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

4 adriceps, abdominals, and extensor digitorum longus.

5 in tibialis anterior and extensor digitorum longus.

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

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

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

9 r force generation in the extensor digitorum longus.

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

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

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

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

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

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

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

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

18 g a greater inter-limb asymmetry of peroneus longus activity (contact phase) (P = 0.003) and gluteus

19 ed glucose transport into extensor digitorum longus and gastrocnemius muscle.

20 We measured extensor digitorum longus and soleus muscle forces, fatigue, and contractil

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

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

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

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

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

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

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

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

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

30 emius, tibialis anterior, extensor digitorum longus, and soleus) was utilized to classify diseased ti

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

32 mius, quadriceps, soleus, extensor digitorum longus, and tibialis anterior muscles was determined.

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

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

35 Gracilis and adductor longus biopsies were collected from children with CP und

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

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

38 ammalian muscles (soleus, extensor digitorum longus, diaphragm and digastric) with varying biomechani

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

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

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

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

43 ons are different in fast extensor digitorum longus (EDL) and slow soleus (SOL) muscle, being complet

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

45 lysis of fast-contracting extensor digitorum longus (EDL) and slow-contracting soleus (SOL) muscles w

46 different in fast-twitch extensor digitorum longus (EDL) and slow-twitch soleus (SOL) muscles derive

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

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

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

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

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

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

53 isolated soleus (SOL) and extensor digitorum longus (EDL) contractile function.

54 In situ extensor digitorum longus (EDL) contractility and femoral blood flow were a

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

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

57 antly reduced in isolated extensor digitorum longus (EDL) from C2(-/-) mice.

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

59 hly induced in glycolytic extensor digitorum longus (EDL) muscle during exercise.

60 ure fast-twitch-fibre rat extensor digitorum longus (EDL) muscle during twitch and tetanic contractio

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

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

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

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

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

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

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

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

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

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

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

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

73 mus, tibialis anterior or extensor digitorum longus (EDL) muscle.

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

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

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

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

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

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

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

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

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

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

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

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

86 k filaments switch OFF in extensor digitorum longus (EDL) muscles of the mouse in response to decreas

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

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

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

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

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

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

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

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

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

96 istribution in soleus and extensor digitorum longus (EDL) muscles.

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

98 myotonia than either the extensor digitorum longus (EDL) or the soleus muscles.

99 m as compared to fast rat extensor digitorum longus (EDL) skeletal muscle under relaxed conditions an

100 The extensor digitorum longus (EDL) was isolated from stimulated (Stim) and con

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

102 vascular perfusion of the extensor digitorum longus (EDL) were determined in a chronic rat model of c

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

104 capillary density in the extensor digitorum longus (EDL), and assessed acute and chronic effects on

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

106 Soleus, extensor digitorum longus (EDL), tibialis anterior (TA), gastrocnemius and

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

108 rformed in the soleus and extensor digitorum longus (EDL): targeted metabolomics, mitochondrial respi

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

110 witch fibre dominant) and extensor digitorum longus (EDL; fast-twitch fibre dominant) muscles.

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

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

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

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

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

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

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

118 Finally, we show that palmaris longus fails to form from early in development.

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

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

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

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

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

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

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

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

127 activity of the tibialis anterior, peroneus longus, medial gastrocnemius, and gluteus medius were re

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

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

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

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

132 ll 15 min for all but the extensor digitorum longus muscle and a significant decrease at 45 or 75 min

133 aximal activation in fast extensor digitorum longus muscle and slow porcine cardiac muscle.

134 ies on PAK2 in glycolytic extensor digitorum longus muscle By contrast to previous reports, PAK1 is d

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

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

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

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

139 -1R) activation in single extensor digitorum longus muscle fibers from adult C57BL/6 mice.

140 pression and release from extensor digitorum longus muscle fibres.

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

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

143 ed from an isolated mouse extensor digitorum longus muscle in the absence of gamma-motoneuron activit

144 ed in isolated glycolytic extensor digitorum longus muscle lacking PAK2 alone (-18%) or in combinatio

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

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

147 h force of the stimulated extensor digitorum longus muscle on n = 11 Wistar rats with intra- and cros

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

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

150 eases EcSOD expression in extensor digitorum longus muscle via muscle-derived IL-1beta-induced upregu

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

152 A diagnosis of hypertrophied palmaris longus muscle was made.

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

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

155 mus, tibialis anterior or extensor digitorum longus muscle was then injured with local injection of B

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

157 onses from isolated mouse extensor digitorum longus muscle were recorded in the absence of fusimotor

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

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

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

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

162 n contrast, in glycolytic extensor digitorum longus muscle, AMPK deficiency reduced contraction-stimu

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

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

165 inal mitochondria in the mouse levator auris longus muscle.

166 non-atrophic fast-twitch extensor digitorum longus muscle.

167 not the atrophy-resistant extensor digitorum longus muscle.

168 and disintegration in the extensor digitorum longus muscle.

169 olytic and cachexia prone extensor digitorum longus muscle.

170 ase in the cachexia-prone extensor digitorum longus muscle.

171 obliteration in the mouse extensor digitorum longus muscle.

172 ction measurements of the extensor digitorum longus muscle.

173 2+) sensitivity of the KO extensor digitorum longus muscle.

174 duced injury than mdx4cv extensor digitorium longus muscle.

175 imes in adult fast twitch extensor digitalis longus muscle.

176 g slow (soleus) and fast (extensor digitorum longus) muscle fibers in situ and determined cellular di

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

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

179 ished force production in extensor digitorum longus muscles and a greater decay of Ca(2+) transients

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

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

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

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

184 old male C57BL/6J mice of extensor digitorum longus muscles during cancer cachexia.

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

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

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

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

189 Extensor digitorum longus muscles from Ryr1(TM/SC-DeltaL) mice exhibit decr

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

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

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

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

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

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

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

197 2-deoxyglucose uptake in extensor digitorum longus muscles of control mice (0.47 +/- 0.07 micromol/m

198 served in the fast-twitch extensor digitorum longus muscles of R58Q vs. wild-type-RLC mice, but mutan

199 that approach using whole extensor digitorum longus muscles of the mouse contracting tetanically at 2

200 on of myosin filaments in extensor digitorum longus muscles of the mouse is delayed by imposing rapid

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

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

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

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

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

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

207 no effect on fast twitch extensor digitorum longus muscles.

208 OL muscles but not in the extensor digitorum longus muscles.

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

210 satellite cell number on extensor digitorum longus myofibres did not differ between groups.

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

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

213 uscle stiffness) than the extensor digitorum longus or soleus muscles.

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

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

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

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

218 temperatures in murine M. extensor digitorum longus single fibers.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

236 oth tibialis anterior and extensor digitorum longus that was associated with maintenance of fibre siz

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

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

239 he synaptic cleft of the mouse levator auris longus using viral expression of the pseudoratiometric p

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

241 aphy (EMG) of the gastrocnemius and peroneus longus were recorded in 14 PD patients during sitting, s

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