ライフサイエンスコーパス: sheath

1 lycoprotein (MOG that is a protein in myelin sheath).

2 l and functional role in the neuronal myelin sheath.

3 e ovulatory contraction of the myoepithelial sheath.

4 elastic energy stored in a contractile tail sheath.

5 ripheral nervous system that form the myelin sheath.

6 , can dispose of a whole sperm mitochondrial sheath.

7 adjacent cytoplasmic membranes of the myelin sheath.

8 ll compared with both guard cells and bundle sheath.

9 o target cells upon contraction of its TssBC sheath.

10 the L1 at the developing margins of the leaf sheath.

11 itical for the genesis of the central myelin sheath.

12 icult requiring manipulation via a steerable sheath.

13 or the periepithelial intestinal mesenchymal sheath.

14 required for the proper growth of the myelin sheath.

15 s caused by immune-mediated damage of myelin sheath.

16 y local translation at the developing myelin sheath.

17 uld result in radial fractures of the myelin sheath.

18 ps affecting the structure of the gelatinous sheath.

19 es are also found in vivo in diseased myelin sheaths.

20 e layers is conserved between T6SS and phage sheaths.

21 iation and properties of Schwann cell myelin sheaths.

22 minant-negative Fbxw7 produced longer myelin sheaths.

23 nt ability to differentiate and form initial sheaths.

24 round axons to generate multilamellar myelin sheaths.

25 ature cells capable of generating new myelin sheaths.

26 mechanism involving the inner and outer root sheaths.

27 was performed through transcaval introducer sheaths.

28 vacuolated cells surrounded by an epithelial sheath [1-3].

29 alloon occlusion catheter placed through the sheath (10 patients) simultaneously during each coronary

30 either via Pluronic gel (2-week), or polymer sheath (3-month), effectively reduced IH without causing

31 An epicardially placed steerable sheath/4 mm-catheter combination (5 patients) or a vascu

32 iration was done directly from a transseptal sheath (8 patients) or through a balloon occlusion cathe

33 lse propagation is facilitated by the myelin sheath, a compact membrane surrounding the axon.

34 The influence on both sheath-accelerated and radiation pressure-accelerated pr

35 In both cases typical Target Normal Sheath Acceleration emission patterns with exponential p

36 the standard and commonly used Target Normal Sheath Acceleration technique (TNSA), or more explorator

37 iolysis was required in 10 patients with the sheath, access wire, and pigtail or ablation catheter.

38 caused by the greater proportion of stem and sheath acting as a physical barrier to bite formation.

39 To predict the behavior of the cement sheath after CO2 injection and the potential for leakage

40 (aHR, 10, 95% CI, 3.0-33), retinal vascular sheathing (aHR, 2.6, 95% CI, 1.4-4.9), and exudative ret

41 The archaeal sheath amyloids do not share homology with any of the cu

42 ry both for the formation of a normal embryo sheath and for embryo-endosperm separation.

43 The TssA1 ring complex binds the T6SS sheath and impacts its behaviour in vivo In the phage, t

44 ncentrating mechanism divided between bundle sheath and mesophyll cells increases photosynthetic effi

45 ppaB activity was observed in the inner root sheath and unilaterally clustered in the HF matrix, whic

46 es whose dimensions match those of the TssBC sheath and which can accommodate the inner Hcp tube.

47 The 4-French vascular sheaths and 4F-catheters were introduced under fluorosco

48 ed fascicles of needle leaves with deciduous sheaths and bulbous bases are recognized as Pinus sp. an

49 d BCCAO-induced damage to hippocampal myelin sheaths and oligodendrocytes, enhanced expression of the

50 structural damage is initiated at the myelin sheaths and only later spreads to the oligodendrocyte ce

51 seen in remyelination; that is, thin myelin sheaths and short internodes.

52 the persistence and longevity of thin myelin sheaths and the importance of remyelination to the long-

53 fecting the integrity of the axon and myelin sheaths and thus preventing proper remyelination.

54 es were gradually released from aging myelin sheaths and were subsequently cleared by microglia.

