ライフサイエンスコーパス: fiber

1 ate fasciculus, cingulum and fronto-striatal fibers).

2 ation of the DNA region within the chromatin fiber.

3 teria resulting from fermentation of dietary fiber.

4 tructure onto the unclad core of the optical fiber.

5 mode fiber directly spliced to a single mode fiber.

6 1-mediated eviction of H1 from the chromatin fiber.

7 by condensing, degrading, and aligning these fibers.

8 signaling and disorganized radial glial cell fibers.

9 the primary GC subtypes, even beneath nerve fibers.

10 ized, multilayered thin film around the axon fibers.

11 the muscle tissue and composed of intrafusal fibers.

12 the surface of commercial microporous carbon fibers.

13 al administration of DEPs activated airway C-fibers.

14 eminal ganglia (TG) neurons, and their nerve fibers.

15 ntiation and de novo myelination of parallel fibers.

16 expected roles for distinct planarian muscle fibers.

17 eceptor potential ankyrin-1 on nociceptive C-fibers.

18 d for the analysis of synthetic polymers and fibers.

19 bers, ceramic fibers, and synthetic vitreous fibers.

20 estication for directional selection of long fibers.

21 ystals allows them to readily exfoliate into fibers.

22 ial of KJM may be greater than that of other fibers.

23 hypertrophy of both glycolytic and oxidative fibers.

24 timulus information is distributed over many fibers.

25 icated the likely origin of some peptidergic fibers.

26 difference in IBDQ-B scores between the high-fiber (+0.1 +/- 14.5) and the habitual-fiber (-8.4 +/- 1

27 contain significant amounts of total dietary fibers (41.69%) and antioxidants as polyphenols and flav

28 high-fiber (+0.1 +/- 14.5) and the habitual-fiber (-8.4 +/- 13.3) groups was significant (P = 0.004)

29 ly to the mechanochemical behavior of stress fibers, actin arcs, and cortical actin-based structures.

30 ical stimulation of mossy fiber and climbing fiber afferents as CS and US, while alternating between

31 s vibrating ion-selective electrodes, carbon fiber amperometry, and magnetic resonance imaging, we mo

32 tioned using electrical stimulation of mossy fiber and climbing fiber afferents as CS and US, while a

33 f the novel flour with high protein, dietary fiber and fat content results in a unique combination of

34 lp meet future demands for plant-based food, fiber and fuel production, but requires a greater unders

35 low mean purchases of fruit, vegetables, and fiber and high mean purchases of junk foods, saturated f

36 was predominantly attributable to intake of fiber and red meat.

37 arkedly changed after further adjustment for fiber and total fruit and vegetable intakes.

38 n-style diets (WD) high in fat and scarce in fiber and vitamin D increase risks of colorectal cancer.

39 We therefore quantified AVP- and OT-ir fibers and cell bodies in 22 subregions of the forebrain

40 knockout podocytes demonstrated fewer stress fibers and impaired migration compared to wild type podo

41 hods, thanks to the light guiding in optical fibers and small distance between the fiber tips and tra

42 matergic transporter profiles of DCN A and C fibers and their relationship to calcitonin gene-related

43 involved in the cellular structure of muscle fibers and, along with DMD, forms part of the dystrophin

44 turated fats, sodium, added sugars, protein, fiber, and calcium.

45 s [carbohydrate, fat, saturated fat, dietary fiber, and glycemic load derived from self-report of die

46 formed that links together the muskeg, wood fibers, and added silicates yielding a load-bearing and

47 y the immediate relaxation of chromosomes, k-fibers, and microtubule speckles.

48 rbon fibers, carbon-nanotube fibers, ceramic fibers, and synthetic vitreous fibers.

49 ver, mitosis continues even when kinetochore fibers are not obviously discernable, and cytokinesis ta

50 k chemistry, either before or after the silk fibers are self-assembled.

51 Elastic fibers are typically decreased.

52 with the D-periodic banding of higher-order fibers assemblies.

53 s revealed the transformation of an extended fiber assembly into discrete flakes after incorporation

54 To do so, we laser-ablate single k-fibers at different spindle locations and in different m

55 up at day 10, the SAAs of both Adelta- and C-fibers at the "ascending" phase of microcontractions wer

56 -[Formula: see text]m thick) "supramolecular fibers" at room temperature.

