ライフサイエンスコーパス: longus

1 Li) in frozen sections of extensor digitorum longus.

2 2.52-2.66 microm for the extensor digitorum longus.

3 for salt- and glucose-mediated regulation of Longus.

4 or and, to a lesser degree, flexor digitorum longus.

5 adriceps, abdominals, and extensor digitorum longus.

6 f their respective Type IV pili, CFA/III and Longus.

7 r force generation in the extensor digitorum longus.

8 hia coli produces a long type 4 pilus called Longus.

9 (ETEC) strains produce a type IV pilus named Longus.

10 uscle types including the extensor digitorum longus (13-fold over basal), plantaris (5.8-fold), red g

11 used fed controls in both extensor digitorum longus (2.01 +/- 0.34 vs. 0.68 +/- 0.11, P = 0.002) and

12 ake was increased by 17% (extensor digitorum longus), 34% (soleus), and 90% (epitrochlearis) in trans

13 oleus (a slow muscle) and extensor digitorum longus (a fast muscle) of the rat.

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

15 motoneurones supplying the extensor hallucis longus, a muscle comprised primarily of slow twitch musc

16 esiding in separate muscles (flexor pollicis longus, a thumb muscle, and flexor digitorum profundus,

17 Extensor digitorum longus and soleus muscles of MSTN(Delta/Delta) rats demo

18 intracellular calcium of extensor digitorum longus and soleus muscles of SHRs were differently alter

19 Ex vivomuscle function in extensor digitorum longus and soleus muscles, including peak stress and tim

20 of mtDNA deletion products in two (adductor longus and soleus) of the four muscles examined compared

21 The force produced by the extensor digitorum longus and tibialis anterior (EDL-TA) muscle groups was

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

23 Adductor longus and/or rectus femoris, whose involvement can go c

24 and white gastrocnemius, extensor digitorum longus, and diaphragm by immunoblot.

25 expression in quadriceps, extensor digitorum longus, and soleus approximately 10-fold, and approximat

26 compared with diaphragm, extensor digitorum longus, and soleus.

27 skeletal muscles (soleus, extensor digitorum longus, and tibialis anterior) were taken for the measur

28 of NMJs in ankle flexors, extensor digitorum longus, and tibialis anterior.

29 xed red gastrocnemius and extensor digitorum longus both fell 60%, and beta1 fell 25%.

30 in tibialis anterior and extensor digitorum longus but not soleus muscles.

31 Soleus, extensor digitorum longus, diaphragm, and heart ventricle proteins were oxi

32 m 26 single motor units in extensor hallucis longus during sustained (60-180 s) maximal dorsiflexions

33 s tibialis anterior (TA), extensor digitorum longus (EDL) and extensor hallucis proprius (EHP) were u

34 ated fibres obtained from extensor digitorum longus (EDL) and flexor digitorum brevis (FDB) muscles o

35 ivity, we denervated fast extensor digitorum longus (EDL) and slow soleus (SOL) muscles of adult rats

36 atigue assays of isolated extensor digitorum longus (EDL) and soleus (SOL) muscles.

37 actile function of intact extensor digitorum longus (EDL) and soleus muscles from Mtm1delta4 mice, wh

38 en sodium influx into rat extensor digitorum longus (EDL) and soleus muscles was facilitated by the s

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

40 in situ contraction of m. extensor digitorum longus (EDL) and treadmill exercise increased muscle and

41 extensor digitorum longus (EDL) and treadmill exercise increased muscle and

42 Extensor digitorum longus (EDL) fibre bundles obtained from chronic high-fa

43 hat in both rat and mouse extensor digitorum longus (EDL) fibres, action potential firing leads to su

44 ucose transport in murine extensor digitorum longus (EDL) muscle (+121%, +164% and +184%, respectivel

45 Extensor digitorum longus (EDL) muscle isolated from skeletal-actin-deficie

46 bundles obtained from the extensor digitorum longus (EDL) muscle of adult mice.