55 n, the main component of the spirochete's PF sheath, and a key determinant of the flagella's coiled s

56 ree qualitative traits: glossy spike, glossy sheath, and black hull color were mapped with high resol

57 the hair follicle, especially the inner root sheath, and that the Q30R substitution affects enzyme pr

58 en leaves within a stem, between laminae and sheaths, and between the mainstem and axillary tillers)

59 omoter, exhibited thicker PNS and CNS myelin sheaths, and PNS myelin abnormalities, such as tomacula

60 ination and spatial learning, thinner myelin sheaths, and reduced myelin gene expression.

61 dominant constituents in cytoplasmic myelin sheaths, and shed new light on mechanisms disrupting lip

62 odal length, and the thickness of the myelin sheath are powerful structural factors that control the

63 sheaths than controls and that their myelin sheaths are 50% shorter than controls.

64 T6SS sheaths are cytoplasmic tubular structures composed of s

65 Surgical sutures with highly porous sheaths are developed using a swelling and freeze-drying

66 Robust relationships between laminae and sheath areas also were found, highlighting the tight con

67 Schwann cells produce myelin sheath around peripheral nerve axons.

68 polymer self-assembly strategy for forming a sheath around the proteins and then tracelessly releasin

69 ificant reduction in the thickness of myelin sheaths around small-diameter axons was observed in indi

70 structures impair the functional role of the sheath as an insulating layer for proper nerve conductio

71 uitously expressed in all tissues except the sheath at heading stage.

72 ee distinct rice diseases, bacterial blight, sheath blight, and rice blast.

73 ct widely used in China for controlling rice sheath blight, Rhizoctonia solani.

74 The blade-sheath boundary disruption, shorter ligule, and disrupte

75 lastin fibers of periosteum, the soft tissue sheath bounding all nonarticular bone surfaces in our bo

76 g mechanism between mesophyll (M) and bundle sheath (BS) cells of leaves.

77 ular species, among mesophyll (M) and bundle sheath (BS) cells, are compared across the leaf developm

78 coordinated across mesophyll (M) and bundle sheath (BS) cells, respectively.

79 become restricted to mesophyll (M) or bundle sheath (BS) cells.

80 o effects on hydraulic pathlength and bundle sheath (BS) surface area; (2) palisade mesophyll remains

81 re exhibited distinct short- and long-period sheath buckling that occurred reversibly out of phase in

82 The filter was then removed through the sheath by using the endobronchial forceps.

83 hloroplasts of mesophyll (C3 plants), bundle-sheath (C4 plants), and guard cells.

84 s fields of epidermal scales and intact horn sheaths capping the body armor.

85 ossible with a balloon; however, a steerable sheath/catheter combination was ultimately successful.

86 In total, 334 sheath/catheter manipulations (transseptal puncture, she

87 gnals in carotid artery were observed during sheath/catheter manipulations especially in saline/contr

88 respiration enabled estimation of the bundle sheath cell CO2 concentration (Cb) using a simple kineti

89 VPR-1 MSPd acts at least in part on gonadal sheath cell precursors in L1 to early L2 stage hermaphro

90 s released by dying vacuolated cells promote sheath cell vacuolization and trans-differentiation.

91 -limited photosynthesis in the mutant bundle sheath cell.

92 to developing leaf veins, to include bundle sheath cells encircling the vein.

93 Here we show that tendon sheath cells harbor stem/progenitor cell properties and

94 In contrast, glial sheath cells harboring the sensory endings of C. elegans

95 sensory organs exhibiting transformation of sheath cells into ectopic neurons.

96 Then, sheath cells invade the inner notochord and differentiat

97 HSS has been localized in the bundle sheath cells of specific leaves.

98 ells were depleted, the surviving outer root sheath cells rapidly acquired an SC-like state and fuele

99 requires an increase in organelle volume in sheath cells surrounding leaf veins.

100 d mitochondrial development in rice vascular sheath cells through constitutive expression of maize GO

101 cS isoforms expressed in mesophyll or bundle-sheath cells.

102 nflux into vacuoles of endodermal and bundle sheath cells.

103 root forming HERS (Hertwig's epithelial root sheath) cells.

104 mesophyll chloroplasts compared with bundle sheath chloroplasts, and MET1 mRNA and protein levels in

105 condary pollution by Pd nanoparticles in the sheath-coating process.

