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1 ents, spontaneous kicking and weight-bearing stepping.
2 e motor head binds to the microtubule during stepping.
3 fundamentally from that of plus-end-directed stepping.
4 minus end-directed to net plus end-directed stepping.
5 from minus end-directed to plus end-directed stepping.
6 eps to detachments without affecting forward stepping.
7 numerical modeling of myosin V diffusion and stepping.
8 xplain the accelerated triggering of induced stepping.
9 al ladder, a complex task requiring accurate stepping.
10 their involvement in control of accuracy of stepping.
11 I4 depolarization never elicited stepping.
12 es of inability to produce effective forward stepping.
13 y, processivity, and probability of backward stepping.
14 across different cycle durations of neonate stepping.
15 lly limited by the need for mechanical phase stepping.
16 slow step for KIF3C resulting in asymmetric stepping.
17 ilateral limb pairs move out-of-phase during stepping.
18 es locomotor speed and ultimately terminates stepping.
19 y modulation recorded in this nucleus during stepping.
20 he STN is involved in the dynamic control of stepping.
21 onformation of dynein optimal for processive stepping.
22 e the effectiveness of random, uncoordinated stepping: (1) the formation of three-headed and four-hea
23 spends 65% of its time undergoing processive stepping, 4% undergoing 1D diffusion, and the remaining
25 echanism and coordination of KIF3A and KIF3B stepping, a presteady-state kinetic analysis was pursued
26 s showed significant improvement in hindlimb stepping ability, quadrupedal weight support, and all me
29 r neighbors inhibit their minus end-directed stepping action, but not their plus end-directed steppin
33 ental data from GFP-labeled kinesin-1 motors stepping along immobilized microtubules, we show 1) that
34 kinesin-1 and kinesin-2 neck-linker chimeras stepping along microtubules in the absence or presence o
36 e the ability to switch protofilaments while stepping along the microtubule when challenged by an obs
37 ve functions are linked to delayed voluntary stepping, alterations in the coupling of posture and loc
38 ull-length GiKIN14a has significantly higher stepping and ATP hydrolysis rates than does GiKIN14a-Del
39 rface, a task that does not require accurate stepping and can be accomplished without the motor corte
40 o show that Lis1 does not directly alter the stepping and force production of individual dynein motor
41 errors in the parametric control of induced stepping and its effectiveness in stabilizing balance wo
44 he rhythmic output required for coordinating stepping and stabilizing the body axis during movements.
45 he rhythmic output required for coordinating stepping and stabilizing the body axis during movements.
46 remarkably consistent alignment between the stepping and stimulation cycle when the stimulation spee
47 e gating mechanism, the pathway for backward stepping, and the energy consumption as a function of AT
52 ed out using a model that incorporated motor stepping, attachment/detachment rates, and intermotor fo
53 , chemical and torsional barriers, sometimes stepping back and cleaving off nucleotides from the grow
54 Pase rate, microtubule-binding affinity, and stepping behavior of dynein, and that microtubule bindin
55 -molecule microscopy to directly observe the stepping behavior of kinesin-1 and -2 family motors with
56 e consistent with a model wherein the normal stepping behavior of the myosin is supplemented by the p
58 the model still shows processive directional stepping, but it becomes uncoordinated and the stepping
60 at ATP hydrolysis in the bound head precedes stepping by the tethered head, leading to a mechanochemi
62 lts, we propose a quantitative model for the stepping characteristics of dynein and its response to c
65 elongation rate intrinsic to the ribosome's stepping cycle and the actual elongation rate that takes
66 dates an essential role for AAA4 in dynein's stepping cycle and underscores the complexity and crosst
67 ics of structural transitions underlying the stepping cycle of kinesin-1 at physiological ATP, we use
68 rimental grounds, the repercussions of their stepping cycle on the collective dynamics still remains
69 aturating ATP, kinesin-1 spends half of each stepping cycle with one head bound, specifying a structu
70 the energy requirements for the fundamental stepping cycle, which likely includes energy from glycos
74 that trigger the two key transitions in the stepping cycle: detachment of the trailing head from the
77 for full-length Cut7, the key determinant of stepping direction is the degree of motor crowding on th
78 yeast kinesin-5 motors, Cut7 can reverse its stepping direction, by mechanisms that are currently unc
79 s presented show that the kinesin processive stepping distance decreases 40-60% with EC50 values <100
80 Institute and Harvard Dental School, and his stepping down as editor of the "Discovery!" section of t
82 We sought to compare the safety and costs of stepping down asthma controller medications with maintai
87 general asthma population and assess whether stepping down medication increased exacerbations or reli
89 patients were drawn to assess the impact of stepping down medication: mean age 50.4 years, 39.4% mal
90 rmation.Objectives: Report ACM and impact of stepping down therapy, following collection of additiona
91 95% or more of the Cyt c population folds by stepping down through the same set of foldon-dependent p
92 with the other factors to reduce chances of stepping down, but did not constitute a problem factor w
94 germane to the findings of our Report: that stepping dynamics provided a better statistical descript
95 e-trial analysis of licking behavior reveals stepping dynamics with variable onset times, which is re
101 was not expressed during swimming, treadmill stepping, exploratory locomotion, or walking on an uncoa
103 ons of this analysis include molecular-motor stepping, fluorophore bleaching, electrophysiology, part
104 rvation of enzymatic memory in translocation stepping, for the kinetics of translocation steps of dif
106 onding to random thermal fluctuations of the stepping head while it searched for its next actin-bindi
108 zed into a hierarchy that precisely controls stepping in a stereotypic, speed-dependent fashion.
