ライフサイエンスコーパス: soleus

1 nhanced insulin-stimulated glucose uptake in soleus.

2 re types with the greatest loss (55%) in the soleus.

3 iglyceride glycerol in the gastrocnemius and soleus.

4 p-regulation of fast-twitch fiber program in soleus.

5 much higher extent than was observed in the soleus.

6 w fibers was increased in PLN-overexpressing soleus.

7 inase 4 mRNA abundance in the heart, EDL and soleus.

8 The same was observed for ccl9 and cxcl13 in soleus.

9 relaxed skeletal muscle sarcomeres from rat soleus.

10 alpha (PGC1alpha) were investigated only in soleus.

11 )) were 0.034 +/- 0.001 and 0.064 +/- 0.001 (soleus), 0.031 +/- 0.001 and 0.060 +/- 0.001 (vastus), a

12 The lipid content of both the soleus (2.99 +/- 0.37 g/dL) and the MHG (3.80 +/- 0.68 g

13 s on slow fibers, precedes wasting of mutant soleus; (3) denervation is likely to drive this wasting,

14 trocnemius (24 +/- 5 versus 21 +/- 2) or the soleus (54 +/- 6 versus 70 +/- 7).

15 cific insulin-stimulated glucose uptake (71% soleus, 58% gastrocnemius) and peripheral glucose cleara

16 3 +/- 4% (mean +/-s.e.m.) of total fibres in soleus, 59 +/- 3% in vastus lateralis and 22 +/- 2% in t

17 rocnemius (39 +/- 7 versus 22 +/- 6) and the soleus (98 +/- 13 versus 65 +/- 13).

18 nscription factor, fail to accumulate in the soleus, a slow muscle, compared with fast muscles (e.g.,

19 he liver (where SIRT1 rises) or heart or the soleus, a type I muscle (where SIRT1 is unchanged).

20 ) revealed the surface-recorded amplitude of soleus action potentials was 6% of that of gastrocnemius

21 Changes in soleus activation rate correlated with changes in users'

22 ll seven measured leg muscles (p >= 0.146)), soleus active muscle volume (p = 0.538; d = 0.241), or a

23 type composition (vastus lateralis, triceps, soleus) after an overnight fast and during infusion of a

24 rophy was initiated by bilateral ablation of soleus agonists 1 week before sacrifice.

25 ng) revealed significant differences between soleus and both gastrocnemii across the whole stride cyc

26 ted glucose uptake in mouse muscle by 55% in soleus and by 20-58% in extensor digitorum longus (EDL;

27 Intriguingly, the soleus and diaphragm muscles are spared of any abnormal

28 eventing the loss of function of slow-twitch soleus and diaphragm muscles.

29 Based on the similar findings in soleus and EDL muscles, fibre type does not appear to de

30 eased by 27% (P = 0.1) and 40% (P < 0.05) in soleus and EDL muscles, respectively, of muscle-specific

31 glucose uptake by 100% and 62% (P < 0.01) in soleus and EDL muscles, respectively.

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

33 action-stimulated glucose transport in mouse soleus and extensor digitorum longus (EDL) muscle.

34 ransport, and increased insulin signaling in soleus and extensor digitorum longus (EDL) muscles from

35 nsulin-stimulated glucose transport in mouse soleus and extensor digitorum longus muscles ex vivo.

36 imulated glucose uptake into the slow-twitch soleus and fast-twitch extensor digitorum longus (EDL)mu

37 In humans, during standing the calf muscles soleus and gastrocnemius actively prevent forward toppli

38 vealed that foot strike pattern affected the soleus and gastrocnemius differently.

39 We show that soleus and gastrocnemius do indeed move paradoxically, s

40 uscle hypertrophy by surgically removing the soleus and gastrocnemius muscles in rats.

41 lipid, glucose metabolism and fiber size in soleus and gastrocnemius muscles of aged rats.

42 -stress in the feed arteries perforating the soleus and gastrocnemius muscles.

