ライフサイエンスコーパス: extensor digitorum longus

1 ly fast muscles: quadriceps, abdominals, and extensor digitorum longus.

2 ated muscle atrophy in tibialis anterior and extensor digitorum longus.

3 dx mice, but similar force generation in the extensor digitorum longus.

4 terstitial nuclei (Li) in frozen sections of extensor digitorum longus.

5 bialis anterior and 2.52-2.66 microm for the extensor digitorum longus.

6 ation in multiple muscle types including the extensor digitorum longus (13-fold over basal), plantari

7 red with saline-infused fed controls in both extensor digitorum longus (2.01 +/- 0.34 vs. 0.68 +/- 0.

8 mulated glucose uptake was increased by 17% (extensor digitorum longus), 34% (soleus), and 90% (epitr

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

10 d from the soleus (a slow-twitch muscle) and extensor digitorum longus (a fast-twitch muscle) of the

11 mitant with increased glucose transport into extensor digitorum longus and gastrocnemius muscle.

12 We measured extensor digitorum longus and soleus muscle forces, fati

13 Extensor digitorum longus and soleus muscles of MSTN(Del

14 stasis; the resting intracellular calcium of extensor digitorum longus and soleus muscles of SHRs wer

15 no acid metabolism.Ex vivomuscle function in extensor digitorum longus and soleus muscles, including

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

17 ssion and capillary-to-fibre ratio (C: F) in extensor digitorum longus and tibialis anterior muscles

18 ured in soleus, red and white gastrocnemius, extensor digitorum longus, and diaphragm by immunoblot.

19 mutation decreased expression in quadriceps, extensor digitorum longus, and soleus approximately 10-f

20 uadriceps, gastrocnemius, tibialis anterior, extensor digitorum longus, and soleus) was utilized to c

21 was highest in EOM compared with diaphragm, extensor digitorum longus, and soleus.

22 nction in gastrocnemius, quadriceps, soleus, extensor digitorum longus, and tibialis anterior muscles

23 clusion of clamps, skeletal muscles (soleus, extensor digitorum longus, and tibialis anterior) were t

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

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

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

27 tionships of four mammalian muscles (soleus, extensor digitorum longus, diaphragm and digastric) with

28 Soleus, extensor digitorum longus, diaphragm, and heart ventricl

29 The fast muscles tibialis anterior (TA), extensor digitorum longus (EDL) and extensor hallucis pr

30 enzymatically isolated fibres obtained from extensor digitorum longus (EDL) and flexor digitorum bre

31 muscle impulse activity, we denervated fast extensor digitorum longus (EDL) and slow soleus (SOL) mu

32 OFF to ON transitions are different in fast extensor digitorum longus (EDL) and slow soleus (SOL) mu

33 Single myofiber analysis of fast-contracting extensor digitorum longus (EDL) and slow-contracting sol

34 s of these isoforms different in fast-twitch extensor digitorum longus (EDL) and slow-twitch soleus (

35 ected in force or fatigue assays of isolated extensor digitorum longus (EDL) and soleus (SOL) muscles

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

37 When sodium influx into rat extensor digitorum longus (EDL) and soleus muscles was f

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

39 extensor digitorum longus (EDL) and treadmill exercise i

40 e found that prior in situ contraction of m. extensor digitorum longus (EDL) and treadmill exercise i

41 supplementation on isolated soleus (SOL) and extensor digitorum longus (EDL) contractile function.

42 In situ extensor digitorum longus (EDL) contractility and femora

43 Extensor digitorum longus (EDL) fibre bundles obtained f

44 It is shown that in both rat and mouse extensor digitorum longus (EDL) fibres, action potential

45 ction were significantly reduced in isolated extensor digitorum longus (EDL) from C2(-/-) mice.

46 sphorylation and glucose transport in murine extensor digitorum longus (EDL) muscle (+121%, +164% and

47 selectively and highly induced in glycolytic extensor digitorum longus (EDL) muscle during exercise.

