ライフサイエンスコーパス: digitorum

1 graphy on antagonistic muscles (right flexor digitorum and extensor digitorum) together with 64-chann

2 of single motor units in the human extensor digitorum and tibialis anterior during repetitive triang

3 basis of the preservation of their extensor digitorum brevis (EDB) muscle seen on MRI and the respon

4 2+) concentration ([Ca(2+)](rest)) in flexor digitorum brevis (FDB) and vastus lateralis prepared fro

5 In flexor digitorum brevis (FDB) fibers isolated from JP45-CASQ1-C

6 We apply our method to isolated mouse flexor digitorum brevis (FDB) fibers that are embedded in 10 mg

7 scle, we overexpressed Rad and Rem in flexor digitorum brevis (FDB) fibers via in vivo electroporatio

8 Myotubes, adult flexor digitorum brevis (FDB) fibers, and sarcoplasmic reticulu

9 elicit Ca(2+) release from the SR of flexor digitorum brevis (FDB) fibers, either a ryanodine recept

10 We used Flexor Digitorum Brevis (FDB) isolated from young (~2-months ol

11 To this end, short flexor digitorum brevis (FDB) muscle fibers from 5-7- and 21-24

12 c1-green fluorescent protein (GFP) in flexor digitorum brevis (FDB) muscle fibres from adult mouse.

13 the preceding paper, we reported that flexor digitorum brevis (FDB) muscle fibres from S100A1 knock-o

14 charge movement currents in isolated flexor digitorum brevis (FDB) muscle fibres from wild-type and

15 k we hypothesized that denervation in flexor digitorum brevis (FDB) muscle from ageing mice is more e

16 orce in single intact fibres from the flexor digitorum brevis (FDB) muscle from the mouse.

17 ully dissociated from the fast-twitch flexor digitorum brevis (FDB) muscle or in small bundles from t

18 e examined in dissociated fibres from flexor digitorum brevis (FDB) muscle using the whole-cell patch

19 Skeletal muscle fibers from the flexor digitorum brevis (FDB) muscle were obtained from 5-7-, 1

20 PMA in fibres from predominantly fast flexor digitorum brevis (FDB) muscle, but did in FDB fibres exp

21 atically dissociated from adult mouse flexor digitorum brevis (FDB) muscles and maintained in culture

22 m extensor digitorum longus (EDL) and flexor digitorum brevis (FDB) muscles of normal and mdx mice.

23 Interestingly, the intrinsic flexor digitorum brevis (FDB) muscles of the foot are identical

24 a(2+) transients in adult dissociated flexor digitorum brevis (FDB) skeletal muscle fibers and human

25 e measured Ca(2+) transients in mouse flexor digitorum brevis (FDB) skeletal muscle fibres under volt

26 Flexor digitorum brevis (FDB)muscles were transfected by in viv

27 ult mouse skeletal muscle fibers from flexor digitorum brevis (predominantly fast-twitch).

28 Murine diaphragm and limb muscle (flexor digitorum brevis [FDB]) preparations were used to determ

29 cnemius, soleus, tibialis anterior, extensor digitorum brevis and flexor digitorum brevis.

30 cium entry (ECCE) in both adult mouse flexor digitorum brevis fibers and primary myotubes.

31 yocytes, skeletal myotubes, and adult flexor digitorum brevis fibers TCS depresses electrically evoke

32 esistant charge movement densities in flexor digitorum brevis fibers.

33 Isolated mouse flexor digitorum brevis fibres showed a rapidly developing, rev

34 Overexpression of miR-19b-3p in mouse flexor digitorum brevis muscle enhances contraction-induced glu

35 greater decay of Ca(2+) transients in flexor digitorum brevis muscle fibers during repetitive stimula

36 Here, we used flexor digitorum brevis muscle fibers from transgenic mice with

37 have been recorded simultaneously in flexor digitorum brevis muscle fibers of adult mice, using the

38 ng us to monitor SR luminal Ca(2+) in flexor digitorum brevis muscle fibers to determine the mechanis

39 against Orai1 were delivered into the flexor digitorum brevis muscle in live mice and knockdown of Or

40 ector genomes) was delivered to the extensor digitorum brevis muscle of 3 subjects with documented SG

41 Muscle fibres were isolated from the flexor digitorum brevis muscle of mice and intracellular NO pro

42 rAAV1.tMCK.hSGCA injected into the extensor digitorum brevis muscle was conducted.