43 joint which is prevented by activity in the soleus and gastrocnemius muscles.

44 ted to the 21 and 18% decline in V(0) in the soleus and gastrocnemius type I fibres.

45 of ultrasound images to resolve calf muscle (soleus and gastrocnemius) length changes as small as 10

46 eptive information than the active agonists (soleus and gastrocnemius).

47 th a decrease in body fat and an increase in soleus and hepatic fat content (p < 0.05).

48 (P < 0.05) compared to the control, whereas soleus and liver glycogen contents were less (P < 0.01 a

49 affected to the same extent (P > .05) as the soleus and medial gastrocnemius.

50 ty both increased, whereas in the shortening soleus and plantaris (PLN) muscles the increase was sign

51 The morphology of the soleus and quadriceps muscles from MGSKO mice appeared n

52 ections showed gamma2 immunostaining in both soleus and TA motoneurons and astrocytes.

53 gamma2 immunoreactivity on the soma of soleus and TA motoneurons in spinal rats was differentia

54 monitored single motor unit contractions in soleus and vastus lateralis muscles of healthy individua

55 gh significant statistically (triceps versus soleus and vastus lateralis, P < 0.05), were within appr

56 f Bcl-2, HSP70, and Mn-SOD increased in both soleus and ventricle muscles of TR animals when compared

57 We have studied mouse living slow (soleus) and fast (extensor digitorum longus) muscle fibe

58 in weight of the quadriceps, gastrocnemius, soleus, and even the heart itself.

59 s of interest in the tibialis anterior (TA), soleus, and medial head of the gastrocnemius (MHG) muscl

60 time to peak perfusion in the gastrocnemius, soleus, and peroneus muscles, and in the anterior compar

61 or group of hindlimb muscles (gastrocnemius, soleus, and plantaris) were evaluated in mice after comp

62 Soleus (ankle extensor) and tibialis anterior (TA, ankle

63 bly action potentials from gastrocnemius and soleus are represented in surface EMGs detected with dif

64 nsion in the calf muscles (gastrocnemius and soleus) are unlikely to signal postural sways on account

65 Expression of endothelial NOS (eNOS) mRNA in soleus arterioles was unaltered by ageing, whereas eNOS

66 fect how locomotion was produced: it changed soleus burst amplitude and may have induced compensatory

67 H-reflex up-conditioning increased the right soleus burst and corrected the locomotor asymmetry.

68 placement in the tongue, adductor magnus and soleus can be helpful for differential diagnosis.

69 Also in soleus, ccl2, interleukin (il)6, il1beta, and cluster of

70 therapy in heart, quadriceps, diaphragm, and soleus, compared with vector alone.

71 activity without substantial attenuation of soleus crosstalk.

72 rrelated with low tibialis anterior and high soleus EMG with no significant coupling between the anta

73 Anatomical analysis indicated that 50% of soleus end plates were completely denervated 1-4 weeks p

74 licit H-reflex in leg muscles other than the soleus, especially during movement.

75 tractions (strength) of the plantar flexors, soleus evoked V-waves (cortical drive), and H-reflexes w

76 Rat soleus feed arteries were isolated, removed and mounted

77 are shown to be resistant to the decrease in soleus fiber cross-sectional area that results from 10 d

78 e cycling and MgADP release rates in skinned soleus fibers using stochastic length-perturbation analy

79 tion and after substitution into rat skinned soleus fibers.

80 For the soleus, forefoot striking decreased tendon energy storag

81 soleus from either genotype.

82 n did not increase insulin sensitivity in m. soleus from either genotype.

83 a larger increase in HSP70 expression in the soleus, gastrocnemius and lung of the WPH-fed rats than

84 Soleus H-reflex conditioning did not affect the duration

85 Over the 30 sessions, the soleus H-reflex decreased in two-thirds of the DC subjec

86 Further, the soleus H-reflex depression did not vary with the contral

87 ic and antagonistic group I afferents on the soleus H-reflex during imposed sinusoidal hip movements.