47 transport in the isolated extensor digitorum longus (EDL) muscle of alpha2(R/R) mice was lower at res

48 ctate accumulation in the extensor digitorum longus (EDL) muscle of rats infused with lipopolysacchar

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

50 Rat extensor digitorum longus (EDL) muscle was incubated with different concent

51 using parameters for rat extensor digitorum longus (EDL) muscle when oxygen consumption by tissue re

52 ual fibers within a whole extensor digitorum longus (EDL) muscle, exhibited significantly reduced amp

53 affect TSC number in the extensor digitorum longus (EDL) muscle, where endplate area was unaffected

54 ely androgen-unresponsive extensor digitorum longus (EDL) muscle.

55 sport in mouse soleus and extensor digitorum longus (EDL) muscle.

56 inned fibres from the rat extensor digitorum longus (EDL) muscle.

57 nantly in the fast-twitch extensor digitorum longus (EDL) muscle.

58 Extraocular and extensor digitorum longus (EDL) muscles from adult Sprague-Dawley rats were

59 n signaling in soleus and extensor digitorum longus (EDL) muscles from rats fed a high-fat diet.

60 ways, isolated soleus and extensor digitorum longus (EDL) muscles from rats were treated with various

61 Extensor digitorum longus (EDL) muscles from wild type and TG mice were iso

62 ally denervated soleus or extensor digitorum longus (EDL) muscles in some animals.

63 tion interval <0.002) rat extensor digitorum longus (EDL) muscles in vitro (95% N2-5% CO2, 37 degrees

64 rations of rat soleus and extensor digitorum longus (EDL) muscles in which muscle action potentials w

65 after transplantation of extensor digitorum longus (EDL) muscles into nude mice.

66 s muscles and fast-twitch extensor digitorum longus (EDL) muscles isolated from C57BL/6J mice.

67 maximum tetanic force of extensor digitorum longus (EDL) muscles of adult and old wild-type (WT) and

68 s were tested by exposing extensor digitorum longus (EDL) muscles of mice deficient in CD18 (CD18(-/-

69 e shifted to the right in extensor digitorum longus (EDL) muscles of the mutant mice.

70 ngle stretches of in situ extensor digitorum longus (EDL) muscles of young, adult and old mice.

71 expression in the SOL and extensor digitorum longus (EDL) muscles when the E-box was mutated.

72 ubation of isolated mouse extensor digitorum longus (EDL) muscles with 2 mM AICAR for 20 min or elect

73 e increased in soleus and extensor digitorum longus (EDL) muscles with Intralipid infusion in both cl

74 In rat extensor digitorum longus (EDL) muscles, (a) AMPK activator, 5-aminoimidazo

75 ed muscle fibres from rat extensor digitorum longus (EDL) muscles.

76 -yloxy)-2-p ropylamine in extensor digitorum longus (EDL) muscles.

77 isolated mouse soleus and extensor digitorum longus (EDL) muscles.

78 y, comparing those of the extensor digitorum longus (EDL) of the limb with satellite cells from the m

79 Rat extensor digitorum longus (EDL) was overloaded by (a) extirpation of the sy

80 Incubation of rat extensor digitorum longus (EDL), a predominantly fast twitch muscle, with g

81 r junctions of diaphragm, extensor digitorum longus (EDL), and soleus from C57 BL/6J dy2J/dy2J mice a

82 l muscle fibres from rat extensor digitorium longus (EDL).

83 ch soleus and fast-twitch extensor digitorum longus (EDL)muscles, activation of insulin signalling in

84 n soleus and by 20-58% in extensor digitorum longus (EDL; P < 0.01).

85 ncluding soleus (P<0.01), extensor digitorum longus (EDL; P<0.001), and tibialis anterior (P<0.05) fo

86 Three muscles (soleus, extensor digitorum longus [EDL], and epitrochlearis) from male and female m

87 mental signals controlling the expression of Longus-encoding genes are unknown.

88 of a complex regulatory network controlling Longus expression, involving both local and global regul

89 and sodium chloride had a positive effect on Longus expression.

90 ied H-NS, CpxR and CRP global regulators, on Longus expression.

91 r hallucis longus (FHL) and flexor digitorum longus (FDL) muscles during locomotion we recorded Ia an

92 were analyzed in wild-type flexor digitorum longus (FDL) tendons.

