ライフサイエンスコーパス: muscle tissue

1 ly lead to greater fatigue and stress of the muscle tissue.

2 ass spectrometry in patient-derived skeletal muscle tissue.

3 ofibers is a necessary step in the repair of muscle tissue.

4 ch for the functional restoration of damaged muscle tissue.

5 tories, Wilmington, Mass) for development of muscle tissue.

6 insulin-stimulated glucose uptake in fat and muscle tissue.

7 oietic cells and mesenchymal stem cells from muscle tissue.

8 ecretion of this critical synaptic enzyme in muscle tissue.

9 to elevate NAD levels in plasma, liver, and muscle tissue.

10 reduced mortality and lower parasite load in muscle tissue.

11 ntiating human muscle cells and regenerating muscle tissue.

12 ner that is reminiscent of the sarcomeres of muscle tissue.

13 ng of neural tissue, as well as other smooth muscle tissue.

14 of sodium-limited traits, such as neural and muscle tissue.

15 lyzed methylation of AARS1 in mouse skeletal muscle tissue.

16 pressed in fetal versus adult human skeletal muscle tissue.

17 lease behavior, characteristic of functional muscle tissue.

18 enabling functional improvement of ischaemic muscle tissue.

19 re not correlated with CTG expansion size in muscle tissue.

20 ansporter-4 (GLUT4) localization in skeletal muscle tissue.

21 37)Cs (2.0 +/- 0.5 Bq kg(-1)) in their white muscle tissue.

22 n structural proteins and their hydration in muscle tissue.

23 ffuse 'volume' neurotransmission in a smooth muscle tissue.

24 lly cooked before consumption, and mostly in muscle tissue.

25 MV is mainly expressed in smooth and cardiac muscle tissue.

26 ion was detected in PPARbeta/delta-null mice muscle tissue.

27 s of interest around ankles, carcinomas, and muscle tissue.

28 lly important for regeneration of dystrophic muscle tissue.

29 persistent factor IX expression in injected muscle tissue.

30 or satellite cell response observed in older muscle tissue.

31 sultant swelling within the fascicles of the muscle tissue.

32 utical distribution and accumulation in fish muscle tissue.

33 not in unaffected control myogenic cells and muscle tissue.

34 n form actin filaments, in intestinal smooth muscle tissue.

35 f tumor growth of >50% even under 1 cm thick muscle tissue.

36 f WT and alanine-expanded PABPN1 in skeletal muscle tissue.

37 (9.0%), and 18:0-18:1-22:6 (16.4%) in salmon muscle tissue.

38 was expressed at extremely low level in the muscle tissue.

39 e and human osteoblasts, as well as in human muscle tissue.

40 is in the regulation of protein synthesis in muscle tissue.

41 terminants of the phenotypes seen in various muscle tissues.

42 is found phosphorylated in vivo in bone and muscle tissues.

43 er concentrations in liver and gonad than in muscle tissues.

44 aldosterone, is also increased in dystrophic muscle tissues.

45 nsive analysis of alpha-actin extracted from muscle tissues.

46 reside in anatomically defined niches within muscle tissues.

47 with tension development in tracheal smooth muscle tissues.

48 resulted in greater MC content in liver and muscle tissues.

49 hogenesis and function of cardiac and smooth muscle tissues.

50 nted the M2c macrophage phenotype in injured muscle tissues.

51 f penicillins in bovine, porcine and chicken muscle tissues.

52 tological analyses of both bone and skeletal muscle tissues.

53 osphate in muscles, which provides energy to muscle tissues.

54 y other strategies to enhance ASO potency in muscle tissues.

55 transcriptomic analyses on white adipose and muscle tissues.

56 Total of 2102 proteins were identified in muscle tissues.

57 cterized by weakness and wasting of skeletal muscle tissues.

58 alamus) as well as in the peripheral (liver, muscle) tissues.

59 tion (uncorrected for fat fraction) of thigh muscle tissue (112-124 mmol/L) lies within the expected

60 ed integrated synthesis rates of proteins in muscle tissue across the proteome to be measured over se

61 Muscle tissue adenosine triphosphate decreased in all gr

62 We show that muscle tissue affects the immune response by acting as a

63 -to-noise ratio (DeltaCNR) between liver and muscle tissue after CM-101 injection was used to quantif

64 ents of the endogenous antioxidant system of muscle tissues, alpha-tocopherol (alpha-TOH) and ascorbi

65 MDSC that combines 3-dimensional artificial muscle tissue (AMT) culture with temporally controlled b

66 y exosomes determined its restoration within muscle tissues, an overall recovery of alpha-DG glycosyl

67 ng a hypermethylated state with age, in both muscle tissue and cells on genes KIF15, DYRK2, FHL2, MRP

68 the muscle spindle, which is embedded in the muscle tissue and composed of intrafusal fibers.