88 Specifically, we down-conditioned the soleus H-reflex during the swing-phase of locomotion in

89 e swing phase of walking as observed for the soleus H-reflex elicited by tibial nerve stimulation.

90 In rats in which the soleus H-reflex elicited in the conditioning protocol (i

91 studied the impact of down-conditioning the soleus H-reflex in people with impaired locomotion cause

92 After a baseline period in which soleus H-reflex size was measured and locomotion was ass

93 The soleus H-reflex was also conditioned by medial gastrocne

94 The soleus H-reflex was conditioned by stimulating the commo

95 The soleus H-reflex was evoked every 4 s during bilateral sy

96 In each conditioning session, the soleus H-reflex was measured while the subject was or wa

97 The ipsilateral soleus H-reflex was profoundly depressed in all conditio

98 eciprocal and pre-synaptic inhibition of the soleus H-reflex, respectively.

99 We assessed the soleus H-reflex, shear modulus (ultrasound elastography)

100 ount of inhibition acting on the ipsilateral soleus H-reflex, supporting cross-leg reflex and heteron

101 onditioned increase or decrease in the right soleus H-reflex-and examined an old behavior-locomotion.

102 alateral hip oscillations on the ipsilateral soleus H-reflex.

103 - and post-alpha motoneuronal control of the soleus H-reflex.

104 Furthermore, the PLN-overexpressing soleus had smaller muscle size, mass, and cross-sectiona

105 l selection were differentially expressed in soleus in meldonium vs. control, and a number of cellula

106 expression of class II HDAC proteins in the soleus in vivo.

107 This study compared soleus intramyocellular lipid (IMCL) concentrations afte

108 rrelated with change in the amplitude of the soleus locomotor burst, and the correlation was consiste

109 between three ankle plantar flexor muscles (soleus, medial and lateral gastrocnemius) and quantify t

110 the primary findings from the work on rabbit soleus MHC-II-1.

111 ioning protocol that greatly increased right soleus motoneuron response to primary afferent input, an

112 levels of gamma2 in TA, and lower levels in soleus motoneurons.

113 Furthermore, the soleus motor responses were inhibited during the swing p

114 ll exercise failed to induce PGC-1a fully in soleus muscle (1.9- vs. 2.8-fold; P < 0.05), and in prim

115 -stimulated glucose uptake in isolated mouse soleus muscle (P < 0.001).

116 ontent (+48%, p < 0.001) was observed in the soleus muscle (predominantly type I fibers).

117 are overactivated at disease-resistant NMJs [soleus muscle (SOL)] in SOD1(G37R) mice.

118 ssTnT-deficient soleus muscle also contains significant numbers of small

119 genesis in response to T3 was similar in the soleus muscle and heart of the young and old animals, bu

120 in indirect calorimetry chambers after which soleus muscle and liver were harvested.

121 d in fibres isolated from predominantly slow soleus muscle and maintained for 4 days in culture, we n

122 s PGC-1a mRNA levels (1.5- to 5-fold) in rat soleus muscle and white gastrocnemius muscle and in mous

123 The soleus muscle and, in particular, oxidative fibres were

124 ce, increased m-calpain levels in dystrophic soleus muscle are associated with loss of Tmod1 from the

125 required for flow-induced vasodilatation in soleus muscle arterioles from young and old rats.

126 ) and l-arginine content, were determined in soleus muscle arterioles.

127 nitric oxide (NO)-mediated vasodilatation of soleus muscle arterioles.

128 sodilatation and levels of NO and O(2)(-) in soleus muscle arterioles.

129 n in endothelium-dependent vasodilatation in soleus muscle arterioles.

