戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 d integration of phospholipid synthesis into artificial cells.
2 ems which are difficult to reconstitute into artificial cells.
3  mimetic chemistry serves the development of artificial cells.
4  autonomous memory transactions in DNA-based artificial cells.
5 nimal triggers of topological transitions in artificial cells.
6  tackle the bottom-up assembly of autonomous artificial cells.
7 could be tailored for memory transactions in artificial cells.
8 , at single vesicles further used to develop artificial cells.
9 y of types of cellular machinery in in vitro artificial cells.
10 of cell-mimetic biosensors, bioreactors, and artificial cells.
11 nced drug delivery vehicles, bioreactors and artificial cells.
12 ields ranging from targeted drug delivery to artificial cells.
13 s/oil/aqueous) to prototype mechanosensitive artificial cells.
14 processing with low-power consumption inside artificial cells.
15 ons of synthetic reaction systems, including artificial cells.
16 selection of restriction endonucleases using artificial cells.
17                                              Artificial cells (ACs) offer a powerful platform to repr
18 unaddressed in the bottom-up construction of artificial cells (ACs).
19                                The resulting artificial cells act as microreactors for enzymatic reac
20 d by oxidative stress, lipid scrambling, and artificial cell aging modulate the cell response to the
21 c biology, vesicles define the boundaries of artificial cells and are increasingly being used as bioc
22 used to develop novel bioreactors, primitive artificial cells and plausible pathways to prebiotic org
23 r opens up new routes for lipid synthesis in artificial cells and sheds light on the origin and evolu
24  could transform the development of lifelike artificial cells and unlock new ways to explore lipid fu
25 cluding drug delivery, membrane bioreactors, artificial cells, and biosensors.
26 ications, including biosensing, constructing artificial cells, and engineering biological batteries.
27 s, which hold great promise as components in artificial cells, and in synthetic biology more widely.
28 ssays useful for drug delivery, for building artificial cells, and in synthetic biology.
29 ibuted system of on-chip DNA compartments as artificial cells, and measured reaction-diffusion dynami
30 lated droplet interface bilayers (eDIBs), or artificial cells, and the bioluminescence tracked in rea
31 tial and temporal behavior of assemblies of "artificial cells," and allows us to design a rich variet
32 tic cells, ranging from simple protocells to artificial cells approaching the complexity of bacteria,
33                                              Artificial cells are biomimetic microstructures that mim
34                                              Artificial cells are biomimetic structures formed from m
35                                          The artificial cells are generated in the form of a water-in
36  and comprehensive analysis of droplet-based artificial cells are still rare.
37 o cell-like containments aiming to assemble "artificial cells" are addressed.
38 omes offers an exceptional platform to build artificial cells as exemplified by the in vitro transcri
39 ogram and operate increasingly sophisticated artificial cells as life-like materials.
40                                        Here, artificial cells (as opposed to bacterial cells themselv
41 ted from the numerical model, we designed an artificial cell based on an optimized selection of condu
42 , we have also discussed the construction of artificial cells based on biomimetic materials, from sim
43 ne-based materials with applications such as artificial cells, biosensors, and therapeutic nanopartic
44  a step forward in the bottom-up creation of artificial cells, building analogous intracellular archi
45 y activated and deactivated in the levitated artificial cell by the application of acoustic and magne
46                   It seems natural to ask if artificial cells can be built to use ion transport as ef
47 these systems in synthetic membranes to form artificial cells can reintroduce features of the cellula
48                    However, it is clear that artificial cells cannot currently match the power and be
49 uggests a potential route to the assembly of artificial cells capable of evolution.
50                              The assembly of artificial cells capable of executing synthetic DNA prog
51 -scale-integration of genetically programmed artificial cells capable of exhibiting collective expres
52                          Building autonomous artificial cells capable of homeostasis requires regulat
53 al DNA compartments fabricated in silicon as artificial cells capable of metabolism, programmable pro
54 Bottom-up synthetic biology aims to engineer artificial cells capable of responsive behaviors by usin
55 er through cannabinoid CB(1) receptors in an artificial cell-cell communication assay that was develo
56 in eukaryotes, we developed and analyzed two artificial cell-cell communication systems in yeast.
57 ht become useful components for constructing artificial cell-cell communication systems that program
58  uses a common metabolite to achieve tunable artificial cell-cell communication.
