ライフサイエンスコーパス: extensor

1 No changes occurred in the finger extensor.

2 elbow, wrist, or finger flexors or shoulder extensors.

3 esting reduced corticospinal inputs to elbow extensors.

4 nd knee rotation dominated input to the knee extensors.

5 rating large currents in both ankle and knee extensors.

6 -motor control is common to both flexors and extensors.

7 d flexors and for elbow flexors versus elbow extensors.

8 at different joints, and between flexors and extensors.

9 tends to favour flexor and hand muscles over extensors.

10 t has the gradient: hand muscles > flexors > extensors.

11 muscle strength in hip and knee flexors and extensors.

12 elbow rostrally (C5-C7), along with flexors, extensors, abductors and adductors acting on the digits,

13 ) muscle-dependent effects, we used constant extensor activations in these simulations.

14 and the rhythmic, alternating hip flexor and extensor activities underlying locomotion and scratching

15 Alternation of flexor and extensor activity in the mammalian spinal cord is mediat

16 Alternating flexor and extensor activity represents the fundamental property un

17 ns were accompanied by sustained ipsilateral extensor activity, whereas rhythmic flexor bursting was

18 voluntary motor control of wrist and finger extensors after stroke.

19 in vitro and in vivo have shown that flexor-extensor alternation during locomotion involves two clas

20 anisms make distinct contributions to flexor-extensor alternation in half-center networks.

21 ation of their connectivity providing flexor-extensor alternation in the spinal cord.

22 of these neuron types did not abolish flexor-extensor alternation.

23 ion of V1 interneurons did not affect flexor-extensor alternation.

24 ocomotor rhythm and in organizing flexor and extensor alternation.

25 The V2b interneurons are involved in flexor-extensor alternations in both intact cord and hemicords.

26 They secure flexor-extensor alternations in the intact cord but lose this f

27 e a higher potential to show plasticity than extensors, although only when plasticity is induced by s

28 ce electromyographic signals (EMGs) from the extensor and flexor muscles of the contralateral forearm

29 Results Macroscopically, all extensor and flexor tendons crossing MTP joints demonstr

30 e MEPs recorded from forearm flexor, forearm extensor and intrinsic hand muscles.

31 s measured before and after 12 weeks of knee extensor and plantar flexor muscles' PS training by sing

32 muscle atrophy, and relatively isolated neck extensor and respiratory weakness.

33 Quantitative muscle strength of knee extensor and the IBM functional rating scale seem to be

34 ral extensors, while suppressing ipsilateral extensors and contralateral flexors.

35 Movement kinematics and EMG from the wrist extensors and flexors and sternocleidomastoid muscles we

36 Soleus (ankle extensor) and tibialis anterior (TA, ankle flexor) motor

37 sions confirmed that instantaneous velocity, extensor, and flexor muscle activity had a significant e

38 and elbow extensors, weak to wrist and digit extensors, and almost absent to the intrinsic muscles of

39 mb, knee flexors were relatively weaker than extensors, and plantar extensors were weaker than planta

40 eurons sometimes inhibited the corresponding extensors, and vice versa.

41 specific roles in left-right (V1) and flexor-extensor (both V2b and V1) interactions in the spinal co

42 l pattern in control recordings in which the extensor bursts were longer than the flexor bursts.

43 tions to the flexor carpi radialis (FCR) and extensor carpi radialis (ECR) muscles of right human for

44 erline thickening of the leading edge of the extensor carpi radialis brevis.

45 were significantly reduced in the soleus and extensor carpi radialis muscles at 8-11 weeks.

46 MEPs) and motor threshold were recorded from extensor carpi radialis using transcranial magnetic stim

47 Tenosynovitis of the extensor carpi ulnaris (odds ratio, 3.21) and flexor ten

48 ous disorders, with De Quervain syndrome and extensor carpi ulnaris tendon disorders being the most c

49 ep variability of the EMG, as well as flexor-extensor coactivation.

50 contributes to the high occurrence of flexor-extensor cocontractions in SCI patients.

51 ry show limited functional recovery of elbow extensors compared with elbow flexor muscles, to date, t

52 ot injured during the fascial opening of the extensor compartment.

53 emales experienced lesser reductions in knee-extensor contractile function, and following heavy inten

54 tionship during intermittent, isometric knee extensor contractions.

55 vity shows increased variability, but flexor-extensor coordination is unaffected.

