ライフサイエンスコーパス: grasp

1 y margins by squeezing before relaxing their grasp.

2 surements, reveals how birds stabilize their grasp.

3 e developed GRASPx, which is 30X faster than GRASP.

4 population of RP patients with mobility and grasp.

5 f pattern formation have been much harder to grasp.

6 maintaining the original high recall rate of GRASP.

7 uning neural communication seem difficult to grasp.

8 bringing its experimental realization within grasp.

9 ne immune cell differentiation is beyond our grasp.

10 ual and visuomotor computations of precision grasps.

11 stal movement components to achieve accurate grasping.

12 exclusion of hand-specific behaviors such as grasping.

13 ry motor area, plays a direct role in object grasping.

14 tic object exploration and haptically guided grasping.

15 correctly decoding information relevant for grasping.

16 communication to achieve transformation for grasping.

17 distal representation controls the hand for grasping.

18 k is necessary for motor coordination during grasping.

19 efficiency of visuomotor transformations for grasping.

20 edback and enable the dexterity of the human grasp(2) remain difficult to replicate in robots.

21 Evaluated were 101 prostate cancer lesions (GRASP, 61 lesions; VIBE, 40 lesions).

22 complex surfaces, yet it is unclear how they grasp a perch reliably.

23 somatosensory and motor cortices as monkeys grasp a variety of objects.

24 behaving primate paradigm in which subjects grasped a handle and moved purposefully to targets in di

25 ssumed to invoke a mental simulation (e.g., "grasping a peanut").

26 er subjects performed straight-ahead reaches grasping a robotic manipulandum.

27 ghborhood Strategy to Predict binding sites (GRaSP), a novel residue centric and scalable method to p

28 The ability to cling requires important grasping abilities and is essential to survive in specie

29 patients, 47/102 patients showed hemiparetic grasping ability and 52/102 patients could not grasp wit

30 iented in the same direction as the prepared grasping action (congruent) or not (incongruent).

31 y was observing an experimenter performing a grasping action and orienting his gaze either toward (co

32 pants were cued to prepare oriented reach-to-grasp actions before discriminating target stimuli orien

33 cuted, observed, or withheld (NoGo) reach-to-grasp actions.

34 F5 maintained a similar representation of grasping actions during both execution and observation.

35 is information appears to be used in guiding grasping actions toward targets after a delay.SIGNIFICAN

36 sable digits results in relatively imprecise grasping actions when compared with those observed in Ol

37 ly developed controls performed reaching and grasping actions with their dominant effector.

38 allow human patients to dexterously perform grasping actions.

39 s with frontal cortex damage inappropriately grasp affording objects.

40 roprostheses for restoration of reaching and grasping after paralysis.

41 In addition to a gene-centric assembly tool, GRASP also serves as a homolog search tool when using th

42 To reach and grasp an object, 'gross' arm and 'fine' dexterous moveme

43 CS) while human participants selected how to grasp an object.

44 For example, how do we grasp an unstable object while eye movements are simulta

45 This extends to abstract concepts, as well ("grasping an idea").

46 uting grasp movements.SIGNIFICANCE STATEMENT Grasping an object requires the brain to perform visual-

47 arget or towards two potential targets while grasping an object.

48 find that Golgi reassembly stacking protein (GRASP), an unconventional secretion pathway component, i

49 Single-cell GRASP analyses reveal that Li4 receives synaptic contact

50 When we grasp and manipulate an object, populations of tactile n

51 ect's location, and later both are shaped to grasp and manipulate.

52 e dysplasia or early adenocarcinoma, a novel grasp and snare EMR technique utilizing a novel over the

53 pear to signal self and other's intention to grasp and the most likely grip type that will be perform

54 alogous movements from each limb (e.g., hand grasp and toe curl) were represented similarly.

55 Using the activity-dependent GRASP and trans-Tango techniques, we confirm that DRA R7

56 to control the robotic arm when reaching to grasp and transport objects.

57 ient and inefficient reaches when the person grasped and displaced an object.

58 ception on motor coordination during routine grasping and grasping under uncertainty.

59 in response to mechanical loads produced by grasping and hanging from branches.

60 In doing so, we reveal strong evidence that grasping and lift force are not represented by spatially

61 Here, we test the extent to which grasping and lifting are represented in a spatially or t

62 he grasped object was instrumented to record grasping and lifting forces and its weight was either co

63 cipatory efforts to integrate and coordinate grasping and lifting of object interactions, all before

64 remity control influenced by LPMC, including grasping and manipulation, must occur through indirect n

65 rgical applications and tasks such as tissue grasping and manipulation.