69 ing lipid metabolites was comparable between muscle tissue and cultured myotubes, and temporal lipid

70 d in delta(202)Hg values between pilot whale muscle tissue and Faroese whalers' hair but no mass-inde

71 the methylomes were vastly different between muscle tissue and HDMCs, we identified a small number of

72 rossover study design, where paired skeletal muscle tissue and plasma specimens were collected at thr

73 ong correlation of TAG incorporation between muscle tissue and primary myotubes (r = 0.848, P = 0.008

74 ads to accumulation of triglycerides in both muscle tissue and the liver.

75 ss response induced by spaceflight involving muscle tissue and the proinflammatory setting, where inf

76 an accurate classifier of young versus older muscle tissue and this healthy ageing RNA classifier per

77 ncy of IFN-gamma-producing CD4(+) T cells in muscle tissues and draining lymph nodes as well as reduc

78 of genes that are specifically expressed in muscle tissues and found that these genes are depleted o

79 Expression levels in animal muscle tissues and in Escherichia coli vary widely for n

80 hat GBF1 is present in mouse spinal cord and muscle tissues and is particularly abundant in neuropath

81 o reach its target organs (e.g., adipose and muscle tissues) and is rate limiting in insulin action.

82 s of a free-standing soft scaffold, skeletal muscle tissue, and optogenetic stem cell-derived neural

83 jury, exit quiescence, proliferate to repair muscle tissue, and self-renew to replenish the satellite

84 matched expected values for subcutaneous and muscle tissue, and that the compliance of the subcutaneo

85 signals from electrodes implanted on viable muscle tissue, and to stimulate severed afferent nerve f

86 METTL2C was almost exclusively expressed in muscle tissue, and, accordingly, we detected METTL21C-ca

87 6243, accumulated triglycerides in liver and muscle tissues, and had reduced rates of beta-oxidation.

88 standing balance, although the properties of muscle tissue are highly labile.

89 Muscle tissues are classically divided into two major ty

90 Ideally, because muscle tissues are extremely long-lived, CRISPR technolo

91 pattern (SHG-AIP) of healthy and proteolysed muscle tissues are simulated and imaged here for the fir

92 on of muscle precursor cells into engineered muscle tissue as a potential noninvasive monitoring tool

93 5 protein levels were higher in tumor versus muscle tissue as determined by Western blot and immunohi

94 d incorporation into lipids were measured in muscle tissue as well as in primary myotubes.

95 of degenerative diseases affecting bone and muscle tissue as well as the central nervous system.

96 enteral nutrition reduced the quality of the muscle tissue, as reflected by the attenuation, revealin

97 n and inhibition of insulin signaling in the muscle tissue at multiple points in the pathway.

98 confirmed histologically, with formation of muscle tissue at the site of injection.

99 ed like AAV2i8 while selectively transducing muscle tissues at high efficiency, comparable with AAV9.

100 e identified in post-mortem human kidney and muscle tissue based on simultaneous screening and confir

101 pHIFU and thermal parameters in bulky normal muscle tissues based on a rabbit model and a preclinical

102 ressed alternatively spliced genes in ribeye muscle tissue between Nelore cattle that differed in the

103 d analysis of electrolytes from mass-limited muscle tissue biopsies (~2 mg dried mass) when multisegm

104 ovel noninvasive diagnostic methods based on muscle tissue biopsies to assess the effects of water po

105 both MeHg and THg increased continuously in muscle tissues but decreased in liver during depuration,

106 sed in growth plate cartilage in addition to muscle tissue, but not in brain, intestine, liver, or lu

107 RRV-T48-nsP1(6M) loads in skeletal muscle tissue, but not in other tissues, decreased drama

108 ) T cells had elevated RRV loads in skeletal muscle tissue, but not joint-associated tissues, at 14 d

109 unication network exists between adipose and muscle tissue, but the effect of active breaks in prolon

110 ls in the hypodermis and at low level in the muscle tissue, but the physiological function of this su

111 We investigated Cys-loop gene expression in muscle tissue by qPCR and localized this expression in m

112 e, through a 20 mm thick specimen of porcine muscle tissue by surface-enhanced spatial offset Raman s

113 ptase polymerase chain reaction performed in muscle tissue (c.1016 + 3A > G).

