ライフサイエンスコーパス: gastrocnemius muscle

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

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

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

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

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

6 hysiological types as established in the cat gastrocnemius muscle.

7 expression of insulin signaling proteins in gastrocnemius muscle.

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

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

10 anisms involved in mRNA translation in mouse gastrocnemius muscle.

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

12 he apoptotic responses to denervation in rat gastrocnemius muscle.

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

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

15 the feed arteries perforating the soleus and gastrocnemius muscles.

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

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

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

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

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

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

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

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

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

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

26 5- to 5-fold) in rat soleus muscle and white gastrocnemius muscle and in mouse soleus muscle, which w

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

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

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

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

31 In gastrocnemius muscle arterioles, ageing did not alter ma

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

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

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

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

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

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

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

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

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

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

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

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

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

45 4c lentivirus into mice caused repression of gastrocnemius muscle development.

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

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

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

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

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

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

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

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

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

55 Following hMDSPC therapy, gastrocnemius muscles from mice exhibited substantially

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

57 MTII treatment increased gastrocnemius muscle heat dissipation during controlled

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 In the gastrocnemius muscle of castrated animals, HB treatment

77 2SC and fumarate in gastrocnemius muscle of control and streptozotocin-induc

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

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

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

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

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

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

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

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

86 < 0.05 vs. control), in both soleus and red gastrocnemius muscles of lean rats infused with either A

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

88 In the gastrocnemius muscle, oxfenicine increased pyruvate dehy

89 .31 +/- 0.06 mmol/kg/min during clamp in red-gastrocnemius muscle, P < 0.05).

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

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

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

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

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

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

96 In gastrocnemius muscle, resveratrol increased the gene exp

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

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

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

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

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

102 -16.1%) within single muscle fibers from the gastrocnemius muscle, the maximum rate of mitochondrial

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

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

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

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

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

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

109 Gastrocnemius muscle was extracted immediately after acu

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

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

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

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

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

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

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

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

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

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

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

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

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

123 The gastrocnemius muscles were evaluated in the patients wit

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

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

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

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

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

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