66 ensations that are naturally perceived while grasping and moving.

67 o a wide range of novel human or conspecific grasping and non-grasping motor acts.

68 Is) have the potential to restore functional grasping and object interaction capabilities in individu

69 ty recorded from the grasping circuit during grasping and paralleled the similarities between brain r

70 human participants as they perform two tasks-grasping and signing in American Sign Language.

71 endently and solely focusing on reaching and grasping and the neural principles that guide them.

72 faster than GRASPx (and 250-fold faster than GRASP) and uses 8-fold less memory while maintaining the

73 vide instructions to perform specific reach, grasp, and manipulate movements.

74 ormance of GRASPx is consistent with that of GRASP, and that both of them significantly outperform ot

75 effect changes in the world by reaching for, grasping, and picking up objects.

76 atory premotor interneurons, the CLIs formed GRASP- and ChAT-positive putative synapses with motoneur

77 M.C. shows near-normal scaling of in-flight grasp aperture to object size despite changes in viewing

78 sition in the evolution of primate reach and grasp behavior.

79 y students from diverse fields struggle with grasping bioinformatic concepts only from classroom lect

80 l locomotion, losing an opposable digit that grasped branches in favor of a longitudinal arch (LA) th

81 etails about processes that are difficult to grasp by bulk biochemical assays that yield ensemble-ave

82 Fingerprints may be difficult to grasp by visual analysis but could be learned from large

83 eal visual and motor features encoded in the grasping circuit and their communication to achieve tran

84 resembled neural activity recorded from the grasping circuit during grasping and paralleled the simi

85 r to those observed in lesion studies of the grasping circuit, providing a potential model for how br

86 ld give insight into the computations of the grasping circuit.

87 ficient for recapitulating processing in the grasping circuit.

88 In nutrient-rich fat cells, GRASP clusters in close proximity to the apical side of

89 his explains how many animals and robots may grasp complex surfaces reliably.

90 In contrast, grasp computations involved a chain of generators attain

91 was to investigate how the brain represents grasp configuration and lift force during a dexterous ob

92 The extent to which grasp configuration and lift force varied between left a

93 cal and cerebellar regions were sensitive to grasp configuration or lift force differences between Co

94 ion of antagonistic muscle pairs and skilled grasping deficits but normal reaching and retrieval beha

95 GRASP depletion also increases cell growth and total pro

96 Interestingly, GRASP depletion reduces the protein level of alpha5beta1

97 BE)- or golden-angle radial sparse parallel (GRASP)-derived dynamic contrast agent-enhanced (DCE) MRI

98 thout grasping different objects, or else on grasping different objects all at the same location.

99 cations can alter distal hand kinematics and grasping different objects can affect kinematics of the

100 her on reaching to various locations without grasping different objects, or else on grasping differen

101 Humans can feel, weigh and grasp diverse objects, and simultaneously infer their ma

102 he structures revealed a ubiquitin-like beta-grasp domain that precedes the proteasome-activating car

103 vel diSUMO polypeptide bearing two SUMO beta-grasp domains in tandem.

104 As a cam, the PTS may increase grasping efficiency in dorsiflexed foot postures by incr

105 One ATP-grasp enzyme, d-alanine-d-alanine ligase (Ddl), catalyze

106 insight into the catalytic mechanism of ATP-grasp enzymes.

107 nions and aromatic rings in SIFSIX materials grasp every atom of SO2 firmly via S(delta+) ...F(delta-

108 sk-dependent saccade modulations and, during grasp execution, they were specifically sensitive to cha

109 the objects, the delay before movement, and grasp execution.

110 Males use the comb to grasp females during copulation, and ablation experiment

111 hanges their structure and causes difficulty grasping females prior to copulation.

112 djacent residues in strand beta2 of the beta-grasp fold whose mutation abrogated induction of MDCK ce

113 ong extension upstream of the signature beta-grasp fold, with cereals also expressing a novel diSUMO

114 cal nucleotide-binding site known as the ATP-grasp fold.

115 ted neural activity to a greater extent than grasping force.

116 eedback combined with a potential for strong grasping forces can result in excessive tissue damage.

117 , and attempt to produce three discrete hand grasping forces with the dominant hand.

118 esigned and tested in an attempt to diminish grasping forces, but the results still fall short of nat

119 Observation of erroneous grasping from a first-person perspective enhanced error-

120 e these issues, we have previously developed GRASP (Guided Reference-based Assembly of Short Peptides

121 veloped a homology detection algorithm named GRASP (Guided Reference-based Assembly of Short Peptides

122 ers ADC with K(trans) or K(ep) acquired with GRASP had higher diagnostic performance compared with di

123 applied to the hemisphere ipsilateral to the grasping hand, compared with other stimulation condition

124 rtex contralaterally or ipsilaterally to the grasping hand.