43 n single intact fibers from the mouse flexor digitorum brevis muscle.

44 Single intact muscle fibres from flexor digitorum brevis muscles from young (2-6 months) and old

45 RNA against CSQ1 was introduced into flexor digitorum brevis muscles using electroporation.

46 and ryanodine receptor disruption in flexor digitorum brevis myofibers isolated from ferlin mutant m

47 mmalian skeletal muscle cells (murine flexor digitorum brevis myofibers) and confocal imaging to dete

48 nner membrane of nuclei isolated from flexor digitorum brevis skeletal muscle fibers of adult mice.

49 terior, extensor digitorum brevis and flexor digitorum brevis.

50 The extensor digitorum communis (EDC) is a multi-compartment muscle t

51 r digitorum superficialis (FDS) and extensor digitorum communis (EDC).

52 of flexor digitorum superficialis, extensor digitorum communis and first dorsal interosseous during

53 multiple muscle types including the extensor digitorum longus (13-fold over basal), plantaris (5.8-fo

54 saline-infused fed controls in both extensor digitorum longus (2.01 +/- 0.34 vs. 0.68 +/- 0.11, P = 0

55 from the soleus (a slow muscle) and extensor digitorum longus (a fast muscle) of the rat.

56 e soleus (a slow-twitch muscle) and extensor digitorum longus (a fast-twitch muscle) of the rat.

57 ast muscles tibialis anterior (TA), extensor digitorum longus (EDL) and extensor hallucis proprius (E

58 cally isolated fibres obtained from extensor digitorum longus (EDL) and flexor digitorum brevis (FDB)

59 N transitions are different in fast extensor digitorum longus (EDL) and slow soleus (SOL) muscle, bei

60 mpulse activity, we denervated fast extensor digitorum longus (EDL) and slow soleus (SOL) muscles of

61 ofiber analysis of fast-contracting extensor digitorum longus (EDL) and slow-contracting soleus (SOL)

62 e isoforms different in fast-twitch extensor digitorum longus (EDL) and slow-twitch soleus (SOL) musc

63 force or fatigue assays of isolated extensor digitorum longus (EDL) and soleus (SOL) muscles.

64 Contractile function of intact extensor digitorum longus (EDL) and soleus muscles from Mtm1delta

65 When sodium influx into rat extensor digitorum longus (EDL) and soleus muscles was facilitate

66 After 4 or 12 h, extensor digitorum longus (EDL) and soleus muscles were removed a

67 extensor digitorum longus (EDL) and treadmill exercise increased

68 hat prior in situ contraction of m. extensor digitorum longus (EDL) and treadmill exercise increased

69 tation on isolated soleus (SOL) and extensor digitorum longus (EDL) contractile function.

70 In situ extensor digitorum longus (EDL) contractility and femoral blood f

71 Extensor digitorum longus (EDL) fibre bundles obtained from chron

72 is shown that in both rat and mouse extensor digitorum longus (EDL) fibres, action potential firing l

73 e significantly reduced in isolated extensor digitorum longus (EDL) from C2(-/-) mice.

74 ion and glucose transport in murine extensor digitorum longus (EDL) muscle (+121%, +164% and +184%, r

75 ly and highly induced in glycolytic extensor digitorum longus (EDL) muscle during exercise.

76 SOL) and pure fast-twitch-fibre rat extensor digitorum longus (EDL) muscle during twitch and tetanic

77 Extensor digitorum longus (EDL) muscle isolated from skeletal-act

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

79 se active transport in the isolated extensor digitorum longus (EDL) muscle of alpha2(R/R) mice was lo

80 ion and lactate accumulation in the extensor digitorum longus (EDL) muscle of rats infused with lipop

81 letal muscle using an incubated rat extensor digitorum longus (EDL) muscle preparation as a tool.

