ライフサイエンスコーパス: gastrocnemius

1 (e.g. diaphragm) and locomotor muscles (e.g. gastrocnemius).

2 rmation than the active agonists (soleus and gastrocnemius).

3 f acidic saline, pH 4, into the right medial gastrocnemius.

4 gastrocnemius but was decreased in the white gastrocnemius.

5 of any stretch reflex response in soleus, or gastrocnemius.

6 an inhibition initially observed in the red gastrocnemius.

7 me extent (P > .05) as the soleus and medial gastrocnemius.

8 Gs detected from multiple skin regions along gastrocnemius.

9 ns with extreme values of 22% in the central gastrocnemius.

10 different between WT and G4(+/-) mice in the gastrocnemius (24 +/- 5 versus 21 +/- 2) or the soleus (

11 ly, p = 0.02 glycerol versus glucose) and in gastrocnemius (25 +/- 5 versus 9 +/- 2 nmol/micromol tri

12 8-fold), red gastrocnemius (4.7-fold), white gastrocnemius (3.3-fold), and soleus (1.6-fold).

13 d heart but declined with age in the lateral gastrocnemius (-32%, p < 0.05).

14 as absent in HKTg + G4(+/-) mice in both the gastrocnemius (39 +/- 7 versus 22 +/- 6) and the soleus

15 -fold over basal), plantaris (5.8-fold), red gastrocnemius (4.7-fold), white gastrocnemius (3.3-fold)

16 ly in the soleus muscle of sham-operated vs. gastrocnemius-ablated rats.

17 ast-twitch plantaris muscles (via unilateral gastrocnemius ablation) of old (O; 30 months) versus you

18 Gastrocnemius action potentials were more likely detecte

19 during standing the calf muscles soleus and gastrocnemius actively prevent forward toppling about th

20 the detection of surface EMGs insensitive to gastrocnemius activity without substantial attenuation o

21 and capillary density, respectively, in the gastrocnemius and a 61% decrease in cardiac muscle capil

22 In particular, the role of the gastrocnemius and biarticular hamstrings in permitting a

23 or to the tendon of the lateral head of the gastrocnemius and blended with the posterolateral joint

24 ECG, respiration, EMG of rectus femoris and gastrocnemius and contraction force of triceps surae.

25 f soleus action potentials was 6% of that of gastrocnemius and did not decrease for inter-electrode d

26 crease in specific intracellular peptides in gastrocnemius and epididymal adipose tissue, which likel

27 increase in HSP70 expression in the soleus, gastrocnemius and lung of the WPH-fed rats than WP or ca

28 , which includes veins and their valves, the gastrocnemius and other lower leg and foot muscles as we

29 cal anisotropic shear moduli for the lateral gastrocnemius and plantaris muscles in a 7-T MR imager,

30 such as kidney, heart, diaphragm, lung, fat, gastrocnemius and quadriceps.

31 tigate how comparably action potentials from gastrocnemius and soleus are represented in surface EMGs

32 Biopsies were obtained from the gastrocnemius and soleus muscles of nine International S

33 muscle spindle primary afferents from medial gastrocnemius and soleus muscles of the cat to study the

34 Following landing on the solid surface, the gastrocnemius and soleus muscles showed peak responses a

35 ection between the aponeuroses of the medial gastrocnemius and soleus muscles without muscle rupture

36 Gastrocnemius and soleus Rg were greater in exercising c

37 Gastrocnemius and soleus were usually (duration 71 +/- 2

38 tified from intramuscular EMGs detected from gastrocnemius and soleus while five participants stood u

39 scle length and tension in the calf muscles (gastrocnemius and soleus) are unlikely to signal postura

40 vity in skeletal muscles (medial and lateral gastrocnemius and soleus), liver, and heart in 6- and 27

41 nd slow type I fibres were prepared from the gastrocnemius and soleus, respectively, mounted between

42 the majority of triglyceride glycerol in the gastrocnemius and soleus.

