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1 rientation increasing with the length of the cytoskeletal filament.
2 s that ballistically move along a network of cytoskeletal filaments.
3 sis to generate force and haul cargoes along cytoskeletal filaments.
4 ructural complexes, regulatory proteins, and cytoskeletal filaments.
5 e force (PMF) and depends on actin-like MreB cytoskeletal filaments.
6 overed class of bacterial proteins that form cytoskeletal filaments.
7 ins that form effective interactions between cytoskeletal filaments.
8 an be segregated by three different types of cytoskeletal filaments.
9 within the cytosol to active transport along cytoskeletal filaments.
10 ize their contents through trafficking along cytoskeletal filaments.
11 oteins that interact with all three types of cytoskeletal filaments.
12 y organize stable regions of overlap between cytoskeletal filaments.
13 P-hydrolyzing motor proteins that move along cytoskeletal filaments.
14 ociated protein 2 (MAP2) and the collapse of cytoskeletal filaments.
15 of the cell membrane flanked by a network of cytoskeletal filaments.
16 containing soluble proteins and a network of cytoskeletal filaments.
17 onal changes to produce force and move along cytoskeletal filaments.
18 es at improper cell surfaces and disoriented cytoskeletal filaments.
19 tions that are associated with the action of cytoskeletal filaments.
20 localize in the cytoplasm, and interact with cytoskeletal filaments.
21 es within growth cones that colocalized with cytoskeletal filaments.
22 y forming an extensive intermeshed system of cytoskeletal filaments analogous to that formed by actin
23 y forming an extensive intermeshed system of cytoskeletal filaments analogous to that formed by actin
24 tracellular signals that are channeled along cytoskeletal filaments and activate the non-receptor tyr
25 negative role by sequestering CBFalpha2 into cytoskeletal filaments and aggregates, thereby disruptin
26 ble was found to be binding of the asters to cytoskeletal filaments and directed transport toward the
27 ough collective interactions among different cytoskeletal filaments and extracellular adhesions in li
28  anti-vinculin and phalloidin revealed clear cytoskeletal filaments and focal adhesions for cells att
29 ed mechanism necessary for rapid assembly of cytoskeletal filaments and for morphological polarity du
30                                              Cytoskeletal filaments and molecular motors facilitate t
31      Biomolecular transport systems based on cytoskeletal filaments and motor proteins have become pr
32                       It remains unclear how cytoskeletal filaments and motor proteins organize into
33 teins, respectively, connects the nucleus to cytoskeletal filaments and performs diverse functions in
34 are strongly influenced by interactions with cytoskeletal filaments and their associated motor protei
35 myosin molecular motors, which bind to actin cytoskeletal filaments and use chemical energy to exert
36     Molecular connections between integrins, cytoskeletal filaments, and nuclear scaffolds may theref
37 he ligand chemistry and interaction with the cytoskeletal filament are key to understanding the mecha
38 re may represent the case in which different cytoskeletal filaments are cross-linked whereas the loop
39                                              Cytoskeletal filaments are often capped at one end, regu
40           Molecular motors translocate along cytoskeletal filaments, as in the case of kinesin motors
41 Modulated polarization microscopy visualizes cytoskeletal filaments based on their birefringence but
42 netosome chain, and an anomalous build-up of cytoskeletal filaments between magnetosomes.
43                                 In bacteria, cytoskeletal filament bundles such as MreB control the c
44  and filament bending of a membrane-attached cytoskeletal filament can be sufficient to prescribe ori
45 insight into the positions and structures of cytoskeletal filaments, cell wall elements, motility mac
46 ethods for bacteria have shown that distinct cytoskeletal filaments composed of actin and tubulin hom
47 ent study was carried out to examine whether cytoskeletal filaments contribute to this response.