93 us (S and FR MU); and the extensor digitorum longus (FF MU).

94 c) of fusimotor drive to the flexor hallucis longus (FHL) and flexor digitorum longus (FDL) muscles d

95 ical studies, harvesting the flexor hallucis longus (FHL) tendon may cause nerve injury.

96 of synergists in humans, the flexor hallucis longus (FHL, a toe flexor) and the anal sphincter, as a

97 is occurs we examined neonatal levator auris longus (LAL) and 4th deep lumbrical (4DL) muscles, as we

98 e transversus abdominis (TVA), levator auris longus (LAL) and lumbrical muscles were disrupted in bot

99 ion potentials were studied in levator auris longus motor terminals using Ca2+-sensitive fluorescent

100 ve, and kidney, heart and extensor digitorum longus muscle (EDL) and soleus muscles were collected.

101 ctively contracting mouse extensor digitorum longus muscle (EDL) than soleus (SOL), but we find these

102 assessed in incubated rat extensor digitorum longus muscle after preincubation for 4 h in media conta

103 expression in fast-twitch extensor digitorum longus muscle containing type IIa and IIb fibers, with c

104 mulated glucose uptake in extensor digitorum longus muscle during the euglycemic-hyperinsulinemic cla

105 e force production of the extensor digitorum longus muscle ex vivo was higher in mice after treatment

106 istics were determined in extensor digitorum longus muscle ex vivo.

107 -1R) activation in single extensor digitorum longus muscle fibers from adult C57BL/6 mice.

108 Incubation of extensor digitorum longus muscle for 1 h with 2 mm 5-aminoimidazole-4-carbo

109 an ex vivo preparation of the levator auris longus muscle from male and female late-stage R6/2 mice

110 ents were measured in the extensor digitorum longus muscle of normal and mdx mice, which lack the pro

111 analysis reveals that the extensor digitorum longus muscle of transgenic mice exhibits significantly

112 Surprisingly, mdx3cv extensor digitorium longus muscle showed significantly higher tetanic force

113 ose transport in isolated extensor digitorum longus muscle tissues and adipocytes.

114 tion frequency, intact KO extensor digitorum longus muscle was able to produce wild-type levels of fo

115 A diagnosis of hypertrophied palmaris longus muscle was made.

116 r hours after trauma, the extensor digitorum longus muscle was microsurgically exposed and analyzed b

117 Moreover, the action of the fibularis longus muscle was more like its homolog in Old World mon

118 The extensor digitorum longus muscle weight and axon counts for the three types

119 (FBF) and tension in the extensor digitorum longus muscle were recorded; isometric twitch and tetani

120 and force potentiation in extensor digitorum longus muscle with low frequency electrical stimulation.

121 action of the fast-twitch extensor digitorum longus muscle yet had no effect on the slow-twitch soleu

122 on (in the expected location of the palmaris longus muscle).

123 mulated glucose uptake in extensor digitorum longus muscle, and adipocytes isolated from IRAP-/- mice

124 ppearance of normal variants of the palmaris longus muscle, as this can obviate surgery.

125 not the atrophy-resistant extensor digitorum longus muscle.

126 and disintegration in the extensor digitorum longus muscle.

127 obliteration in the mouse extensor digitorum longus muscle.

128 ction measurements of the extensor digitorum longus muscle.

129 2+) sensitivity of the KO extensor digitorum longus muscle.

130 duced injury than mdx4cv extensor digitorium longus muscle.

131 imes in adult fast twitch extensor digitalis longus muscle.

132 inal mitochondria in the mouse levator auris longus muscle.

133 ased protein synthesis in extensor digitorum longus muscles (13.21 +/- 1.09%; P<0.05), markedly enhan

134 +]i ratios in fast-twitch extensor digitorum longus muscles 24 hrs after CLP compared with sham opera

135 old transgenic soleus and extensor digitorum longus muscles are 50% higher than in old nontransgenic

136 s determined in incubated extensor digitorum longus muscles as release of tyrosine and 3-methylhistid

137 is reproduced in control extensor digitorum longus muscles by selectively inhibiting alpha2 enzyme a

138 es in force generation in extensor digitorum longus muscles compared with those from mdx mice.