43 lateralis, biceps femoris posterior, lateral gastrocnemius and tibialis anterior in mice from postnat

44 th IMCL and EMCL content was observed in the gastrocnemius and tibialis anterior muscles (with mixed

45 re reduced by 90 and 80% in skeletal muscle (gastrocnemius) and cardiac muscle, respectively, compare

46 n-stimulated glucose uptake (71% soleus, 58% gastrocnemius) and peripheral glucose clearance as docum

47 r flexor muscles (soleus, medial and lateral gastrocnemius) and quantify thickness changes at multipl

48 teral and contralateral leg muscles (lateral gastrocnemius) and systemic muscles (spinotrapezius).

49 (30 min daily RAMT over the stroke-affected gastrocnemius) and were followed up to poststroke d 14.

50 es, including kidney, adipose tissue, liver, gastrocnemius, and hypothalamus, is shown.

51 rophin expression was detected in diaphragm, gastrocnemius, and intercostal muscles.

52 the synapses in the ankle extensors, medial gastrocnemius, and soleus, remained intact, with little

53 At 150 min, soleus, gastrocnemius, and superficial vastus lateralis were exc

54 idative fibre density and capillarity in the gastrocnemius, and used a comprehensive substrate titrat

55 ck the strain patterns of the turkey lateral gastrocnemius aponeurosis during active and passive forc

56 ted gastrocnemius while the Vehicle injected gastrocnemius appeared to show reduced uptake.

57 y high values (e.g. red fibre section of the gastrocnemius: approximately 7 ml min(-1) (100 g)(-1) mm

58 clusion that both biarticular hamstrings and gastrocnemius are extensors of the lower limb.

59 arms of both the biarticular hamstrings and gastrocnemius are smaller at the knee than at the hip or

60 reased perfusion 1.5-fold in stroke-affected gastrocnemius as compared to RAMT(-) controls.

61 s protein and mitochondrial content of their gastrocnemius as predictors of mortality rate.

62 expression (0.6-fold) in the stroke-affected gastrocnemius, as compared to the contralateral one.

63 n concentration and mitochondrial content in gastrocnemius biopsies from patients with peripheral art

64 n synthase activity was increased in the red gastrocnemius but was decreased in the white gastrocnemi

65 3)C]glycerol) was complete in quadriceps and gastrocnemius, but not soleus, within 2 h after beginnin

66 gastrocnemius by 1H-MRS and HPLC to compare signal quali

67 minutes of intense stimulation of the mouse gastrocnemius caused PCr, ATP, and pH to fall and ADP an

68 Subsequently, the gastrocnemius complex and soleus muscles were excised an

69 The gastrocnemius complex of nine anaesthetised, ventilated

70 Isometric tetanic contractions of the gastrocnemius complex of six anaesthetised, ventilated d

71 foot strike pattern affected the soleus and gastrocnemius differently.

72 We show that soleus and gastrocnemius do indeed move paradoxically, shortening w

73 reaction to analyze changes in mRNA from rat gastrocnemius during disuse atrophy induced by denervati

74 ars old, differences appeared at 6 months in gastrocnemius (EIM phase slope = -0.83 degrees /kHz/mo,

75 t accumulation in liver and skeletal muscle (gastrocnemius) evaluated by measurements of triglyceride

76 In gastrocnemius, exercise increased the cross-sectional ar

77 The gastrocnemius exhibits altered force and work output in

78 e, we test this through direct recordings of gastrocnemius fascicle length (using sonomicrometry), mu

79 .001), but was similar between groups in the gastrocnemius feed arteries (GFA, P = 0.79).

80 Popliteal arteries, subsequent gastrocnemius feed arteries, and first and second order

81 Gastrocnemius first-order arterioles were removed from y

82 For the gastrocnemius, forefoot striking increased muscle activa

83 y 2.4-fold (P < 0.05 vs. control) in the red gastrocnemius from obese rats, whereas insulin had no ef

84 , nuclear factor-kappa B (NF-kappaB)) in the gastrocnemius (G).

85 oss-sectional area and tension output in the gastrocnemius (GA) after DEX treatment.