56 Flexor and extensor deletions showed marked asymmetry: flexor delet

57 mic flexor bursting was not perturbed during extensor deletions.

58 Knee-extensors demonstrate greater fatigue resistance in fema

59 i minimi, biceps brachii, tibialis anterior, extensor dig. brevis, abductor hallucis) were measured e

60 on and relaxation times in adult fast twitch extensor digitalis longus muscle.

61 Surprisingly, mdx3cv extensor digitorium longus muscle showed significantly h

62 ntric contraction-induced injury than mdx4cv extensor digitorium longus muscle.

63 nt forces of single motor units in the human extensor digitorum and tibialis anterior during repetiti

64 ed on the basis of the preservation of their extensor digitorum brevis (EDB) muscle seen on MRI and t

65 al gastrocnemius, soleus, tibialis anterior, extensor digitorum brevis and flexor digitorum brevis.

66 0(1)(1) vector genomes) was delivered to the extensor digitorum brevis muscle of 3 subjects with docu

67 ial using rAAV1.tMCK.hSGCA injected into the extensor digitorum brevis muscle was conducted.

68 The extensor digitorum communis (EDC) is a multi-compartment

69 es: flexor digitorum superficialis (FDS) and extensor digitorum communis (EDC).

70 Single myofiber analysis of fast-contracting extensor digitorum longus (EDL) and slow-contracting sol

71 s of these isoforms different in fast-twitch extensor digitorum longus (EDL) and slow-twitch soleus (

72 ected in force or fatigue assays of isolated extensor digitorum longus (EDL) and soleus (SOL) muscles

73 Contractile function of intact extensor digitorum longus (EDL) and soleus muscles from

74 e found that prior in situ contraction of m. extensor digitorum longus (EDL) and treadmill exercise i

75 extensor digitorum longus (EDL) and treadmill exercise i

76 Extensor digitorum longus (EDL) fibre bundles obtained f

77 It is shown that in both rat and mouse extensor digitorum longus (EDL) fibres, action potential

78 sphorylation and glucose transport in murine extensor digitorum longus (EDL) muscle (+121%, +164% and

79 letal muscle fibre bundles obtained from the extensor digitorum longus (EDL) muscle of adult mice.

80 Na,K-ATPase active transport in the isolated extensor digitorum longus (EDL) muscle of alpha2(R/R) mi

81 ) inhibition and lactate accumulation in the extensor digitorum longus (EDL) muscle of rats infused w

82 on in skeletal muscle using an incubated rat extensor digitorum longus (EDL) muscle preparation as a

83 Rat extensor digitorum longus (EDL) muscle was incubated wit

84 ulated glucose transport in mouse soleus and extensor digitorum longus (EDL) muscle.

85 nd increased insulin signaling in soleus and extensor digitorum longus (EDL) muscles from rats fed a

86 train/120 s contraction interval <0.002) rat extensor digitorum longus (EDL) muscles in vitro (95% N2

87 rior (TA) muscle or after transplantation of extensor digitorum longus (EDL) muscles into nude mice.

88 Additionally, incubation of isolated mouse extensor digitorum longus (EDL) muscles with 2 mM AICAR

89 a different ontology, comparing those of the extensor digitorum longus (EDL) of the limb with satelli

90 The extensor digitorum longus (EDL) was isolated from stimul

91 Rat extensor digitorum longus (EDL) was overloaded by (a) ex

92 ction in functional capillary density in the extensor digitorum longus (EDL), and assessed acute and

93 into the slow-twitch soleus and fast-twitch extensor digitorum longus (EDL)muscles, activation of in

94 soleus (Sol; slow-twitch fibre dominant) and extensor digitorum longus (EDL; fast-twitch fibre domina

95 use muscle by 55% in soleus and by 20-58% in extensor digitorum longus (EDL; P < 0.01).

96 skeletal muscles, including soleus (P<0.01), extensor digitorum longus (EDL; P<0.001), and tibialis a

97 ttermates: the soleus (S and FR MU); and the extensor digitorum longus (FF MU).

98 mitant with increased glucose transport into extensor digitorum longus and gastrocnemius muscle.

99 We measured extensor digitorum longus and soleus muscle forces, fati

100 Extensor digitorum longus and soleus muscles of MSTN(Del

101 stasis; the resting intracellular calcium of extensor digitorum longus and soleus muscles of SHRs wer

102 no acid metabolism.Ex vivomuscle function in extensor digitorum longus and soleus muscles, including

103 antibody at 160 kDa in tibialis anterior and extensor digitorum longus but not soleus muscles.