114 Even at a mature age, muscle tissue can undergo a robust rebuilding process th

115 lded significant lymphocytic infiltration of muscle tissue comparable to that produced in C57BL/6 wil

116 extensive and reciprocal cross-talk between muscle tissue compartments, including satellite cells, a

117 t for genes expressed in vascular and smooth muscle tissues, consistent with a predominant theory of

118 The sturgeon muscle tissue contained HUFA in proportions comparable t

119 es in the fatty acid composition of the fish muscle tissue, contributing to increase its nutritional

120 al three-dimensional model of human skeletal muscle tissue could accelerate progress towards new and

121 rotomy with cecetomy and femur fracture with muscle tissue damage (polytrauma).

122 P inhibitors suppress mitochondrial defects, muscle tissue damage and cell death associated with IBMP

123 oss of Fer1l6 led to deformation of striated muscle tissues, delayed development of the heart, and hi

124 Skeletal muscle tissue demonstrates global hypermethylation with

125 We confirmed our results in intact muscle tissue, demonstrating that nuclei of transgenic D

126 protein were expressed in myogenic cells and muscle tissues derived from FSHD affected subjects, incl

127 hat even the fastest events involving animal muscle tissues do not surpass a few hundred hertz.

128 mmunity, quantitative PCR (qPCR) analysis of muscle tissue, draining lymph nodes, spleen, spinal cord

129 ay whereby increased inflammation within the muscle tissue during ischemia/reperfusion injury sensiti

130 O-ribose-methylation, is increased in murine muscle tissue during postischemic neovascularization.

131 , neutrophils also accumulate in adipose and muscle tissues during high-fat diets and contribute to a

132 cells, including epithelia, vascular smooth muscle tissue, electrically excitable cells, and some tu

133 In muscle tissue, electrodes were placed exactly parallel,

134 both mitochondria and myofibrils in skeletal muscle tissues engineered on micromolded gelatin hydroge

135 nd cell therapy, and it could be extended to muscle tissue engineering and disease modeling.

136 strategies in neural, skin, connective, and muscle tissue engineering are explored.

137 view of fundamental concepts associated with muscle-tissue engineering and the current status of musc

138 utility of anisotropic materials in skeletal-muscle-tissue engineering are highlighted, along with th

139 tissue engineering and the current status of muscle-tissue-engineering approaches is provided.

140 were measured in mitochondria isolated from muscle tissue ex vivo with chemoluminescence and fluores

141 Individual myofibers that make up muscle tissue exhibit variation in their metabolic and c

142 The developing muscle tissue exhibited increasing MT values during the

143 CsGABArdl and CspHCl2 subunits, whereas the muscle tissue expressed a wider variety of subunits, esp

144 R imaging correlated qualitatively well with muscle tissue expression of specific skeletal markers, a

145 Their effects were evaluated in muscle tissue extracts and freshly dissociated SM cells.

146 se heart, kidney, brain, liver, and skeletal muscle tissue extracts as examples.

147 ad higher percentage of EPA and DHA in their muscle tissue (filets) compared to that of triploids and

148 Red coloration of muscle tissue (flesh) is a unique trait in several salmo

149 stantial accumulation in the interstitium of muscle tissue followed by relatively rapid clearance and

150 Sampling skeletal muscle tissue for analyses of SERCA activity as well as

151 dy determines the levels of total mercury in muscle tissue from 268 reared Atlantic bluefin tuna in t

152 Recently, we obtained muscle tissue from a subject injected 10 years earlier w

153 In a separate experiment, skeletal muscle tissue from muscle-specific Rac1 knockout (Rac1 m

154 o P4ha1 null mice, which die prenatally, the muscle tissue from P1 and P2 was found to have reduced c

155 espite greatly decreased oxidative capacity, muscle tissue from patients deficient in the Fe-S cluste

156 needles were also observed when tested using muscle tissue from pigs.