86 seline levels; however, VEGF was elevated in gastrocnemius (GA), but not the soleus (SOL) or plantari

87 on the locomotor discharges of single medial gastrocnemius gamma-motoneurones has been investigated i

88 Isolated soleus (SOL) and gastrocnemius (GAS) muscle arterioles were studied in vi

89 or contracture to either the soleus (SOL) or gastrocnemius (GAS) or both of these major plantarflexor

90 c receptive field, but not the contralateral gastrocnemius (GN) or front leg muscles, sensitized resp

91 with the moment-angle characteristics of the gastrocnemius (GS) and tibialis anterior (TA) muscles in

92 t was associated with an enhanced ability of gastrocnemius (GTN) muscles to maintain force during a p

93 uscle, and pyruvate oxidation was similar in gastrocnemius homogenates from Acsl1(M) (-/-) and contro

94 on, and a reduction in ROS production in red gastrocnemius in response to palmitoyl carnitine.

95 nts (63.2%) and a muscular branch (soleus or gastrocnemius) in 215 (56.0%).

96 ntricle and soleus) and a glycolytic muscle (gastrocnemius) in control and vdac1(-/-) mice.

97 levels, UCP3 mRNA and protein levels in the gastrocnemius increased 1.7- (p < 0.01) and 2.9-fold (p

98 he post-landing activity in m. soleus and m. gastrocnemius is a short-latency spinal reflex triggered

99 Gastrocnemius K(+) channel alpha subunit remodeling aris

100 Gastrocnemius length and force return to level running m

101 nd images to resolve calf muscle (soleus and gastrocnemius) length changes as small as 10 mum in stan

102 MTU) length, and EMG activity of SO, lateral gastrocnemius (LG) and medial gastrocnemius (MG) were me

103 ad (BL), tibialis anterior (TA), and lateral gastrocnemius (LG) during walking were recorded.

104 These changes in gastrocnemius mechanics suggest that runners planning to

105 nt of the myotendinous junction (MTJ) of the gastrocnemius medialis muscle was measured by ultrasonog

106 single muscle spindle afferents from medial gastrocnemius (MG) and tibialis anterior (TA) muscles of

107 firing patterns in the ankle extensor medial gastrocnemius (MG) have therefore been repeated in the f

108 from muscle spindle afferents of the medial gastrocnemius (MG) muscle during locomotion in decerebra

109 luntary isometric contractions of the medial gastrocnemius (MG) muscle in chronic stroke survivors.

110 In the medial gastrocnemius (MG) muscle of homozygous HCSMA animals, m

111 olor power Doppler ultrasound) of the medial gastrocnemius (MG) muscle on either paretic or non-paret

112 ng and motion analysis to examine how medial gastrocnemius (MG) muscle-tendon unit behavior is adjust

113 as significantly decreased in paretic medial gastrocnemius (MG) muscles compared to non-paretic MG mu

114 leus H-reflex was also conditioned by medial gastrocnemius (MG) nerve stimulation at C-T intervals ra

115 The axotomized medial gastrocnemius (MG) nerve was provided with NT-3 or NT-4/

116 of SO, lateral gastrocnemius (LG) and medial gastrocnemius (MG) were measured during level and slope

117 d from the heel to the ankle extensor medial gastrocnemius (MG), has been studied during antigen-indu

118 the EMG activity of the soleus (SOL), medial gastrocnemius (MG), tibialis anterior (TA), medial hamst

119 G) activity from the soleus (SOL) and medial gastrocnemius (MG).

120 were recorded from the ankle extensor medial gastrocnemius (MG).

121 20) soleus (Sol, slow-twitch, type I), mixed gastrocnemius (MG, fast-twitch, type IIa) and white gast

122 nterior (TA), soleus, and medial head of the gastrocnemius (MHG) muscle groups.

123 subcutaneous 200-microg injections) reduced gastrocnemius mitochondrial ROS generation and inflammat

124 In the isolated canine gastrocnemius model, we evaluated the effects of acute n

125 drenal sympathetic preganglionic neurons and gastrocnemius motoneurons, were observed in several area

126 with aging in the less oxidative mixed fiber gastrocnemius muscle (-17-22%, p < 0.05).

127 tential was higher in tibialis anterior than gastrocnemius muscle (chi(2) = 87.12, p < 0.001).

128 ); TNF-alpha and NF-kappaBp65 content in the gastrocnemius muscle (GM) by western blotting; IKKalpha/

129 s of autogenic proprioception in the lateral gastrocnemius muscle (LG) using self-reinnervation.

