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1 rientation increasing with the length of the cytoskeletal filament.
2  of taking several consecutive steps along a cytoskeletal filament.
3 n of the halting of motility of microns-long cytoskeletal filaments.
4  destinations by stepping along a network of cytoskeletal filaments.
5 cal systems, exemplified by the formation of cytoskeletal filaments.
6 etween motor forces and the mechanics of the cytoskeletal filaments.
7 a three-dimensional network of F-actin proto-cytoskeletal filaments.
8  with large, collective displacements of the cytoskeletal filaments.
9  protein that is involved in a condensate on cytoskeletal filaments.
10     Tropomyosin binds to actin in muscle and cytoskeletal filaments.
11 go pulled by molecular motors stepping along cytoskeletal filaments.
12 overed class of bacterial proteins that form cytoskeletal filaments.
13 f root hairs, including the rearrangement of cytoskeletal filaments.
14 s that ballistically move along a network of cytoskeletal filaments.
15 sis to generate force and haul cargoes along cytoskeletal filaments.
16 ructural complexes, regulatory proteins, and cytoskeletal filaments.
17 es and co-assemble into hetero-oligomers and cytoskeletal filaments.
18 e force (PMF) and depends on actin-like MreB cytoskeletal filaments.
19 ins that form effective interactions between cytoskeletal filaments.
20 an be segregated by three different types of cytoskeletal filaments.
21 within the cytosol to active transport along cytoskeletal filaments.
22 ize their contents through trafficking along cytoskeletal filaments.
23 oteins that interact with all three types of cytoskeletal filaments.
24 y organize stable regions of overlap between cytoskeletal filaments.
25 P-hydrolyzing motor proteins that move along cytoskeletal filaments.
26 ociated protein 2 (MAP2) and the collapse of cytoskeletal filaments.
27 of the cell membrane flanked by a network of cytoskeletal filaments.
28 containing soluble proteins and a network of cytoskeletal filaments.
29 onal changes to produce force and move along cytoskeletal filaments.
30 es at improper cell surfaces and disoriented cytoskeletal filaments.
31 ranging from metabolism to the nucleation of cytoskeletal filaments.
32 tions that are associated with the action of cytoskeletal filaments.
33 localize in the cytoplasm, and interact with cytoskeletal filaments.
34 es within growth cones that colocalized with cytoskeletal filaments.
35 y forming an extensive intermeshed system of cytoskeletal filaments analogous to that formed by actin
36 y forming an extensive intermeshed system of cytoskeletal filaments analogous to that formed by actin
37 tracellular signals that are channeled along cytoskeletal filaments and activate the non-receptor tyr
38 negative role by sequestering CBFalpha2 into cytoskeletal filaments and aggregates, thereby disruptin
39 we simulate tens to hundreds of thousands of cytoskeletal filaments and crosslinking motors, recapitu
40 ble was found to be binding of the asters to cytoskeletal filaments and directed transport toward the
41 ough collective interactions among different cytoskeletal filaments and extracellular adhesions in li
42  anti-vinculin and phalloidin revealed clear cytoskeletal filaments and focal adhesions for cells att
43 ed mechanism necessary for rapid assembly of cytoskeletal filaments and for morphological polarity du
44                                              Cytoskeletal filaments and molecular motors facilitate t
45                                   Bundles of cytoskeletal filaments and molecular motors generate mot
46      Biomolecular transport systems based on cytoskeletal filaments and motor proteins have become pr
47                       It remains unclear how cytoskeletal filaments and motor proteins organize into
48 teins, respectively, connects the nucleus to cytoskeletal filaments and performs diverse functions in
49 are strongly influenced by interactions with cytoskeletal filaments and their associated motor protei
50 myosin molecular motors, which bind to actin cytoskeletal filaments and use chemical energy to exert
51     Molecular connections between integrins, cytoskeletal filaments, and nuclear scaffolds may theref
52 ial force directions, thus stabilizing those cytoskeletal filament architectures that result in shear
53 he ligand chemistry and interaction with the cytoskeletal filament are key to understanding the mecha
54 re may represent the case in which different cytoskeletal filaments are cross-linked whereas the loop
55                                              Cytoskeletal filaments are often capped at one end, regu
56 ections from chromatin to nuclear lamina and cytoskeletal filaments as a single mechanical unit.