106 Sheaths composed of VipB and VipA fused to an antigen of

107 The tail sheath contraction induces conformational changes of the

108 However, the tail sheath contraction of Myoviridae phages is not sufficien

109 These downsized sheath-core fibers provide the demonstrated basis for gl

110 components such as Hertwig's epithelial root sheath, cranial neural crest cells and stem cells residi

111 s that we propose results in the same myelin sheath deficiencies as seen in remyelination; that is, t

112 -like kinases GSO1 and GSO2 are required for sheath deposition at the embryo surface but not for prod

113 cture of a native contracted Vibrio cholerae sheath determined by cryo-electron microscopy.

114 Thus, [Ca(2+)]i controls myelin sheath development.

115 Optic nerve sheath diameter (ONSD) evaluated in CT imaging as well a

116 nICP was assessed using optic nerve sheath diameter (ONSD), venous transcranial Doppler (vTC

117 Sheaths displaying heterologous antigens generated bette

118 A stiff guidewire and a large sheath distorted the anatomy, which resulted in an incom

119 ition to the more commonly observed electron-sheath driven proton acceleration.

120 l-subdeltoid bursa/long head of bicep tendon sheath effusion (44.4%), and long head of bicep tendon s

121 usion (44.4%), and long head of bicep tendon sheath effusion only (40%).

122 inniped optic nerve, those with thick myelin sheaths (elephant seal: 9%, sea lion: 7%) and thin myeli

123 hant seal: 9%, sea lion: 7%) and thin myelin sheaths (elephant seal: 91%, sea lion: 93%).

124 ing oligodendrocytes in vivo and that myelin sheath elongation is promoted by a high frequency of [Ca

125 Sheath elongation occurs 1 h after [Ca(2+)]i elevation.

126 Contraction of the tail sheath enables the tail tube to penetrate through the ba

127 er insertion, pulmonary vein venography, and sheath exchange) and 333 radiofrequency applications (po

128 ion (CSA) to a boost procured by a TNSA-like sheath field in the downward density ramp of the target,

129 using laser-induced fluorescence (LIF) in a sheath flow cuvette.

130 imately 200 mum from each other) generates a sheath flow that confines the analyte molecules eluting

131 tic fluids to increase the displacement of a sheath flow-focused particle mixture for a high-purity s

132 mplished by combining line focus optics with sheath-flow SERS detection.

133 ficantly higher microbubble volume than slow sheath flushing (median, 12 200 versus 121 nL; P<0.0001)

134 Fast sheath flushing produced significantly higher microbubbl

135 atheter manipulations (transseptal puncture, sheath flushing, catheter insertion, pulmonary vein veno

136 ensuring the timely generation of new myelin sheaths following demyelinating injury in the adult CNS.

137 uppress Cas9 and may function like molecular sheaths for the Cas9 scalpel.

138 imulating neuronal activity increased myelin sheath formation by individual oligodendrocytes.

139 We present a model in which sheath formation depends on the coordinated production o

140 tivity-dependent secretion stabilized myelin sheath formation on select axons.

141 cally decreased MBP and P0 levels and myelin sheath formation without affecting expression of Krox20/

142 of MBP that correlates with a lack of myelin sheath formation.

143 Nascent sheaths formed on silenced axons were shorter in length,

144 samples resulted in the enrichment of both, sheath-forming and stalk-forming Zetaproteobacteria.

145 We demonstrate in this work a continuous sheath-free separation of both a binary and a ternary pa

146 ve thermal transfer (between the superheated sheath gas and the solvent) is predominant and stronger

147 ectrostatic lens and a manifold for internal sheath gas distribution and delivery.

148 Cartridges with and without a sheath gas manifold and an electrostatic lens are compar

149 the cartridge with an electrostatic lens and sheath gas manifold compared to the cartridge without (1

150 -phase reactions in microdroplets sheared by sheath gas without using a phase-transfer catalyst.

151 pH imaging and RNA sequencing of the amphid sheath glia of Caenorhabditis elegans to reveal a novel

152 ibe our discovery that the C. elegans amphid sheath glia regulate intracellular pH via HCO3 (-) flux

153 Following stabilization, myelin sheaths grow along axons, and we find that higher-freque

154 ing axons was also suppressed, inhibition of sheath growth was relieved.