130 Counts of motor units to the soleus muscle as well as of axons in the soleus muscle n

131 Added foot stiffness also altered soleus muscle behaviour, leading to greater peak force (

132 NAs regulating fuel selection was altered in soleus muscle by meldonium, highlighting the modulation

133 Na(+) and Cl(-) were quantified in the soleus muscle by using three phantoms that contained 10-

134 The KO animals also exhibited soleus muscle cell hypertrophy and a 2.5-fold increase i

135 ucose oxidation and metabolic flexibility in soleus muscle cells from ABA-treated mice with DIO.

136 , with comparable expressions in slow-twitch soleus muscle containing type I and IIa fibers.

137 and measure how exoskeleton stiffness alters soleus muscle contractile dynamics and shapes the user's

138 Surprisingly, overexpression of skMLCK in soleus muscle did not recapitulate the fast-twitch poten

139 cluded the use of ultrasonography to examine soleus muscle dynamics in vivo.

140 Not surprisingly, T32KO soleus muscle expressed an elevated type I slow myosin i

141 Permeabilized rat soleus muscle fibers were subjected to rapid shortening/

142 During the unloading period, soleus muscle fibre cross-section decreased by 38%.

143 3.0 T of L4 for bone marrow fat content, of soleus muscle for intramyocellular lipids (IMCL), and li

144 We measured extensor digitorum longus and soleus muscle forces, fatigue, and contractile kinetics

145 skeletal muscle because ex vivo exposure of soleus muscle from chow-fed lean mice to compound A incr

146 lated glucose uptake is elevated in isolated soleus muscle from Hfe(-/-) mice (p < 0.03).

147 sitivity and reduced proinflammatory tone in soleus muscle from obese Zucker rats fed a 2DG-supplemen

148 nNOS gene expression in atrophic slow-twitch soleus muscle from the mouse leg.

149 hronic hypoxia and pulmonary inflammation on soleus muscle hypertrophic capacities, we challenged mal

150 ype 1 skeletal muscle fibers, we studied the soleus muscle in mice genetically deficient for myofiber

151 Using a rat strain whose soleus muscle is innervated by two nerves, we chronicall

152 tion profile of sMyBP-C in mouse slow-twitch soleus muscle isolated from fatigued or non-fatigued you

153 Slow oxidative soleus muscle maintained muscle mass, whereas fast glyco

154 the soleus muscle as well as of axons in the soleus muscle nerve showed no loss of motor neurons.

155 reased the proportion of fast-type fibers in soleus muscle of both control and LLC-bearing mice.

156 tor binding protein, was up-regulated in the soleus muscle of high sucrose diet (HSD) induced insulin

157 creased the proportion of fast-type fiber in soleus muscle of mice.

158 ne whether electrotransfer of Hsp27 into the soleus muscle of rats, prior to skeletal muscle disuse,

159 mid-mediated overexpression of Hsp70, in the soleus muscle of rats, was sufficient to regulate specif

160 ed alterations of calcium homeostasis in the soleus muscle of SHRs occurred with changes of some func

161 chain (MHC) phenotype are observed in EDL or soleus muscle of the FKBP12-deficient mice, but diaphrag

162 irst-order arterioles were isolated from the soleus muscle of young (6 months old) and old (24 months

163 As exoskeleton stiffness increased, the soleus muscle operated at longer lengths and improved ec

164 hronic exercise training (6 weeks) increased soleus muscle PGC-1a mRNA levels ( approximately 25%) an

165 The soleus muscle PGC-1a response to chronic exercise was al

166 ed to study how myosin activators may affect soleus muscle relaxation.

167 e physically active than respective GC while soleus muscle showed expected atrophy.