57           Molecular motors translocate along cytoskeletal filaments, as in the case of kinesin motors
58                                              Cytoskeletal filaments assemble into dense parallel, ant
59 Modulated polarization microscopy visualizes cytoskeletal filaments based on their birefringence but
60 netosome chain, and an anomalous build-up of cytoskeletal filaments between magnetosomes.
61                                 In bacteria, cytoskeletal filament bundles such as MreB control the c
62  and filament bending of a membrane-attached cytoskeletal filament can be sufficient to prescribe ori
63 econdary antibodies, the 'extensions' on the cytoskeletal filaments can achieve considerable lengths
64   Active changes in the curvature of elastic cytoskeletal filaments can lead to filament perversions
65 engths (longer than several diameters of the cytoskeletal filament carrier), thus geometrically impai
66 insight into the positions and structures of cytoskeletal filaments, cell wall elements, motility mac
67         The architecture and connectivity of cytoskeletal filaments change in response to mechanical
68                     Microtubules are dynamic cytoskeletal filaments composed of aB-tubulin heterodime
69 ethods for bacteria have shown that distinct cytoskeletal filaments composed of actin and tubulin hom
70 ent study was carried out to examine whether cytoskeletal filaments contribute to this response.
71 ree-dimensional spheroid model, we show that cytoskeletal filaments do not actively support compressi
72            Contractile rings are formed from cytoskeletal filaments during cell division.
73 anization and functions of each of the three cytoskeletal filaments during the key events that shape
74 ssembly of macromolecular assemblies such as cytoskeletal filaments (e.g., microtubules and actin) or
75                                              Cytoskeletal filaments form diverse superstructures that
76                                  Septins are cytoskeletal filament-forming proteins that typically as
77            Far from being homogeneous beams, cytoskeletal filaments have complex mechanical propertie
78 omologous to all three classes of eukaryotic cytoskeletal filaments have recently been discovered.
79 lf-propelled biological molecular motors and cytoskeletal filaments hold significant promise in these
80 ns are small beta-helical proteins that form cytoskeletal filaments in a range of bacteria.
81  developed to study the self-organization of cytoskeletal filaments in in vitro systems of purified c
82                    In an effort to visualize cytoskeletal filaments in living cells, we have develope
83 nterplay of cell wall growth, mechanics, and cytoskeletal filaments in shaping the bacterial cell.
84  mechanisms that dictate the localization of cytoskeletal filaments is crucial for elucidating cell s
85 otein machines whose directed movement along cytoskeletal filaments is driven by ATP hydrolysis.
86 omechanical network based on the microtubule cytoskeletal filament - itself a non-equilibrium chemica
87 a significant departure from prior models of cytoskeletal filament length control and presents a diff
88 ghts into the physical principles underlying cytoskeletal filament localization and suggest design pr
89  review, we summarize decades of research on cytoskeletal filament mechanics, highlighting their most
90             The neuronal axon is packed with cytoskeletal filaments, membranes, and organelles, many
91 e cell mechanics, trafficking, and motility, cytoskeletal filaments must assemble into higher-order n
92 tional proteins that stabilize and crosslink cytoskeletal filament networks.
93 ins, growth factor receptors, myosin motors, cytoskeletal filaments, nuclei, extracellular matrix, an
94  the Akt/Src signaling pathway and deranging cytoskeletal filaments of endothelial cells.
95 cts that depends on the local density of the cytoskeletal filaments on which motors operate.
