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1 the newly formed geminate radical ion pairs (GRIPs).
2 ith pore loops synergistically to strengthen grip.
3 t during index finger abduction or precision grip.
4 ical inhibition, but not CMEPs, during power grip.
5 x finger abduction, precision grip and power grip.
6 of finger muscles during precision and power grip.
7  but not index finger abduction or precision grip.
8 ger abduction, a precision grip, and a power grip.
9  corticospinal output during human precision grip.
10 spital, who agreed to assessment of gait and grip.
11 nship between receptor density and precision grip.
12  core that contributes most significantly to grip.
13 king individual objects to multiple possible grips.
14 alignment and coupling of ATP binding to DNA gripping.
15 amic nucleus (STN) unit activity during hand gripping.
16  logged NT-proBNP was associated with weaker grip (-0.63 kg, 95% CI, -0.99 to -0.28); the equivalent
17 corticoid receptor (GR)-interacting protein (GRIP)1-cooperates with GR to repress inflammatory genes.
18 ysical performance battery, Zubrod, and hand grip; 6 mo: short physical performance battery, Zubrod)
19 nt substrate engagement steps allow ClpXP to grip a wide variety of sequences to ensure efficient unf
20 d a central target object: using a precision grip, a power grip, or touching the object without hand
21 s was that they do not precisely scale their grip according to the dimensions of the target object wh
22 ctrical actuation, enabling novel designs of gripping actuators for soft robotics.
23 unctional deficits consisting of weaker hand grip (adjusted difference vs community controls -1.7 kg,
24 ubunits to constrict into a tight helix that grips an 80 A stretch of unfolded protein.
25 F) contributions to action comprehension for grip and context encoding, respectively, the negative co
26  affected by grip context (no contact, light grip and firm grip), as well as how they are co-ordinate
27 ed during power grip compared with precision grip and index finger abduction, suggesting a cortical o
28 ed during power grip compared with precision grip and index finger abduction.
29  During a subsequent test phase, we examined grip and load force coordination during corrective arm m
30                 However, in natural actions, grip and object type are often confounded, and the few e
31 , frequently used as a benchmark quantity in grip and perceptual studies, is a poor reflection of the
32                        We also evaluated his grip and pinch force.
33 cle during index finger abduction, precision grip and power grip.
34 rtical inhibition decreased during precision grip and spinal motoneuron excitability remained unchang
35 ct of PKC on the dissociation of AMPARs from GRIP and thus their availability for trafficking.
36 ic field and, at a second temperature, could grip and transport a cargo.
37  suggests a paradigm for soft adhesion-based gripping and transfer-printing systems that achieves are
38 roficiently and forcefully perform precision grips and in-hand manipulation of objects.
39 rios as defined by the compatibility between grips and intentions afforded by the contextual objects.
40 uman-like (MHL) hand anatomy, its associated grips and the invention and use of stone tools by early
41 eins-glutamate receptor-interacting protein (GRIP) and protein interacting with C kinase 1 (PICK1)-re
42 xterity: index finger abduction, a precision grip, and a power grip.
43 tivities of daily living (ADLs), falls, hand-grip, and chair-stands.
44  was also associated with higher BMI, weaker grip, and more comorbid illnesses (p < 0.05 for all).
45 thogonally manipulated object properties and grip, and revealed the visual dimension (object elongati
46 /- 9, and 38 +/- 9 minutes in the glue, self-gripping, and suture groups, respectively (P < 0.001).
47 ns are captured by a coordinated protein-DNA grip-and-release cycle to produce DNA translocation.
48                       Two of them state that grip aperture and the movement of the hand are controlle
49 cating the horizontal size of each target by grip aperture and, in a further experiment, a verbal siz
50    Predictive modeling revealed that maximum grip aperture, time to reach peak velocity and hand use
51 lnerability to cocaine relapse and highlight GRIP as a novel target for the development of cocaine ad
52 rip context (no contact, light grip and firm grip), as well as how they are co-ordinated with the low
53 e the colony and perform a stereotyped death grip behavior, where they bite onto vegetation over fora
54 reasingly modern anatomy prevented them from gripping branches with their feet.