168 The atrophy of the soleus muscle was reduced in the laser treated rats.

169 Soleus muscle was taken for measurement of mitochondrial

170 Soleus muscle was used to determine maximal rates of ATP

171 Thus, we measured body and soleus muscle weight, food intake, and diaphragm contrac

172 tion task, the H-reflexes were evoked on the soleus muscle when the amplitude of the APA exceeded 10-

173 ivities were derived specifically within the soleus muscle with PET images and magnetic resonance ima

174 t insulin sensitivity was improved in heart, soleus muscle, adipose tissue, and liver of BTBR SCD1-de

175 ease in the time to peak T2* measured in the soleus muscle, and (3) a prolongation of the posterior t

176 ional assessments of TAG levels in serum and soleus muscle, hepatic levels of adenosine triphosphate,

177 In the soleus muscle, however, which were richer in nuclei, pos

178 In isolated soleus muscle, recombinant CTRP1 activated AMPK signalin

179 ression by 80% and 154% in the plantaris and soleus muscle, respectively.

180 , whereas Tmod4 additionally disappears from soleus muscle, resulting in thin filament length increas

181 However, in the treated mdx soleus muscle, the percentage of slow fibers was signifi

182 In soleus muscle, we reported a greater capacity to cultiva

183 y observable in the non-weight-bearing (NWB) soleus muscle, which undergoes a slow-to-fast fiber type

184 and white gastrocnemius muscle and in mouse soleus muscle, which was prevented by pretreatment with

185 aracterized the resulting changes in in vivo soleus muscle-tendon mechanics using ultrasonography.

186 ficantly reduced the tolerance to fatigue in soleus muscle.

187 d concentrations of TAG in liver, serum, and soleus muscle.

188 used male rats and induced an injury of the soleus muscle.

189 nd mitochondrial biogenesis in the oxidative soleus muscle.

190 in mitochondria isolated from the liver and soleus muscle.

191 and Akt (Ser(473) and Thr(308)) in liver and soleus muscle.

192 diated increases of the same antioxidants in soleus muscle.

193 or (BDNF) in both the lumbar spinal cord and soleus muscle.

194 muscle yet had no effect on the slow-twitch soleus muscle.

195 ary densities (angiogenesis) in the ischemic soleus muscle.

196 requency in the measured oscillations of the soleus muscle; one of the main human ankle plantar flexo

197 peed (p = 0.002) of the major plantarflexor (Soleus) muscle, indicating a shift in its force-velocity

198 contractile force (30%) in adult slow twitch soleus muscles (SOL) with no effect on fast twitch exten

199 ated glucose uptake in tibialis anterior and soleus muscles and brown adipose tissue, suggesting that

200 an index of vasoconstriction in slow-twitch soleus muscles and fast-twitch extensor digitorum longus

201 ections did not affect macrophage numbers in soleus muscles at 2 days of reloading, macrophages were

202 tion in fast-twitch muscle were activated in soleus muscles by treatment with the nitric oxide (NO) d

203 Overexpression of dominant negative Nedd4 in soleus muscles completely reversed the unloading-induced

204 t confirmed increased mRNA expression in rat soleus muscles due to 1-14 days of hind limb unloading.

205 In both mdx and mdx/mTR mice, both TA and soleus muscles exhibit normal localization of alpha-acti

206 f intact extensor digitorum longus (EDL) and soleus muscles from Mtm1delta4 mice, which produce no my

207 vation was explored by partially denervating soleus muscles in mice lacking presynaptic NCAM (Hb9(cre

208 HGF significantly enhanced DOGU in mouse soleus muscles in vitro.

209 Fibers (n = 16) were obtained from the soleus muscles of adult male rats and the middle portion

210 Bundles of intact fibres from soleus muscles of adult mice were isolated by dissection

211 Soleus muscles of constitutive Orai-KO mice exhibited a

212 Extensor digitorum longus and soleus muscles of MSTN(Delta/Delta) rats demonstrated 20

213 The soleus muscles of Myo-Cre/Flox-MCIP1 mice fatigued more

214 ies were obtained from the gastrocnemius and soleus muscles of nine International Space Station crew

215 In addition, soleus muscles of SHR showed reduced activity of the sar

216 lar calcium of extensor digitorum longus and soleus muscles of SHRs were differently altered with res

217 In diaphragm and soleus muscles of the knockdown and knockout mouse model

218 expression was elevated in the plantaris and soleus muscles of the trained animals compared to the se