104 ater (n = 8) as above, and kidney, heart and extensor digitorum longus muscle (EDL) and soleus muscle

105 l times faster in actively contracting mouse extensor digitorum longus muscle (EDL) than soleus (SOL)

106 e uptake partly relies on PAK2 in glycolytic extensor digitorum longus muscle By contrast to previous

107 in skMLCK protein expression in fast-twitch extensor digitorum longus muscle containing type IIa and

108 Insulin-stimulated glucose uptake in extensor digitorum longus muscle during the euglycemic-h

109 Absolute force production of the extensor digitorum longus muscle ex vivo was higher in m

110 ntractile characteristics were determined in extensor digitorum longus muscle ex vivo.

111 ferents were recorded from an isolated mouse extensor digitorum longus muscle in the absence of gamma

112 was slightly reduced in isolated glycolytic extensor digitorum longus muscle lacking PAK2 alone (-18

113 scle physiological analysis reveals that the extensor digitorum longus muscle of transgenic mice exhi

114 mal tetanic stimulation frequency, intact KO extensor digitorum longus muscle was able to produce wil

115 Twenty-four hours after trauma, the extensor digitorum longus muscle was microsurgically exp

116 indle afferent responses from isolated mouse extensor digitorum longus muscle were recorded in the ab

117 femoral blood flow (FBF) and tension in the extensor digitorum longus muscle were recorded; isometri

118 LC phosphorylation and force potentiation in extensor digitorum longus muscle with low frequency elec

119 ific force of contraction of the fast-twitch extensor digitorum longus muscle yet had no effect on th

120 and in vitro contraction measurements of the extensor digitorum longus muscle.

121 zed myofilament Ca(2+) sensitivity of the KO extensor digitorum longus muscle.

122 ere not detected in non-atrophic fast-twitch extensor digitorum longus muscle.

123 r ischemia-induced obliteration in the mouse extensor digitorum longus muscle.

124 29%; P<0.05), increased protein synthesis in extensor digitorum longus muscles (13.21 +/- 1.09%; P<0.

125 alpha2(-/-) muscles is reproduced in control extensor digitorum longus muscles by selectively inhibit

126 ulated glucose transport in mouse soleus and extensor digitorum longus muscles ex vivo.

127 nimals were terminally anaesthetized and the extensor digitorum longus muscles from both hindlimbs we

128 lso be hyperactivated in O vs YA fast-twitch extensor digitorum longus muscles from Fischer(344) x Br

129 mpletely restore the function of fast-twitch extensor digitorum longus muscles in dystrophic mdx mice

130 ndles of fibres were manually dissected from extensor digitorum longus muscles of 7- to 14-week-old m

131 rce that was not observed in the fast-twitch extensor digitorum longus muscles of R58Q vs. wild-type-

132 Isolated mutant extensor digitorum longus muscles were abnormally sensit

133 ane potential (RMP) in uninjured and injured extensor digitorum longus muscles were made to determine

134 muscles (SOL) with no effect on fast twitch extensor digitorum longus muscles.

135 ylation among soleus, tibialis anterior, and extensor digitorum longus muscles.

136 I/type II only in SOL muscles but not in the extensor digitorum longus muscles.

137 ic range at higher temperatures in murine M. extensor digitorum longus single fibers.

138 studied mouse living slow (soleus) and fast (extensor digitorum longus) muscle fibers in situ and det

139 minals in a subset of NMJs in ankle flexors, extensor digitorum longus, and tibialis anterior.

140 dx mice, but similar force generation in the extensor digitorum longus.

141 gonistic muscles (right flexor digitorum and extensor digitorum) together with 64-channel electroence

142 s of fictive locomotion that were flexor vs. extensor dominated, demonstrating that asymmetric lockin

143 tion in an opposing manner to control flexor-extensor-driven movements.

144 mediated by lesser deoxygenation of the knee extensors during exercise.

145 group of neurons that were coactivated with extensors during PLRs before RS and exhibited a dramatic

146 % of peak work-rate) using a single-leg knee-extensor ergometer situated inside the bore of a 1.5 T s

147 nd during two workloads of steady-state knee-extensor exercise (7 W and 27 W).