55 ticulospinal tract, while performing a power grip but not during index finger abduction or precision
56 uring a startle cue while performing a power grip but not index finger abduction or precision grip.
57  resolution, we identify the determinants of grip by measuring how substrate tail sequences alter the
58 reveal the essential tubulin tail glutamates gripped by a double spiral of electropositive loops lini
59            The N terminus of gp120, which is gripped by gp41 in the pre-fusion or CD4-bound Env, flip
60                                    Different grips can be used, and different objects require differe
61 f ensemble patterns reflecting unique object-grip combinations.
62 mb postures that may reflect habitual use of grips commonly used for hafted tools.
63 ticospinal excitability present during power grip compared with fine finger manipulations are largely
64 timulation were more suppressed during power grip compared with precision grip and index finger abduc
65  not CMEPs, was more suppressed during power grip compared with precision grip and index finger abduc
66 cal inhibition was more reduced during power grip compared with the other tasks.
67 cal inhibition was more reduced during power grip compared with the other tasks.
68 erms of action type (whole-hand or precision grip), concurrent tactile stimulation (stimulation or no
69 his study, we show that signals representing grip configurations can be reliably decoded from neural
70 s in corticospinal excitability during these gripping configurations.
71  a phenomenon we call "grip constancy." Does grip constancy, like perceptual constancy, depend on V1
72 tual object constancy, it is unnecessary for grip constancy, which is mediated instead by separate vi
73 ce [31-41] (Figure 1), a phenomenon we call "grip constancy." Does grip constancy, like perceptual co
74 termined how these responses are affected by grip context (no contact, light grip and firm grip), as
75 termined how these responses are affected by grip context, as well as how they are co-ordinated with
76  not compromise the kinetochore's ability to grip depolymerizing microtubules.
77  the degradation of Arl1 and dissociation of GRIP domain-containing proteins Golgin-97 and Golgin-245
78 outside the cell with the protease-sensitive GRIP domains in the periphery (Noreng et al., 2018).
79 nctional module consisting of the finger and GRIP domains.
80                    The design of such tissue gripping drug delivery devices offers an effective strat
81 m for strand separation, and show Csm3/Tof1 "grip" duplex DNA ahead of CMG via a network of interacti
82 underlying sand layer where they gained more grip during progression.
83            Handgrip strength was tested by a grip dynamometer and used to classify adults as fit or u
84            Following a bout of rhythmic hand grip exercise, post exercise circulatory occlusion (PECO
85 no contact, light grip (< 1 N) (LG) and firm grip (FG).
86 S that position mtClpX and provide it with a grip for acting on ALAS.
87                  To reduce the risk of slip, grip force (GF) control includes a safety margin above t
88 ed, we found that the participants generated grip force adjustments tightly coupled, both spatially a
89  in the control of the corrective responses, grip force changes would anticipate the unusual load for
90 is human study, we examined rapid, precision grip force contractions to determine whether feedforward
91                                   After each grip force exertion, participants had the opportunity to
92 targets either side of midline and a minimal grip force for midline movements.
93 ficial skin-stretch increases the predictive grip force modulation in anticipation of the load force.
94      Critically, on these trials the initial grip force was minimal, appropriate for the midline move
95 top of inducing short latency disturbance of grip force, single-pulse TMS should also quickly disrupt
96  development of the predictive modulation of grip force.
97 t whose horizontal motion is driven by their grip force.
98 al differences in socially-induced change in grip force.
99 g their slippage using predictive control of grip force.
100 ed in the planning, execution and control of gripping force and movement vigour.
101 nglia control signal for force and to decode gripping force based on local field potential (LFP) acti
102 derstanding of how the basal ganglia control gripping force, and also suggest that deep brain LFPs co
103 13-30m Hz) bands were most informative about gripping force, and that a first order dynamic linear mo
104 an be used to decode the temporal profile of gripping force.
105 imilarly exacerbated force tremor during the grip-force task in dystonic tremor and essential tremor
106 e experimental paradigm included a precision grip-force task wherein online visual feedback related t
107 ial tremor patients produced exacerbation of grip-force tremor and associated changes in functional a
108 ly compared the effect of visual feedback on grip-force tremor and associated functional network-leve
109 at the system can help users achieve average grip forces closer to those normally possible with the h
110 l elastic load to the object requiring large grip forces for reaches to targets either side of midlin
111 on, while measuring effort perception during grip forces of different intensities.
