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 op 2 increased actin affinity and processive run length.
2 ity of myosin V for actin and the processive run length.
3 charge on the neck coiled-coil decreases the run length.
4 in, plays an important role in governing the run length.
5 ng to KIF1A's characteristic superprocessive run length.
6 of mononucleotide runs increase change with run length.
7 onal positive charge to loop-12 enhanced the run length.
8 ivity depends nonmonotonically on the cell's run length.
9 tamylation reduced KIF1A pausing and overall run length.
10 median run length, and standard deviation of run length.
11 ommonly used to determine motor velocity and run length.
12 distances large compared with the swimmers' run length.
13 kinesin from the perspective of velocity and run length.
14 cluding stepping velocity and characteristic run length.
15 d slower than myoVa alone and with twice the run length.
16 t of Vamp2, a cargo of Kif1a, with decreased run length.
17 s motility, increasing both KHC velocity and run length.
18 ot all of which inhibit kinesin's processive run length.
19 diffusion may non-trivially influence motor run length.
20 rostatics, initial placement of solvent, and run lengths.
21 FPt, and mApple) cause aberrantly long motor run lengths.
22 track length has on observed characteristic run lengths.
23 Two of the 3 patients who died had very long run lengths (28.8 and 24.7 days, respectively), whereas
25 ted published force-dependent velocities and run lengths, along with mechanical interactions between
26 y to associate motors appears to enhance the run length and attachment time of the quantum dot, impro
27 as no direct correlation between homopolymer run length and frameshift accumulation in the wild-type
28 olecule motility in vitro but with decreased run length and slightly increased unloaded velocity comp
32 in-1, -2, -3, -5, and -7 motors and measured run length and velocity in a single-molecule fluorescenc
35 iation from the microtubule, we measured Eg5 run lengths and also compared the duration of the last s
36 As a result, these phagosomes have shorter run lengths and are not successful in reaching the lysos
38 activate cytoplasmic dynein, inducing longer run lengths and higher velocities than the previously ch
39 antly bundled, and bundling enhances kinesin run lengths and provides a greater number of available k
40 ment of APP vesicles, increasing anterograde run lengths and reducing retrograde runs and segmental v
43 merical simulations, the mean velocity, mean run length, and mean dwell time of the kinesin-1 motors
46 increase in the number of motile particles, run length, and stimulated anterograde moving ZBP1 parti
47 ntrolled optical trap to probe the velocity, run length, and unbinding kinetics of mouse KIF3A/B unde
49 mutant motors display decreased velocities, run lengths, and landing rates and delayed cargo transpo
50 trap assays but exhibited increased speeds, run lengths, and landing rates under unloaded conditions
51 sin Va by examining the velocity, processive run-length, and individual steps of a Qdot-labeled myosi
52 optimal spreading, which emerges when their run lengths are comparable to the longest straight path
53 s the limitations of the traditional average run length (ARL) in reflecting the differences in sampli
57 C loop L11 (KIF3ACDeltaL11) exhibited longer run lengths at approximately 1.55 mum than wild-type KIF
58 state, as well as the walking velocities and run lengths at various concentrations of ATP and ADP.
60 e structural features that affect processive run length by analyzing the properties of chimeras of mo
62 tive charge in loop-12 of KIF1A enhances the run length by stabilizing binding of the motor in its vu
64 in VI homodimerization and processivity with run lengths comparable with constitutive myosin VI dimer
66 -PBWT is an adaptation of techniques for the run-length compressed BWT for the PBWT (RLPBWT) and it i
67 A loop-12 into kinesin-1 did not enhance its run length, consistent with the two motor families using
69 suggest that multiple myosin velocities and run lengths depend on both the compliance and the effect
70 he specific factors that determine kinesin's run length (distance traveled per microtubule encounter)
72 lymers vastly outnumber G and C HPs, and the run-length distributions of A and T homopolymers differ
74 ient method for constructing and storing the run-length encoded PBWT, and computing set maximal match
76 of VCF with judicious entropy reduction and run-length encoding, delivering >10x size reduction for
77 ces might determine the average velocity and run-length even when they are outnumbered by wild type m
78 om a sharp decrease in microtubule minus-end run length followed by a gradual decrease in plus-end ru
79 ty, resulting in significant decrease in the run length for conventional kinesin-1 and kinesin-2.