155 Here we report that the myoepithelial sheath has a distinct myosin population containing nonmu

156 The sheath has a quaternary structure with handedness opposi

157 ition, loss and/or dysfunction of the myelin sheath has been associated with a variety of neurologic

158 Therefore, although the myoepithelial sheath has smooth muscle-like contractile apparatuses, i

159 s iron accumulates, a degeneration of myelin sheaths has been observed in the elderly, but the relati

160 raction of the tripod proteins with the tail sheath, hence triggering its contraction.

161 nation between the Hertwig's epithelial root sheath (HERS) and apical papilla (AP) is crucial for pro

162 r) is expressed in Hertwig's epithelial root sheath (HERS) during root development, with mutant mice

163 can cell wall is a major protective external sheath in bacteria and a key target for antibiotics(1).

164 thogenic autoimmune cells that attack myelin sheath in experimental autoimmune encephalomyelitis (EAE

165 The myoepithelial sheath in the somatic gonad of the nematode Caenorhabdit

166 e critical role of Hertwig's epithelial root sheath in tooth root formation.

167 In the first, we have followed thin myelin sheaths in a model of delayed myelination during a perio

168 The presence of thin myelin sheaths in the adult CNS is recognized as a marker of re

169 erved in the vicinity of sperm mitochondrial sheaths in the zygotes and increased in the embryos trea

170 ribe the fine spatial organization of myelin sheaths in vivo.

171 Thinner myelin sheaths, indicated by increased G-ratio of myelin, were

172 m ulcerans who developed a right hand flexor sheath infection and symptoms of sepsis such as fever, t

173 nd changes in cell shape that lead to myelin sheath initiation and formation.

174 evel, but not on the axonal tracts or myelin sheath integrity.

175 The sheath is deposited outside the embryonic cuticle and in

176 on, and longitudinal extension of the myelin sheath is disrupted.

177 The myelin sheath is highly enriched in galactosylceramide (GalCer)

178 s, but not in supra/proximal bulb outer root sheath K15+ progenitors.

179 y including other rubber and carbon nanotube sheath layers, we demonstrated strain sensors generating

180 on that axon diameters correlate with myelin sheath length, as well as reports that PNS axonal neureg

181 oligodendrocyte myelination and appropriate sheath lengths.

182 separation medium, and as an additive to the sheath liquid of the electrospray interface (ESI), gener

183 re needed for the development of these nerve sheath malignancies.

184 Catheter/sheath manipulations in left atrium were performed in 25

185 ecific stages during initiation of the basal sheath margins from the tubular disc of insertion (DOI).

186 the embryo surface but not for production of sheath material in the endosperm.

187 two lines of evidence here that thin myelin sheaths may persist indefinitely in long-lived animal mo

188 coordinate gene expression across the bundle sheath, mesophyll, and guard cells in the C4 leaf.

189 diazirine can be hyperpolarized by the SABRE-SHEATH method, sustaining both singlet and magnetization

190 The notochord sheath mineralizes normally, supporting the idea of an o

191 The prepared ZnO@ZIF-CoZn core-sheath nanowire arrays show greatly enhanced performance

192 As a result, these devices often require a sheathing needle to prepuncture robust sample matrixes a

193 henocopies Notch loss of function during the sheath-neuron cell fate decision, suggesting the miRNAs

194 f adult HF stem cells and the dermal papilla/sheath niche, along with lineage-related keratinocytes a

195 ization of glycolytic enzymes on the fibrous sheath of mammalian sperm, here we show a complex reacti

196 tion electrode directly through the neuronal sheath of nerves and ganglia in insects.

197 n/absorption of electromagnetic waves by the sheath of plasma created by a high speed vehicle re-ente

198 ponent of the perichromosomal layer (PCL), a sheath of proteins surrounding condensed chromosomes dur

199 with handedness opposite that of contracted sheath of T4 phage tail and is organized in an interlace

200 hich separates the distal blade and proximal sheath of the leaf.

201 formed, which showed a defect in the fascial sheath of the muscle through which the tibialis anterior

202 of a fluorescent particle to the insulating sheath of the SECM tip extends this technique to nonfluo

203 nge mediated by Fc(2+) adsorbed on the glass sheath of the tip.