112 e movement, and not the average of the large grip forces required for movements to the individual tar
113 tracking task, we show that tracking errors, grip forces, and learning curves are consistent with pre
114             When GVS was applied during firm grip, hand and ground reaction forces were generated.
115 ntly associated with waiting list mortality: grip (hazard ratio = 0.89, 95% confidence interval 0.83-
116 ly, transcription of lncRNAs could serve as "grip holds" for nuclear proteins to pull the genome into
117  (DORC, Zuidland, The Netherlands) using end-gripping ILM forceps.
118 rst study to demonstrate a role for accumbal GRIP in behavior.
119 of finger muscles during precision and power grip in humans but the neural mechanisms involved remain
120 ed delay periods for object presentation and grip instruction.
121                                     Afferent grip-intensity levels are also decoded from M1, enabling
122                           Distinct substrate-gripping interactions are identified for NBD1 and NBD2 p
123   These results show that a minimum level of grip is necessary before the upper limb plays an active
124 sults support a mechanism in which unfolding grip is primarily mediated by non-specific van der Waal'
125  results demonstrate that a minimum level of grip is required before the upper limb becomes active in
126 y for forceful precision and power "squeeze" gripping is linked to two key evolutionary transitions i
127  did we observe CSE modulations according to grip kinematics.
128                                         ClpX grips large hydrophobic and aromatic side chains strongl
129 o enable robotic (machine) functions such as gripping, lifting, or motility (walking, crawling, swimm
130 ith an earth-fixed object: no contact, light grip (&lt; 1 N) (LG) and firm grip (FG).
131            When GVS was applied during light grip (&lt; 1 N), hand forces were secondary to body movemen
132 anoacrylate glue (Histoacryl, n = 216), self-gripping mesh (Parietex ProGrip, n = 202), or convention
133             To evaluate the effect of a self-gripping mesh (Progrip) on the incidence of chronic post
134 ever, during action observation of the pinch-grip movement, the increase of corticospinal excitabilit
135 tations (M392A, M392L, and M392V) and primer grip mutations (K375R and R376K) exhibited divergent RNA
136 rent frequencies during an index-thumb pinch-grip observation task.
137 nputs to spinal motoneurons during precision grip of a small object.
138 so, today, most of Antarctica remains in the grip of continental ice sheets, with only about 0.2% of
139 all clinging defect, mutant males often lose grip of the female abdomen during copulation.
140 ty near the active site, the extended primer grip of the polymerase has the potential to distinguish
141          We conclude that an extended primer grip of the polymerase, including L420, M392, K375, and
142              We implicate an extended primer grip of the viral polymerase in sexual RNA replication m
143  size, these "hopping heads" use a vice-like grip of their jaws to restrain and immobilize prey.
144 hy) environmental stresses, have an integral grip on cell fate, and have shaped the ecological succes
145 ne is a transcription factor with a powerful grip on cellular growth and proliferation.
146 ole of the Ska complex in maintaining a firm grip on dynamic microtubules.
147  mechanism, the kinetochore can modulate its grip on microtubules over mitosis and yet retain its abi
148 strands and then closes to establish a tight grip on the DNA template.
149  and clamp opening, RNA polymerase loses its grip on the RNA:DNA hybrid and is inactivated.
150 pull-ups with the body suspended by the arms gripped on a bar; 3) sit-ups in which the upper and lowe
151 tropomyosin superhelices as they "lose their grip" on F-actin.
152 rget object: using a precision grip, a power grip, or touching the object without hand preshaping.
153 keys through the process of passive viewing, grip planning, and grasping movement execution.
154 al inguinal hernia were randomized to a self-gripping polyester mesh or a sutured polyester mesh.
155                                           As grip progressed along this continuum, we observed an inc
156                                     The self-gripping Progrip mesh does not reduce CPIP rates.
157 ty levels are also decoded from M1, enabling grip reanimation regulated by touch signaling.