130 mius muscle (MHG) and/or lateral head of the gastrocnemius muscle (LHG) and adductor magnus tendon by

131 ) in contracting fast-twitch oxidative mixed gastrocnemius muscle (MG: 9% type I+IIa fibres).

132 femoral attachment of the medial head of the gastrocnemius muscle (MHG) and/or lateral head of the ga

133 croL, pH 4.0) were given unilaterally in the gastrocnemius muscle 2 days apart in male Sprague-Dawley

134 versus 119 micrometer) were observed in rat gastrocnemius muscle after 5 min of contraction, induced

135 prepared from both rat and mouse (wild-type) gastrocnemius muscle after a single bout of exercise plu

136 hin and increase perfusion of ischemic mouse gastrocnemius muscle after femoral artery ligation.

137 multiple mtDNA deletions was investigated in gastrocnemius muscle and eye specimens harvested from 2-

138 5- to 5-fold) in rat soleus muscle and white gastrocnemius muscle and in mouse soleus muscle, which w

139 who undergo US, abnormalities of the medial gastrocnemius muscle appear to be more common than those

140 In gastrocnemius muscle arterioles, ageing did not alter ma

141 provement of the bioenergetic reserve of the gastrocnemius muscle as assessed by (31)P NMR spectrosco

142 w that raising the heel by 13cm shortens the gastrocnemius muscle by 5% while the Achilles tendon rem

143 In contrast, unloading the gastrocnemius muscle by hindlimb suspension, which promo

144 ed in lower levels of vastus medialis-medial gastrocnemius muscle co-contractions (P = 0.089).

145 city and muscle grip strength and that their gastrocnemius muscle contains myocytes with central nucl

146 Transmission electron microscopy on red gastrocnemius muscle demonstrated that Pus1(-/-) mice al

147 4c lentivirus into mice caused repression of gastrocnemius muscle development.

148 Essential amino acid levels of the gastrocnemius muscle did not reach significance, with th

149 esis rates were measured in the human medial gastrocnemius muscle during high intensity exercise usin

150 strates and cofactors onto permeabilized rat gastrocnemius muscle fibers, as well as isolated mitocho

151 e tibial nerve projected axons to denervated gastrocnemius muscle fibers, where they formed functiona

152 ctivity of alpha1 AMPK remained unchanged in gastrocnemius muscle from AICAR-treated animals compared

153 UCP-3 mRNA expression in gastrocnemius muscle from diabetic rats was increased fo

154 carboxylase phosphorylation was increased in gastrocnemius muscle from gamma3(R225Q) mutant mice inde

155 cerol and ceramide content were unaltered in gastrocnemius muscle from ob/ob-gamma3(R225Q) mice, wher

156 s significantly reduced in extracts from red gastrocnemius muscle from Pus1(-/-) mice.

157 At rest, perfusion and T(2)* in gastrocnemius muscle group within calf muscle were 5 +/-

158 MTII treatment increased gastrocnemius muscle heat dissipation during controlled

159 GH treatment increased gastrocnemius muscle IGF-1 mRNA levels significantly in

160 thelial cells (ECs) in protein gels into the gastrocnemius muscle improves local reperfusion in immun

161 s included rupture of the medial head of the gastrocnemius muscle in 94 patients (66.7%), fluid colle

162 content were observed in C2C12 myotubes and gastrocnemius muscle in vivo, indicating that they were

163 maximum isometric specific force measured in gastrocnemius muscle is significantly reduced in the mKO

164 e turkey, much of the force generated by the gastrocnemius muscle is stored as elastic energy during

165 g (with Evans blue dye) of the diaphragm and gastrocnemius muscle isolated from treated mdx mice, and

166 th wild-type mice at 2 and 4 weeks following gastrocnemius muscle laceration injury.

167 n of rabies-G pseudotyped vectors to the rat gastrocnemius muscle leads to gene transfer in motoneuro

168 ntake, body weight gain, lean body mass, and gastrocnemius muscle mass as compared with vehicle-treat

169 gery, by improved blood flow to the ischemic gastrocnemius muscle measured by radioactive microsphere

170 The deletion frequency was quantified in gastrocnemius muscle of 8 patients with unilateral PAD a

171 Here we have examined NMJs from gastrocnemius muscle of adult rat using immunofluorescen

172 Mitochondria isolated from gastrocnemius muscle of apoA-I ko mice displayed markedl

173 e-related transcriptional alterations in the gastrocnemius muscle of C57BL/6 mice.