80 rest for the following high-order gray-level run-length (GLRL) gray-level zone size matrix (GLZSM) an
81 s large compared with the swimmers' size and run length has been an experimental challenge, as standa
82 lity of slippage is strongly correlated with run length, however, it was not clear whether shorter ru
84 observer marginalizes over both the current run length (i.e., time since last change) and the curren
85 trate that Tau inhibits kinesin's processive run length in an isoform-dependent manner on GDP-microtu
87 s a potent inhibitor of kinesin's processive run length in vitro suggests that it may actively partic
91 entional wisdom, the measured characteristic run length is directly coupled to the characteristic tra
93 , V, randomness, r, stalling force, and mean run length, L, reveal a need for improved theoretical un
94 Particularly, well-designed incremental and run-length-limited encoding schemes are utilized to comp
96 hasis (SRE) and long run emphasis (LRE) from run length matrix (RLM); and HH wavelet coefficient ener
97 consistently repeatable, whereas gray-level run length matrix and gray-level zone length matrix feat
98 consistently repeatable, whereas gray-level run length matrix and gray-level zone length matrix feat
100 l co-occurrence matrix (GLCM) and gray-level run-length matrix (GLRLM) models, and iii) calculation o
101 matrix cluster shade (P < .001), gray-level run-length matrix low gray-level run emphasis (P = .049)
102 ay-level run emphasis (P = .049), gray-level run-length matrix run entropy (P = .003), gray-level siz
105 sed methods (minimum spanning tree and graph run-length matrix) to characterize spatial heterogeneity
106 , gray-level cooccurrence matrix, gray-level run-length matrix, gray-level size-zone matrix, and neig
107 (unharmonized), respectively, for gray-level run-length matrix; 87.6% and 85.6% (harmonized), respect
108 on of the MT results in decreased processive run lengths measured using single-molecule fluorescence
109 mous run length properties including average run length, median run length, and standard deviation of
112 been reported to be responsible for shorter run lengths observed for another heterotrimeric kinesin-
113 .78 +/- 0.11 microm/s and display an average run length of 1.17 +/- 0.38 microm, which agrees well wi
115 he plus end of microtubules, with an average run length of 2.6 +/- 0.2 mum, in a hand-over-hand fashi
116 ve analytic expressions for the velocity and run length of a general model of finitely processive hel
118 is linearly correlated with the velocity and run length of dynein, and we use this linearity to predi
119 e level how calcium regulates the processive run length of full-length myosin V (dFull) and a truncat
120 F3AA and KIF3CC are processive, although the run length of KIF3AC exceeds that of KIF3AA and KIF3CC.
123 onformational transition, and the processive run length of myosin V, and thus, it is important to und
124 als disease-induced deficits in the flux and run length of retrogradely transported endosomes in both
126 fect on motor activity, although the average run length of single kinesin molecules decreased by 30-5
128 ets as a function of sample size, processive run length of the motor, and distribution of track lengt
129 to account; 3) that the interaction time and run length of the motors can be estimated independent of
131 led-coil formation is highly processive with run lengths of approximately 1.23 mum and matching those
132 helix alpha7 is also highly processive with run lengths of approximately 1.62 mum and exceeding thos
133 ults in superprocessive motion, with average run lengths of approximately 10 mum, and that this prope
136 ns with kinesin-1 motors, the velocities and run lengths of peroxisomes driven by multiple myosinVa m
138 7A and produces a motor in which the average run length on actin at physiological concentrations of A
140 h ionic strength there was not a decrease in run length or any selective inhibition of the diffusiona
141 C-terminal region of tubulin increased motor run length (processivity) by inhibiting "detachment" but
142 As in studies of multiple kinesins, the run lengths produced by two myosins are only slightly la
143 symmetric distributions by using some famous run length properties including average run length, medi
144 100 000-fold with increasing homonucleotide run length, representing the greatest effect on replicat
145 nalytical expressions, we derive the optimal run length, revealing an intuitive dependence on environ
146 linker was replaced, kinesin-1 and kinesin-2 run lengths scaled identically with neck linker length,
147 he distinctive features of myosin VIIa (long run lengths, slow motility) will be very useful in video
148 esis at rates that increase as a function of run length, suggesting the involvement of misaligned int
149 -type KIF3AC and were more similar to KIF3AB run lengths, suggesting that L11 also contributes to tun
151 ve kinesin mutants that have fourfold longer run lengths than the wild-type motor, but that have norm
152 r complexes on actin bundles, which showed a run length that was even shorter than that of a single m
153 l observable quantities (the distribution of run length, the distribution of velocity [[Formula: see
155 neck-linker has been correlated with longer run lengths, the structural data to support this hypothe
156 ymmetry in the sensitivity of single-kinesin run length to load direction, raising the intriguing pos
158 Best Overlap Graph) is robust to homopolymer run length uncertainty, high read coverage and heterogen
160 o microtubules was decreased threefold, bead run length was decreased over fourfold, and there was a
161 of KLC1 did not inhibit phagosome speed, but run length was decreased, and phagosome localization and
162 y 27% as compared to a single motor, whereas run length was increased by only 37%, much less than exp
163 lpha,omega-diene monomer with a 36 methylene run length was synthesized and polymerized, and the unsa
165 tage and lead to an increase in the expected run-length when the load on the cargo is in the vicinity
166 f kinesin-1 resulted in a 6-fold decrease in run length, whereas adding additional positive charge to
167 adding free P(i)) nearly doubled the kinesin run length, whereas reducing either the ATP binding rate
168 orous media can be optimized by tuning their run lengths, which we rationalize using a coarse-grained
169 elevant quantities like average velocity and run-length without resorting to Monte Carlo simulations.