158 y adjacent to L420 and the polymerase primer grip region, led us to engineer additional polymerase mu
159 luenced by its interactions with the "primer grip" region and could be influenced by the M230I mutati
160 erceptual object properties onto categorical grip representations.
161               In this study, 4486 adults had grip scores at baseline indicating adequate function (26
162                             This mechanisms' grip slips, however, when the feedback loop is intermitt
163 tion, lung function, physical capacity (hand grip, step test, and physical activity), and blood marke
164  We used objects affording multiple possible grip strategies.
165 ates information related to object shape and grip strategy as it becomes available, revealing a trans
166 >/=30) in the lowest tertile of sex-specific grip strength (<35.3 kg for men and <19.6 kg for women).
167                  The risk of developing weak grip strength (assessed as a binary yes or no outcome) o
168                                       Higher grip strength (GS) is associated with lower mortality ri
169 .21; 95% CI: 1.32, 3.71) and/or reduced hand grip strength (HR: 1.53; 95% CI: 10.07, 2.17) than in th
170 nce intervals -16.786 to -4.482) decrease in grip strength (kg force) (P < 0.001) and -8.74 (95% conf
171      Participants with CMT2A had the weakest grip strength (P < .05), while those with CMT2A and CMT4
172 (P = .03) and B (P = .05), right-sided Jamar grip strength (P = .02), Rapid Pace Walk (P = .03), Brak
173 viduals and identify 16 loci associated with grip strength (P<5 x 10(-8)) in combined analyses.
174                         For example, greater grip strength (per 6 kg) had an odds ratio (95% CI) of 0
175 ss index (Spearman r=0.28, P<0.0001), weaker grip strength (Spearman r=-0.34, P<0.01), and slower wal
176 Ab levels were significantly correlated with grip strength (Spearman r=-0.57, P<0.005), walking speed
177 sed risk (95% CI, 1%-23%) of developing weak grip strength and a 14% decreased risk (95% CI, 8%-20%)
178 ligible patients had low performance on hand grip strength and chair rise tests, tested with the proc
179  observed for cardiovascular mortality.Lower grip strength and excess adiposity are both independent
180 ured using dual energy x-ray absorptiometry; grip strength and information on lifestyle indicators, i
181                                     In fact, grip strength and maximum isometric tetanic force are ev
182 ination reduced or prevented disease-related grip strength and object recognition deficits, mHTT accu
183 that likely relate to self-selection such as grip strength and self-rated health.
184  to reduce the likelihood of developing weak grip strength and slow walking speed because purpose has
185 ssociated with lower risk of developing weak grip strength and slow walking speed over time.
186 ted with a decreased risk of developing weak grip strength and slow walking speed, although the findi
187 paired voluntary running capacity and muscle grip strength and that their gastrocnemius muscle contai
188 nsight into the mechanistic underpinnings of grip strength and the causal role of muscular strength i
189  pressure and attenuation of decline in both grip strength and time to death.
190 g speed, chair rise speed, balance time, and grip strength assessed at ages 60 to 64 and 69 years.
191 ce, however, JQ1 had no effect on rotarod or grip strength but exacerbated weight loss and worsened p
192 icantly increased body weight, lean mass and grip strength by 60-80% over vehicle-treated mdx mice.
193 ed reduced body and muscle mass and impaired grip strength compared with controls, which was accompan
194                                  Significant grip strength declines observed in HRHF-Untreated and HR
195 9; 95% CI, 0.83-0.95), but associations with grip strength did not reach conventional levels of stati
196 pollution, poor diet, low education, and low grip strength had stronger effects on cardiovascular dis
197 mouse or change gait, motor coordination, or grip strength in adult mice of both sexes.
198 -related somatic changes are correlated with grip strength in men, suggesting blood-derived whole gen
199 on, in conjunction with a relatively tighter grip strength in the manual claws.
200                                         Hand grip strength is a widely used proxy of muscular fitness
201                     In contrast to Hyp mice, grip strength is preserved.
202      Galactosylceramide resulted in enhanced grip strength of forelimbs in male and female mice, bett
203 ausal effect of higher genetically predicted grip strength on lower fracture risk.