96 res subjected to directed transport, such as cytoskeletal filaments or elongated organelles transport
97 case of a single type of molecular motor and cytoskeletal filaments oriented in one dimension in oppo
98                                              Cytoskeletal filaments propelled by surface-bound motor
99                          The distribution of cytoskeletal filaments puts constraints on the likely pr
100 tructural proteins localize to the cVAC, and cytoskeletal filaments radiate from a microtubule organi
101 ipulating bound microbeads or micropipettes, cytoskeletal filaments reoriented, nuclei distorted, and
102                             Microtubules are cytoskeletal filaments responsible for cell morphology a
103 re imposed on their movements, the propelled cytoskeletal filaments show dynamic patterns distinct fr
104     Thus, our multiscale modeling correlates cytoskeletal filament size with conformational changes i
105 ns, especially the orientation and length of cytoskeletal filaments such as FtsZ and MreB in rod-shap
106 alized in granules that were associated with cytoskeletal filament systems and distributed throughout
107 n the cytoskeleton and it involves all three cytoskeletal filament systems as well as nuclear scaffol
108 (suspended) cells, indicating that these two cytoskeletal filament systems can cooperate to promote c
109 organization requires the interaction of the cytoskeletal filament systems.
110  assembly of the stromal Z ring, composed of cytoskeletal Filamenting temperature-sensitive Z (FtsZ)
111                                          The cytoskeletal Filamenting temperature-sensitive Z (FtsZ)
112                             Microtubules are cytoskeletal filaments that are dynamically assembled fr
113   Non-centrosomal microtubules are essential cytoskeletal filaments that are important for neurite fo
114 ell motility is driven by rapidly elongating cytoskeletal filaments that are persistently tethered at
115                                  Septins are cytoskeletal filaments that assemble at the inner face o
116           Neurofilaments (NFs) are important cytoskeletal filaments that consist of long flexible C-t
117    Bactofilins are rigid, nonpolar bacterial cytoskeletal filaments that link cellular processes to s
118 portant role in PRRSV binding with the other cytoskeletal filaments that mediate transportation of th
119  encodes a tubulin homolog (TubZ) that forms cytoskeletal filaments that move rapidly with treadmill
120 cells assemble diverse proteins into dynamic cytoskeletal filaments that perform essential cellular f
121                             Microtubules are cytoskeletal filaments that provide structural support f
122                   AlfA-GFP assembles dynamic cytoskeletal filaments that rapidly turn over (t(1/2)< a
123                     Microtubules are dynamic cytoskeletal filaments that undergo stochastic switching
124          Bacteria use homologs of eukaryotic cytoskeletal filaments to conduct many different tasks,
125 anophores regulate melanosome trafficking on cytoskeletal filaments to generate a range of spatiotemp
126 t to quantify the mechanical behavior of the cytoskeletal filaments to get a better insight into cell
127 n the family of proteins that could organize cytoskeletal filaments to include any filamentous-actin-
128      Thus, it seems that prokaryotes can use cytoskeletal filaments to position organelles within the
129 e shape mutants restores the ability of MreB cytoskeletal filaments to properly orient the synthesis
130 wide variety of subcellular structures, from cytoskeletal filaments to three-dimensional organelles.
131 in cellular electric potential can stimulate cytoskeletal filaments to transmit ionic currents along
132 operty that distinguishes IFs from the other cytoskeletal filament types, actin filaments and microtu
133 crease the likelihood of unraveling of large cytoskeletal filaments under physiological forces, molec
134  cell nucleus can be moved or reorganized by cytoskeletal filaments under various conditions (for exa
135 a macropinocytosis to impede the dynamics of cytoskeletal filaments via promiscuous interactions with
136                                          The cytoskeletal filament vimentin is inherent to the endoth
137  components of the 7G10 MAb-bound complex as cytoskeletal filaments: vimentin, cytokeratin 8, cytoker
138 eins kinesin and myosin and their associated cytoskeletal filaments, we review recent work aiming for
139 organelles to a newly recognized prokaryotic cytoskeletal filament which organizes magnetosomes into
140 a surface with immobilized motors propelling cytoskeletal filaments, which are decorated with antibod
141      Septin hetero-oligomers polymerize into cytoskeletal filaments with essential functions in many
142 ament curvature can alter the interaction of cytoskeletal filaments with regulatory proteins, suggest
143 analytes by integrating microtubules, one of cytoskeletal filaments, with nanofluidic technologies.
144   Microtubules are the least flexible of the cytoskeletal filaments, yet they are occasionally seen t

 
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