57 ill patients have manifest diaphragm muscle fiber atrophy and weakness in the absence of mitochondri

58 Skeletal muscle fiber atrophy develops in response to severe sepsis, but

59 ers to detect fibrotic tissue deposition and fiber atrophy in dystrophic strains.

60 is triggers more severe and sustained muscle fiber atrophy in limb muscles when compared with respira

61 In addition, the muscle fiber atrophy was associated with high levels of inflamm

62 length and the alignment of nanofibers along fiber axis.

63 the pathologic retrograde sprouting of mossy fiber axons, both hallmarks of temporal lobe epilepsy.

64 released histamine was quantified by a glass fiber-based fluorometric method; passive HR-IgE-stripped

65 late an object, populations of tactile nerve fibers become activated and convey information about the

66 Soluble fiber beneficially affects metabolism, and fiber supplem

67 so that we explore the mechanism that causes fiber branching.

68 s spectrometry (CFI-MS), which uses a carbon fiber bundle as the ion source, is useful for the analys

69 tractography, we describe novel methods for fiber bundle reconstruction and graph-based connectivity

70 bution changes of chemical components on the fiber bundle surface during the process, indicating that

71 We also model the formation of fiber bundles and domains so that we explore the mechani

72 d experimental results suggest that multiple fiber bundles can be formed under the condition of a low

73 We also demonstrate that these piezoelectric fiber bundles can serve as ultra-flexible textile sensor

74 s fiber bundles, but increased in homozygous fiber bundles compared to wildtype mice.

75 illar tension were decreased in heterozygous fiber bundles, but increased in homozygous fiber bundles

76 serrated teeth on the formation of multiple fiber bundles, three-dimensional finite element simulati

77 decreased FA in multiple major white matter fiber bundles, which connect the fronto-parietal control

78 esults in a higher preferential formation of fiber bundles.

79 d is not decorated with glycosylated surface fibers, but features 30 A-long surface protrusions that

80 was developed for innervation of intrafusal fibers by human gamma-MNs and demonstrated by morphologi

81 the mechanical properties of polymerized HbS fibers by the mesoscopic model, thus providing a means o

82 ate) or indicators of quality (e.g., dietary fiber) by use of self-report or objective biomarkers of

83 The fouled fibers can be easily regenerated by backwash of water wi

84 m polymers, gel spun fibers, modified carbon fibers, carbon-nanotube fibers, ceramic fibers, and synt

85 fect, linking MTOR signaling to induction of fiber cell differentiation by TGFbeta.

86 ition and cell migration but did not prevent fiber cell differentiation.

87 ilitating the transport of water across lens fiber cell membranes.

88 ong longitudinal actin cables, the short Li1 fiber cells accumulated disoriented transverse cables.

89 to undergo differentiation into either lens fiber cells or myofibroblasts.

90 ccCP, M3 fibers were located medially and M1 fibers centromedially, with M2, LPMCv, and M4 pathways o

91 ers, modified carbon fibers, carbon-nanotube fibers, ceramic fibers, and synthetic vitreous fibers.

92 The study of fiber clustering of natural flocs could be useful for im

93 set carbon fiber composites, which allow the fiber component of a resin and carbon fiber fluid to be

94 f printing high performance thermoset carbon fiber composites, which allow the fiber component of a r

95 xperimentally measured alteration in elastic fiber composition, alveolar geometry and surfactant comp

96 The hydrogel fibers consist of poly(acrylamide-co-poly(ethylene glyco

97 thermodynamic point of view, the calculated fiber constants further corroborate the hypothesis that

98 Fibers containing orexins project to brain structures th

99 ancement of the resistant starch and dietary fiber content with the replacement of green banana flour

100 Regarding fiber content, it is unclear whether the intake of solub

101 Stress fibers-contractile actomyosin bundles-are important for

102 rmore, different conformations of phage tail fibers correlated with the aforementioned orientations o

103 combined with RBC models, the generated HbS fibers could be applied to study the morphologies and me

104 ns: the microscale model represents a single fiber cross-section; the macroscale model represents a t

105 Defects in this BM lead to muscle fiber damage from the force of contraction.

106 Recent sequencing of the fiber-degrading Ruminococcus flavefaciens FD-1 genome re

107 e binds carbon monoxide in both micelles and fibers, demonstrating that the heme active site in both

108 be associated with a loss of epidermal nerve fiber density (ENFD).