219 mRNA levels increased in both ventricle and soleus muscles of TR animals, and Bax mRNA levels decrea

220 Overexpression of wild-type Nedd4 in soleus muscles of weight bearing rats caused a decrease

221 We observed that MPO-/-soleus muscles showed a significant 52% reduction in mem

222 a dominant negative (d.n.) IKKbeta into rat soleus muscles showed complete inhibition of 7-day disus

223 was measured from the tibialis anterior and soleus muscles together with knee and ankle joint positi

224 d extensor digitorum longus muscle (EDL) and soleus muscles were collected.

225 Rat soleus muscles were electroporated with green fluorescen

226 Subsequently, the gastrocnemius complex and soleus muscles were excised and all feed arteries were c

227 trocnemius, superficial vastus lateralis and soleus muscles were excised at 120 min to determine 2-(3

228 When atrophied soleus muscles were injected intramuscularly with M-CSF,

229 or 12 h, extensor digitorum longus (EDL) and soleus muscles were removed and subjected to a (normally

230 re and capillary density in the fetal TB and soleus muscles, and mRNA levels in the TB of insulin rec

231 months, vastus lateralis, rectus femoris and soleus muscles, from AL-fed rats, had significant muscle

232 le function in extensor digitorum longus and soleus muscles, including peak stress and time to fatigu

233 In soleus muscles, incubation with phenylephrine (PE) or UK

234 Js in partially denervated Hb9(cre)NCAM(flx) soleus muscles, one with high (mature) quantal content,

235 Like the soleus muscles, plantaris muscles from Nfkb1(-/-) and Bc

236 oximately 10 and approximately 12% in TA and soleus muscles, respectively.

237 sites in old wild type and young or old mdx soleus muscles, respectively.

238 ic sites in young fatigued wild type and mdx soleus muscles, respectively.

239 nted ends in both tibialis anterior (TA) and soleus muscles, whereas Tmod4 additionally disappears fr

240 d a decrease in fiber size of weight-bearing soleus muscles, while muscles overexpressing w.t. IKKbet

241 ays of reloading, compared with PBS-injected soleus muscles.

242 lin (450 microU/ml) was measured in isolated soleus muscles.

243 terior and extensor digitorum longus but not soleus muscles.

244 rts tetanic force development in slow twitch soleus muscles.

245 of flexor (tibialis anterior) and extensor (soleus) muscles associated with a fixed-trajectory and a

246 tus lateralis and rectus femoris but not the soleus of AL-fed rats.

247 d mitochondrial biogenesis were increased in soleus of apelin-treated mice.

248 ivo T2 relaxation data was acquired from the soleus of eight healthy volunteers using a localized Car

249 The soleus of the immobilized-reambulated hindlimb was found

250 he TR group decreased by 15% whereas that in soleus of the TR group tended to decrease (P=0.058) when

251 nimals, and Bax mRNA levels decreased in the soleus of TR animals when compared with CON animals.

252 densities were lower in the TB, but not the soleus, of PI and L fetuses.

253 diaphragm of the mutant mice but not in the soleus or EDL.

254 243 patients (63.2%) and a muscular branch (soleus or gastrocnemius) in 215 (56.0%).

255 me of aerobic energy consuming muscle in the soleus, or any other leg muscle, during running.

256 ent was lower in skeletal muscles, including soleus (P<0.01), extensor digitorum longus (EDL; P<0.001

257 , starvation, and diabetes led to atrophy of soleus, plantaris, and gastrocnemius muscles, but only u

258 On the seventh day, the gastrocnemius-soleus-plantaris muscle group was isolated and snap froz

259 and DNA fragmentation) were investigated in soleus (predominately Type I fiber), and superficial vas

260 e ankle extensors, medial gastrocnemius, and soleus, remained intact, with little pre- or postsynapti

261 res were prepared from the gastrocnemius and soleus, respectively, mounted between a force transducer

262 Gastrocnemius and soleus Rg were greater in exercising compared with seden

263 ce and their wild-type (WT) littermates: the soleus (S and FR MU); and the extensor digitorum longus

264 the number of mitochondria in white and red (soleus) skeletal muscle.

