ライフサイエンスコーパス: gastrocnemius

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

2 (e.g. diaphragm) and locomotor muscles (e.g. 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 level or high/low Mr isoform ratio in sheep 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 min-1 (100 g tissue)-1; n = 6; n.s.) or the gastrocnemius (62.9 +/- 7.9 ml min-1 (100 g tissue)-1; n

17 min-1 (100 g tissue)-1; n = 6; n.s.) or the gastrocnemius (62.9 +/- 7.9 ml min-1 (100 g tissue)-1; n

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

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

20 Gastrocnemius action potentials were more likely detecte

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

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

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

24 expression was reciprocal: highest in white gastrocnemius and barely detectable in soleus and diaphr

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

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

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

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

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

30 put to gamma-motoneurones innervating medial gastrocnemius and four other hindlimb muscles revealed d

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

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

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

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

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

36 of obese animals increased glucose uptake in gastrocnemius and soleus muscles by 44 and 47%, respecti

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

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

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

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

41 Gastrocnemius and soleus Rg were greater in exercising c

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

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

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

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

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

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

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

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

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

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

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

53 (30 min daily RAMT over the stroke-affected gastrocnemius) and were followed up to poststroke d 14.

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

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

56 nmol/micromol triglyceride/h for quadriceps, gastrocnemius, and soleus muscle, respectively).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

72 The gastrocnemius complex of nine anaesthetised, ventilated

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

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

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

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

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

78 In gastrocnemius, exercise increased the cross-sectional ar

79 The gastrocnemius exhibits altered force and work output in

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

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

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

83 Gastrocnemius first-order arterioles were removed from y

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

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 rotocol 2 (n = 4), IT concentrations in Sol, gastrocnemius (Gast) and tibialis (Tib) muscles were 46.

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

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

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

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

97 Gastrocnemius K(+) channel alpha subunit remodeling aris

98 The gastrocnemius medialis (GM), gastrocnemius lateralis (GL) and soleus (SOL) muscles of

99 Gastrocnemius length and force return to level running m

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

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

102 The gastrocnemius medialis (GM), gastrocnemius lateralis (GL

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

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

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

106 te group I EPSPs evoked in intact rat medial gastrocnemius (MG) motoneurons by stimulation of the lat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 5- to 5-fold) in rat soleus muscle and white gastrocnemius muscle and in mouse soleus muscle, which w

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

129 In gastrocnemius muscle arterioles, ageing did not alter ma

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

131 ow (stenosis), electrical stimulation of the gastrocnemius muscle at a rate of one per second (stimul

132 min-1 (100 g tissue)-1 (n = 6; P < 0.01) and gastrocnemius muscle blood flow increased from 15.8 +/ 3

133 min-1 (100 g tissue)-1 (n = 6; P < 0.01) and gastrocnemius muscle blood flow increased from 15.8 +/-

134 min-1 (100 g tissue)-1 (n = 6; P < 0.02) and gastrocnemius muscle blood flow increased from 24.8 +/-

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

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

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

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

139 4c lentivirus into mice caused repression of gastrocnemius muscle development.

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

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

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

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

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

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

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

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

148 MTII treatment increased gastrocnemius muscle heat dissipation during controlled

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

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

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

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

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

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

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

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

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

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

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

160 lso reversed the increase in PDK4 protein in gastrocnemius muscle mitochondria.

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

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

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

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

165 In the gastrocnemius muscle of castrated animals, HB treatment

166 2SC and fumarate in gastrocnemius muscle of control and streptozotocin-induc

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

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

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

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

171 nts of force and fiber length in the lateral gastrocnemius muscle of running turkeys revealed that th

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

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

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

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

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

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

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

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

180 whereas the lack of decreased SERCA1 mRNA in gastrocnemius muscle suggests translational regulation.

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

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

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

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

185 Gastrocnemius muscle was extracted immediately after acu

186 sue)-1, n = 6; n.s.) white blood flow in the gastrocnemius muscle was reduced to 21.8 +/- 6.0 ml min-

187 ue)-1; n = 6; n.s.) whilst blood flow in the gastrocnemius muscle was reduced to 21.8 +/- 6.0 ml min-

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

189 richment measurements by 1H NMR in heart and gastrocnemius muscle were also highly correlated with in

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

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

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

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

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

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

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

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

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

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

200 also increased the abundance of PDK4 mRNA in gastrocnemius muscle, and refeeding and insulin treatmen

201 In the gastrocnemius muscle, oxfenicine increased pyruvate dehy

202 .31 +/- 0.06 mmol/kg/min during clamp in red-gastrocnemius muscle, P < 0.05).

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

204 In gastrocnemius muscle, resveratrol increased the gene exp

205 -16.1%) within single muscle fibers from the gastrocnemius muscle, the maximum rate of mitochondrial

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

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

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

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

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

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

212 expression of insulin signaling proteins in gastrocnemius muscle.

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

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

215 anisms involved in mRNA translation in mouse gastrocnemius muscle.

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

217 he apoptotic responses to denervation in rat gastrocnemius muscle.

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

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

220 in mammalian tissues, in the mitochondria of gastrocnemius muscle.

221 hysiological types as established in the cat gastrocnemius muscle.

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

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

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

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

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

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

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

229 Following hMDSPC therapy, gastrocnemius muscles from mice exhibited substantially

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

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

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

233 < 0.05 vs. control), in both soleus and red gastrocnemius muscles of lean rats infused with either A

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

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

236 sis of the tibialis anterior, diaphragm, and gastrocnemius muscles showed a decrease in SERCA1 protei

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

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

239 The gastrocnemius muscles were evaluated in the patients wit

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

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

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

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

244 the feed arteries perforating the soleus and gastrocnemius muscles.

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

246 There was no change in SERCA1 mRNA levels in gastrocnemius muscles.

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

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

249 and diaphragm) as in fast glycolytic (white gastrocnemius) muscles, and beta2 expression was recipro

250 Stimulation of the gastrocnemius nerve and sural nerve revealed significant

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

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

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

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

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

256 four leg muscles (tibialis anterior, medial gastrocnemius, rectus femoris and biceps femoris).

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

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

259 0.06 in the predominantly red portion of the gastrocnemius (RG) during rest.

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

261 In mouse gastrocnemius skeletal muscle, alpha1- and beta1-syntrop

262 recorded intracellularly from MG or lateral gastrocnemius soleus (LGS) motoneurons in response to st

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

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

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

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

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

268 Gastrocnemius, soleus, heart, and liver of untreated obe

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

270 1-rostral L3), whereas group II afferents of gastrocnemius-soleus and hamstring nerves evoked their m

271 d potentials evoked by group II afferents of gastrocnemius-soleus and hamstring nerves were restricte

272 malonyl-CoA formation, were examined in rat gastrocnemius-soleus muscles at rest and during contract

273 G) motoneurons by stimulation of the lateral gastrocnemius-soleus nerve (LG-S).

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

275 nd interscapular brown adipose tissue and in gastrocnemius/soleus muscle preparations from the obesit

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 acidic in their NH2-terminal segment versus gastrocnemius TnTs.

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

282 21 and 18% decline in V(0) in the soleus and gastrocnemius type I fibres.

283 I > soleus type II > gastrocnemius type I > gastrocnemius type II.

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

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

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

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

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

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

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

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

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

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

294 inantly glycolytic muscle groups such as the gastrocnemius when flow is restricted.

295 inantly glycolytic muscle groups such as the gastrocnemius when flow is restricted.

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

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