174 In the gastrocnemius muscle of castrated animals, HB treatment

175 2SC and fumarate in gastrocnemius muscle of control and streptozotocin-induc

176 Here, we injected cardiotoxin into gastrocnemius muscle of Hmox1(+/+) and Hmox1(-/-) animal

177 ravascular tracer washout data obtained from gastrocnemius muscle of lean Zucker rats (LZRs) and obes

178 ctions of acidic saline, 5 d apart, into the gastrocnemius muscle of male Sprague Dawley rats.

179 ate experimental protocol using the isolated gastrocnemius muscle of mongrel dogs (n= 6) K(+) infusio

180 us-SERCA2a (AAV-SERCA2a) gene therapy in the gastrocnemius muscle of Sgcd(-/-) mice mitigated dystrop

181 We report in vivo recordings of the gastrocnemius muscle of the guinea fowl (Numida meleagri

182 tic sensitivity using von Frey filaments and gastrocnemius muscle pinch, respectively.

183 ogical recovery at 1 month as well as better gastrocnemius muscle recovery at 5 months than the acell

184 Twa is associated with longer fibers in the gastrocnemius muscle relative to those of neighboring, n

185 Injection of acid into the gastrocnemius muscle results in a persistent, mechanical

186 Microarray and qPCR analysis of gastrocnemius muscle RNA revealed that ablation of Zip14

187 le saline injections of pH 4.0 or 7.4 in the gastrocnemius muscle starting at postnatal day 8.

188 Moreover, injection of the peptide into the gastrocnemius muscle strongly enhanced acid-induced musc

189 etaII mRNA levels in Akt2(+/+) and Akt2(-/-) gastrocnemius muscle tissues were compared using quantit

190 ine (PCr) onset kinetics in exercising human gastrocnemius muscle under varied fractions of inspired

191 tic nerve was measured by contraction of the gastrocnemius muscle upon electrical stimulation.

192 Hypertrophy in the Mtm1 p.R69C gastrocnemius muscle was associated with increased level

193 Gastrocnemius muscle was extracted immediately after acu

194 activation of Akt1 signaling in normal mouse gastrocnemius muscle was sufficient to promote myofiber

195 force production, and pathology of isolated gastrocnemius muscle were analysed at the end point.

196 Blood and gastrocnemius muscle were collected in non-exercised con

197 Total DNA and RNA contents of the gastrocnemius muscle were greater for transgenic mice th

198 Group 1a muscle afferents supplying the gastrocnemius muscle were impaled with microelectrodes i

199 Arterioles (1A) from the red portion of the gastrocnemius muscle were isolated, cannulated and press

200 atory parameters for desmin-null fast twitch gastrocnemius muscle were unaffected.

201 velocities between the sciatic notch and the gastrocnemius muscle were unchanged in paralyzed mice.

202 increases glucose transport activity in red gastrocnemius muscle while suppressing endogenous glucos

203 n and decreased malonyl CoA concentration in gastrocnemius muscle within 15-30 min.

204 The weight of the medial gastrocnemius muscle, a hindlimb muscle activated during

205 First, we locally injected MG-132 into the gastrocnemius muscle, and observed the outcome after 24

206 In the gastrocnemius muscle, oxfenicine increased pyruvate dehy

207 .31 +/- 0.06 mmol/kg/min during clamp in red-gastrocnemius muscle, P < 0.05).

208 In the gastrocnemius muscle, pri-miR487b editing increased from

209 In gastrocnemius muscle, resveratrol increased the gene exp

210 -16.1%) within single muscle fibers from the gastrocnemius muscle, the maximum rate of mitochondrial

211 as their wild-type littermates in liver and gastrocnemius muscle, they have reduced expression of ge

212 protein, was injected into sympathectomized gastrocnemius muscle, whereas PRV-BaBlu, which expresses

213 protein (PRV-152) was injected into the left gastrocnemius muscle, which was surgically sympathectomi

214 protein, was injected into sympathectomized gastrocnemius muscle, while PRV-BaBlu, which expresses b

215 but did coincide with passive stretch of the gastrocnemius muscle-tendon units.