59 el systems are becoming increasingly used as artificial cell chassis and as biomimetic constructs for
60 the development of small-scale, bio-inspired artificial cell components that recreate the function of
61 otein (red dots, see scheme) is expressed in artificial cells composed of biocompatible polymersomes,
62  the fabrication of microfluidic devices for artificial cell construction in bottom-up synthetic biol
63 ed on the efforts of bottom-up strategies in artificial cell construction.
64  non-equilibrium processes in communities of artificial cells could provide a step to life-like syste
65 -level QC workflow enables identification of artificial cells created not only by staining or imaging
66 microfluidic device to mechanically activate artificial cells creates new opportunities in force-acti
67 orts to create advanced cell mimics, namely, artificial cells, demands strategies for constructing si
68 the critical bottlenecks in the synthesis of artificial cell, depends on the properties of phospholip
69 tions for nanobiotechnology applications and artificial cell design.
70                                              Artificial cells designed for specific applications comb
71                                              Artificial cell development ultimately aims to produce m
72 hydrogels can be leveraged in the context of artificial cell development.
73                                          The artificial cells expand the senses of Escherichia coli b
74  storage or detoxification) organelles or as artificial cell factories for in situ biocatalysis.
75                          The construction of artificial cells from inanimate molecular building block
76               The attractions of engineering artificial cells from scratch, as opposed to re-engineer
77 uce a platform for constructing membraneless artificial cells from the self-assembly of synthetic DNA
78  that it may be possible to construct simple artificial cells from two subsystems: a self-replicating
79 en substantial efforts aimed at constructing artificial cells from various molecular components with
80 occurs in polyploid hepatocytes generated by artificial cell fusion.
81 ology and bionic technology, the research of artificial cells has gradually become a subclass.
82 scale biological inspiration in the field of artificial cells has great potential for successes in th
83                           The development of artificial cells has led to fundamental insights into th
84 uli-responsive elements compartmentalized in artificial cells has potential applications in therapeut
85 zing decision-making with a few molecules in artificial cells has remained a challenge.
86                                              Artificial cells have generated much interest since the
87 d cell models to decipher the rules of life, artificial cells have the potential to be designed as mi
88 ral living matter and work toward rebuilding artificial cells in vitro.
89 t, we apply this platform to build DNA-based artificial cells in which a prototypical nucleus synthes
90   Parallel efforts to construct more complex artificial cells, incorporating translational machinery
91 compartments, abiogenesis, and the design of artificial cell-inspired systems are considered.
92 sion system with a 30 x 30 square lattice of artificial cells interconnected by thin capillaries for
93 sults highlight a new strategy for designing artificial cell interfaces that can nondestructively pen
94 n polymerizes in the vesicles and alters the artificial cells' internal structure by creating interna
95            The problem of a self-replicating artificial cell is a long-lasting goal that might imply
96                A common method of generating artificial cells is to encapsulate protein expression sy
97                                              Artificial cell-like communities participate in diverse
98  paving the way towards rudimentary forms of artificial cell-like entities (protocells).
99 ms of collective behaviour in communities of artificial cell-like entities (synthetic protocells).
100 ad to new types of chemical bio-reactors and artificial cell-like entities, and bring new insights co
101                      Coacervation creates an artificial cell-like environment in which the rate of mR
102 s atomic scale observation, we have built an artificial cell-like environment with nano-scale enginee
103 porters enable control over catalysis inside artificial cell-like systems, which could form the basis
104  has been restricted in higher eukaryotes to artificial cell lines and reporter genes.
105 R signaling is traditionally investigated in artificial cell lines which do not provide sufficient ph
106 ollowing transplantation in vivo arises from artificial cell manipulations ex vivo.
107 trast, the growth of tumor cells grown on an artificial cell matrix (Matrigel) was unaffected by deco
108 lar and extracellular environments across an artificial cell membrane construct.
109 he detection of gadolinium spin labels in an artificial cell membrane under ambient conditions using
110 ated into supported lipid bilayers (SLBs, an artificial cell membrane), which in turn were interfaced
111 ements of the interactions between SERMs and artificial cell membranes and independent observations o
112 cles through the integration of bio-inspired artificial cell membranes and naturally derived cell mem
113       Upon light or temperature stimulation, artificial cell membranes are activated, releasing signa
114 network that generates and maintains dynamic artificial cell membranes.