148 Six men performed bilateral knee-extensor exercise (estimated to require 110% peak aerobi

149 eletal muscle VO2 max during single leg knee extensor exercise (KE VO2 max , direct Fick by femoral a

150 sessed at peak effort during single-leg knee-extensor exercise (KE), where ventilation is assumed to

151 ticipants performed two-legged isolated knee-extensor exercise at 20 +/- 1 W ( approximately 50% maxi

152 ate days: one day with prior one-legged knee-extensor exercise to local exhaustion (~2.5 h) and anoth

153 young male subjects, 1 h of one-legged knee-extensor exercise was followed by 7 h of saline or intra

154 y men during (1) incremental one-legged knee-extensor exercise, (2) step-wise femoral artery ATP infu

155 g of the torque signal during isometric knee extensor exercise.

156 d) and eight controls during single-leg knee-extensor exercise.

157 ectively) equalled those during maximal knee-extensor exercise.

158 r MRC score) in thumb abductors versus elbow extensors, for hand extensors versus hand flexors and fo

159 equalization of the duty cycle in flexor and extensors from an asymmetrical pattern in control record

160 OA patients showed reduced (P < 0.01) knee extensor function.

161 nfiltration (MFI) of the deep cervical spine extensors has been observed in cervical spine conditions

162 nstant task of raising the foot, whereas the extensors have the more variable task of support and pro

163 Extensor imagination with TMS increased MEPs in extensor

164 ema or atrophy within muscles (supinator and extensors) innervated by the posterior interosseous nerv

165 nd V2b neuron populations involved in flexor-extensor interactions on each cord side.

166 d to make them critically involved in flexor-extensor interactions.

167 Flexor and extensor involvement was documented for each joint.

168 Knee extensor (KE) torque, voluntary activation (VA), cross-s

169 xors [PF], 62% vs 78% vs 89%; P < .001; knee extensors [KE], 73% vs 95% vs 93%; P < .001).

170 gated localization of damage within the knee extensors (KEs) and plantar flexors (PFs) induced by dow

171 Demographic data and extensor mechanism features were compared, including tro

172 mic gamma-motor firing patterns in the ankle extensor medial gastrocnemius (MG) have therefore been r

173 dinosus (ST), and from the heel to the ankle extensor medial gastrocnemius (MG), has been studied dur

174 eral L5, which contains many of the hindlimb extensor MNs activated by the LVST.

175 or and extensor moment arms, and an existing extensor model to simulate FT joint swing.

176 and older men during two-legged dynamic knee-extensor moderate-intensity exercise, as well as changes

177 We combined these data, the flexor and extensor moment arms, and an existing extensor model to

178 ably reduced the excessive stance-phase knee extensor moment present during crouch gait by a mean of

179 ionally, persons with TTA had a reduced knee extensor moment relative to uninjured persons (P < 0.001

180 extensor muscle group I afferents increases extensor motoneurone activity and prolongs the extensor

181 alternating rhythmic activity of flexor and extensor motoneurones in the absence of rhythmic input a

182 cuits controlling the activity of flexor and extensor motoneurones.

183 Extensor motoneurons are densely innervated by 5-HT and

184 tic electrophysiological parameters in ankle extensor motoneurons in nontrained and treadmill-trained

185 s, here we show that dendritic PICs in ankle extensor motoneurons in the cat are reduced about 50% by

186 birth, almost all ( approximately 80%) ankle extensor motoneurons recorded in whole-cell configuratio

187 ed the rhythmic synaptic drive to flexor and extensor motoneurons, increased the spiking in each cycl

188 ll organization was clearly present in ankle extensor motoneurons, producing increased peak-to-peak m

189 2, which is 2.3- and 1.4-fold less than neck extensor motoneurons.

190 ways differentially control elbow flexor and extensor motoneurons; therefore, it is possible that reo

191 ttern generator (CPG) that coordinate flexor-extensor motor activity.

192 ng that they can generate alternating flexor-extensor motor neuron firing in the absence of glutamate

193 r and intrinsic hand muscles, not in forearm extensor motor neurons.

194 for the production of an alternating flexor-extensor motor output.

195 tended to be focused for the ankle and knee extensor motor pools studied.

196 that the production of an alternating flexor-extensor motor rhythm depends on the composite activitie

197 engthening of connections to flexor, but not extensor, motor neurons mirrors the extensor weakness an

198 During swing, the FT joint extensor muscle actively shortens and the flexor muscle

199 Knee extensor muscle activity decreased slightly during exosk

200 Pairing stimulation of a finger flexor or extensor muscle at the motor point with transcranial mag

201 Rectified forearm extensor muscle EMG and physiological hand tremor were r

202 in), the peak expiratory flow (11%), and the extensor muscle exercise capacity (464 J).