82 Rat extensor digitorum longus (EDL) muscle was incubated with differe

83 ar network using parameters for rat extensor digitorum longus (EDL) muscle when oxygen consumption by

84 in individual fibers within a whole extensor digitorum longus (EDL) muscle, exhibited significantly r

85 ls did not affect TSC number in the extensor digitorum longus (EDL) muscle, where endplate area was u

86 he relatively androgen-unresponsive extensor digitorum longus (EDL) muscle.

87 nically skinned fibres from the rat extensor digitorum longus (EDL) muscle.

88 T4 predominantly in the fast-twitch extensor digitorum longus (EDL) muscle.

89 uteus maximus, tibialis anterior or extensor digitorum longus (EDL) muscle.

90 ucose transport in mouse soleus and extensor digitorum longus (EDL) muscle.

91 Extraocular and extensor digitorum longus (EDL) muscles from adult Sprague-Dawley

92 sed insulin signaling in soleus and extensor digitorum longus (EDL) muscles from rats fed a high-fat

93 aling pathways, isolated soleus and extensor digitorum longus (EDL) muscles from rats were treated wi

94 Extensor digitorum longus (EDL) muscles from wild type and TG mic

95 the partially denervated soleus or extensor digitorum longus (EDL) muscles in some animals.

96 s contraction interval <0.002) rat extensor digitorum longus (EDL) muscles in vitro (95% N2-5% CO2,

97 scle preparations of rat soleus and extensor digitorum longus (EDL) muscles in which muscle action po

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

99 itch soleus muscles and fast-twitch extensor digitorum longus (EDL) muscles isolated from C57BL/6J mi

100 The maximum tetanic force of extensor digitorum longus (EDL) muscles of adult and old wild-typ

101 hypotheses were tested by exposing extensor digitorum longus (EDL) muscles of mice deficient in CD18

102 n and thick filaments switch OFF in extensor digitorum longus (EDL) muscles of the mouse in response

103 curves are shifted to the right in extensor digitorum longus (EDL) muscles of the mutant mice.

104 n after single stretches of in situ extensor digitorum longus (EDL) muscles of young, adult and old m

105 uciferase expression in the SOL and extensor digitorum longus (EDL) muscles when the E-box was mutate

106 nally, incubation of isolated mouse extensor digitorum longus (EDL) muscles with 2 mM AICAR for 20 mi

107 levels were increased in soleus and extensor digitorum longus (EDL) muscles with Intralipid infusion

108 In rat extensor digitorum longus (EDL) muscles, (a) AMPK activator, 5-am

109 ally skinned muscle fibres from rat extensor digitorum longus (EDL) muscles.

110 -mannose-4-yloxy)-2-p ropylamine in extensor digitorum longus (EDL) muscles.

111 bolism in isolated mouse soleus and extensor digitorum longus (EDL) muscles.

112 ber-type distribution in soleus and extensor digitorum longus (EDL) muscles.

113 nt ontology, comparing those of the extensor digitorum longus (EDL) of the limb with satellite cells

114 m had less myotonia than either the extensor digitorum longus (EDL) or the soleus muscles.

115 myocardium as compared to fast rat extensor digitorum longus (EDL) skeletal muscle under relaxed con

116 The extensor digitorum longus (EDL) was isolated from stimulated (Sti

117 Rat extensor digitorum longus (EDL) was overloaded by (a) extirpation

118 and microvascular perfusion of the extensor digitorum longus (EDL) were determined in a chronic rat

119 Incubation of rat extensor digitorum longus (EDL), a predominantly fast twitch musc

120 functional capillary density in the extensor digitorum longus (EDL), and assessed acute and chronic e

121 uromuscular junctions of diaphragm, extensor digitorum longus (EDL), and soleus from C57 BL/6J dy2J/d

122 Soleus, extensor digitorum longus (EDL), tibialis anterior (TA), gastrocn

123 ys were performed in the soleus and extensor digitorum longus (EDL): targeted metabolomics, mitochond

124 slow-twitch soleus and fast-twitch extensor digitorum longus (EDL)muscles, activation of insulin sig

125 ol; slow-twitch fibre dominant) and extensor digitorum longus (EDL; fast-twitch fibre dominant) muscl

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

127 muscles, including soleus (P<0.01), extensor digitorum longus (EDL; P<0.001), and tibialis anterior (

128 the flexor hallucis longus (FHL) and flexor digitorum longus (FDL) muscles during locomotion we reco

129 n patterns were analyzed in wild-type flexor digitorum longus (FDL) tendons.