109 Corneal nerve fiber density (mean [SE] difference, -6.78 [2.14] fibers

110 ated that fractional anisotropy and apparent fiber density in tracts connecting bilateral SMA were ne

111 of miRNA regulatory roles in the process of fiber development, which is helpful to increase fiber yi

112 Dietary fiber (DF), protein and lipid-bound antioxidants, obtain

113 1 also prevented premature initiation of the fiber differentiation process mediated by the NAC SECOND

114 y of a graded-index and large core multimode fiber directly spliced to a single mode fiber.

115 ared using 90% of beef and 10% of an aqueous fiber dispersion and were determined for HAA-levels afte

116 analysis to detect the precise time at which fibers distort ("sickle") the cells.

117 l sampling and deconvolution of high-density fiber electrical activity to decode accurate alpha-motor

118 ation of proton reduction on an inert carbon fiber electrode.

119 Fiber enhanced Raman spectroscopy (FERS) is an arising n

120 rneurons, these results reveal that climbing fibers exert control over inhibition at both the input a

121 of intramolecular triple helix formation or fiber-fiber aggregation.

122 al investigations, microscale single-crystal fiber field-effect transistors were also fabricated.

123 deling of sparse and filopodia-bearing mossy fibers, finding that these circuit features uniquely con

124 Using fiber-FISH, we demonstrate that parents transmitting the

125 pounds from commercial samples of chia seed, fiber flour and oil were extracted using an ultrasound-a

126 ow the fiber component of a resin and carbon fiber fluid to be aligned in three dimensions via contro

127 Few-mode fibers (FMFs) have been recently employed in classical o

128 Multinucleated skeletal muscle fibers form through the fusion of myoblasts during devel

129 ouse podocytes with Bis-T-23 promoted stress fiber formation and focal adhesion maturation in a dynam

130 ing, sticky particles, we demonstrate robust fiber formation for a variety of particle shapes and agg

131 ntegrin alpha9beta1, abolishing actin stress fiber formation, inhibiting YAP and its target gene expr

132 ng with the Abeta peptide to inhibit Abeta42 fiber formation.

133 forming aggregate glands were divergent from fiber-forming glands.

134 Diaphragm muscle fibers from critically ill patients displayed significan

135 it is unclear whether the intake of soluble fibers from foods or supplements has an equally benefici

136 rs small aggregates, thereby preventing long fibers from forming.

137 We address this gap by analyzing descending fibers from injections of an anterograde tracer in the r

138 the posteromedial tibia condyle, merged with fibers from the semimembranosus tendon, the other origin

139 mechanisms involved [5, 6], we propose that fibers generically arise from the aggregation of irregul

140 substantial innervation by trigeminal nerve fibers immunoreactive for calcitonin gene-related peptid

141 loit the external perturbation on large core fiber in various applications.

142 f polyplexes resulted in dystrophin-positive fibers in a mouse model of Duchenne muscular dystrophy w

143 e tissue is involved in driving regenerating fibers in a single direction, outlining for them a well-

144 xpression and a switch toward type I and IIa fibers in rat muscle and myotubes in vitro.

145 y of the invading cells and the alignment of fibers in the matrix, suggesting that cell polarization

146 tment changed the ultrastructure of collagen fibers in the vessel basement membrane, and the kinetics

147 s a critical step in the assembly of elastic fibers in vivo, preceding chemical cross-linking.

148 ultiple degenerating and regenerating muscle fibers, increased central nuclei, elevated creatine kina

149 ype Xu-142, 26 miRNAs are involved in cotton fiber initiation and 48 miRNAs are related to primary wa

150 tivity of individual motor units (the muscle fibers innervated by a single motor neuron) and manipula

151 entum and rostral rhombencephalon, and their fibers innervated the brain and pituitary profusely.

152 response that would be produced in the nerve fiber innervating that receptor.

153 del to simulate the responses of all tactile fibers innervating the glabrous skin of the hand to any

154 e with normalized striatal TH-immunoreactive fiber innervation and bidirectional synaptic connectivit

155 tiotemporal information transmitted by mossy fiber inputs with a wide variety of firing patterns.