203 afferents appear to determine the pattern of extensor muscle firing.

204 r phase of fictive locomotion, activation of extensor muscle group I afferents increases extensor mot

205 ees of motoneurons innervating a dorsal neck extensor muscle, splenius, in the adult cat are densely,

206 ied model system: the locust hind leg tibial extensor muscle.

207 rin function disrupts the limb trajectory of extensor-muscle-innervating motor axons the guidance of

208 sociated with an increased activation of leg extensor muscles (medial and lateral gastrocnemius, vast

209 fat infiltration (MFI) in the deep cervical extensor muscles (multifidus and semispinalis cervicis)

210 tance (P<0.02), the strength testing of knee extensor muscles (P=0.008), and the ventilatory threshol

211 ymmetrical recovery between elbow flexor and extensor muscles after cervical spinal cord injury.

212 pinal cord MN pools for lower leg flexor and extensor muscles and the electromyograms (EMGs) of the c

213 duce the excessive burden placed on the knee extensor muscles as measured by knee moments.

214 Reciprocal activation of flexor and extensor muscles constitutes the fundamental mechanism t

215 t reduced the rate of fatigue for six lumbar extensor muscles during leaning.

216 ordinated contraction of antagonistic flexor-extensor muscles in the adult, indicating that accurate

217 comotion, alternating activity of flexor and extensor muscles is largely regulated by a spinal neuron

218 ansplantation involved all of the flexor and extensor muscles of the forearm.

219 ensor imagination with TMS increased MEPs in extensor muscles only.

220 this perturbation suggested that distal leg extensor muscles play a key role in stabilisation.

221 erial properties of tendons from k-rat ankle extensor muscles to those of similarly sized white rats.

222 g the pathway transynaptically from hindlimb extensor muscles using rabies virus (RV).

223 uscles, while the EMG activity of all finger extensor muscles were modulated in a similar way across

224 t coordination and alternation of flexor and extensor muscles.

225 the end of swing in all proximal and distal extensor muscles.

226 flexors and, to a much lesser extent, elbow extensor muscles.

227 from right ankle dorsiflexor and right wrist extensor muscles.

228 ontraction of heteronymous (elbow flexor and extensor) muscles compared with a unilateral contraction

229 d unilaterally or independently in flexor or extensor networks.

230 of high-energy phosphates and pH in the knee extensors of seven young (22.7 +/- 1.2 years; six women)

231 biarticular hamstrings and gastrocnemius are extensors of the lower limb.

232 muscle groups were hip and knee flexors and extensors on strength testing.

233 ry light responses, corneal reflexes, and an extensor or absent motor response at Day 3 after cardiac

234 (absent corneal reflex, absent cough reflex, extensor or absent motor response, and an oxygenation in

235 eflex (4.16, 1.79-9.70; p=0.0009; 2 points), extensor or absent motor responses (2.99, 1.22-7.34; p=0

236 f V1 interneurons suppressed both flexor and extensor oscillations.

237 Leucine protected knee extensor peak torque (CON compared with LEU group: -15%

238 d-dependent asymmetric changes of flexor and extensor phase durations.

239 During the extensor phase of fictive locomotion, activation of exte

240 This extensor phase prolongation may occur with or without a

241 tles if the tap occurred during the swim hip extensor phase.

242 tensor motoneurone activity and prolongs the extensor phase.

243 as reduced or eliminated during the swim hip extensor phase.

244 ospinal tract signs were frequent, including extensor plantar reflexes and/or diffuse tendon reflexes

245 , marked pyramidal signs including bilateral extensor plantar reflexes, occasionally spasticity, and

246 development for all muscles (knee flexor and extensor, plantar and dorsiflexor) increased from pre- t

247 for a Glasgow Coma Scale motor score showing extensor posturing or worse (false-positive rate, 0.09;

248 overvalued, such as absent motor response or extensor posturing, which 87% of respondents considered

249 .07) and 11% (P<0.05) increases in peak knee extensor power at the 2 highest movement velocities test

250 in the medial portions of the deep cervical extensors regardless of WAD recovery, but the magnitude

251 ic activation of V2b interneurons suppressed extensor-related activity, while similar activation of V

252 chronous pattern of L2 flexor-related and L5 extensor-related locomotor activity.