216 RNAseq analysis was performed on the gastrocnemius muscle.

217 hysiological types as established in the cat gastrocnemius muscle.

218 expression of insulin signaling proteins in gastrocnemius muscle.

219 nge of either HFE2 mRNA or protein levels in gastrocnemius muscle.

220 ked potentials (MEPs) were recorded from the gastrocnemius muscle.

221 anisms involved in mRNA translation in mouse gastrocnemius muscle.

222 ucleosome ELISA was increased by 100% in the gastrocnemius muscle.

223 he apoptotic responses to denervation in rat gastrocnemius muscle.

224 ctively, in the T(3)-treated vs. control rat gastrocnemius muscle.

225 ase activity, PDK4 protein, and PDK4 mRNA in gastrocnemius muscle.

226 transport into extensor digitorum longus and gastrocnemius muscle.

227 ion was decreased in laminin-alpha2 dyW null gastrocnemius muscle.

228 ograde marker cholera toxin B (CTB) into the gastrocnemius muscle/sciatic nerve of SOD1 rats before d

229 nd PKC phospho-sites in the DA-1 AH, but not gastrocnemius, muscle.

230 endothelial growth factor gene expression in gastrocnemius muscles after acute exercise.

231 emitendinosus, vastus lateralis, and lateral gastrocnemius muscles at four treadmill speeds: 0.2, 0.4

232 and histological evidence of hypertrophy in gastrocnemius muscles but not in quadriceps or triceps.

233 ilis muscles, and immunostaining for CD31 in gastrocnemius muscles cross-sections, we found that ther

234 Treatment-responsive Mtm1 p.R69C gastrocnemius muscles displayed lower levels of phosphor

235 Following hMDSPC therapy, gastrocnemius muscles from mice exhibited substantially

236 gen metabolism were studied in red and white gastrocnemius muscles from rats treated with 5-aminoimid

237 trophy by surgically removing the soleus and gastrocnemius muscles in rats.

238 Isolated canine gastrocnemius muscles in situ (n = 8) were studied durin

239 cose metabolism and fiber size in soleus and gastrocnemius muscles of aged rats.

240 s) was injected into nonischemic or ischemic gastrocnemius muscles of C57Bl/6J mice following unilate

241 < 0.05 vs. control), in both soleus and red gastrocnemius muscles of lean rats infused with either A

242 II, a murine fibrosarcoma, were grown in the gastrocnemius muscles of male nude mice.

243 In red and white gastrocnemius muscles of offspring, we are the first to

244 Inoculation of the vaccine DNA into the gastrocnemius muscles resulted in intense mononuclear ce

245 emma of the microdystrophin(DeltaR4-R23)/mdx gastrocnemius muscles was highly protected from experime

246 Brains and gastrocnemius muscles were collected from young (3-5 mon

247 The gastrocnemius muscles were evaluated in the patients wit

248 (proximal leg, lumbar paraspinal and medial gastrocnemius muscles).

249 tes led to atrophy of soleus, plantaris, and gastrocnemius muscles, but only unloaded and denervated

250 membrane GLUT4 content in both red and white gastrocnemius muscles, the TBC1D1 ablation did not alter

251 corporation into EDL, tibialis anterior, and gastrocnemius muscles, was normal in alpha2i TG mice.

252 the feed arteries perforating the soleus and gastrocnemius muscles.

253 h is prevented by activity in the soleus and gastrocnemius muscles.

254 e than double that of a birdcage coil in the gastrocnemius muscles.

255 Arterioles were isolated from the soleus and gastrocnemius muscles; luminal diameter changes were det

256 Stimulation of the gastrocnemius nerve and sural nerve revealed significant

257 Samples from the gastrocnemius of PAD patients were used for all analyses

258 t and glucose uptake were lower in the white gastrocnemius of the KO animals.

