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1 ither by a chaperone such as EF1A or through macromolecular crowding.
2 cessivity are not upregulated or hindered by macromolecular crowding.
3 three environmental variables: pH, salt, and macromolecular crowding.
4 tes are nearly equally adversely affected by macromolecular crowding.
5 h osmolality, presumably as a consequence of macromolecular crowding.
6 trates and protect them from the problems of macromolecular crowding.
7  our understanding of the functional role of macromolecular crowding.
8 arious macromolecules, a phenomenon known as macromolecular crowding.
9 f the brain that have limited solvent due to macromolecular crowding.
10 ing both theory and experiment to studies of macromolecular crowding.
11 vesting efficiency of photosystem (PS) II on macromolecular crowding.
12 rnatively as the "depletion interaction" or "macromolecular crowding."
13         Herein, we assessed the influence of macromolecular crowding, a biophysical phenomenon that r
14                    However, it is known that macromolecular crowding, a key feature in natural cells,
15                                              Macromolecular crowding affects most chemical equilibria
16                         Theory predicts that macromolecular crowding affects protein behavior, but ex
17                        The results show that macromolecular crowding affects protein-folding dynamics
18  state of gp45 is, however, increased by the macromolecular crowding agent polyethylene glycol.
19 resence of 220 mg/mL dextran 70, a synthetic macromolecular crowding agent that occupies space but do
20 , we investigated the effects of a synthetic macromolecular crowding agent, dextran 20, on the folded
21 ClpB in the absence and presence of an inert macromolecular crowding agent.
22  presence of high concentrations of an inert macromolecular crowding agent.
23                                We introduced macromolecular crowding agents into reconstituted fusion
24  solutions containing high concentrations of macromolecular crowding agents would give new insights i
25 lding speed for apoazurin in the presence of macromolecular crowding agents, a result that points to
26 g reaction is carried out in the presence of macromolecular crowding agents, such as Ficoll and dextr
27 ein, apoflavodoxin, in the presence of inert macromolecular crowding agents, using in silico and in v
28 glycosaminoglycans or high concentrations of macromolecular crowding agents.
29 nscript length and was greatly stimulated by macromolecular crowding agents.
30 in machinery is sensitive to the presence of macromolecular crowding agents.
31 nd on the nanoscale organization assumed for macromolecular crowding agents.
32 es fundamental differences between small and macromolecular crowding agents.
33 n with FIH in the presence of cell lysate or macromolecular crowding agents.
34 unfolded-state compaction in the presence of macromolecular crowding along with its energetic and kin
35 tro results obtained on isolated mRNAs, both macromolecular crowding and a high ionic strength favor
36 lytes via specific transporters both reduces macromolecular crowding and ionic strength, thus leading
37       The encapsulation results suggest that macromolecular crowding and molecular confinement are ac
38 perimental system for testing the effects of macromolecular crowding and molecular confinement on pro
39                     Here, we discovered that macromolecular crowding and reducing agents increase ove
40 radict predictions from accepted theories of macromolecular crowding and show that cosolutes commonly
41 e of amyloidogenesis may be affected by both macromolecular crowding and spatial heterogeneity (e.g.
42 ents can critically influence the outcome of macromolecular crowding and that the structure of the am
43 ossibly enabling cellular cargos to overcome macromolecular crowding and to navigate obstacles along
44 y cooperative process, strongly dependent on macromolecular crowding, and involves back-to-back stack
45      Although the excluded-volume effects of macromolecular crowding are expected to cause compaction
46 mplicating the commonly overlooked aspect of macromolecular crowding as a possible factor in the etio
47 s on the available volume can be affected by macromolecular crowding, but the effects of crowding in
48 mimic intracellular compartmentalization and macromolecular crowding by partitioning RNA in an aqueou
49  scattering was used to study the effects of macromolecular crowding by two globular proteins, i.e.,
50                                              Macromolecular crowding can alter the structure and func
51 heir native intracellular environments where macromolecular crowding can drastically change reaction
52 te if combined application of ultrasound and macromolecular crowding can improve efficiency of MR.
53              Theoretical models predict that macromolecular crowding can increase protein folding sta
54                    Here, we demonstrate that macromolecular crowding can increase the robustness of g
55 can be inferred from their observations that macromolecular crowding can lead to robustness in gene e
56  ligands of different sizes (actin and ATP), macromolecular crowding can modulate the kinetics of ind
57 , ligand affinity, switching free energy and macromolecular crowding collectively control riboswitch
58                                              Macromolecular crowding conditions accelerate reactions
59            Here we have investigated whether macromolecular crowding conditions are able to promote h
60 ciency, we varied the salt concentration and macromolecular crowding conditions.
61  protein domain, intracellular viscosity and macromolecular crowding dictate its in vivo behavior.
62                                    Increased macromolecular crowding does not activate OpuA but acts
63 periment and computer simulation to show how macromolecular crowding dramatically affects the structu
64 s at different fixed temperatures showed the macromolecular crowding effect to be temperature-indepen
65 ation of polyvalent binding and the enhanced macromolecular crowding effect using nanoparticles.
