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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
23 unctional deficits consisting of weaker hand grip (adjusted difference vs community controls -1.7 kg,
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
29 During a subsequent test phase, we examined grip and load force coordination during corrective arm m
31 , frequently used as a benchmark quantity in grip and perceptual studies, is a poor reflection of the
34 rtical inhibition decreased during precision grip and spinal motoneuron excitability remained unchang
37 suggests a paradigm for soft adhesion-based gripping and transfer-printing systems that achieves are
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
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.
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
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
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
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
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
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).
81 m for strand separation, and show Csm3/Tof1 "grip" duplex DNA ahead of CMG via a network of interacti
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
93 ficial skin-stretch increases the predictive grip force modulation in anticipation of the load force.
95 top of inducing short latency disturbance of grip force, single-pulse TMS should also quickly disrupt
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
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
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
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
119 of finger muscles during precision and power grip in humans but the neural mechanisms involved remain
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
129 o enable robotic (machine) functions such as gripping, lifting, or motility (walking, crawling, swimm
132 anoacrylate glue (Histoacryl, n = 216), self-gripping mesh (Parietex ProGrip, n = 202), or convention
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
138 so, today, most of Antarctica remains in the grip of continental ice sheets, with only about 0.2% of
140 ty near the active site, the extended primer grip of the polymerase has the potential to distinguish
144 hy) environmental stresses, have an integral grip on cell fate, and have shaped the ecological succes
147 mechanism, the kinetochore can modulate its grip on microtubules over mitosis and yet retain its abi
150 pull-ups with the body suspended by the arms gripped on a bar; 3) sit-ups in which the upper and lowe
152 rget object: using a precision grip, a power grip, or touching the object without hand preshaping.
154 al inguinal hernia were randomized to a self-gripping polyester mesh or a sutured polyester mesh.
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
163 tion, lung function, physical capacity (hand grip, step test, and physical activity), and blood marke
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).
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
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
182 ination reduced or prevented disease-related grip strength and object recognition deficits, mHTT accu
184 to reduce the likelihood of developing weak grip strength and slow walking speed because purpose has
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
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
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
198 -related somatic changes are correlated with grip strength in men, suggesting blood-derived whole gen
202 Galactosylceramide resulted in enhanced grip strength of forelimbs in male and female mice, bett
205 udy aimed to evaluate whether gait speed and grip strength predicted clinical outcomes among older ad
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
218 ge, sex, race, cognition, comorbidities, and grip strength, AMD subjects showed an increased likeliho
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.
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).
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
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
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
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
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
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
266 nction findings in his right/left hand were: grip strength: 10/13 kg; key pinch: 3/3 kg; Kapandji sco
268 ies have explored primates with precise hand grips, such as higher apes, few have considered primates
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
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
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
295 aten) mice demonstrated decreased body size, grip weakness, abnormal gait, joint laxity, and early-on
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.