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

131 redominantly type I fiber muscles), extensor digitorum longus (predominantly type II fiber muscles),

132 Three muscles (soleus, extensor digitorum longus [EDL], and epitrochlearis) from male an

133 th increased glucose transport into extensor digitorum longus and gastrocnemius muscle.

134 We measured extensor digitorum longus and soleus muscle forces, fatigue, and

135 Extensor digitorum longus and soleus muscles of MSTN(Delta/Delta)

136 he resting intracellular calcium of extensor digitorum longus and soleus muscles of SHRs were differe

137 etabolism.Ex vivomuscle function in extensor digitorum longus and soleus muscles, including peak stre

138 The force produced by the extensor digitorum longus and tibialis anterior (EDL-TA) muscle g

139 capillary-to-fibre ratio (C: F) in extensor digitorum longus and tibialis anterior muscles of mice.

140 ely; in mixed red gastrocnemius and extensor digitorum longus both fell 60%, and beta1 fell 25%.

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

142 8) as above, and kidney, heart and extensor digitorum longus muscle (EDL) and soleus muscles were co

143 aster in actively contracting mouse extensor digitorum longus muscle (EDL) than soleus (SOL), but we

144 take were assessed in incubated rat extensor digitorum longus muscle after preincubation for 4 h in m

145 u phase till 15 min for all but the extensor digitorum longus muscle and a significant decrease at 45

146 upon sub-maximal activation in fast extensor digitorum longus muscle and slow porcine cardiac muscle.

147 partly relies on PAK2 in glycolytic extensor digitorum longus muscle By contrast to previous reports,

148 K protein expression in fast-twitch extensor digitorum longus muscle containing type IIa and IIb fibe

149 nsulin-stimulated glucose uptake in extensor digitorum longus muscle during the euglycemic-hyperinsul

150 Absolute force production of the extensor digitorum longus muscle ex vivo was higher in mice after

151 characteristics were determined in extensor digitorum longus muscle ex vivo.

152 eptor (IGF-1R) activation in single extensor digitorum longus muscle fibers from adult C57BL/6 mice.

153 -1beta) expression and release from extensor digitorum longus muscle fibres.

154 Incubation of extensor digitorum longus muscle for 1 h with 2 mm 5-aminoimidazo

155 ere recorded from an isolated mouse extensor digitorum longus muscle in the absence of gamma-motoneur

156 htly reduced in isolated glycolytic extensor digitorum longus muscle lacking PAK2 alone (-18%) or in

157 ssium currents were measured in the extensor digitorum longus muscle of normal and mdx mice, which la

158 iological analysis reveals that the extensor digitorum longus muscle of transgenic mice exhibits sign

159 ized twitch force of the stimulated extensor digitorum longus muscle on n = 11 Wistar rats with intra

160 lated glucose transport in isolated extensor digitorum longus muscle tissues and adipocytes.

161 hexia increases EcSOD expression in extensor digitorum longus muscle via muscle-derived IL-1beta-indu

162 ic stimulation frequency, intact KO extensor digitorum longus muscle was able to produce wild-type le

163 Twenty-four hours after trauma, the extensor digitorum longus muscle was microsurgically exposed and

164 uteus maximus, tibialis anterior or extensor digitorum longus muscle was then injured with local inje

165 The extensor digitorum longus muscle weight and axon counts for the t

166 erent responses from isolated mouse extensor digitorum longus muscle were recorded in the absence of

167 blood flow (FBF) and tension in the extensor digitorum longus muscle were recorded; isometric twitch

168 orylation and force potentiation in extensor digitorum longus muscle with low frequency electrical st

169 e of contraction of the fast-twitch extensor digitorum longus muscle yet had no effect on the slow-tw

170 In contrast, in glycolytic extensor digitorum longus muscle, AMPK deficiency reduced contrac

171 nsulin-stimulated glucose uptake in extensor digitorum longus muscle, and adipocytes isolated from IR

172 uscle but not the atrophy-resistant extensor digitorum longus muscle.