110 tivity in the lumbosacral spinal cord during stepping in newborns, toddlers, preschoolers, and adults
111 f the track does not automatically instigate stepping in the absence of an additional stimulus (heat
112 evocation of spontaneous and actively driven stepping, including optimization of these behaviors in d
113 Furthermore, a remarkable feature of newborn stepping is a higher overall activation of lumbar versus
116 The basic rhythmic activity that underlies stepping is generated by a neural network, situated in t
117 g and falls, initiation slowing of voluntary stepping is observed together with perturbation-induced
118 epresent an event-triggering process whereby stepping is released according to the occurrence of a pe
119 rference (i.e., load-dependent modulation of stepping kinetics and binding-site exclusion), whereas f
120 ase cycle suggesting that within KIF3AC, the stepping kinetics are similar for each head during the p
125 nt study was designed to further compare the stepping-like movements generated via epidural (ES) and/
128 of the spinal cord at L3-L7 induced hindlimb stepping-like movements on a moving treadmill belt, but
131 in rotational mobility were detected during stepping, likely corresponding to random thermal fluctua
132 examine the structural dynamics of dynein's stepping mechanism in real time, we used polarized total
133 her, these observations demonstrate that the stepping mechanism of dynein is fundamentally different
134 many of the critical unknown aspects of the stepping mechanism of myosin 5 including head-head coord
135 ctivity with functional implications for its stepping mechanism, and also reveal a previously unappre
137 ation, in which a translocating RNAP uses a "stepping" mechanism, has been studied extensively, but p
138 f dynein is fundamentally different from the stepping mechanisms of other well-studied MT motors, bec
140 n transitions dynamically between the active stepping mode and this weak surface-associated mode enha
141 e window of evidence accumulation, and their stepping model cannot explain existing data as effective
145 Toward this end, single-molecule, in vitro stepping-motility assays are commonly used to determine
148 he geometry, we propose a diffusive sideward stepping motion of Kip3 on the microtubule lattice, asym
149 synthase (FOF1) is comprised of two rotary, stepping motors (FO and F1) coupled by an elastic power
150 activity in the STN could entrain patients' stepping movements as evidence of the STN's involvement
155 he numerous possibilities of how to regulate stepping movements to achieve different walking goals.
156 ic pattern when Parkinson's patients perform stepping movements, raising the question whether the STN
158 at the conditional knock-outs used alternate stepping, not hopping, during overground locomotion, sug
159 are consistent with a mechanism in which the stepping of KIF3C can be activated by KIF3A in a strain-
160 In contrast to other processive motors, stepping of the dynein motor domains (heads) is not prec
161 synthase, and explain the need for the finer stepping of the F1 motor in the mammalian system, as see
163 port system to allow bipedal and quadrupedal stepping on a treadmill and in an open field environment
165 molecular motor myosin V transports cargo by stepping on actin filaments, executing a random diffusiv
167 transfer from simple locomotion to accurate stepping on the ladder slow-conducting PTNs more profoun
168 ransition from simple locomotion to accurate stepping on the ladder, slow-conducting PTNs respond in
169 ses ATP hydrolysis, like other kinesins, for stepping on the microtubule lattice, but at the plus end
172 nce, rats avoid a tone-signaled footshock by stepping onto a nearby platform, delaying access to sucr
174 y binding their barbed ends and processively stepping onto incoming actin monomers to incorporate the
175 ass platform; forelimb use was unbiased when stepping onto the glass surface but biased when stepping
177 ions of neurons are well described by either stepping or nonlinear ramping, which may be less categor
181 f the PPC of cats walking on a treadmill and stepping over a moving obstacle whose speed of advance w
185 mbers translocate nucleosomes with a similar stepping pattern maintained by the catalytic subunit of
186 structure fully consistent with the variable stepping pattern observed as dynein moves along the MT.