204 ere was no significant change of either hand grip strength or leg extension power.
205 udy aimed to evaluate whether gait speed and grip strength predicted clinical outcomes among older ad
206 the risk of all-cause mortality increased as grip strength reduced within each BMI category.
207                 All animals underwent weekly grip strength testing and were sacrificed 14 weeks follo
208 ced skeletal muscle function, as measured by grip strength tests 4 weeks after injection.
209 ted more strongly with exercise capacity and grip strength than with lung function.
210                                              Grip strength was assessed using Smedley spring-type han
211                       Every 5-kg decrease in grip strength was associated with worse survival (adjust
212                                              Grip strength was improved significantly for both hands
213 ural and environmental risk factors and hand grip strength were assessed as factors interfering with
214 t physical performance battery; Zubrod; hand grip strength) and health-related quality of life (EuroQ
215 er 3 months on the waiting list: -0.38 kg in grip strength, -0.05 meters/second in gait, 0.03 seconds
216 ters, comorbidities, Clinical Frailty Scale, grip strength, 5-meter walk test, and pulmonary function
217             We also collected lung capacity, grip strength, a series of balance tests, and a timed wa
218 ge, sex, race, cognition, comorbidities, and grip strength, AMD subjects showed an increased likeliho
219 basic behavioral activities, impaired muscle grip strength, and defects in motor coordination.
220 hy Impairment Score of the Lower Limbs, hand grip strength, and evaluation of vegetative dysfunction,
221 ors (ie, education, symptoms of depression), grip strength, and household and ambient pollution.
222        Treadmill exercise capacity, forelimb grip strength, and in vivo maximum tetanic force were al
223 played reduced spontaneous activity, loss of grip strength, and increased circulating levels of muscl
224 -min walking distance, fast gait speed, hand grip strength, and isometric leg extension strength).
225 ce resulted in growth retardation, decreased grip strength, and loss of vocalization.
226 otor activity, contextual fear conditioning, grip strength, and motor learning, mainly in Tg but not
227 ipants were stratified by country, age, hand grip strength, and performance on the chair rise test, a
228 e walls of the vials, suggesting a defect in grip strength, and repeat the cycle of climbing and fall
229 low physical activity, exhaustion, decreased grip strength, and slow gait speed.
230          FE65 family KO mice show attenuated grip strength, and the nuclei of DKO muscle cells freque
231        The final frailty index consisted of: grip strength, chair stands, and balance.
232                     The liver frailty index (grip strength, chair stands, balance) was measured at ev
233 but other measurements of strength (forelimb grip strength, ex vivo measurements of contractile funct
234 ds ratio = 2.43; 95% CI, 1.17-5.03) and poor grip strength, exhaustion, and slowed walking speed (haz
235  across several movement qualities including grip strength, fine motor skills, and synergies and was
236 ater adverse changes in physical capability (grip strength, gait speed, and physical activity), senso
237 ailty was measured on a scale from 0 to 5 by grip strength, gait speed, exhaustion, shrinkage, and ph
238 (HDL) cholesterol, forced expiratory volume, grip strength, HbA1c, longevity, obesity, self-rated hea
239 mmonia, increase in lean body mass, improved grip strength, higher skeletal muscle mass and diameter,
240 Truncal flexion and extension strength, hand grip strength, leg extension power, and quality of life
241             The most common pattern was poor grip strength, low physical activity, and slowed walk sp
242 serum biochemistry, tissue weight, voluntary grip strength, maximal aerobic capacity (VO(2max)), body
243 gnificant defects in motor skills, including grip strength, motor coordination, and gait and also rel
244 cin markedly improved their wellness scores, grip strength, neuropathology, and survival.