156 type III predominance, and lack of collagen fiber insertion in the necrotic bone were associated wit

157 indicating that supplementation may improve fiber intake and health in these individuals.

158 y was to compare the acute effect of soluble fiber intake from foods or supplements after a common me

159 s strong epidemiologic evidence that dietary fiber intake is protective against overweight and obesit

160 terized by high protein, sugar, fat, and low fiber intake, and is widely believed to contribute to th

161 ed linear mixed models, which controlled for fiber intake, sex, age, body mass index, and repeated sa

162 esses of HbS nucleation, polymerization, HbS fiber interaction, and subsequent distortion of RBCs is

163 SEM, on solid samples, showed arrangement of fibers into nanorods.

164 Carbon fiber ionization mass spectrometry (CFI-MS), which uses

165 filtering approach using modified cellulosic fibers is desirable for purification of natural water.

166 nsory modalities and function of regenerated fibers is uncertain.

167 t-attached fibers, resulting in formation of fiber kinks.

168 onlinear system with complexity, mode-locked fiber lasers are known for their complex behaviour.

169 to SSPiM appeared more frequently in Henle's fiber layer (HFL) than the inner nuclear layer (INL) and

170 thickness of the peripapillary retinal nerve fiber layer (NFL) and ganglion cell complex (GCC).

171 To quantify retinal nerve fiber layer (RNFL) changes in patients with multiple scl

172 s were compared with regard to retinal nerve fiber layer (RNFL) thickness, drusen morphology, size, e

173 hyperopic refractive error shifts, and nerve fiber layer infarcts.

174 ameters, minimum rim width and retinal nerve fiber layer thickness, in addition to peripapillary chor

175 ing severity of IOP elevation, retinal nerve fiber layer thinning, or electrodiagnostic findings.

176 sitive staining was present within the nerve fiber layer, inner plexiform layer, and inner and outer

177 A diet high in fiber led to changes in the gut microbiota that played a

178 2; 95% CI, -28.77 to -7.10; P = .001), nerve fiber length (mean [SE] difference, -3.03 [0.89] mm/mm2;

179 The optimal fiber length for Raman gas sensing was found to be 15 cm

180 include proteoglycans, polysaccharides, and fibers like collagen, all of which makeup the extracellu

181 these projections allows us to identify the fibers likely to be affected by experimental manipulatio

182 inated sensory neurons (nonpeptidergic and C-fiber low-threshold mechanoreceptor neurons) resistant t

183 ched with the mode of almost any single mode fiber, making this approach highly versatile and integra

184 The favorable effects of fiber may be explained by the generation and distributio

185 nd reversibly control small-diameter sensory fibers may have many applications, both for the analysis

186 S and ZCS cells developed increased climbing fiber (MCS) or parallel fiber (ZCS) input during visual

187 tinic exposure prolongs superior laryngeal C-fiber-mediated apnea and bradycardia through enhancing n

188 rous nonwoven spunbonded poly(l-lactic acid) fiber mesh scaffolds.

189 is composed of approximately 67% fast-twitch fibers (MHC IIa+IId).

190 de array and dopamine dynamics from a carbon-fiber microelectrode.

191 yclic voltammetry (FSCV) coupled with carbon-fiber microelectrodes.

192 y methyl cellulose, locust bean gums, potato fiber, milk, potato and soy proteins) were added to toma

193 ntrations of lipids, proteins, total dietary fiber, minerals and vitamin E.

194 to detect signatures for the hexon, penton, fiber, minor capsid, and core proteins.

195 density (mean [SE] difference, -6.78 [2.14] fibers/mm2; 95% CI, -11.04 to -2.52; P = .002), nerve br

196 re typically derived from polymers, gel spun fibers, modified carbon fibers, carbon-nanotube fibers,

197 NF-kappaB activity is also involved in hair fiber morphogenesis during HF cycling.

198 hologs in zebrafish embryos disrupted muscle fiber morphology and resulted in abnormal eye developmen

199 g extracellular matrix (ECM), remodeling ECM fiber network structure by condensing, degrading, and al

200 The newly developed tight UF hollow fibers not only possess a small mean pore diameter of 1.

201 n immersion of a solid-phase microextraction fiber of PDMS/DVB into the oil matrix, followed by Gas C

202 O- to C-state transition in fully activated fibers of fast skeletal muscle of the rabbit occurs duri

203 e inhibitory effect of Lm211 is seen only in fibers of small caliber.