125 enameloid to preserve an efficient shape for grasping hard prey.

126 GRASP has significantly improved recall rate (60-80% vs.

127 at MethylNet can study cellular differences, grasp higher order information of cancer sub-types, esti

128 Our minds limit how much information we grasp in an instant.

129 nitiation of movement from representation of grasp in order to flexibly guide behaviour.

130 s, suggesting that the division of reach and grasp in PMd and PMv, respectively, cannot be made based

131 ng that this classical division of reach and grasp in PMd and PMv, respectively, does not accurately

132 Moreover, if the object is grasped in the dark after a delay, these areas show "rea

133 are part of a network involved reaching and grasping in primates.

134 ifocal representation of object geometry for grasping in the PMC and expand our understanding of how

135 ifocal representation of object geometry for grasping in the PMC that matches the known multifocal pa

136 hese results demonstrate a critical role for GRASPs in maintaining the stacked structure of the Golgi

137 However, GRASP is both time- and space-consuming.

138 Thinking about what the senses cannot grasp is one of the hallmarks of human cognition.

139 e proposed a third theory, which states that grasping is a combination of two goal-directed single-di

140 jects and, upon its reappearance, reached to grasp it with the thumb and index finger along one of it

141 y the role of different brain regions during grasping, it is necessary to disentangle the processing

142 y cells from simple to complex organisms, he grasped its significance in the host response to injury

143 the role of tactile information in the human grasp itself-for example, how tactile maps are used to i

144 Golgi stacking proteins; however, subsequent GRASP knockdown experiments yielded inconsistent results

145 Additionally, the GRASP knockout cell lines developed in this study will b

146 rea activity patterns evolve during reach-to-grasp learning in rats.

147 tro reconstitution approach based on two ATP-grasp ligases that were constitutively activated using c

148 nction is sufficient to allow the patient to grasp lightweight and medium-sized objects.

149 (CaMKII) phosphorylation, inhibits proximal GRASP localization to LDs.

150 Results show that GRaSP made compatible or superior predictions when compa

151 discriminate videos showing grasping or non-grasping manual motor acts in a two-alternative categori

152 Accordingly, in order to grasp, measure, and handle overdiagnosis, we should revi

153 A new dynamic grasping model, which integrates our detailed measuremen

154 novel human or conspecific grasping and non-grasping motor acts.

155 ional specialization of the human PMC during grasping movement.

156 Coordinated reach-to-grasp movements are often accompanied by rapid eye movem

157 ally, it has been hypothesized that reach-to-grasp movements arise from two discrete parietofrontal c

158 re arbitrarily assigned to control reach and grasp movements, respectively.

159 se areas.SIGNIFICANCE STATEMENT For reach-to-grasp movements, the dorsal premotor cortex (PMd) has be

160 ns over the course of planning and executing grasp movements.SIGNIFICANCE STATEMENT Grasping an objec

161 There are three main theories on how human grasping movements are controlled.

162 The frontoparietal networks underlying grasping movements have been extensively studied, especi

163 PMv) has been associated with the control of grasping movements of the hand.

164 PMv) has been associated with the control of grasping movements of the hand.

165 roprosthesis for restoring both reaching and grasping movements to people with chronic tetraplegia du

166 nal cord injury who coordinated reaching and grasping movements using his own paralysed arm and hand,

167 er similar dynamics are also observed during grasping movements, which involve fundamentally differen

168 on during single-digit pointing movements to grasping movements.

169 hat M1 does not exhibit such dynamics during grasping movements.

170 elimb motor circuit and skilled reaching and grasping movements.

171 ary for transforming visual information into grasping movements.

172 are integral part of the so-called "lateral grasping network." In the present study, we analyzed the

173 n provided by the context in which the to-be-grasped object is presented.

174 The grasped object was instrumented to record grasping and l

175 The ability of humans to reach and grasp objects in their environment has been the mainstay

176 Studying the mechanics of how humans grasp objects will complement vision-based robotic objec

177 required muscle dynamics used by primates to grasp objects would give insight into the computations o

178 fundamental to a variety of behaviours from grasping objects to navigating.

179 fundamental to the control of movement: From grasping objects to speech production, sensing guides ac

180 nsfers to the hand opening when subsequently grasping objects, leaving the movement of the hand unaff

181 de daily hand actions, like reaching for and grasping objects.

182 e typical tactile patterns that emerge while grasping objects.

183 tactile information that humans rely on when grasping objects.