115 the bottom-up construction of hydrogel-based artificial cell microsystems which replicate fundamental
116 art materials, autonomous micromachinery and artificial cell-mimics.
117 e observations were collected in vitro using artificial cell models transfected with cloned receptors
118 ug delivery of proteins, and the creation of artificial cell networks.
119  drug/gene/protein delivery, biosensors, and artificial cells often requires the combination of lipid
120 with a 2D layout of 1024 DNA compartments as artificial cells on a 5 x 5 mm(2) area.
121 hetic lipid membranes as key constituents of artificial cells or to develop new tools for remodeling
122 rmacologic agents, recombinant proteins, and artificial cell-permeable proteins have been developed t
123 nd provide a step towards the development of artificial cell platforms capable of multiple operations
124 d sensors and establishes the feasibility of artificial cell platforms to detect environmentally rele
125 escribes the state and the development of an artificial cell project.
126                                   Typically, artificial cells rely on a bilayer membrane chassis and
127                 The bottom-up engineering of artificial cells requires a reconfigurable cytoskeleton
128  way for solid-liquid interaction studies in artificial cell research.
129 volves a mechano-transduction axis including artificial cell rigidity, pseudopodia, and macrophage in
130 tworks is a crucial step towards engineering artificial cell-scale devices and systems.
131                                  We describe artificial cells, selected current applications and how
132 gohistidine affinity tags, we synthesized an artificial cell surface receptor comprising an N-alkyl d
133 ng membrane transport mechanisms relevant to artificial cell systems and drug screening.
134 ein and protein-nucleic acid interactions in artificial cell systems comprising water-in-oil emulsion
135    Whereas initial studies were performed in artificial cell systems, recent publications are shiftin
136 on/translation for applications of DIB-based artificial cell systems.
137 mploying receptor/arrestin overexpression in artificial cell systems.
138  broader engineering biology applications in artificial cell technologies.
139 sible to design and construct communities of artificial cells that can perform different tasks relate
140       We suggest methods for producing these artificial cells that could potentially be used to power
141                         As such, engineering artificial cells that possess this behavior has been at
142 tic polymers to construct advanced biohybrid artificial cells that provide insights into phase segreg
143 and remaining challenges in the synthesis of artificial cells, the possibility of creating new forms
144                 Engineering mechanosensitive artificial cell through bottom-up in vitro reconstitutio
145  as a response of our mechanically activated artificial cell through thinning of oil.
146 sins can be used for genetically programming artificial cells to display interacting peptide pairs, e
147 e incorporated within the next generation of artificial cells to engineer improved biological mimics
148 : is it possible to interface biological and artificial cells together to create hybrid living/synthe
149                     We propose CITE-sort, an artificial-cell-type aware surface marker clustering met
150 tly and reliably separates multiplet-induced artificial-cell-type droplet clusters from real BCT drop
151 tely, multiplets in CITE-seq datasets create artificial cell types (ACT) and complicate the automatio
152                            Multiplets create artificial cell types in the dataset.
153 eer complex emulsion-based, multicompartment artificial cells, using microfluidics and acoustic levit
154  In order to demonstrate mechanosensation in artificial cells, we develop a novel microfluidic device
155                                              Artificial cells were synthesized using biocatalytic ato
156  and functional scaffolds inside natural and artificial cells, where RNA produced by gene networks co
157                  Efforts to create life-like artificial cells will likely involve mimicking the struc
158 mble biocompatible cell-sized hydrogel-based artificial cells with a variety of different embedded fu
159 ttom-up synthetic biology seeks to construct artificial cells with biomimetic or novel functionalitie
160 systems is a critical step towards preparing artificial cells with collective behaviour.
161 ecision-making by a bistable gene network in artificial cells with constant protein turnover.
162 ng the spontaneous bottom-up construction of artificial cells with high organizational complexity and
163                            By incubating the artificial cells with macrophages, we investigate the me
164  study actin-based positioning mechanisms in artificial cells with persistently contracting actomyosi
165 port enzymatically synthesized polymer-based artificial cells with the ability to express proteins.
166              The bottom-up development of an artificial cell would provide a minimal system with whic

 
Page Top