253 eal a bias in the innervation of flexor- and extensor-related motor neurons by V1 and V2b INs that li

254 r limb flexor muscles show good recovery but extensors remain weak, with this being a major contribut

255 rons representing left and right, flexor and extensor rhythm-generating centers interacting via commi

256 activation of flexor (tibialis anterior) and extensor (soleus) muscles associated with a fixed-trajec

257 Knee extensor strength and H:Q ratio at baseline significantl

258 Knee extensor strength and work output during 30 maximal isok

259 strength by 119%, chair stands by 30%, knee extensor strength by 25%, arm curls by 23%, and walk tim

260 Isometric knee extensor strength declined to a greater extent in IMB (-

261 untary contractions held at 25% maximal knee extensor strength in 22 young (mean +/- SD, 25.3 +/- 4.8

262 y OA, higher body mass index, and lower knee extensor strength independently increased the risk of tr

263 Neither knee extensor strength nor the H:Q ratio was predictive of in

264 lowest tertile, the highest tertile of knee extensor strength protected against development of incid

265 The primary outcome was maximal knee extensor strength; secondary outcomes were muscle power

266 h V1 and V2b interneurons resulted in flexor-extensor synchronization, whereas selective inactivation

267 n of only V2b interneurons led to the flexor-extensor synchronization, while inactivation of V1 inter

268 and low strain rarely injured common digital extensor tendon (CDET) in a group of horses with a wide

269 ammation in the collateral ligaments and the extensor tendons and more severe changes at the correspo

270 d bodies were examined at flexor tendons and extensor tendons for the presence and course of tendon s

271 Moreover, a subset of extensor tendons initially form as fused structures due

272 d OR of 3.1 (95% CI: 1.9, 5.2; P < .001) for extensor tendons.

273 synovitis and 0.15, 0.98, 0.63, and 0.86 for extensor tenosynovitis, respectively.

274 n produced larger synaptic currents in ankle extensors than knee or hip rotations and knee rotation d

275 its synaptic drive to a leg motoneuron, fast extensor tibiae (FETi), always had the same maximum ampl

276 bodies located close to the soma of the fast extensor tibiae motoneuron likely belong to strand recep

277 gs from an identified motor neuron, the fast extensor tibiae motor neuron, show increased spike laten

278 leg kick force, produced by stimulating the extensor tibiae muscle, was reduced following exposure,

279 ese neurons are responsible for reduction of extensor tone and postural reflexes during spinal shock.

280 pinal shock, that is a dramatic reduction of extensor tone and spinal reflexes, including PLRs.

281 The passive calf muscles provided: (i) an extensor torque capable of sustaining unstable balance w

282 During human standing, tonic ankle extensor torque is required to support the centre of mas

283 eton designed to provide appropriately-timed extensor torque to the knee joint during walking in a mu

284 dly demonstrated a 15% increase in peak knee extensor torques within the first five MVEs with minimal

285 b abductors versus elbow extensors, for hand extensors versus hand flexors and for elbow flexors vers

286 (reduction in mechanical power) of the knee extensors was closely associated with a greater accumula

287 r unit mass of muscle in the exercising knee extensors was greater in the older (12.5 +/- 6.2 ml min(

288 erse phase, so that recruitment of the wrist extensors was minimized.

289 od flow heterogeneity in the exercising knee extensors was significantly lower in the older (56 +/- 2

290 (reductions in mechanical power) of the knee extensors was ~1.8-fold greater with age and was accompa

291 retch of the loaded antagonist muscle (i.e., extensor) was accompanied by increased afferent firing r

292 urons innervating shoulder muscles and elbow extensors, weak to wrist and digit extensors, and almost

293 but not extensor, motor neurons mirrors the extensor weakness and flexor spasm which in neurological

294 dysarthria, dysphagia, tongue atrophy, neck extensor weakness, and weakness of jaw closure during a

295 eal and distal distribution, including wrist extensor weakness, finger and foot drop, scapular wingin

296 elatively weaker than extensors, and plantar extensors were weaker than plantar flexors.

297 ighest levels of activity observed in finger extensors when the wrist was extended.

298 The coactivation period of leg flexors and extensors, which is used to store the energy required fo

299 itated ipsilateral flexors and contralateral extensors, while suppressing ipsilateral extensors and c

300 -five subjects completed 100 ECs of the knee extensors with 1 leg, and muscle biopsies were taken fro