66                                              Macromolecular crowding effects may be a tool for the ma
67                                  To quantify macromolecular crowding effects on protein folding mecha
68       Recent results support the notion that macromolecular 'crowding' enhances protein aggregation,
69 ing condition, the excluded volume effect of macromolecular crowding favors aggregation, whereas incr
70                          Most theories about macromolecular crowding focus on two ideas: the macromol
71  a qualitatively different dependence on the macromolecular crowding for high and low values of the r
72                               We studied how macromolecular crowding guides protein between different
73                                              Macromolecular crowding has a profound effect upon bioch
74                                              Macromolecular crowding has long been known to significa
75                 This study demonstrates that macromolecular crowding has structural effects on the fo
76 al implications, few experimental studies of macromolecular crowding have been reported.
77                                   Studies of macromolecular crowding have shown its important effects
78 mbles a fractal structure with its origin in macromolecular crowding in the cell membrane.
79 n important factor in limiting the degree of macromolecular crowding in the cell.
80 e roles of cytoplasmic osmolytes, water, and macromolecular crowding in the growth of osmotically str
81 n be regulated jointly by the local level of macromolecular crowding in the nucleus, together with th
82             We seek to elucidate the role of macromolecular crowding in transcription and translation
83                 Our results demonstrate that macromolecular crowding in two dimensions can play a sig
84  structures because milder water deficit and macromolecular crowding induce high alpha-helix levels i
85 hese findings have profound implications for macromolecular crowding inside cells.
86                                              Macromolecular crowding intensifies oxidative modificati
87                                              Macromolecular crowding is a critical parameter affectin
88                                              Macromolecular crowding is commonly understood in terms
89                                              Macromolecular crowding is expected to have a significan
90                                              Macromolecular crowding is known to profoundly influence
91                                              Macromolecular crowding is one of the key characteristic
92             This volume exclusion because of macromolecular crowding is predicted to affect both equi
93 ere, we present an unexpected discovery that macromolecular crowding is required for reconstituting t
94                              With increasing macromolecular crowding levels, the precision of particl
95                               To explore how macromolecular crowding may influence cellular protein f
96                  Our results demonstrate how macromolecular crowding may influence protein folding by
97 asound, biophysical properties of tissue and macromolecular crowding of insonated zone of tissue are
98 s generally assumed to be anomalous due high macromolecular crowding of the milieu.
99 the importance of approaching the effects of macromolecular crowding on a case-by-case basis.
100                          Thus, the effect of macromolecular crowding on activity and structure need t
101                  We addressed the effects of macromolecular crowding on alpha-synuclein by combining
102 mental question we investigate the effect of macromolecular crowding on cell metabolism.
103 s attention has been given to the effects of macromolecular crowding on cell physiology.
104  the present study we analyzed the effect of macromolecular crowding on fibrillation of four proteins
105                      To study the effects of macromolecular crowding on folding thermodynamics and ki
106               We have studied the effects of macromolecular crowding on protein folding kinetics by s
107                 We investigate the effect of macromolecular crowding on protein folding, using purely
108 esidue-level interrogation of the effects of macromolecular crowding on protein stability.
109 s for the effects of spatial confinement and macromolecular crowding on protein stability.
110                       However, the effect of macromolecular crowding on protein structure is poorly u
111 udy the effects of cellular architecture and macromolecular crowding on signal transduction in Escher
112                Here we analyze the effect of macromolecular crowding on structure and function of the
113           To investigate the consequences of macromolecular crowding on the behavior of a globular pr
114                                The effect of macromolecular crowding on the binding of ligands to a r
115 rom effects of preferential interactions and macromolecular crowding on the membrane or on ProP.
116                      The observed effects of macromolecular crowding on the myosin-ligand interaction
117                                The effect of macromolecular crowding on the rates of association reac
118 ive transition-state ensemble, the effect of macromolecular crowding on the relative stability betwee
119 l-angle scattering to measure the effects of macromolecular crowding on the size of a protein complex
120 he effect of intermolecular excluded volume (macromolecular crowding) on protein stability and confor
121                                              Macromolecular crowding opens new avenues for a more rat
122 pic, excluded-volume effect variously called macromolecular crowding or depletion attraction.
123                                              Macromolecular crowding ought to stabilize folded forms
124       Although it is still underappreciated, macromolecular crowding plays a critical role in life as
125                                Consequently, macromolecular crowding plays a major role in determinin
126                   In vitro studies show that macromolecular crowding, rather than changes in monolaye
127                        Our results show that macromolecular crowding reduces noise (as measured by th
128                                 Accordingly, macromolecular crowding should constitute an integral el
129 lisecond time resolution under conditions of macromolecular crowding similar to those within cells.
130        Our data reinforce the assertion that macromolecular crowding stabilizes the protein by destab
131 d HIV-1 CA-NC complexes is not due solely to macromolecular crowding, suggesting the presence of spec
132                                   Models for macromolecular crowding tend to focus on the steric effe
133 robes provides more detailed readouts on the macromolecular crowding than a single sensor.
134 o-collective hydration transition induced by macromolecular crowding that slows the hydration dynamic
135                 However, the contribution of macromolecular crowding to receptor retention remains po
136                              Here we examine macromolecular crowding using the replication system of
137    Specifically, we demonstrate that, during macromolecular crowding, viscosity dominates over the ex
138          At high osmolarity, the increase in macromolecular crowding which accompanies the reduction
139 an might be anticipated considering the high macromolecular crowding within the cell.

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