184 onkeys viewed and grasped (or refrained from grasping) objects, and then observed a human doing the s

185 nstructional approach to best hone learners' grasp of concepts and skills.

186 diiron (NHFe(2)) enzymes is still beyond the grasp of contemporary computational and experimental tec

187 and matrix manipulation in R and a moderate grasp of core statistical principles.

188 Having a better grasp of how these immune cells are lost is therefore of

189 and showing that as a society we have a good grasp of how we interact.

190 tissue - "negative emotions" - is beyond the grasp of the authors' largely literary approach.

191 These correlations give us a better grasp of the hitherto obscure Chinese family structure t

192 A focus on establishing a better grasp of the physicochemical cues governing differentiat

193 A better grasp of the risk of antibiotic resistance on outcomes t

194 e to offer chemists the tools to have a good grasp of this singular functionality and open the door t

195 etics with other disciplines may improve our grasp of TRF hyperdiversity in the future.

196 exhibited significantly more frequent manual grasping of food items.

197 ns may coordinate during the visually guided grasping of objects.

198 17 male and female human participants during grasping of three objects of different sizes.

199 ue that network analysis offers a high-level grasp on a wide area of pharmacological aspects, indicat

200 at drive cortical neurons, we have a limited grasp on the structure of our brains' internal models.

201 at drive cortical neurons, we have a limited grasp on the structure of the brain's internal models.

202 types fairly well in advance with respect to grasping onset.

203 s could actively discriminate videos showing grasping or non-grasping manual motor acts in a two-alte

204 exploration of objects and action execution (grasping or reaching) separated by an 18 s delay.

205 number of untrained, novel videos depicting grasps or other manual motor acts.

206 rons with a task in which monkeys viewed and grasped (or refrained from grasping) objects, and then o

207 ch as a non-biological effector performing a grasp, or a human hand touching an object with the back

208 Grasp orientation classifiers relied on a system of occi

209 ulations during unexpected changes in object/grasp orientation, and functional connectivity with fron

210 anipulated object visual characteristics and grasp orientation, and used multivariate EEG analysis to

211 GRaSP outperformed six other residue-centric methods, in

212 subjects perform an action (e.g., a reach-to-grasp pantomime) congruent with that afforded by a prese

213 ts demonstrated a variety of consistent hand grasp patterns including single finger movement and coor

214 mulation technique in eliciting various hand grasp patterns.

215 sis, in order to classify the different hand grasp patterns.

216 ontrolling a variety of finger movements and grasp patterns.

217 The kinematics of their reaching and grasping patterns were recorded for offline analysis.

218 The object-grasping performance improved to 100% by the third trial

219 r cortex neuron activity associated with the grasping phase of a skilled motor task.

220 egrates saccade and visual signals to update grasp plans in additional intraparietal/superior parieta

221 and visual orientation signals for updating grasp plans is unknown.

222 , that integrates visuospatial updating into grasp plans, and may help to explain some of the more co

223 radigm, where saccades sometimes interrupted grasp preparation toward a briefly presented object that

224 ptorial limbs of C. serrata were adapted for grasping prey employing a descending stroke for transpor

225 shape of the rostrum, reflecting its use in grasping prey, whereas snakes show a correlation between

226 Using the ATP-grasp protein as a bioinformatic handle, we identified h

227 ate production from ATP catalyzed by the ATP-grasp protein encoded in the Y. bercovieri Anbu operon.

228 rotease family and an iteratively acting ATP-grasp protein.

229 We show that double knockout of GRASP proteins disperses the Golgi stack into single cis

230 Depletion of GRASP proteins disrupts Golgi stack formation and impair

231 More recently, GRASP proteins have drawn extensive attention from resea

232 ill be useful tools for studying the role of GRASP proteins in other important cellular processes.

233 Here, we report that depletion of GRASP proteins reduces cell attachment and migration.

234 that FABP4 secretion is also independent of GRASP proteins, autophagy, and multivesicular bodies but

235 emerging and divergent roles for individual GRASP proteins, focusing on GRASP65 in cell migration an

236 ying seven manipulative actions (drag, drop, grasp, push, roll, rotate, squeeze) in four visual forma

237 GRaSP ranked second when compared with five state-of-the

238 ings indicate that naturalistic reaching and grasping, rather than being spatially segregated process

239 a preference based on action type (reaching/grasping) regardless of the effector used in the associa

240 Right SMG and several parietal grasp regions, namely, left anterior intraparietal sulcu

241 Rather, the grasp-related neuronal dynamics in M1 are similar to the

242 Grasping-related activity is represented in a diffuse, v

243 The accuracy of reaching and grasping relies on internal feedback pathways that updat

244 a premotor counterpart of a similar diffuse grasping representation is available.

