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1 tributing to the ease with which AR 6 "loses grip".
2 the newly formed geminate radical ion pairs (GRIPs).
3 corticospinal output during human precision grip.
4 used to program and execute the appropriate grip.
5 ical inhibition, but not CMEPs, during power grip.
6 e grip, or in some cases for both object and grip.
7 on the rake task with that during precision grip.
8 t during index finger abduction or precision grip.
9 x finger abduction, precision grip and power grip.
10 of finger muscles during precision and power grip.
11 but not index finger abduction or precision grip.
12 ger abduction, a precision grip, and a power grip.
13 king individual objects to multiple possible grips.
14 alignment and coupling of ATP binding to DNA gripping.
15 hages is mediated by GR-interacting protein (GRIP)1, a transcriptional coregulator of the p160 family
16 corticoid receptor (GR)-interacting protein (GRIP)1-cooperates with GR to repress inflammatory genes.
17 d a central target object: using a precision grip, a power grip, or touching the object without hand
19 se region of RT, and the 428, RNase H Primer Grip Adjacent, and 507 sites, located in the RNase H reg
20 unctional deficits consisting of weaker hand grip (adjusted difference vs community controls -1.7 kg,
23 affected by grip context (no contact, light grip and firm grip), as well as how they are co-ordinate
24 ed during power grip compared with precision grip and index finger abduction, suggesting a cortical o
26 During a subsequent test phase, we examined grip and load force coordination during corrective arm m
29 , frequently used as a benchmark quantity in grip and perceptual studies, is a poor reflection of the
31 rtical inhibition decreased during precision grip and spinal motoneuron excitability remained unchang
33 suggests a paradigm for soft adhesion-based gripping and transfer-printing systems that achieves are
34 uman-like (MHL) hand anatomy, its associated grips and the invention and use of stone tools by early
35 eins-glutamate receptor-interacting protein (GRIP) and protein interacting with C kinase 1 (PICK1)-re
37 was also associated with higher BMI, weaker grip, and more comorbid illnesses (p < 0.05 for all).
38 ized clinical evaluations of extremity, hand grip, and respiratory muscle strength; anthropometrics (
39 thogonally manipulated object properties and grip, and revealed the visual dimension (object elongati
40 /- 9, and 38 +/- 9 minutes in the glue, self-gripping, and suture groups, respectively (P < 0.001).
41 groups for "onset time," "time after maximum grip," and "time after maximum velocity," indicating tha
44 cating the horizontal size of each target by grip aperture and, in a further experiment, a verbal siz
47 lnerability to cocaine relapse and highlight GRIP as a novel target for the development of cocaine ad
48 rip context (no contact, light grip and firm grip), as well as how they are co-ordinated with the low
52 ticulospinal tract, while performing a power grip but not during index finger abduction or precision
53 uring a startle cue while performing a power grip but not index finger abduction or precision grip.
54 on, such as grasping an object using a power grip, but also when the animal passively observes a simi
57 slow gait, muscle weakness (defined as weak grip), cognitive impairment, and depressive symptoms.
59 ticospinal excitability present during power grip compared with fine finger manipulations are largely
60 ullary MEP size was reduced during precision grip compared with index finger abduction in uninjured h
61 timulation were more suppressed during power grip compared with precision grip and index finger abduc
62 not CMEPs, was more suppressed during power grip compared with precision grip and index finger abduc
66 ht to independently control either reach and grip components (a functional dissociation), or planning
67 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 termined how these responses are affected by grip context (no contact, light grip and firm grip), as
72 termined how these responses are affected by grip context, as well as how they are co-ordinated with
79 scharged during both object presentation and grip execution, displaying selectivity for either the ob
81 ate brainstem pathways (BS); (2) distal limb-grip exercises preferentially stimulating CST pathways (
87 errors are necessary for trajectory but not grip force adaptation, and that kinetic errors are suffi
89 ed, we found that the participants generated grip force adjustments tightly coupled, both spatially a
90 rticipants continued to effectively modulate grip force but exhibited substantial kinematic errors, e
92 in the control of the corrective responses, grip force changes would anticipate the unusual load for
93 is human study, we examined rapid, precision grip force contractions to determine whether feedforward
97 he channel, participants learned to modulate grip force in synchrony with load force and this learnin
100 Critically, on these trials the initial grip force was minimal, appropriate for the midline move
101 s in motivational responding, as measured by grip force, although subjective liking responses to the
103 top of inducing short latency disturbance of grip force, single-pulse TMS should also quickly disrupt
104 nticipatory downscaling but not upscaling of grip force, suggesting an inhibitory role of PMd in anti