173 etected in non-atrophic fast-twitch extensor digitorum longus muscle.

174 and in Z-band disintegration in the extensor digitorum longus muscle.

175 more glycolytic and cachexia prone extensor digitorum longus muscle.

176 vels increase in the cachexia-prone extensor digitorum longus muscle.

177 a-induced obliteration in the mouse extensor digitorum longus muscle.

178 tro contraction measurements of the extensor digitorum longus muscle.

179 lament Ca(2+) sensitivity of the KO extensor digitorum longus muscle.

180 05), increased protein synthesis in extensor digitorum longus muscles (13.21 +/- 1.09%; P<0.05), mark

181 [Na+]i/[K+]i ratios in fast-twitch extensor digitorum longus muscles 24 hrs after CLP compared with

182 ited diminished force production in extensor digitorum longus muscles and a greater decay of Ca(2+) t

183 force in old transgenic soleus and extensor digitorum longus muscles are 50% higher than in old nont

184 eolysis was determined in incubated extensor digitorum longus muscles as release of tyrosine and 3-me

185 -) muscles is reproduced in control extensor digitorum longus muscles by selectively inhibiting alpha

186 ar increases in force generation in extensor digitorum longus muscles compared with those from mdx mi

187 n 13-week-old male C57BL/6J mice of extensor digitorum longus muscles during cancer cachexia.

188 ucose transport in mouse soleus and extensor digitorum longus muscles ex vivo.

189 re terminally anaesthetized and the extensor digitorum longus muscles from both hindlimbs were remove

190 Incubated extensor digitorum longus muscles from CLP, sham-operated, or nor

191 peractivated in O vs YA fast-twitch extensor digitorum longus muscles from Fischer(344) x Brown Norwa

192 Extensor digitorum longus muscles from Ryr1(TM/SC-DeltaL) mice ex

193 e analysis of the nerve terminal in extensor digitorum longus muscles from senescent mice showed that

194 of the junctions in rat soleus and extensor digitorum longus muscles have one TSC soma.

195 restore the function of fast-twitch extensor digitorum longus muscles in dystrophic mdx mice, a murin

196 Last, extensor digitorum longus muscles isolated from normal rats were

197 In addition, extensor digitorum longus muscles isolated from normal rats were

198 fibres were manually dissected from extensor digitorum longus muscles of 7- to 14-week-old mice.

199 ncrease in 2-deoxyglucose uptake in extensor digitorum longus muscles of control mice (0.47 +/- 0.07

200 was not observed in the fast-twitch extensor digitorum longus muscles of R58Q vs. wild-type-RLC mice,

201 ratio of that approach using whole extensor digitorum longus muscles of the mouse contracting tetani

202 Activation of myosin filaments in extensor digitorum longus muscles of the mouse is delayed by impo

203 ctural genes was measured in rabbit extensor digitorum longus muscles subjected to different mechanic

204 Isolated mutant extensor digitorum longus muscles were abnormally sensitive to th

205 hours after operation, fast-twitch extensor digitorum longus muscles were isolated and incubated in

206 tial (RMP) in uninjured and injured extensor digitorum longus muscles were made to determine if a chr

207 Rat extensor digitorum longus muscles were preincubated for 4 h in Kr

208 Last, incubation of extensor digitorum longus muscles with GF109203X or rottlerin sig

209 mong soleus, tibialis anterior, and extensor digitorum longus muscles.

210 only in SOL muscles but not in the extensor digitorum longus muscles.

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

212 Resident satellite cell number on extensor digitorum longus myofibres did not differ between groups

213 tio (C: F) and muscle blood flow in extensor digitorum longus of rats that had undergone unilateral l

214 yotonia (muscle stiffness) than the extensor digitorum longus or soleus muscles.

215 at higher temperatures in murine M. extensor digitorum longus single fibers.