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

49 Extensor digitorum longus (EDL) muscle isolated from ske

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

51 Na,K-ATPase active transport in the isolated extensor digitorum longus (EDL) muscle of alpha2(R/R) mi

52 ) inhibition and lactate accumulation in the extensor digitorum longus (EDL) muscle of rats infused w

53 on in skeletal muscle using an incubated rat extensor digitorum longus (EDL) muscle preparation as a

54 Rat extensor digitorum longus (EDL) muscle was incubated wit

55 al vascular network using parameters for rat extensor digitorum longus (EDL) muscle when oxygen consu

56 imaging in individual fibers within a whole extensor digitorum longus (EDL) muscle, exhibited signif

57 rone levels did not affect TSC number in the extensor digitorum longus (EDL) muscle, where endplate a

58 press GLUT4 predominantly in the fast-twitch extensor digitorum longus (EDL) muscle.

59 n into gluteus maximus, tibialis anterior or extensor digitorum longus (EDL) muscle.

60 ulated glucose transport in mouse soleus and extensor digitorum longus (EDL) muscle.

61 that of the relatively androgen-unresponsive extensor digitorum longus (EDL) muscle.

62 in mechanically skinned fibres from the rat extensor digitorum longus (EDL) muscle.

63 Extraocular and extensor digitorum longus (EDL) muscles from adult Sprag

64 nd increased insulin signaling in soleus and extensor digitorum longus (EDL) muscles from rats fed a

65 dent signaling pathways, isolated soleus and extensor digitorum longus (EDL) muscles from rats were t

66 Extensor digitorum longus (EDL) muscles from wild type a

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

68 train/120 s contraction interval <0.002) rat extensor digitorum longus (EDL) muscles in vitro (95% N2

69 nerve-muscle preparations of rat soleus and extensor digitorum longus (EDL) muscles in which muscle

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

71 n slow-twitch soleus muscles and fast-twitch extensor digitorum longus (EDL) muscles isolated from C5

72 The maximum tetanic force of extensor digitorum longus (EDL) muscles of adult and old

73 These hypotheses were tested by exposing extensor digitorum longus (EDL) muscles of mice deficien

74 uscle thin and thick filaments switch OFF in extensor digitorum longus (EDL) muscles of the mouse in

75 frequency curves are shifted to the right in extensor digitorum longus (EDL) muscles of the mutant mi

76 ared 1 min after single stretches of in situ extensor digitorum longus (EDL) muscles of young, adult

77 ange in luciferase expression in the SOL and extensor digitorum longus (EDL) muscles when the E-box w

78 Additionally, incubation of isolated mouse extensor digitorum longus (EDL) muscles with 2 mM AICAR

79 (G-6-P) levels were increased in soleus and extensor digitorum longus (EDL) muscles with Intralipid

80 In rat extensor digitorum longus (EDL) muscles, (a) AMPK activa

81 mechanically skinned muscle fibres from rat extensor digitorum longus (EDL) muscles.

82 1,3-bis(D-mannose-4-yloxy)-2-p ropylamine in extensor digitorum longus (EDL) muscles.

83 (FA) metabolism in isolated mouse soleus and extensor digitorum longus (EDL) muscles.

84 (MHC) fiber-type distribution in soleus and extensor digitorum longus (EDL) muscles.

85 a different ontology, comparing those of the extensor digitorum longus (EDL) of the limb with satelli

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

87 n porcine myocardium as compared to fast rat extensor digitorum longus (EDL) skeletal muscle under re

88 The extensor digitorum longus (EDL) was isolated from stimul

89 Rat extensor digitorum longus (EDL) was overloaded by (a) ex

90 low (FBF) and microvascular perfusion of the extensor digitorum longus (EDL) were determined in a chr

91 Incubation of rat extensor digitorum longus (EDL), a predominantly fast tw

92 ction in functional capillary density in the extensor digitorum longus (EDL), and assessed acute and

93 of the neuromuscular junctions of diaphragm, extensor digitorum longus (EDL), and soleus from C57 BL/