204 uronal nitric oxide synthase (nNOS) in nerve fibers of the murine vaginal wall.

205 ical misinnervation of the lateral rectus by fibers of the oculomotor nerve in DRS is secondary to ab

206 m and the remainder terminate into the sling fibers of the stomach.

207 A structures were integrated within portable fiber optic detection system, what is important for the

208 and experimental realization of a SPR based fiber optic nicotine sensor having coatings of silver an

209 ular in vivo biosensing when using ultrathin fiber optic probes for research purposes.

210 ization of a surface plasmon resonance based fiber optic xanthine sensor using entrapment of xanthine

211 Fiber optic-based near-infrared spectroscopy (FONIRS) se

212 A 3.7 Fr catheter with a fiber-optic channel was constructed based on a 40 MHz cl

213 present a short immunoassay (10 min) using a fiber-optic surface plasmon resonance (FO-SPR) biosensor

214 er we have described a potentially miniature fiber-optic vibrometer based on a modified Michelson int

215 nduced elongation, and promoted actin stress fiber organization.

216 tions of adhesion lifetime, which depends on fiber orientation.

217 tiate and integrate into the host, extending fibers over a long distance.

218 podia repeatedly contacted off-target muscle fibers over several hours during late embryogenesis, wit

219 fruits, vegetables and foods rich in dietary fiber (p-trends < 0.01).

220 e strength of the arcuate fasciculus (AF), a fiber pathway interlinking the left-hemispheric language

221 d and fabricated air-silica photonic crystal fiber (PCF).

222 drug that appears to be selective for Adelta-fibers (peripherally) and HT neurons (centrally).

223 l (moisture, ash, protein, fructans, dietary fibers, phenolic contents and antioxidant activity) prop

224 hese projections and observed phasic VTA-PFC fiber photometry signals after the delivery of rewards.

225 When attached to multiple fibers, platelets densify the fibrin network by pulling

226 high protein, carbohydrates, minerals, crude fibers, polyphenols and antioxidants thus can be used as

227 h 1 healthy and 1 endodontically treated and fiber post-restored abutment.

228 -y clinical performance of ETT restored with fiber posts.

229 The microscopic fibers present in organogel and hydrogel have different

230 The fibers presented different structural, crystallinity, an

231 Incorporation of NM-II into actin stress fiber provides a traction force to promote actin retrogr

232 in-part by long-term depression of parallel fiber-Purkinje cell synapse and induction of long-term p

233 helpful to increase fiber yield and improve fiber quality.

234 genome, and identified 19 candidate loci for fiber-quality-related traits through a genome-wide assoc

235 age respectively), insoluble/soluble dietary fiber ratio (4.3 and 1.79 seeds and mucilage respectivel

236 approach to study the nonlinear vibration of fiber reinforced composite laminates containing an embed

237 idermis, and stiffness anisotropy within the fiber-reinforced dorso-ventral epidermis are critical in

238 al cyclic stretch results in an actin stress fiber reinforcement response that stabilizes the actin c

239 activation exhibit a higher density of nerve fibers relative to biopsies during virological and clini

240 identification of the glycans found in viral fibers remain incomplete.

241 long SCs processes and reduced numbers of C-fibers/Remak bundle.

242 and late responses, mediated by Adelta and C fibers, respectively, based on required stimulation stre

243 An equitoxic binary mixture of beads and fibers resulted in a toxic unit of 1.85 indicating less

244 shortening and bending of platelet-attached fibers, resulting in formation of fiber kinks.

245 ecruitment of LIMCH1 into contractile stress fibers revealed its localization complementary to actini

246 Fiber sections (2.5 mm) were loaded with 10 pg of New Br

247 al of NCS-when constrained by food security, fiber security, and biodiversity conservation-is 23.8 pe

248 parameters such as excitation threshold and fiber selectivity.

249 assembly and mechanics of actomyosin stress fibers (SFs) depend on myosin regulatory light chain (RL

250 Actomyosin stress fibers (SFs) play key roles in driving polarized motilit

251 Herein, knittable fiber-shaped zinc-air batteries with high volumetric ene

252 eveloped to prepare the key component of the fiber-shaped zinc-air battery, i.e., a bifunctional cata

253 r neurons of SMA model mice increases muscle fiber size, enhances the post-synaptic NMJ area, reduces

254 noperated controls and those with selective, fiber-sparing lesions of either the OFC or VLPFC.