204 NAcylation is mislocalized within the myelin sheath of these mutant animals.

205 eposits in the muzzle skin containing dermal sheath of vibrissae and in aorta.

206 filarial protein (MfP) was isolated from the sheath of W. bancrofti microfilariae through ultrafiltra

207 f compact, multilamellar myelin and generate sheaths of physiological length.

208 fibers, comprising a buckled carbon nanotube sheath on a rubber core, are fabricated, characterized,

209 r fibers, comprising buckled carbon nanotube sheaths on a rubber core, can be used as glucose sensors

210 RG (defined as the radius of the insulating sheath over the radius of the active metal electrode).

211 Laminins colocalized with NP41 within nerve sheath, particularly perineurium, where laminin-421 is p

212 45 catheterizations with successful PCA and sheath placement, 44 interventions were performed, the m

213 igher-frequency Ca(2+) transient activity in sheaths precedes faster elongation.

214 mplitude, long-duration Ca(2+) transients in sheaths prefigure retractions, mediated by calpain.

215 , antigen-specific antibodies raised against sheaths presenting Neisseria meningitidis factor H bindi

216 Sheath production is dependent upon the activity of ZHOU

217 lignment transfer to heteronuclei" or "SABRE-SHEATH", promises to be a simple, cost-effective way to

218 )) orthologous to regions in the major outer sheath protein (MOSP(N) and MOSP(C)) of Treponema dentic

219 The major outer sheath protein (MOSP) is a prominent constituent of the

220 and accumulate improperly assembled fibrous sheath proteins.

221 We also found that the bundle sheath provides a significant minority of evaporation (1

222 t membrane proteins from entering the myelin sheath region.

223 eceptors that drive the growth of the myelin sheath remain poorly understood in the CNS.

224 We show that the myelin sheaths remain thin and stable on many axons throughout

225 in the presence of apparently normal myelin sheaths, remain unknown.

226 multivalent nanoparticles based on the T6SS sheath represent a versatile scaffold for vaccine applic

227 igodendrocytes produce myelin, an insulating sheath required for the saltatory conduction of electric

228 ogen-15 in a variety of molecules with SABRE-SHEATH (SABRE in shield enables alignment transfer to he

229 promoted the differentiation of glial nerve sheath Schwann cells and induced their migration by acti

230 Sheath shortening is associated with a low frequency of

231 d with preferential expression in the bundle sheath showed continually decreasing expression from bun

232 in metronidazole is demonstrated using SABRE-SHEATH (Signal Amplification by Reversible Exchange in S

233 ivo In the phage, the first disc of the gp18 sheath sits on a baseplate wherein gp6 is a dodecameric

234 alcin (Bglap) can be used as an adult tendon-sheath-specific marker in mice.

235 ynamics) representation of a fraction of the sheath structure to generate a continuum model of the en

236 ge or dysregulation of the insulating myelin sheath surrounding spinal motor axons, causing pain, ine

237 ing reticulospinal neurons have fewer myelin sheaths than controls and that their myelin sheaths are

238 to generate a continuum model of the entire sheath that also couples to a model of the viral capsid

239 scribe a structure we refer to as the embryo sheath that forms on the surface of the embryo as it sta

240 crucial role in holding together the myelin sheath that insulates peripheral nerves.

241 produce myelin, a lipid-rich, multilamellar sheath that surrounds axons and promotes the rapid propa

242 e contractile activity of the tubular muscle sheath that surrounds developing egg chambers.

243 ostasis, a major lipid constituent of myelin sheaths that are formed by oligodendrocytes.

244 The resulting smooth and uniform C-coatings sheathing the inner core metal oxide NPs are made of wel

245 with a curious evolutionary innovation: they sheath themselves in a cell wall made largely of silica.

246 remains uncertainty about whether these thin sheaths thicken with time and whether they remain viable

247 ng axon numbers, axonal calibers, and myelin sheath thickness by electron microscopy.

248 ensheathment and in the regulation of myelin sheath thickness in the PNS.

249 recovery from demyelination to normal myelin sheath thickness remains unknown.

250 and nanostructure as well as a tunable CeO2 sheath thickness were obtained by a biomolecule-assisted

251 g together to drive the growth of the myelin sheath, thus increasing myelin thickness.SIGNIFICANCE ST

252 ecular function of Hh signaling in extrinsic sheath tissues for tendon repair.