48 ree-dimensional spheroid model, we show that cytoskeletal filaments do not actively support compressi
49 ssembly of macromolecular assemblies such as cytoskeletal filaments (e.g., microtubules and actin) or
50                                              Cytoskeletal filaments form diverse superstructures that
51 omologous to all three classes of eukaryotic cytoskeletal filaments have recently been discovered.
52 lf-propelled biological molecular motors and cytoskeletal filaments hold significant promise in these
53  developed to study the self-organization of cytoskeletal filaments in in vitro systems of purified c
54                    In an effort to visualize cytoskeletal filaments in living cells, we have develope
55 nterplay of cell wall growth, mechanics, and cytoskeletal filaments in shaping the bacterial cell.
56 otein machines whose directed movement along cytoskeletal filaments is driven by ATP hydrolysis.
57 omechanical network based on the microtubule cytoskeletal filament - itself a non-equilibrium chemica
58 tional proteins that stabilize and crosslink cytoskeletal filament networks.
59 ins, growth factor receptors, myosin motors, cytoskeletal filaments, nuclei, extracellular matrix, an
60                          The distribution of cytoskeletal filaments puts constraints on the likely pr
61 tructural proteins localize to the cVAC, and cytoskeletal filaments radiate from a microtubule organi
62 ipulating bound microbeads or micropipettes, cytoskeletal filaments reoriented, nuclei distorted, and
63                             Microtubules are cytoskeletal filaments responsible for cell morphology a
64 ns, especially the orientation and length of cytoskeletal filaments such as FtsZ and MreB in rod-shap
65 alized in granules that were associated with cytoskeletal filament systems and distributed throughout
66 n the cytoskeleton and it involves all three cytoskeletal filament systems as well as nuclear scaffol
67 (suspended) cells, indicating that these two cytoskeletal filament systems can cooperate to promote c
68 organization requires the interaction of the cytoskeletal filament systems.
69                                          The cytoskeletal Filamenting temperature-sensitive Z (FtsZ)
70                             Microtubules are cytoskeletal filaments that are dynamically assembled fr
71 ell motility is driven by rapidly elongating cytoskeletal filaments that are persistently tethered at
72           Neurofilaments (NFs) are important cytoskeletal filaments that consist of long flexible C-t
73 portant role in PRRSV binding with the other cytoskeletal filaments that mediate transportation of th
74  encodes a tubulin homolog (TubZ) that forms cytoskeletal filaments that move rapidly with treadmill
75 cells assemble diverse proteins into dynamic cytoskeletal filaments that perform essential cellular f
76                   AlfA-GFP assembles dynamic cytoskeletal filaments that rapidly turn over (t(1/2)< a
77          Bacteria use homologs of eukaryotic cytoskeletal filaments to conduct many different tasks,
78 anophores regulate melanosome trafficking on cytoskeletal filaments to generate a range of spatiotemp
79 t to quantify the mechanical behavior of the cytoskeletal filaments to get a better insight into cell
80      Thus, it seems that prokaryotes can use cytoskeletal filaments to position organelles within the
81 operty that distinguishes IFs from the other cytoskeletal filament types, actin filaments and microtu
82 crease the likelihood of unraveling of large cytoskeletal filaments under physiological forces, molec
83 a macropinocytosis to impede the dynamics of cytoskeletal filaments via promiscuous interactions with
84                                          The cytoskeletal filament vimentin is inherent to the endoth
85  components of the 7G10 MAb-bound complex as cytoskeletal filaments: vimentin, cytokeratin 8, cytoker
86 organelles to a newly recognized prokaryotic cytoskeletal filament which organizes magnetosomes into
87      Septin hetero-oligomers polymerize into cytoskeletal filaments with essential functions in many
88 ament curvature can alter the interaction of cytoskeletal filaments with regulatory proteins, suggest
89 analytes by integrating microtubules, one of cytoskeletal filaments, with nanofluidic technologies.
90   Microtubules are the least flexible of the cytoskeletal filaments, yet they are occasionally seen t

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