255 bstrate for phase-dependent binding of mossy fiber spikes to repetitive theta-frequency cycles of gra

256 e cells also contributed to functional mossy fiber sprouting, but exhibited less synaptic depression.

257 ural rearrangements between the oligomer and fiber states.

258 CMOS) integrated circuits are reported on 1D fiber substrates by using selectively chemical-doped sin

259 ners and toppings, SSBs, and total calories, fiber, sugar, and sodium.

260 observed for most outcomes.Isolated soluble fiber supplementation improves anthropometric and metabo

261 controlled trials (RCTs) of isolated soluble fiber supplementation in overweight and obese adults on

262 e fiber beneficially affects metabolism, and fiber supplementation may be a feasible approach to impr

263 Aligned collagen fibers support elevated tensions that promote the foldin

264 resent a thermal drawing approach to achieve fiber surface gratings on a rectangular cross-section.

265 urotransmission through the Drosophila giant fiber system (GFS), a simple escape response neuronal ci

266 gallery-mode (WGM) microdisk resonator and a fiber taper which exchange energies at two distinct regi

267 amolecular composites, opening a window into fiber technology through low-energy manufacturing.

268 Further, these 5-HT3 -expressing nerve fibers terminate in a restricted central-lateral portion

269 cally decreased densities of the small nerve fibers that innervate the epidermis, one hypothesis is t

270 polymerization of hemoglobin S (HbS) to form fibers that make red cells less flexible, most drugs cur

271 anatomically segregated fast and slow muscle fibers that possess different metabolic and contractile

272 mined for the presence and location of nerve fibers that reacted with a labeled antibody against calc

273 on glucose uptake (GU) +/- insulin in single fibers that were also characterized for fiber type.

274 -matrix systems in which cells migrate along fibers, the "hand-over-hand" longitudinal pulling causes

275 l of amyloid secondary structure even if the fibers themselves are too short to be resolved with TEM.

276 omain clusters decompact into mononucleosome fibers through a mechanism that requires Myc and continu

277 ptical fibers and small distance between the fiber tips and trapped particle.

278 ctions, HGF attenuates the linkage of stress fibers to cell-to-cell junctions with concomitant decrea

279 rior olivary (IO) neurons that send climbing fibers to innervate cerebellar Purkinje cells for the co

280 ithin the trapezoid body, a central auditory fiber tract, and determine the influence sensory experie

281 ing to their location (white matter, cortex, fiber tracts, basal ganglia).

282 ets densify the fibrin network by pulling on fibers transversely to their longitudinal axes.

283 While wild-type lint fiber trichome cells contained long longitudinal actin c

284 nsulin resistance and independent of altered fiber type composition.

285 duced insulin resistance was attributable to fiber type selective insulin resistance and independent

286 ngle fibers that were also characterized for fiber type.

287 ene oxide-silica composite reinforced hollow fiber was prepared via sol-gel technology and used as a

288 receptor, a marker for non-peptidergic nerve fibers, was not only significantly reduced but could als

289 ogy, and dynamic imaging of zebrafish muscle fibers, we find significantly reduced DHPR levels, funct

290 In the ccCP, M3 fibers were located medially and M1 fibers centromediall

291 the dynamic process of polymerization of HbS fibers, while maintaining the mechanical properties of p

292 dB in a link comprised of 90 km of installed fiber with additional optical attenuation introduced to

293 Considering a fiber with resonant Bragg gratings as an example, the me

294 separation to fabricate porous multimaterial fibers with complex internal architectures.

295 Using optical fibers with enhanced Rayleigh backscattering profiles as

296 It is shown that a single nozzle can print fibers with resolution much finer than the nozzle diamet

297 We demonstrate that optical fibers with tapered tips can be used to illuminate eithe

298 at muscles rich in type I vs. type II muscle fibers would exhibit similar changes in intramyocellular

299 er development, which is helpful to increase fiber yield and improve fiber quality.

300 d increased climbing fiber (MCS) or parallel fiber (ZCS) input during visual stimulation; SCS cells f