245 atches the known multifocal parietal maps of grasping representations.

246 or rostral forelimb area control reaching or grasping, respectively, and both are required in the tra

247 functional obstacle course and a custom-made grasping setup were used.

248 ex and dorsolateral striatum during reach-to-grasp skill learning in rats.

249 The large body size and high number of grasping spines in C. praetermissus may indicate that mi

250 Chaetognath grasping spines, originally reported as conodonts, occur

251 nctional impairment and recovery in reaching/grasping, spontaneous limb use, and hindlimb placement d

252 Whereas computer-vision-based robot grasping strategies(3-5) have progressed substantially w

253 The ATP-grasp superfamily of enzymes shares an atypical nucleoti

254 ite is structurally conserved within the ATP-grasp superfamily.

255 v encode the kinematics of both reaching and grasping synergies, suggesting that the division of reac

256 v encode the kinematics of both reaching and grasping synergies, suggesting that this classical divis

257 ined to perform an instructed-delay reach-to-grasp task in the dark and in the light toward objects o

258 sion male rats performing a skilled reach-to-grasp task the.

259 aneously while macaques performed a reach-to-grasp task.

260 while rhesus macaques engaged in a reach-to-grasp task.

261 trolling a robotic arm to complete reach-and-grasp tasks efficiently using non-invasive BCI has yet t

262 nkeys performing three-dimensional reach and grasp tasks, PSID revealed that the behaviorally relevan

263 d by the subjects while performing different grasping tasks.

264 ed with diffusion weighting and DCE by using GRASP (temporal resolution, 2.5 seconds) or VIBE (tempor

265 n mobility testing (p = 0.02), and by 70% in grasp testing (p = 0.03).

266 sed for visual/hand coordination with object-grasping tests.

267 derstanding of the complex reaction network, grasp the capability of manipulating structure and combi

268 simple quantitative biophysical models that grasp the different regimes of in vitro gene expression,

269 Yet, we are only beginning to grasp the drivers of terrestrial microbial diversity and

270 ontrast, hippocampal patients were unable to grasp the higher-order structure of the task with the sa

271 ess have been implemented, they do not fully grasp the impacts on ecosystem functioning.

272 he multiple nutrition-related challenges and grasp the opportunities before us.

273 fects need to be taken into account to fully grasp the spin properties (such as spin dependent densit

274 Conversely, grasping the anterior and posterior leaflets did not red

275 Despite having been known for four decades, grasping the functions and features of ISG15 has been a

276 and right CoM conditions was manipulated by grasping the object collinearly (requiring a non-colline

277 Grasping the principles of host-microbiota interactions

278 Grasping their fundamentals can advance a broad range of

279 such as size and shape, into motor plans for grasping them, hence contributing to "pragmatic" afforda

280 the consecutive emergence of sensitivity to grasping, then lifting within the same region.

281 hts from the tactile signatures of the human grasp-through the lens of an artificial analogue of the

282 conditions at differing time points during a grasp to lift action.

283 ty was measured as subjects used a precision-grasp to lift an object with a center of mass (CoM) on t

284 The coordinated grasp to lift effort is shown to be under dorsolateral (

285 GFP reconstitution across synaptic partners (GRASP) to show that pr1 cells in the ventral nerve cord

286 d the future design of prosthetics(7), robot grasping tools and human-robot interactions(1,8-10).

287 a large degree, functionally substitute for GRASP-type Golgi stacking proteins to sustain normal Gol

288 Our classifier was able to discriminate grasp types fairly well in advance with respect to grasp

289 Reaching and grasping typically are viewed as processes that proceed

290 tor coordination during routine grasping and grasping under uncertainty.

291 er, this approach may limit opportunities to grasp unintended drug actions, which can open up channel

292 gration of oculomotor and visual signals for grasp updating.SIGNIFICANCE STATEMENT How does the brain

293 gly developed in extant taxa that habitually grasp vertical supports with strongly dorsiflexed feet.

294 GRASP was developed to implement a simultaneous alignmen

295 pecifying whether and how the object will be grasped, which progressively turns into a broader agent-

296 ow the brain orchestrates and integrates the grasp with lift forces of the fingers in a coordinated m

297 asping ability and 52/102 patients could not grasp with their paretic hands.

298 angutans and consistent with locomotor power-grasping with the fingers, while that of the thumb is co

299 provide strong evidence for our theory that grasping with the thumb and index finger is based on a c

300 onses, particularly at the end of reach when grasping would normally be occurring.