110 nglia control signal for force and to decode gripping force based on local field potential (LFP) acti
111 derstanding of how the basal ganglia control gripping force, and also suggest that deep brain LFPs co
112 13-30m Hz) bands were most informative about gripping force, and that a first order dynamic linear mo
114 l elastic load to the object requiring large grip forces for reaches to targets either side of midlin
116 e movement, and not the average of the large grip forces required for movements to the individual tar
117 ined the adaptation of hand trajectories and grip forces when moving grasped objects with novel dynam
118 tracking task, we show that tracking errors, grip forces, and learning curves are consistent with pre
121 ntly associated with waiting list mortality: grip (hazard ratio = 0.89, 95% confidence interval 0.83-
122 ly, transcription of lncRNAs could serve as "grip holds" for nuclear proteins to pull the genome into
126 of finger muscles during precision and power grip in humans but the neural mechanisms involved remain
127 ts demonstrate that the control of precision grip in humans involves premotoneuronal subcortical mech
130 These results show that a minimum level of grip is necessary before the upper limb plays an active
131 results demonstrate that a minimum level of grip is required before the upper limb becomes active in
132 y for forceful precision and power "squeeze" gripping is linked to two key evolutionary transitions i
136 Taken together, these results indicate that GRIP may modulate addictive phenotypes through its regul
137 anoacrylate glue (Histoacryl, n = 216), self-gripping mesh (Parietex ProGrip, n = 202), or convention
143 hy) environmental stresses, have an integral grip on cell fate, and have shaped the ecological succes
145 Ps on processivity are overcome by the extra grip on DNA provided by the lagging strand polymerases.
147 ence that they function by weakening gp120's grip on gp41 rather than by altering gp120 binding to sp
148 mechanism, the kinetochore can modulate its grip on microtubules over mitosis and yet retain its abi
150 eir unusually straight bill enables a stable grip on tools, and raises the tool tip into their visual
151 pull-ups with the body suspended by the arms gripped on a bar; 3) sit-ups in which the upper and lowe
152 32 degrees C allowing them to spontaneously grip onto tissue when introduced from a cold state into
153 d discrete adhesion sites which can be in a "gripping" or "slipping" mode and integrates the adhesion
155 rget object: using a precision grip, a power grip, or touching the object without hand preshaping.
157 al inguinal hernia were randomized to a self-gripping polyester mesh or a sutured polyester mesh.
164 selectivity in single cells was as strong as grip selectivity, indicating that V6A cells were able to
166 tion, lung function, physical capacity (hand grip, step test, and physical activity), and blood marke
168 ates information related to object shape and grip strategy as it becomes available, revealing a trans
169 >/=30) in the lowest tertile of sex-specific grip strength (<35.3 kg for men and <19.6 kg for women).
170 0.26 kg, P < 0.001; 11 studies, n = 308) and grip strength (5.3%, P < 0.050; 4 studies, n = 156), whi
173 .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
174 nce intervals -16.786 to -4.482) decrease in grip strength (kg force) (P < 0.001) and -8.74 (95% conf
175 articipants viewing TV >/= 6 hrs/d had lower grip strength (Men, B = -1.20 kg, 95% CI, -2.26, -0.14;
176 ast, internet use was associated with higher grip strength (Men, B = 2.43 kg, 95% CI, 1.74, 3.12; Wom
177 Participants with CMT2A had the weakest grip strength (P < .05), while those with CMT2A and CMT4
178 (P = .03) and B (P = .05), right-sided Jamar grip strength (P = .02), Rapid Pace Walk (P = .03), Brak
181 ss index (Spearman r=0.28, P<0.0001), weaker grip strength (Spearman r=-0.34, P<0.01), and slower wal
182 Ab levels were significantly correlated with grip strength (Spearman r=-0.57, P<0.005), walking speed
183 sed risk (95% CI, 1%-23%) of developing weak grip strength and a 14% decreased risk (95% CI, 8%-20%)
184 ulted in significant improvement in hindlimb grip strength and a 30% decrease in inflammation in the
185 idisciplinary expert team measured patients' grip strength and assessed their predicted mobilization
186 ligible patients had low performance on hand grip strength and chair rise tests, tested with the proc
187 decline in normalized forelimb and hindlimb grip strength and declines in in vitro EDL force after r
188 observed for cardiovascular mortality.Lower grip strength and excess adiposity are both independent
189 th performance; those in the lowest fifth of grip strength and highest fifth of BMI having particular
190 ured using dual energy x-ray absorptiometry; grip strength and information on lifestyle indicators, i
193 havioral (Digiscan) and functional outcomes (grip strength and Rotarod) were assessed prior to sacrif
194 to reduce the likelihood of developing weak grip strength and slow walking speed because purpose has
196 ted with a decreased risk of developing weak grip strength and slow walking speed, although the findi
197 nsight into the mechanistic underpinnings of grip strength and the causal role of muscular strength i
199 icantly increased body weight, lean mass and grip strength by 60-80% over vehicle-treated mdx mice.