216 The collagen V-null ACL and flexor digitorum longus tendon both had significant alterations

217 the flexor hallucis longus tendon or flexor digitorum longus tendon is frequently used for the treat

218 igher collagen V content than did the flexor digitorum longus tendon.

219 cruciate ligament (ACL), than in the flexor digitorum longus tendon.

220 Flexor digitorum longus tendons from a haplo-insufficient colla

221 rophy in both tibialis anterior and extensor digitorum longus that was associated with maintenance of

222 f quadriceps, tibialis posterior, and flexor digitorum longus were largest in the dorsal horn (up to

223 ontrast, incubation of isolated rat extensor digitorum longus with naturally formed Acrp30 trimers or

224 ouse living slow (soleus) and fast (extensor digitorum longus) muscle fibers in situ and determined c

225 lucose uptake was increased by 17% (extensor digitorum longus), 34% (soleus), and 90% (epitrochlearis

226 oleus, red and white gastrocnemius, extensor digitorum longus, and diaphragm by immunoblot.

227 decreased expression in quadriceps, extensor digitorum longus, and soleus approximately 10-fold, and

228 , gastrocnemius, tibialis anterior, extensor digitorum longus, and soleus) was utilized to classify d

229 est in EOM compared with diaphragm, extensor digitorum longus, and soleus.

230 gastrocnemius, quadriceps, soleus, extensor digitorum longus, and tibialis anterior muscles was dete

231 f clamps, skeletal muscles (soleus, extensor digitorum longus, and tibialis anterior) were taken for

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

233 of four mammalian muscles (soleus, extensor digitorum longus, diaphragm and digastric) with varying

234 Soleus, extensor digitorum longus, diaphragm, and heart ventricle protein

235 ion of the FHL sheath with the ankle, flexor digitorum longus, or subtalar joint occurred in half the

236 out L6 and L7), gastrocnemius soleus, flexor digitorum longus, posterior biceps-semitendinosus and po

237 d glucose uptake were determined in extensor digitorum longus, soleus, and epitrochlearis muscles.

238 stal tongue, but not in quadriceps, extensor digitorum longus, soleus, or ventricle.

239 e isometric tension measured in the extensor digitorum longus-tibialis anterior muscle group was 6.64

240 l nuclei (Li) in frozen sections of extensor digitorum longus.

241 terior and 2.52-2.66 microm for the extensor digitorum longus.

242 is posterior and, to a lesser degree, flexor digitorum longus.

243 uscles: quadriceps, abdominals, and extensor digitorum longus.

244 le atrophy in tibialis anterior and extensor digitorum longus.

245 but similar force generation in the extensor digitorum longus.

246 is of the distal peroneal nerve and extensor digitorum muscle weight were analyzed 3 months after sur

247 The macaque flexor digitorum profundus (FDP) consists of a muscle belly wit

248 pollicis longus, a thumb muscle, and flexor digitorum profundus, an index-finger muscle) was just as

249 ts in the first dorsal interossei and flexor digitorum profundus.

250 rded from two intrinsic hand muscles: flexor digitorum superficialis (FDS) and extensor digitorum com

251 ind that the extrinsic muscles of the flexor digitorum superficialis (FDS) first differentiate as int

252 NIRS data were obtained from the flexor digitorum superficialis (FDS) muscle on the dominant arm

253 Results from resting flexor digitorum superficialis and calf muscle showed a signifi

254 nalysis of median nerve regeneration, flexor digitorum superficialis atrophy, and neuromuscular junct

255 Individual motor units in flexor digitorum superficialis formed two-three groups (MU-mode

256 om the more superficial tendon of the flexor digitorum superficialis muscle.

257 microdialysis probes implanted in the flexor digitorum superficialis of the forearm in 7 healthy volu

258 Analysis of the response of flexor digitorum superficialis to ischaemic exercise provides e

259 Surface electromyographic signal from flexor digitorum superficialis was recorded and used to identif

260 s exhibited peak muscle excitation of flexor digitorum superficialis, extensor digitorum communis and

261 obic exercise in both calf muscle and flexor digitorum superficialis, phosphocreatine was depleted mo

262 muscles (right flexor digitorum and extensor digitorum) together with 64-channel electroencephalograp