94 Soleus, extensor digitorum longus (EDL), tibialis anterior (TA),

95 wing assays were performed in the soleus and extensor digitorum longus (EDL): targeted metabolomics,

96 into the slow-twitch soleus and fast-twitch extensor digitorum longus (EDL)muscles, activation of in

97 soleus (Sol; slow-twitch fibre dominant) and extensor digitorum longus (EDL; fast-twitch fibre domina

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

99 skeletal muscles, including soleus (P<0.01), extensor digitorum longus (EDL; P<0.001), and tibialis a

100 Three muscles (soleus, extensor digitorum longus [EDL], and epitrochlearis) fro

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

102 ater (n = 8) as above, and kidney, heart and extensor digitorum longus muscle (EDL) and soleus muscle

103 l times faster in actively contracting mouse extensor digitorum longus muscle (EDL) than soleus (SOL)

104 lucose uptake were assessed in incubated rat extensor digitorum longus muscle after preincubation for

105 a plateau phase till 15 min for all but the extensor digitorum longus muscle and a significant decre

106 guration upon sub-maximal activation in fast extensor digitorum longus muscle and slow porcine cardia

107 e uptake partly relies on PAK2 in glycolytic extensor digitorum longus muscle By contrast to previous

108 in skMLCK protein expression in fast-twitch extensor digitorum longus muscle containing type IIa and

109 Insulin-stimulated glucose uptake in extensor digitorum longus muscle during the euglycemic-h

110 Absolute force production of the extensor digitorum longus muscle ex vivo was higher in m

111 ntractile characteristics were determined in extensor digitorum longus muscle ex vivo.

112 tor-1 receptor (IGF-1R) activation in single extensor digitorum longus muscle fibers from adult C57BL

113 1beta (IL-1beta) expression and release from extensor digitorum longus muscle fibres.

114 Incubation of extensor digitorum longus muscle for 1 h with 2 mm 5-ami

115 ferents were recorded from an isolated mouse extensor digitorum longus muscle in the absence of gamma

116 was slightly reduced in isolated glycolytic extensor digitorum longus muscle lacking PAK2 alone (-18

117 Potassium currents were measured in the extensor digitorum longus muscle of normal and mdx mice,

118 scle physiological analysis reveals that the extensor digitorum longus muscle of transgenic mice exhi

119 he normalized twitch force of the stimulated extensor digitorum longus muscle on n = 11 Wistar rats w

120 lin-stimulated glucose transport in isolated extensor digitorum longus muscle tissues and adipocytes.

121 ancer cachexia increases EcSOD expression in extensor digitorum longus muscle via muscle-derived IL-1

122 mal tetanic stimulation frequency, intact KO extensor digitorum longus muscle was able to produce wil

123 Twenty-four hours after trauma, the extensor digitorum longus muscle was microsurgically exp

124 The gluteus maximus, tibialis anterior or extensor digitorum longus muscle was then injured with l

125 The extensor digitorum longus muscle weight and axon counts

126 indle afferent responses from isolated mouse extensor digitorum longus muscle were recorded in the ab

127 femoral blood flow (FBF) and tension in the extensor digitorum longus muscle were recorded; isometri

128 LC phosphorylation and force potentiation in extensor digitorum longus muscle with low frequency elec

129 ific force of contraction of the fast-twitch extensor digitorum longus muscle yet had no effect on th

130 In contrast, in glycolytic extensor digitorum longus muscle, AMPK deficiency reduce

131 sal and insulin-stimulated glucose uptake in extensor digitorum longus muscle, and adipocytes isolate

132 and p94 and in Z-band disintegration in the extensor digitorum longus muscle.

133 ere not detected in non-atrophic fast-twitch extensor digitorum longus muscle.

134 an in the more glycolytic and cachexia prone extensor digitorum longus muscle.

135 EcSOD) levels increase in the cachexia-prone extensor digitorum longus muscle.

136 r ischemia-induced obliteration in the mouse extensor digitorum longus muscle.

137 and in vitro contraction measurements of the extensor digitorum longus muscle.