139 sport in mouse soleus and extensor digitorum longus muscles ex vivo.

140 lly anaesthetized and the extensor digitorum longus muscles from both hindlimbs were removed and snap

141 Incubated extensor digitorum longus muscles from CLP, sham-operated, or normal rats w

142 ed in O vs YA fast-twitch extensor digitorum longus muscles from Fischer(344) x Brown Norway (FBN) ra

143 of the nerve terminal in extensor digitorum longus muscles from senescent mice showed that the decre

144 nctions in rat soleus and extensor digitorum longus muscles have one TSC soma.

145 e function of fast-twitch extensor digitorum longus muscles in dystrophic mdx mice, a murine model of

146 Last, extensor digitorum longus muscles isolated from normal rats were incubated

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

148 e manually dissected from extensor digitorum longus muscles of 7- to 14-week-old mice.

149 taneous application of CNTF to levator auris longus muscles of adult mice evokes sprouting from nearl

150 2-deoxyglucose uptake in extensor digitorum longus muscles of control mice (0.47 +/- 0.07 micromol/m

151 es was measured in rabbit extensor digitorum longus muscles subjected to different mechanical signals

152 Isolated mutant extensor digitorum longus muscles were abnormally sensitive to the Na+/K+ p

153 er operation, fast-twitch extensor digitorum longus muscles were isolated and incubated in normal Kre

154 in uninjured and injured extensor digitorum longus muscles were made to determine if a chronic depol

155 Rat extensor digitorum longus muscles were preincubated for 4 h in Krebs-Hensel

156 Last, incubation of extensor digitorum longus muscles with GF109203X or rottlerin significantly

157 no effect on fast twitch extensor digitorum longus muscles.

158 s, tibialis anterior, and extensor digitorum longus muscles.

159 and muscle blood flow in extensor digitorum longus of rats that had undergone unilateral ligation of

160 We identified two genes lngR and lngS in the Longus operon, whose predicted products share homology w

161 FHL sheath with the ankle, flexor digitorum longus, or subtalar joint occurred in half the cases.

162 L7), gastrocnemius soleus, flexor digitorum longus, posterior biceps-semitendinosus and popliteus (m

163 ly type I fiber muscles), extensor digitorum longus (predominantly type II fiber muscles), and the po

164 ium, appears to be an important stimulus for Longus production.

165 uptake were determined in extensor digitorum longus, soleus, and epitrochlearis muscles.

166 e, but not in quadriceps, extensor digitorum longus, soleus, or ventricle.

167 Alleles of the Longus structural subunit gene lngA demonstrate a divers

168 The collagen V-null ACL and flexor digitorum longus tendon both had significant alterations in mechan

169 Os peroneum fracture and peroneus longus tendon injuries were characterized with US and MR

170 r hallucis longus tendon or flexor digitorum longus tendon is frequently used for the treatment of po

171 The transfer of the flexor hallucis longus tendon or flexor digitorum longus tendon is frequ

172 was associated with full-thickness peroneus longus tendon tear in seven of seven patients (100%).

173 cture and associated full-thickness peroneus longus tendon tear.

174 five, and both peroneus brevis and peroneus longus tendon tears in two.

175 At surgery, isolated peroneus longus tendon tears were seen in four patients, isolated

176 ed detection of peroneus brevis and peroneus longus tendon tears.

177 ariable and included the calcaneus, peroneus longus tendon, peroneus brevis tendon; and cuboid bone.

178 agen V content than did the flexor digitorum longus tendon.

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

180 Flexor digitorum longus tendons from a haplo-insufficient collagen V mous

181 gene cluster involved in the biosynthesis of Longus that has 57 to 95% identity at the protein level

182 c tension measured in the extensor digitorum longus-tibialis anterior muscle group was 6.64 +/- 0.66

183 ar ATP on fully innervated rat levator auris longus using two intracellular microelectrodes.

184 ps, tibialis posterior, and flexor digitorum longus were largest in the dorsal horn (up to 600 microV

185 ncubation of isolated rat extensor digitorum longus with naturally formed Acrp30 trimers or trimeric