ライフサイエンスコーパス: muscle tissue

1 ass and ectopic fat deposition (in liver and muscle tissue).

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

3 oietic cells and mesenchymal stem cells from muscle tissue.

4 ecretion of this critical synaptic enzyme in muscle tissue.

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

6 reduced mortality and lower parasite load in muscle tissue.

7 ntiating human muscle cells and regenerating muscle tissue.

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

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

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

11 pressed in fetal versus adult human skeletal muscle tissue.

12 lease behavior, characteristic of functional muscle tissue.

13 enabling functional improvement of ischaemic muscle tissue.

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

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

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

17 n structural proteins and their hydration in muscle tissue.

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

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

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

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

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

23 lly important for regeneration of dystrophic muscle tissue.

24 persistent factor IX expression in injected muscle tissue.

25 sultant swelling within the fascicles of the muscle tissue.

26 utical distribution and accumulation in fish muscle tissue.

27 not in unaffected control myogenic cells and muscle tissue.

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

29 s upregulated in serum and in bladder smooth muscle tissue.

30 the production of full-length antibody from muscle tissue.

31 mage and dysfunction that occur in myopathic muscle tissue.

32 ha-agonist-mediated ERK activation in smooth muscle tissue.

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

34 ential for formation of contractile skeletal muscle tissue.

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

36 ass spectrometry in patient-derived skeletal muscle tissue.

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

38 ch for the functional restoration of damaged muscle tissue.

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

40 reside in anatomically defined niches within muscle tissues.

41 with tension development in tracheal smooth muscle tissues.

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

43 hogenesis and function of cardiac and smooth muscle tissues.

44 nted the M2c macrophage phenotype in injured muscle tissues.

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

46 Total of 2102 proteins were identified in muscle tissues.

47 the role of fibroblast-like cells in smooth muscle tissues.

48 A from adult mouse brain, liver and skeletal muscle tissues.

49 cterized by weakness and wasting of skeletal muscle tissues.

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

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

52 aldosterone, is also increased in dystrophic muscle tissues.

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

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

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

56 Skin and muscle tissue accounted for 70% of the reduction in whol

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

58 Muscle tissue adenosine triphosphate decreased in all gr

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

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

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

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

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

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

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

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

67 of these cancers might originate outside of muscle tissue and highlight the need for a better unders

68 of a complete device then tested in vitro on muscle tissue and in vivo on a porcine laparoscopic mode

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

70 firmed by weight loss as well as analyses of muscle tissue and serum.

71 amine the expression of ebf genes in Xenopus muscle tissue and show that EBF activity is necessary fo

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

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

74 is highly expressed in cardiac and skeletal muscle tissues and becomes strongly upregulated during c

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

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

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

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

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

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

81 6243, accumulated triglycerides in liver and muscle tissues, and had reduced rates of beta-oxidation.

82 imetic fabrication of three-dimensional (3D) muscle tissue architectures in vitro.

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

84 tramuscular adipose and its interaction with muscle tissue are unclear.

85 Muscle tissues are classically divided into two major ty

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

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

88 5 protein levels were higher in tumor versus muscle tissue as determined by Western blot and immunohi

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

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

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

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

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

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

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

96 indicates rapid onset of ER stress in young muscle tissue but also that gene expression of key muscl

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

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

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

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

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

102 vinculin head domain peptide (Vh) in smooth muscle tissues, but not the talin-binding deficient muta

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

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

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

106 ently published literature examining various muscle tissue cells and their modulators that determine

107 ow cells, circulating monocytes, and injured muscle tissue cells to recruit MOs/MPs into injured musc

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

109 n, with both increased adipose and decreased muscle tissue compared with wild-type mice.

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

111 arge, few hundred micron-thick bioartificial muscle tissues composed of viable, dense, uniformly alig

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

113 sts cultured within 3-dimensional engineered muscle tissue constructs were treated with 10 nM soluble

114 The sturgeon muscle tissue contained HUFA in proportions comparable t

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

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

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

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

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

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

121 study unveils a novel mechanism of skeletal muscle tissue destruction in pathological conditions.

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

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

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

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

126 e structural deterioration of the C. elegans muscle tissues during aging.

