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

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

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

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

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

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

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

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

10 Extensor digitorum longus and soleus muscles of MSTN(Del

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

31 extensor digitorum longus (EDL) and treadmill exercise i

32 Extensor digitorum longus (EDL) fibre bundles obtained f

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

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

35 Extensor digitorum longus (EDL) muscle isolated from ske

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 1,3-bis(D-mannose-4-yloxy)-2-p ropylamine in extensor digitorum longus (EDL) muscles.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

91 The extensor digitorum longus muscle weight and axon counts

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

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

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

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

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

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

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

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

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

101 29%; P<0.05), increased protein synthesis in extensor digitorum longus muscles (13.21 +/- 1.09%; P<0.

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

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

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

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

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

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

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

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

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

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

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

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

114 Last, extensor digitorum longus muscles isolated from normal r

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

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

117 3-fold increase in 2-deoxyglucose uptake in extensor digitorum longus muscles of control mice (0.47

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

119 Isolated mutant extensor digitorum longus muscles were abnormally sensit

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

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

122 Rat extensor digitorum longus muscles were preincubated for

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

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

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

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

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

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

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

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

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