265 ii (TB, slow- and fast-twitch myofibres) and soleus (slow-twitch myofibres) muscles.

266 f any, muscle fascicles of denervated feline soleus (SO) change length during stance of walking when

267 Isolated soleus (SOL) and gastrocnemius (GAS) muscle arterioles w

268 nd electromyographic (EMG) activity from the soleus (SOL) and medial gastrocnemius (MG).

269 y, we assessed the effect of up-conditioning soleus (SOL) H-reflex on SOL and tibialis anterior (TA)

270 cacy at the synapse between Ia afferents and soleus (Sol) motoneurones.

271 ensor digitorum longus (EDL) and slow-twitch soleus (SOL) muscles derived from Sprague-Dawley rats?

272 recorded from the tibialis anterior (TA) and soleus (Sol) muscles during treadmill locomotion and kin

273 digitorum longus (EDL) and slow-contracting soleus (SOL) muscles was conducted 3 weeks post-treatmen

274 isolated extensor digitorum longus (EDL) and soleus (SOL) muscles.

275 R58Q mice is also manifested in slow-twitch soleus (SOL) muscles.

276 muscle weakness or contracture to either the soleus (SOL) or gastrocnemius (GAS) or both of these maj

277 elevated in gastrocnemius (GA), but not the soleus (SOL) or plantaris (PLT) muscles, of D14 mice.

278 extensor digitorum longus muscle (EDL) than soleus (SOL), but we find these rates are not distinguis

279 52 m/s), we measured the EMG activity of the soleus (SOL), medial gastrocnemius (MG), tibialis anteri

280 high intensities (Hi, 4.5 V) in rat (n = 20) soleus (Sol, slow-twitch, type I), mixed gastrocnemius (

281 d by DNA methylation of the nNOS promotor in soleus (Sol; slow-twitch fibre dominant) and extensor di

282 and apparent AS160 PAS phosphorylation among soleus, tibialis anterior, and extensor digitorum longus

283 ralis, rectus femoris, medial gastrocnemius, soleus, tibialis anterior, extensor digitorum brevis and

284 w during early postnatal development and, in soleus, to a reduction in number of fibers generated.

285 A comparison of the soleus transcriptome profiles between spaceflight and a

286 inhibitory effects of PLN on the transgenic soleus twitch kinetics.

287 ower with the hierarchy of the effects being soleus type I > soleus type II > gastrocnemius type I >

288 the loss of peak force (P(0)), which for the soleus type I fibre declined 35% from 0.86 to 0.56 mN.

289 was fibre atrophy, which averaged 20% in the soleus type I fibres (98 to 79 mum diameter).

290 erarchy of the effects being soleus type I > soleus type II > gastrocnemius type I > gastrocnemius ty

291 ponent Hill-type model of the human Achilles-soleus unit.

292 Young adult mutant soleus was drastically wasted, with highly atrophied typ

293 Myopathic alterations in soleus were apparent by 12 mo, including abnormally dist

294 vels and the PLN/SERCA2a ratio in transgenic soleus were comparable with those in cardiac muscle.

295 The tongue, the adductor magnus and the soleus were the most commonly affected muscles.

296 Gastrocnemius and soleus were usually (duration 71 +/- 23 and 81 +/- 16%,

297 uscular EMGs detected from gastrocnemius and soleus while five participants stood upright.

298 [Ca(2+)](rest), and present muscle damage in soleus with a strong sex bias.

299 rest was similar between young and old rats (soleus: Y, 65 +/- 5; O, 64 +/- 5 dynes cm(-2); gastrocne

300 additional feed artery perforating both the soleus (young, 3.3 +/- 0.2; old, 2.6 +/- 0.2 vessels; P