157 from enrofloxacin (ENR) in liver, kidney and muscle tissues from broiler chickens subjected to a phar

158 ell RNA sequencing to profile human skeletal muscle tissues from embryonic, fetal, and postnatal stag

159 nd 1.22mug/kg bw/day) through consumption of muscle tissues from Paso de Ovejas and Puente Nacional d

160 Vascular and intestinal smooth muscle tissues from sm-STIM1-KO mice developed abnormall

161 crease in total omega 3 fatty acids (n-3) in muscle tissue (from 63.6 to 181.5 mg g(-1)) and a decrea

162 the latter was much greater in tumor than in muscle tissue (GLUT1 50:1), the opposite was found for G

163 ical transplantation of CTS but not skeletal muscle tissue grafts.

164 During development, muscle tissue grows by several mechanisms, including hyp

165 in extracellular matrix self-organize into a muscle tissue guided by the geometry of the scaffold, an

166 the exercise transcriptome in human skeletal muscle tissue harvested from the vastus lateralis.

167 Availability of human embryonic muscle tissue has been a limiting factor in investigatin

168 ed cells, and larger coverage arrays in aged muscle tissue have not been undertaken.

169 proximate calculations show that caveolae in muscle tissue have the strength to handle the stress of

170 With aging, muscle tissue homeostasis is progressively disrupted and

171 (SM) myosin II are both expressed in smooth muscle tissues, however the role of NM myosin in SM cont

172 ower rates of turnover such as in adipose or muscle tissue; however, the present report provides inve

173 es within the airways, such as airway smooth muscle tissue hypertrophy.

174 rientations matching those of host abdominal muscle tissue improved graft integration and the mechani

175 ed the reconstruction of functional skeletal muscle tissue in a rodent volumetric muscle loss injury

176 r proteins of various ontologies in skeletal muscle tissue in both rodents and humans.

177 om muscle precursor cells to mature skeletal muscle tissue in muscle cell therapy.

178 human MuSCs and MRCs can generate functional muscle tissue in our VML model.

179 Muscle tissue in the early stages of the differentiation

180 d myogenic and adipogenic differentiation in muscle tissue in the HFrD rats.

181 th known to increase effective stiffness for muscle tissue in vitro, which is consistent with our hyp

182 kipping mutant dystrophin exons in postnatal muscle tissue in vivo, we used adeno-associated virus-9

183 improved cell survival and formed volumetric muscle tissues in an ectopic muscle site.

184 otein in heart muscle compared with skeletal muscle tissues in DMD models.

185 gical analyses revealed greater infection of muscle tissues in Irf1 (-/-) mice than in wild-type mice

186 plied on the adipose, and heart and skeletal muscle tissues in old and young female African green ver

187 LUT4 controls glucose transport into fat and muscle tissues in response to insulin and also into musc

188 ive tracking of hD2R hMPCs and bioengineered muscle tissues in the clinic.

189 in clearing glycogen from numerous skeletal muscle tissues in the Pompe mouse model.

190 Acetylcholine stimulation of tracheal smooth muscle tissues induces the recruitment of vinculin to th

191 pina3n in mouse models of MD and after acute muscle tissue injury.

192 take in pancreatic beta cells, cancer cells, muscle tissues, intestinal tissues and P.

193 ytocin precursor gene expression in skeletal muscle tissue is a valid marker for detection of illicit

194 enne muscular dystrophy, progressive loss of muscle tissue is accompanied by fibrosis, chronic inflam

195 geometry of the scaffold, and the resulting muscle tissue is cocultured in situ with a neural cluste

196 Repair of damaged skeletal-muscle tissue is limited by the regenerative capacity of

197 on of muscle fibers fails progressively, and muscle tissue is replaced with connective tissue.

198 Preservation of smooth muscle tissue is the key to preserving erectile function

199 of anti-angiogenic isoform (VEGF165b) in PAD muscle tissues is a potential cause for the failure of t

200 ptional modules (subnetworks) in adipose and muscle tissues is important for revealing the related me

201 n perturbed gene expression between skin and muscle tissue, it is likely that analysis of a more read

202 up IV afferents to mechanical stimuli at the muscle tissue level, possibly contributing to insulin-in

203 ot only at dorsal root ganglion, but also at muscle tissue levels.

204 as performed with DNA isolated from ischemic muscle, tissue macrophages (Mvarphis), and endothelial c

205 oluminescent organs) embedded throughout the muscle tissue make the entire body glow, thereby backlig

206 early systemic correction to both neural and muscle tissues may be essential for successful correctio

207 ect only the myofibers without affecting the muscle tissue microenvironment.