253 Transplantation of sheath tissues improves tendon repair.

254 Mechanistically, Hh signaling in sheath tissues is necessary and sufficient to promote th

255 ts show that Bglap-expressing cells in adult sheath tissues possess clonogenic and multipotent proper

256 the proliferation of Mkx-expressing cells in sheath tissues, and its action is mediated through TGFbe

257 Treg cells could directly target the myelin sheath to ameliorate EAE.

258 ontinually decreasing expression from bundle sheath to mesophyll to guard cells.

259 ressures among joints through the periosteal sheath to sustain the integrity of the joint contacting

260 odal junction (PNJ) that attaches the myelin sheath to the axon, are present in the shk central nervo

261 The ratio of the insulating sheath to the electroactive core of the UMEs was 2.5-3.6

262 n adaptations to both axons and their myelin sheaths to fully understand how myelinated axon plastici

263 g characteristic models were generated using sheath-to-iliofemoral artery ratios as a variable and SR

264 acterized by focal thickenings of the myelin sheath (tomacula), progressive demyelination, axonal los

265 Malignant peripheral nerve sheath tumor (MPNST) is an aggressive soft tissue sarcom

266 ansformation to a malignant peripheral nerve sheath tumor, an aggressive soft-tissue sarcoma.

267 en established in malignant peripheral nerve sheath tumors (MPNST) where NF1 mutations also occur.

268 cular features of malignant peripheral nerve sheath tumors (MPNST).

269 Malignant peripheral nerve sheath tumors (MPNSTs) are a type of rare sarcomas with

270 Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive neoplasms that com

271 Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive tumors with low su

272 Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive, frequently metast

273 Malignant peripheral nerve sheath tumors (MPNSTs) are devastating sarcomas for whic

274 n differentiating malignant peripheral nerve sheath tumors (MPNSTs) from benign neurofibromas (BNFs)

275 being applied to malignant peripheral nerve sheath tumors (MPNSTs), rare Schwann cell-derived malign

276 In malignant peripheral nerve sheath tumors and CNS tumors, the cancers traditionally

277 ibrosarcomas, and malignant peripheral nerve sheath tumors are characterized by complex genomic chara

278 benign Schwann cell-derived peripheral nerve sheath tumors arising sporadically and within neurofibro

279 Schwannomas are common peripheral nerve sheath tumors that can cause debilitating morbidities.

280 al perineuriomas are benign peripheral nerve sheath tumors that cause progressive debilitating focal

281 eurofibromas, and malignant peripheral nerve sheath tumors, as well as behavioral, cognitive, motor,

282 s of patients with multiple peripheral nerve sheath tumors.

283 in/CTNNA3 in the biology of peripheral nerve sheath tumors.

284 embedded specimens of human peripheral nerve sheath tumors.

285 tail fibers are folded back against the tail sheath until irreversible adsorption, a feature compatib

286 tered structure of Hertwig's epithelial root sheath was also observed.

287 flated with CO2 to displace the lung, an 18F sheath was delivered to the left atrium, and the left at

288 Here, the structure of the VipA/B sheath was exploited to generate immunogenic multivalent

289 Consistent with this, the myelin sheath was thinner, less compact and not properly rolled

290 d 'onion bulb' formations and/or thin myelin sheaths were observed in 14 (67%) of them.

291 r MG132, in which intact sperm mitochondrial sheaths were observed.

292 tory distal tip cells and the proximal gonad sheath, where it becomes enriched in response to tissue

293 that Bph32 was highly expressed in the leaf sheaths, where BPH primarily settles and feeds, at 2 and

294 vy chains are expressed in the myoepithelial sheath, which are also expressed in the body-wall striat

295 drocytes initially over-produce short myelin sheaths, which are either retracted or stabilized.

296 the central nervous system (CNS), the myelin sheaths, which protect axons and allow the fast propagat

297 ghly nonlinear conformational changes of the sheath whose elastic energy drives the injection process

298 -long, single crystal, alpha-Si3N4 nanowires sheathed with amorphous silicon oxide were synthesised b

299 After sheath withdrawal, hemostasis was achieved with manual c

300 The myelin sheaths wrapped around axons by oligodendrocytes are cru