245 -appearing brain was associated with: weaker grip strength, poorer lung function, slower walking spee
246  echocardiography, novel object recognition, grip strength, rotarod, glucose tolerance test (GTT) and
247       Frailty was measured by 4-m walk time, grip strength, self-reported weight loss, exhaustion, an
248  muscle measurements, such as hand pinch and grip strength, show the strongest correlation with disea
249 ced vital capacity, resting heart rate, hand grip strength, sit and reach distance, and time standing
250  or more of the following 5 components: weak grip strength, slowed walking speed, poor appetite, phys
251 e to >=3 of the following 5 components: weak grip strength, slowed walking speed, poor appetite, phys
252 glycated hemoglobin, smoking, education, and grip strength, the opposite sex role of periodontitis an
253         Patients were clinically assessed on grip strength, vibration perception thresholds and postu
254 ate the genetic determinants of variation in grip strength, we perform a large-scale genetic discover
255  physical activity, slow walking speed, poor grip strength, weight loss, and exhaustion) and disabili
256  following criteria: slow walking speed, low grip strength, weight loss, exhaustion, and low physical
257 , 2.17) than in those with stable weight and grip strength, with the highest risk in those with both
258 tion of fibrosis and restoration of forelimb grip strength.
259  were more robust for walking speed than for grip strength.
260 uding robust hind limb elements modified for grip strength.
261 , mechanical hypersensitivity, and decreased grip strength.
262 paired motor control, exercise capacity, and grip strength.
263 d neurological recovery weekly by upper-limb grip strength.
264 l nucleation, fibrosis and declined forelimb grip strength.
265 g telomere length, the epigenetic clock, and grip strength.
266 nction findings in his right/left hand were: grip strength: 10/13 kg; key pinch: 3/3 kg; Kapandji sco
267 02); and greater recovery of motor function (grip strength: p < 0.001).
268 ies have explored primates with precise hand grips, such as higher apes, few have considered primates
269 on that elastomers are commonly used to coat grip surfaces.
270 d deformable gripper body, the proposed soft-gripping system controls the bonding strength by changin
271 e this trade-off with an adhesion-based soft-gripping system that exhibits enhanced fracture strength
272  LFOs during the performance of a visuomotor grip task and motor function in a longitudinal (<5 days,
273 oring of participants' performance of a fine grip task during functional magnetic resonance neuroimag
274  underwent rest and stress OCT-A (i.e., hand-grip test [HGT]).
275  physical function (e.g. rotarod, treadmill, grip test, and wheel running), we observed that mTORC1 a
276 proved motor performance in rotarod and foot grip tests in treated Sh3tc2-/- mice compared to mock ve
277  and beta-chains as tweezers to surround and grip the glucose moiety of GMM, GEM TCRs create a highly
278 if intruding between the two DNA strands and gripping the 3'-overhang while Bax1 interacts with the 5
279   There, a tight web of aromatic amino acids grips the substrate in a sequence-promiscuous, hydrophob
280 lar system, suppressed MEP size during power grip to a lesser extent than during the other tasks and
281 lar system, suppressed MEP size during power grip to a lesser extent than during the other tasks at a
282  manipulating tools, (ii) a strong precision grip to hold tools securely, and (iii) enhanced visually
283 n strength, locally switching adhesions from gripping to slipping and further accelerating actin flow
284 her's intention to grasp and the most likely grip type that will be performed, whereas action-related
285 l devoid of any specificity for the observed grip type.
286  substantially larger when predicting the 20 grip types (planning, 74%; execution, 86%; chance level,
287 te for the first time that a large number of grip types can be decoded from higher cortical areas dur
288 decoding from individual arrays, objects and grip types could be predicted well during movement plann
289                    Offline, we determined 20 grip types from the kinematic data and decoded these han
290         We investigated the decoding of many grip types using spiking activity from the anterior intr
291  across either different object locations or grip types.
292 yes classifier used for decoding objects and grip types.
293 ch restricts the dissociation of AMPARs from GRIP under basal conditions.
294                       The forceful precision grips used by modern humans probably evolved in the cont
295 aten) mice demonstrated decreased body size, grip weakness, abnormal gait, joint laxity, and early-on
296 it is not well-understood how motors produce grip when resisting a folded domain.
297 fingers extension-thumb interface and primer grip, which may contribute their stronger inhibition.
298 sion grip with two or five digits, or coarse grip with five digits) and used representational similar
299 gation) and task (passive viewing, precision grip with two or five digits, or coarse grip with five d
300 perimentalists and theorists have to come to grips with the fact that they rely on different models.

 
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