138 zed myofilament Ca(2+) sensitivity of the KO extensor digitorum longus muscle.

139 soleus muscle but not the atrophy-resistant extensor digitorum longus muscle.

140 studied mouse living slow (soleus) and fast (extensor digitorum longus) muscle fibers in situ and det

141 29%; P<0.05), increased protein synthesis in extensor digitorum longus muscles (13.21 +/- 1.09%; P<0.

142 Na+]i and [Na+]i/[K+]i ratios in fast-twitch extensor digitorum longus muscles 24 hrs after CLP compa

143 ice exhibited diminished force production in extensor digitorum longus muscles and a greater decay of

144 ic muscle force in old transgenic soleus and extensor digitorum longus muscles are 50% higher than in

145 llar proteolysis was determined in incubated extensor digitorum longus muscles as release of tyrosine

146 alpha2(-/-) muscles is reproduced in control extensor digitorum longus muscles by selectively inhibit

147 to similar increases in force generation in extensor digitorum longus muscles compared with those fr

148 gulated in 13-week-old male C57BL/6J mice of extensor digitorum longus muscles during cancer cachexia

149 ulated glucose transport in mouse soleus and extensor digitorum longus muscles ex vivo.

150 nimals were terminally anaesthetized and the extensor digitorum longus muscles from both hindlimbs we

151 Incubated extensor digitorum longus muscles from CLP, sham-operate

152 lso be hyperactivated in O vs YA fast-twitch extensor digitorum longus muscles from Fischer(344) x Br

153 Extensor digitorum longus muscles from Ryr1(TM/SC-DeltaL

154 The analysis of the nerve terminal in extensor digitorum longus muscles from senescent mice sh

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

156 mpletely restore the function of fast-twitch extensor digitorum longus muscles in dystrophic mdx mice

157 In addition, extensor digitorum longus muscles isolated from normal r

158 Last, extensor digitorum longus muscles isolated from normal r

159 ndles of fibres were manually dissected from extensor digitorum longus muscles of 7- to 14-week-old m

160 3-fold increase in 2-deoxyglucose uptake in extensor digitorum longus muscles of control mice (0.47

161 rce that was not observed in the fast-twitch extensor digitorum longus muscles of R58Q vs. wild-type-

162 -to-noise ratio of that approach using whole extensor digitorum longus muscles of the mouse contracti

163 Activation of myosin filaments in extensor digitorum longus muscles of the mouse is delaye

164 two structural genes was measured in rabbit extensor digitorum longus muscles subjected to different

165 Isolated mutant extensor digitorum longus muscles were abnormally sensit

166 enty-four hours after operation, fast-twitch extensor digitorum longus muscles were isolated and incu

167 ane potential (RMP) in uninjured and injured extensor digitorum longus muscles were made to determine

168 Rat extensor digitorum longus muscles were preincubated for

169 Last, incubation of extensor digitorum longus muscles with GF109203X or rott

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

171 ylation among soleus, tibialis anterior, and extensor digitorum longus muscles.

172 I/type II only in SOL muscles but not in the extensor digitorum longus muscles.

173 Resident satellite cell number on extensor digitorum longus myofibres did not differ betwe

174 fibre ratio (C: F) and muscle blood flow in extensor digitorum longus of rats that had undergone uni

175 ch less myotonia (muscle stiffness) than the extensor digitorum longus or soleus muscles.

176 soleus (predominantly type I fiber muscles), extensor digitorum longus (predominantly type II fiber m

177 ic range at higher temperatures in murine M. extensor digitorum longus single fibers.

178 stimulated glucose uptake were determined in extensor digitorum longus, soleus, and epitrochlearis mu

179 ase in distal tongue, but not in quadriceps, extensor digitorum longus, soleus, or ventricle.

180 muscle atrophy in both tibialis anterior and extensor digitorum longus that was associated with maint

181 the muscle isometric tension measured in the extensor digitorum longus-tibialis anterior muscle group

182 In contrast, incubation of isolated rat extensor digitorum longus with naturally formed Acrp30 t