208 and chemically responsive, contractile human muscle tissues ('myobundles') using primary myogenic cel

209 Affected muscle tissue, obtained from 16 patients with IMNM, was

210 hemoatttractants eotaxin-1 and RANTES in the muscle tissue of all three dystrophin-deficient strains;

211 ine the mercury and methylmercury content in muscle tissue of chub (Leuciscus cephalus L.), to assess

212 radioactivity were detected in the blood and muscle tissue of exposed fish.

213 termination of mercury concentrations in the muscle tissue of fish from the Brazilian Amazon using gr

214 A gastropod, Trochus erithreus, and a muscle tissue of fish, Otolithes ruber, were analyzed as

215 osition and lipid profiles were evaluated in muscle tissue of four species of Brazilian fish using th

216 rrection of disease-causing mutations in the muscle tissue of patients with DMD.

217 re capable of reducing RRV loads in skeletal muscle tissue of Rag1(-/-) mice, indicating that T cells

218 Liver and muscle tissue of tusks ( Brosme brosme) have been analyz

219 , and impaired insulin signaling in skeletal muscle tissue of wild-type mice but not in Nox2-null mic

220 n interaction are also observed in liver and muscle tissues of epinephrine/norepinephrine-injected mi

221 ApoA-IV on glucose uptake in the adipose and muscle tissues of mice and cultured 3T3-L1 adipocytes.

222 Few or no abnormalities were found in muscle tissues of SCz+STc24+STc52-immunized mice, wherea

223 stimulus in both white adipose and skeletal muscle tissues of the LPD group compared with the CN gro

224 (DORM-2) and spiking the both Hg species in muscles tissue of a fish.

225 (MeHg) and inorganic mercury (iHg) levels in muscles tissues of 10 freshwater fish species.

226 The concentrations of MeHg and iHg in muscles tissues of ten fish species were found in the ra

227 the tongue and engineered contractile human muscle tissues on thin films.

228 oximately 2-fold higher in the tumor than in muscle tissue or the contralateral mammary fat pad.

229 eneration and subsequent regeneration of the muscle tissue over time.

230 e [FDG]) to quantify, respectively, skeletal muscle tissue perfusion (glucose delivery), kinetics of

231 ls that surround sensory neurons and also in muscle tissue, probably around the nerve endings of the

232 d changes and interindividual differences in muscle tissue proteome dynamics.

233 ure of other pathological features, aged mdx muscle tissue provides reliable benchmarks for disease p

234 In addition, local muscle tissue radioprotection by lead shielding during i

235 ts experienced by ICU survivors originate in muscle tissue rather than the nervous system.

236 L injury model using unbiased assessments of muscle tissue regeneration and functional recovery.

237 nd social behaviours--is required for proper muscle tissue regeneration and homeostasis, and that pla

238 was found to reduce inflammation and promote muscle tissue regeneration compared to a saline control.

239 egradation rates matching the time course of muscle tissue regeneration, and markedly enhanced the en

240 rophage transition dynamics and subsequently muscle tissue regeneration.

241 sfunction and structural changes in skeletal muscle tissue remains to be discovered.

242 been reported to promote functional skeletal muscle tissue remodeling in small and large animal model

243 e capacity of ECMs to orchestrate functional muscle tissue remodeling was interrogated in a porcine V

244 regulate extracellular matrix deposition and muscle tissue remodeling.

245 pic shift, which is indispensable for normal muscle tissue repair dynamics.

246 As in situ reprogramming occurs along with muscle tissue repair, the data provide a link between th

247 ed and control samples of biceps and deltoid muscle tissues, respectively, with 29 genes in common.

248 Fasting skeletal muscle tissue samples were taken before and after 5 and

249 phingosine was identified as a marker in the muscle tissue samples which may offer potential for the

250 f carbon and nitrogen in whole organisms and muscle tissue scale allometrically with body mass raised

251 s 1, 4, 14, and 42 after injury, sampling of muscle tissue served for analysis of proliferation, apop

252 Histological analysis of muscle tissues showed abnormalities such as presence of

253 Muscle tissue shows diurnal variations in function, phys

254 lls, SCs) but surprisingly without affecting muscle tissue size.