188 epping, but it becomes uncoordinated and the stepping pattern shows a greater variability, which repr
191 e to the observed spontaneous improvement of stepping performance after incomplete SCI and are at lea
194 ciates at 2.1 s(-1), 20-fold slower than the stepping rate, demonstrating the presence of rear head g
195 ite release rate of KIF1A was similar to the stepping rate, indicating that during stepping, rear-hea
197 to the stepping rate, indicating that during stepping, rear-head detachment is an order of magnitude
199 ternating stimulation pattern resembling the stepping-related modulation of activity in the STN could
201 ed independently from other core features of stepping, revealing a striking freedom in an otherwise p
202 wever, because sensory feedback entrains the stepping rhythm, it is difficult to reveal central patte
203 rnating DBS (altDBS) could entrain patients' stepping rhythm, suggesting a causal role of the STN in
205 ircling and ameliorated deficits in forelimb stepping similarly to electrical DBS, while optogenetic
206 when the stimulation speed was close to the stepping speed in the five patients that demonstrated si
208 symmetric, sparing the basal ganglia, and a stepping stone appearance in the frontal pericallosal re
209 , we show that wood has served not only as a stepping stone between habitats but also as a bridge bet
213 suggesting that plaque may have served as a stepping stone for environmental microbes to adapt to ho
214 ngst ancient eukaryotes, but also provides a stepping stone for exploration of PTM-reader interaction
216 power of single-cell RNA-seq and provides a stepping stone for future explorations of cellular heter
217 horseradish and watercress represent a first stepping stone for future whole-genome sequencing effort
219 Purified coiled-coil domains of Steppke and Stepping stone heterodimerized through a hydrophobic sur
220 llocation, and this work provides a valuable stepping stone in guiding policy on CSF surveillance and
221 ere that family living acted as an essential stepping stone in the evolution of cooperative breeding
222 We anticipate that our work represents a stepping stone in the understanding and use of recurrent
224 erature and argue that these could provide a stepping stone into the identification of scientific bes
226 itment at the single cell level, a potential stepping stone to improved lineage manipulation through
227 te solution and concentrated gels, acts as a stepping stone to rationally control the organization in
231 C response to radiotherapy and constitutes a stepping stone toward modeling indirect tumor cell death
232 Importantly, this finding also acts as a stepping stone toward understanding the evolution of emp
235 st that the proposed method can be used as a stepping stone towards the development of an accessible
245 al genetic modelling identified two waves of stepping-stone colonization: an eastward wave moving thr
246 This achievement was further employed as a stepping-stone for the characterization of the triflate
249 ude much of the MPA network that may provide stepping-stone protection for species that must shift th
250 In a first step, we simulated the historical stepping-stone spreading dynamics of 40 marine alien spe
251 es acquisition and allocation, and provide a stepping-stone to developing trait-based approaches for
252 stics, these findings serve as a fundamental stepping-stone to the development of the first large-sca
254 erve as an alternative, or even evolutionary stepping-stone, to switching between multiple systems.
255 some of the deleterious mutations served as stepping stones across otherwise impassable fitness vall
256 om land and indicate that islands may act as stepping stones facilitating the transoceanic transport
258 fic and Indian oceans and propose islands as stepping stones for the transoceanic transport of terres
261 The COVID-19 pandemic has provided the vital stepping stones to improve how clinical trials are condu
262 iption factor-DNA interactions are important stepping stones towards a mechanistic understanding of m
263 opulations are only connected via additional stepping stones was supported by contemporary migration
264 Milu searched for vacant habitat patches as "stepping stones" and established refuge populations.
265 els provide intermediate states that act as "stepping stones" for electrons tunnelling across the dio
266 l, persisting populations, which can act as "stepping stones" that enable a rapid population expansio
269 th increasing charge stabilization on their "stepping stones." The presence of mobile anions facilita
270 , Micronesia, and Melanesia, act as critical stepping-stones for dispersal across the Pacific Ocean.
272 als atomically dispersed on oxides are major stepping-stones toward a rational development of single-
274 d that more neurons were better described by stepping than ramping, even when conditioned on evidence
275 Our work reveals features of base triplet stepping that are conserved among these three phylogenet
277 try (SCV), current transients acquired after stepping the potential along the redox wave of interest
279 ysis finds that a number of proteins fold by stepping through a reproducible sequence of native-like
283 and [T] can be quantitatively measured from stepping trajectories with very little prejudice in data
284 eck-linker element that is crucial for motor stepping undergoes discrete, ordered displacements.
286 rovide evidence for the clinical benefits of stepping up patients with COPD from an inhaled corticost
288 models demonstrated clear redundancy between stepping variables, but could not replicate human steppi
292 plete section (T13) in these cats, bilateral stepping was seen on the next day, a skill usually acqui
293 To examine the role of the NL in regulating stepping, we investigated NL mutants of various lengths
296 een well described that prolonged rotational stepping will adapt the podokinetic sense of rotation, t
297 minimal ATPase cycle), the model reproduces stepping with 8-nm steps (even though the motor itself i
299 patterns without bilateral gait training, as stepping with one leg can facilitate adaptive learning t
300 ugh a series of experiments, we observe that stepping with only one leg can facilitate learning of an