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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44 terior, extensor digitorum brevis and flexor digitorum brevis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 extensor digitorum longus (EDL) and treadmill exercise increased

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 tro contraction measurements of the extensor digitorum longus muscle.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 Flexor digitorum longus tendons from a haplo-insufficient colla

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

188 but similar force generation in the extensor digitorum longus.

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

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

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

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

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

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

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

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

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

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

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

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