259 re consistent with Kcne3 deletion increasing gastrocnemius oxidative metabolic gene expression and th

260 uctural characteristics were investigated in Gastrocnemius pars interna (GN) and Iliofiburalis (IF) l

261 imals were sacrificed 16 h postexercise, and gastrocnemius protein synthesis, mTOR signaling, and bio

262 Results from 66 motor units (whereof 31 from gastrocnemius) revealed the surface-recorded amplitude o

263 re confirmed by histological analyses of the gastrocnemius, revealing a decreased muscle fiber size a

264 0.06 in the predominantly red portion of the gastrocnemius (RG) during rest.

265 isms by which heart and skeletal muscle (red gastrocnemius, RG) mitochondria experience differential

266 Eighteen hours later, ileum, jejunum, medial gastrocnemius skeletal muscle, liver, and lung were anal

267 sterior, posterior biceps-semitendinosus and gastrocnemius soleus were also highly effective (dischar

268 , tibialis posterior (throughout L6 and L7), gastrocnemius soleus, flexor digitorum longus, posterior

269 sed a reduction in weight of the quadriceps, gastrocnemius, soleus, and even the heart itself.

270 an increase in time to peak perfusion in the gastrocnemius, soleus, and peroneus muscles, and in the

271 entire posterior group of hindlimb muscles (gastrocnemius, soleus, and plantaris) were evaluated in

272 is, vastus lateralis, rectus femoris, medial gastrocnemius, soleus, tibialis anterior, extensor digit

273 On the seventh day, the gastrocnemius-soleus-plantaris muscle group was isolated

274 g might benefit from a progressive eccentric gastrocnemius strengthening program to avoid injury.

275 FP or mRFP), injected pairwise into male rat gastrocnemius, subcutaneous WAT and interscapular BAT, c

276 ase activity in heart, but not in soleus and gastrocnemius, suggest that distinct metabolic responses

277 Gastrocnemius, superficial vastus lateralis and soleus m

278 In the murine gastrocnemius, the estimated methylation fraction increa

279 l and tibial) or just muscle (lateral/medial gastrocnemius), this pattern was mostly absent.

280 fects being soleus type I > soleus type II > gastrocnemius type I > gastrocnemius type II.

281 21 and 18% decline in V(0) in the soleus and gastrocnemius type I fibres.

282 I > soleus type II > gastrocnemius type I > gastrocnemius type II.

283 eral leg muscles (tibialis anterior, lateral gastrocnemius, vastus lateralis and biceps femoris).

284 patients with GNE-related myopathy, and the gastrocnemius, vastus lateralis, and rectus femoris musc

285 of leg extensor muscles (medial and lateral gastrocnemius, vastus medialis, vastus lateralis and rec

286 When the rat gastrocnemius was contracted, the level of Rac1 activati

287 Muscle mass of the medial gastrocnemius was diminished in the Op-Control group ind

288 rial production in liver and skeletal muscle gastrocnemius was increased in mice with insulin deficie

289 ll for periods of 10, 20 or 30 min, then the gastrocnemius was rapidly removed and analysed for phosp

290 Skeletal muscle (gastrocnemius) was analyzed for insulin sensitivity, cer

291 'final' gait termination EMG activity (right gastrocnemius) was greater in the patient group than con

292 GWI gastrocnemius weight was ~ 35% lower versus controls, wh

293 igher in soleus (0.41 +/- 0.22) versus white gastrocnemius (WG) (0.18 +/- 0.11).

294 nemius (MG, fast-twitch, type IIa) and white gastrocnemius (WG, fast-twitch, type IIb) muscle.

295 rease in the apparent Km((ADP)) in heart and gastrocnemius, whereas the V(max) remained unchanged in

296 supercomplex formation between red and white gastrocnemius, which may be integral to fiber-type speci

297 depot region of the GSK1265744 LAP injected gastrocnemius while the Vehicle injected gastrocnemius a

298 e leg is more extended in the drop step, net gastrocnemius work decreases (-5.2 J kg(-1) versus contr

299 leus: Y, 65 +/- 5; O, 64 +/- 5 dynes cm(-2); gastrocnemius: Y, 329 +/- 22; O, 327 +/- 27 dynes cm(-2)

300 0.2; old, 2.6 +/- 0.2 vessels; P < 0.05) and gastrocnemius (young, 8.8 +/- 0.1; old, 7.5 +/- 0.2 vess