255 c to CTS because transplantation of skeletal muscle tissue slices led to faster dilative remodeling a

256 eprogramming, and hematopoietic and skeletal muscle tissue stem cells, and we discuss the implication

257 Contractile stimulation of tracheal smooth muscle tissues stimulates phosphorylation of the NM myos

258 y included as compared with the tonic smooth muscle tissues, such as the aorta and inferior vena cava

259 2- to 5-fold more abundant in phasic smooth muscle tissues, such as the portal vein, small intestine

260 was markedly lower than its distribution to muscle tissue surrounding the skull (VT, 0.86 +/- 0.10 m

261 nd approached the values for mature skeletal muscle tissue: T1, 1386 msec +/- 88; T2, 32.0 msec +/- 4

262 mm(2)/sec +/- 0.02 (reference erector spinae muscle tissue: T1, 1417 msec +/- 106; T2, 31.0 msec +/-

263 eover, mitochondrial respiration in skeletal muscle tissue tends to be susceptible to complex IV acti

264 rapid innervation and mature into organized muscle tissue that restores normal muscle weight and fun

265 dine-containing dipeptides (anserine) within muscle tissue that was distinctive from dynamic metaboli

266 s a wasting disorder of adipose and skeletal muscle tissues that leads to profound weight loss and fr

267 Within skeletal muscle tissue, these 'cancer' genes predominant function

268 Spike total mercury (THg) persisted in muscle tissue throughout the entire study despite discon

269 receptor SUCNR1 in non-myofibrillar cells in muscle tissue to control muscle-remodeling transcription

270 nsitive FRET probes were expressed in smooth muscle tissues to determine how Tyr(1065) phosphorylatio

271 blood compartment to the interstitium of the muscle tissues to enhance ASO functional uptake.

272 of VSV particles leads to a dose-dependent, muscle tissue-tropic, lethal infection in C. elegans.

273 D31+/CD45-) isolated from uninjured hindlimb muscle tissue undergo in vivo EndMT when transplanted di

274 crease in satellite-cell activation in p75KO muscle tissue up to 10 d after HLI surgery.

275 Results Adipose and thigh muscle tissue volumes of 20 subjects (18 women; age rang

276 The CTG expansion size in muscle tissue was determined by Southern blot.

277 ucture of gilthead sea bream (Sparus aurata) muscle tissue was evaluated over time by transmission el

278 eriodically recaptured and a small amount of muscle tissue was extracted using a nonlethal biopsy.

279 Aged muscle tissue was hypermethylated compared with young ti

280 For the in vivo assays, skeletal muscle tissue was obtained from male rats and maintained

281 R) phosphorylation (activation) in liver and muscle tissues was compared with postinjection of INS or

282 xpression of miR-17-92 in cardiac and smooth muscle tissues was generated.

283 ECs or restoring Dll4 expression in ischemic muscle tissue, we rescued most of the HIF-2alpha-depende

284 Following the study in bulky normal muscle tissues, we further created bulky tumor model wit

285 ication of triacylglycerols (TAGs) in salmon muscle tissue were conducted using electrospray ionizati

286 highest total mercury concentrations in fish muscle tissues were found was the Vltava - Vranany (0.23

287 The two Rbm20 speckles found in nuclei from muscle tissues were identified as aggregates of Rbm20 pr

288 particularly challenging for visceral smooth muscle tissue where progenitor cells have not been clear

289 zes to membrane adhesion junctions in smooth muscle tissues, where its head domain binds to talin and

290 cerbated in some biological systems, such as muscle tissue, which lack adequate cell culture lines to

291 rom Nrf2-deficient or overexpressed skeletal muscle tissues will provide a broader spectrum of Nrf2 t

292 VIEW: Sarcopenia, or the decline of skeletal muscle tissue with age, is one of the most important cau

293 escribes a metalloproteomics study of bovine muscle tissue with different grades of meat tenderness f

294 ed the POP concentrations in their liver and muscle tissue with the corresponding concentrations in t

295 otypic shift and the cross-talk of the local muscle tissue with the infiltrating macrophages during t

296 redicted that this is generally accurate for muscle tissue with uniform oxygen uptake.

297 ing and testing highly functional biomimetic muscle tissues with a resident satellite cell niche and

298 n vivo in awake rats and ex vivo in skeletal muscle tissue, with a superior safety profile compared t

299 hibit MLCP activity in isolated ileal smooth muscle tissues, with additional phosphorylation upon pha

300 .01), reaching levels comparable to those in muscle tissue, without changing (11)C-erlotinib plasma p