200 demonstrated improved downward climbing and grip strength compared with those given vehicle, though
201 9; 95% CI, 0.83-0.95), but associations with grip strength did not reach conventional levels of stati
203 complex to calcium improves muscle force and grip strength immediately after administration of single
211 ded hindlimb and forelimb muscle strength by Grip Strength Meter and quantitative muscle fibrosis par
218 .03), appendicular skeletal muscle mass, and grip strength than did controls, but these differences w
226 er 3 months on the waiting list: -0.38 kg in grip strength, -0.05 meters/second in gait, 0.03 seconds
227 e we examine the morphological correlates of grip strength, a defensive combat trait involved in mate
228 ivation of the Col12a1 gene showed decreased grip strength, a delay in fiber-type transition and a de
230 ge, sex, race, cognition, comorbidities, and grip strength, AMD subjects showed an increased likeliho
233 hy Impairment Score of the Lower Limbs, hand grip strength, and evaluation of vegetative dysfunction,
235 -min walking distance, fast gait speed, hand grip strength, and isometric leg extension strength).
236 ipants were stratified by country, age, hand grip strength, and performance on the chair rise test, a
238 otor functions, including breathing pattern, grip strength, balance beam and rotarod performance.
240 r adults in the home, body mass index (BMI), grip strength, cognitive ability, mood, or comorbid illn
241 walk, 5 chair stands, standing balance, and grip strength, each scored from 0 to 4 (0, unable to per
242 but other measurements of strength (forelimb grip strength, ex vivo measurements of contractile funct
243 ds ratio = 2.43; 95% CI, 1.17-5.03) and poor grip strength, exhaustion, and slowed walking speed (haz
244 ailty was measured on a scale from 0 to 5 by grip strength, gait speed, exhaustion, shrinkage, and ph
245 (HDL) cholesterol, forced expiratory volume, grip strength, HbA1c, longevity, obesity, self-rated hea
246 mmonia, increase in lean body mass, improved grip strength, higher skeletal muscle mass and diameter,
247 Truncal flexion and extension strength, hand grip strength, leg extension power, and quality of life
249 -appearing brain was associated with: weaker grip strength, poorer lung function, slower walking spee
251 3 weeks after stroke on locomotor activity, grip strength, sensory neglect, gait impairment, motor c
252 ced vital capacity, resting heart rate, hand grip strength, sit and reach distance, and time standing
253 or more of the following 5 components: weak grip strength, slowed walking speed, poor appetite, phys
254 ures of physical capability at age 53 years: grip strength, standing balance, and chair-rise time.
255 ms and four measures of physical capability: grip strength, timed walk or get up and go, chair rises
257 ate the genetic determinants of variation in grip strength, we perform a large-scale genetic discover
258 , 2.17) than in those with stable weight and grip strength, with the highest risk in those with both
268 the best hope to curb the HIV-AIDS epidemic gripping sub-Saharan Africa, but it remains elusive.
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 oring of participants' performance of a fine grip task during functional magnetic resonance neuroimag
273 those with nontremor-dominant PD performed a grip task, and the results obtained were compared using
274 e was assessed during an auxotonic precision grip task; tremor was quantified using accelerometry dur
276 and beta-chains as tweezers to surround and grip the glucose moiety of GMM, GEM TCRs create a highly
277 e of climbing and supporting their weight by gripping the cage bars with the contralesional hand.
278 lar system, suppressed MEP size during power grip to a lesser extent than during the other tasks and
279 lar system, suppressed MEP size during power grip to a lesser extent than during the other tasks at a
280 manipulating tools, (ii) a strong precision grip to hold tools securely, and (iii) enhanced visually
282 n strength, locally switching adhesions from gripping to slipping and further accelerating actin flow
285 substantially larger when predicting the 20 grip types (planning, 74%; execution, 86%; chance level,
286 te for the first time that a large number of grip types can be decoded from higher cortical areas dur
287 decoding from individual arrays, objects and grip types could be predicted well during movement plann
293 Although the incidence of neurons encoding grips was twofold that of neurons encoding objects, obje
294 aten) mice demonstrated decreased body size, grip weakness, abnormal gait, joint laxity, and early-on
295 ion strength, knee extension power, and hand grip were associated with increased mortality in these p
296 fingers extension-thumb interface and primer grip, which may contribute their stronger inhibition.
297 sion grip with two or five digits, or coarse grip with five digits) and used representational similar
298 gation) and task (passive viewing, precision grip with two or five digits, or coarse grip with five d
299 issue of Blood, Safeukui et al have come to grips with an important issue in red blood cell (RBC) bi
300 dy demonstrates that conditional deletion of GRIP within the nucleus accumbens potentiates cue-induce
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