteins that contribute to biomineralization and provide functional information on
83 h in understanding the processes involved in biomineralization and revealing information that is impo
86 n environmental trigger for the evolution of biomineralization and the 'Cambrian explosion' of ecolog
88 m to investigate the processes implicated in biomineralization and to unravel the complex roles of pr
89 vided novel insights into microbial-mediated biomineralization and, therefore, provides a powerful me
90 nding the role of calcium in bone formation, biomineralization, and bone diseases like osteoporosis.
92 offers a new approach to study mechanisms of biomineralization, and perhaps ultimately new techniques
94 llular and molecular mechanisms that support biomineralization, and their evolutionary origins, are d
95 luble molecules for sensing applications, or biomineralization approaches for the controlled formatio
97 nesis, magnetosome protein localization, and biomineralization are placed under discrete genetic cont
100 best model organisms for studying magnetite biomineralization, as their genomes are sequenced and to
101 believed to play an essential role in enamel biomineralization, because defects in KLK4 cause hypomat
102 interactions also play an important role in biomineralization, biomedicine, and in assembling the bu
103 reduced miR-204 expression promotes vascular biomineralization by augmenting the expression of the tr
104 ngs indicate that intracellular Ca-carbonate biomineralization by cyanobacteria has been overlooked b
107 structural information for understanding Mn biomineralization by such unexplored enzymes.Significant
109 calcite--which is of tremendous relevance to biomineralization, carbon sequestration, paleogeochemist
110 stigate biologically induced metal carbonate biomineralization, CdCl2 was contacted with supernatants
111 nt materials and processes, including marine biomineralization, cement hydration, corrosion inhibitio
113 verse areas of inquiry, such as nanoconfined biomineralization, CO2 sequestration in porous aquifers,
114 luding predation and most of its variations, biomineralization, colonial or clonal growth, bioerosion
115 s an important advance in the translation of biomineralization concepts into regimes for in-situ remi
117 genetic requirements for proteolysis causes biomineralization defects, showing that proper regulatio
118 This also indicated species specificity in biomineralization depending on nutrition and physiology.
119 ystalline surfaces play an important role in biomineralization, determine survival of some organisms
120 Cs, but most likely are directly involved in biomineralization during sea urchin embryonic developmen
121 ralized tissues suggest distinct pathways of biomineralization, e.g., the nature of the equilibrium b
122 side chains and resulting metallocluster for biomineralization emerges from the lower iron oxidation
123 bioceramic with unique materials properties, biomineralization exploits cells to create a tissue-spec
124 activation of MamE-dependent proteolysis of biomineralization factors and direct binding to transiti
125 oteolytic processing of itself and two other biomineralization factors in vivo Here, we have analyzed
127 blastic cultures occurs within extracellular biomineralization foci (BMF) within 12 h after addition
128 l extracellular spherical structures, termed biomineralization foci (BMF), containing bone acidic gly
129 r surface of HAp material after hydrothermal biomineralization for 5 days has considerable capability
130 re used to mimic nondestructive detection of biomineralization for intact real-size 3D tissue enginee
131 of vertebrates evolved, but reading this pre-biomineralization fossil record is fraught with difficul
133 In the absence of SRF genes associated with biomineralization, GATA-6, bone morphogenetic protein 4
136 monas stutzeri strain DCP-Ps1 to drive CaCO3 biomineralization has been investigated in a microfluidi
138 natural peptides with the ability to promote biomineralization have the potential to be utilized in h
139 the known functions of amelogenin in enamel biomineralization, i.e., self-assembly, associations wit
140 tence of at least two distinct mechanisms of biomineralization: (i) one with Ca-carbonate inclusions
143 ere, we investigate the process of magnetite biomineralization in Desulfovibrio magneticus sp. RS-1,
150 simple solution-based process that resembles biomineralization in that organic molecules adsorbed on
152 nd demonstrates a central role for bacterial biomineralization in the formation of highly pure Au in
153 ur understanding of the proteins involved in biomineralization in the sea urchin, a powerful model sy
159 n of this matrix is based upon examples from biomineralization in which hydrogels are coupled with fu
160 te explores the fascinating world of otolith biomineralization in zebrafish; revealing the importance
161 rarchical levels of control found in natural biomineralization, including genetic, chemical, spatial,
162 bstrates suggest roles for the kinase beyond biomineralization, including lipid homeostasis, wound he
163 and several secreted proteins implicated in biomineralization, including the small integrin-binding
170 pposed to the complete loss of mamE where no biomineralization is observed, the protease-deficient va
174 nterplay between noncollagenous proteins and biomineralization is widely accepted, yet the contributi
175 for the formation of an inorganic material (biomineralization) is not only a fascinating biological
176 uggest that ectopic calcification, like bone biomineralization, is an actively regulated process.