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

128 In muscle tissue, electrodes were placed exactly parallel,

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

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

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

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

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

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

135 The developing muscle tissue exhibited increasing MT values during the

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

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

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

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

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

141 s and by electron microscopic observation of muscle tissue fixed immediately following isolation, usi

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

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

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

145 numbers were greater in skin than in paired muscle tissue from patients with juvenile DM (P = 0.014)

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

147 between blood in the vessels and surrounding muscle tissue from which the intravascular blood oxygen

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

149 genesis in vitro and in vivo, using myositis muscle tissues from humans and mice.

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

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

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

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

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

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

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

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

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

159 With aging, muscle tissue homeostasis is progressively disrupted and

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

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

162 rtilization, formation of placenta, bone and muscle tissues, immune response, tissue repair, and rege

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

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

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

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

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

168 al fibroblasts, which disturbs normal smooth muscle tissue in radially patterned organs.

169 Muscle tissue in the early stages of the differentiation

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

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

172 R23 is secreted by muscle cells in vitro and muscle tissue in vivo.

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

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

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

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

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

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

179 In human DM muscle tissue, increased Mi-2 expression was found prefe

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

181 S3E) but not wild type cofilin in the smooth muscle tissues inhibited endogenous ADF/cofilin dephosph

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

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

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

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

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

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

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

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

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

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

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

193 However, gene transfer in non-muscle tissues, mainly the liver, was dramatically reduc

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

195 s, carbohydrate versus fat fuel selection in muscle tissues, metabolic changes in muscle during contr

196 In injured mouse muscle tissue, Mi-2 levels were dramatically and persist

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

198 ed that the contractile activation of smooth muscle tissues might regulate the activation of vinculin

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

200 nic mesoderm later differentiates into heart muscle tissue (myocardium) and non-muscular heart tissue

201 bility of T. cruzi to establish infection in muscle tissue nor does it impair the generation of a rob

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

203 N-alpha/beta), have been found abundantly in muscle tissue of adult dermatomyositis and juvenile derm

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

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

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

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

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

209 ion of mononuclear cells in the inflammatory muscle tissue of IIM patients.

210 n dense material in the t-tubules within the muscle tissue of parkin knockdown zebrafish.

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

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

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

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

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

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

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

218 in myoblast cell line C2C12 and in skeletal muscle tissues of transgenic mice.

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

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

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

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

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

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

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

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

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

228 Skeletal muscle tissue provides mechanical force for locomotion o

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

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

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

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

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

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

235 rophage transition dynamics and subsequently muscle tissue regeneration.

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

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

238 regulate extracellular matrix deposition and muscle tissue remodeling.

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

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

241 (Pax7(+)) satellite cells can repair damaged muscle tissue repeatedly after several bouts of acute in

242 on, and assembly into functional ventricular muscle tissue, representing a combination of tissue engi

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

244 tically compared them to the cycloviruses in muscle tissue samples of commonly eaten farm animals in

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

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

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

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

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

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

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

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

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

254 2- to 5-fold more abundant in phasic smooth muscle tissues, such as the portal vein, small intestine

255 patients with juvenile DM, but not in paired muscle tissue, suggests that they have a specific role i

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

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

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

259 genes in neural, skeletal muscle and cardiac muscle tissue tend to have tissue-specific roles.

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

261 ld greater sensitivity to insulin of in vivo muscle tissue than previously reported from intravenous

262 ore broadly to the transcriptional output of muscle tissue than previously thought, offering a partia

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

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

265 a membrane where it functions in adipose and muscle tissue to clear glucose from circulation.

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

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

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

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

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

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

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

273 ry response was muted, and highly functional muscle tissue was formed.

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

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

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

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

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

279 the interaction between adipose and skeletal muscle tissues, we used Myf5-Cre and aP2-Cre mice in com

280 subspecies from human plasma, rat liver, and muscle tissue were 78 to 91%, 70 to 99%, and 71 to 95%,

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

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

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

284 is tightly regulated in all cells, including muscle tissue, where the specialized ER sarcoplasmic ret

285 3 actively shape gene expression patterns in muscle tissue, where they regulate sarcomeric actin orga

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

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

288 factor-alpha, IL-12, and STAT1 levels in the muscle tissue, which may serve as biomarkers and aid in

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

290 chanical and enzymatic digestion of skeletal muscle tissue with collagenase XI, dispase and trypsin f

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

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

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

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

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

296 Stimulation of tracheal smooth muscle tissues with acetylcholine (ACh) induced the recr

297 y transduced cardiac and whole-body skeletal muscle tissues with high efficiency.

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