177 lected for this study due to its key role in biomineralization, is expressed in many species and tiss
178 ves to control crystallization, as occurs in biomineralization, is rarely investigated due to the vas
179 re presumed to play a role in the process of biomineralization, key questions regarding the nature of
180 in all populations and occurred in genes for biomineralization, lipid metabolism, and ion homeostasis
182 c mutants further demonstrate increased iron biomineralization measured by a novel fluorescent geneti
183 Here, we show that bivalves modify the main biomineralization mechanism during the event to continue
189 ar mechanisms of mineral growth that control biomineralization, mineral scaling and industrial materi
193 porated onto template nanotube surfaces, the biomineralization of Ag ions on the nanotubes led the is
196 s Neurospora crassa was investigated for the biomineralization of calcium carbonate and its potential
200 rea and calcium-containing medium, extensive biomineralization of fungal filaments was observed.
202 ivorans bacterial cells served as nuclei for biomineralization of initially spherical vaterite precip
203 On Earth, magnetotactic bacteria perform biomineralization of intracellular magnetite nanoparticl
205 vesicles exist in the absence of magnetite, biomineralization of magnetite proceeds simultaneously i
206 sly showed that this mobilization was due to biomineralization of metallic Cu nanoparticles associate
211 oteins and processes required for the normal biomineralization of otoconia and otoliths in the inner
212 tion of their bivalved bauplan preceding the biomineralization of shell valves in crown brachiopods.
213 lled magnetosomes, which are tasked with the biomineralization of small crystals of the iron oxide ma
214 ame differentiation genes as are used in the biomineralization of the embryo skeleton are also used t
216 Our facile technique, which is analogous to biomineralization, offers a promising and generalized me
217 biological formation of inorganic materials (biomineralization) often occurs in specialized intracell
218 in biogeochemistry models, which often base biomineralization only on SI (caused by biotic or abioti
219 k more efficiently, via increased cell size, biomineralization or increased CN of eukaryotic phytopla
220 as now emerged as a highly regulated form of biomineralization organized by collagenous and elastin e
222 es, but has maintained its distinct skeletal biomineralization pattern for at least 40 My: Well-prese
223 for Otop1 in the initiation of extracellular biomineralization, possibly through the regulation of in
224 s in secondary Au formation, we assessed the biomineralization potential of biofilms growing in quart
225 eds simultaneously in multiple vesicles, and biomineralization proceeds from the same location in eac
226 ials have been synthesized using a fungal Mn biomineralization process based on urease-mediated Mn ca
228 deposits at the surface of the Earth using a biomineralization process that has been almost systemati
229 ormed by the evolutionarily highly conserved biomineralization process that is controlled by extracel
231 thesis of electrode materials using a fungal biomineralization process, thus providing a novel strate
236 iocorrosion have focused on the influence of biomineralization processes taking place on metallic sur
242 uch understanding of biomolecule controls on biomineralization promises new insights into the control
245 enamel development and is thought to be the biomineralization protein controlling the unique elongat
246 s study of a ten member polyanionic sequence biomineralization protein family, Asprich, and the exper
247 within the mineral-recognition domain of the biomineralization protein salivary statherin adsorbed on
248 at proteins) together with five known silica biomineralization proteins (four cingulins and one silaf
255 aining exon4 cause a specific enhancement of biomineralization related to stabilization of early-form
256 ndings suggest a molecular mechanism for how biomineralization-related enantiomers might exert hierar
257 anied by the de novo expression of terminal, biomineralization-related genes in the PMC GRN, as well
258 nts a unique extensive proteomic analysis of biomineralization-related proteins in corals from which
263 ern and fossil cells in order to investigate biomineralization response of ancient coccolithophores t
264 etically heterogeneous group of disorders of biomineralization resulting from failure of normal ename
267 to the devastating effects of inappropriate biomineralization seen in cardiac valvulopathies, calcip
268 s that carry out and regulate cynaobacterial biomineralization should put us in a position where we c
271 lead geomycology and organic phosphates as a biomineralization substrate, and are also relevant to me
272 and phosphate mineralization demonstrates a biomineralization system that provides a versatile route
273 ilaffins and silacidins), analogous to other biomineralization systems, which also depend on diverse
277 nd the ensuing assembly process, inspired by biomineralization templates capable of surface reconfigu
279 almost universally employed measure of coral biomineralization, the rate of linear extension, might n
282 This is the only description of the whole "biomineralization toolkit" of the matrices that, at leas
283 proteins in corals from which we identify a biomineralization "toolkit," an organic scaffold upon wh
284 rom this work have demonstrated that modular biomineralization units can be effective at processing c
285 of culture that is associated with decreased biomineralization, up-regulate expression of cyclin D3 a
287 ent soft collagenous tissue was co-opted for biomineralization using redundant genes resulting from w
290 of a previously unrecognized 'checkpoint' in biomineralization where MamE moderates the completion of
291 ality is ubiquitous in biology, including in biomineralization, where it is found in many hardened st
292 bonate are believed to be central species of biomineralization, which serves as an important inspirat
293 en at the mat surface promotes Fe(III)-oxide biomineralization, which was supported using molecular a
294 he effects of abrupt climate change on shell biomineralization, while also offering an alternative vi
296 to mimic protein-crystal interaction during biomineralization with the use of artificial proteins (d
297 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
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