ライフサイエンスコーパス: sheath

1 e-evolving magnetization of the hot electron sheath.

2 he axon and the terminal loops of the myelin sheath.

3 the airway epithelium as a spatially uniform sheath.

4 PPP is critical for elongation of the myelin sheath.

5 vered over-the-wire with a deflectable 13.5F sheath.

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

7 elastic energy stored in a contractile tail sheath.

8 required for the proper growth of the myelin sheath.

9 d maintenance of the peripheral nerve myelin sheath.

10 suspended a radio-frequency produced plasma sheath.

11 ), the membrane proteins found in the myelin sheath.

12 e structure of the glia-extracellular matrix sheath.

13 cation mechanisms as synapses to form myelin sheaths.

14 that likely form autotypic junctions to seal sheaths.

15 endons for the presence and course of tendon sheaths.

16 mechanism involving the inner and outer root sheaths.

17 ving oligodendrocytes to generate new myelin sheaths.

18 drocytes and specifically phagocytose myelin sheaths.

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

20 participation in the primary Li(+) solvation sheath, abundant Li(2) O, Li(3) N, and LiN(x) O(y) grain

21 ergy of protons resulting from Target Normal Sheath Acceleration is presently still limited to around

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

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

24 A deflectable sheath (Agilis, Abbott) was used to maneuver the ablatio

25 rformed in vivo two-photon imaging of myelin sheaths along single axons of excitatory callosal neuron

26 er, remyelination-the regeneration of myelin sheaths-also depends upon an immune response, and the ef

27 ation, we used Caenorhabditis elegans amphid sheath (AMsh) glia as a model and show that a conserved

28 n potential conduction depends on the myelin sheath and clustered Na(+) channels at nodes of Ranvier.

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

30 Carbonate molecules occupy the solvation sheath and improve the Coulombic efficiencies of both th

31 ied cubic epithelium enclosed in a pigmented sheath and in close contact with the basal cartilage of

32 Albumin (BSA) conjugate incorporated in the sheath and intermediate layers of triaxial fibers was ac

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

34 combinations of focal or elongated segmental sheathing and discontinuity of small and large retinal a

35 hypomyelination with shorter, thinner myelin sheaths and motor coordination deficits.

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

37 ulate the formation and remodeling of myelin sheaths and perhaps additional functions of oligodendroc

38 Fbxw7 mutant SCs make thicker myelin sheaths and sometimes appear to myelinate multiple axons

39 ll walls adjoining the parenchymatous bundle sheath; and the proportion of leaf GLDP invested in the

40 larly to neurons and synapses, excess myelin sheaths are produced and selectively eliminated, but how

41 For % myelination the myelin sheaths are selected using the Frangi vesselness algorit

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

43 , thereby forming and maintaining the myelin sheath around peripheral axons (Grove et al., 2017).

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

45 xternal ultrathin poly(epsilon-caprolactone) sheath as an interposition graft in the abdominal aorta

46 Thus, our study identifies the dermal sheath as smooth muscle that drives follicle regression

47 imaging shows the T6SS as a long contractile sheath assembled around a rigid tube with associated tox

48 arie-Tooth neuropathy, but the mature myelin sheath assembly mechanism is unclear.

49 ciphering the 3D assembly of a mature myelin sheath at the molecular level.

50 that they assemble and fire T6SS contractile sheaths at ~6% of the frequency of rhs (+) cells.

51 s and combinations of critical gas pressure (sheath, auxiliary, sweep) and temperature (ion transfer

52 field significantly and beneficially alters sheath based ion acceleration and creates two distinct s

53 3D fully kinetic simulations of laser driven sheath-based ion acceleration with a kilotesla-level app

54 hermore, we provide the structure of the AFP sheath-baseplate complex in a contracted state.

55 The generation of sheath blight (ShB)-resistant transgenic rice plants thr

56 Rice sheath blight disease caused by Rhizoctonia solani Kuhn

57 ani gives a high level of resistance against sheath blight disease of rice.

58 erference (RNAi)-mediated resistance against sheath blight disease, we identified genes encoding prot

59 silencing of AG1IA_04727 and suppression of sheath blight disease.

60 , the functions of sRNAs in response to rice sheath blight remain unclear.

61 portantly, pre-treatment with auxin enhanced sheath blight resistance by affecting endogenous auxin h

62 ening an alternative strategy for developing sheath blight-resistant rice cultivars.

63 and a positive response to a modified rectus sheath block (>50% pain reduction, 81%).

64 on, combined with a positive modified rectus sheath block, may allow for diagnosing ACNES in patients

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

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

67 eveloping protoxylem of root, stem, and leaf sheath, but not metaxylem, and its expression is induced

68 strate that accurate placement of the myelin sheath by oligodendrocytes requires the coordinated acti

69 cells a suite of genomic RNA segments, each sheathed by the viral nucleocapsid protein and bound by

70 ormation of a relatively thick, smooth oxide sheath can improve the catalytic stability by mitigating

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

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

73 ize synchronization of TDI clocking with the sheathed-cell velocity and to improve sensitivity via th

74 S patients and more precisely the outer root sheath cells (ORSCs).

75 titioned such that leaf mesophyll and bundle sheath cells accumulate different components of the phot

76 of mesophyll cells; and supernumerary bundle sheath cells develop.

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

78 ight perception between mesophyll and bundle sheath cells facilitate differential regulation and accu

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

80 Then, sheath cells invade the inner notochord and differentiat

81 4) enzymes either to mesophyll (M) or bundle sheath cells is considered a crucial step towards the ev

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

83 oration as reflectin proteins distributed in sheath cells that envelop each chromatocyte.

84 f concentrated CO(2) that escapes the bundle-sheath cells, for the chilling-tolerant C(4) plant Misca

85 MP1, increased with aging, whereas in dermal sheath cells, hyaluronic acid synthase 2, HAS2, and PDPN

86 lly accumulated between mesophyll and bundle sheath cells, indicative of differential network activit

87 ion of exocyst components in inner germarial sheath cells, which form the differentiation niche, caus

88 s compartmented between mesophyll and bundle-sheath cells.

89 robably to avoid CO(2) leakiness from bundle sheath cells.

90 ary cultures of dermal fibroblast and dermal sheath cells.

91 ission electron microscopy, a healthy myelin sheath comprises compacted membrane layers spiraling aro

92 ons of mesophyll conductance (g(m) ), bundle-sheath conductance (g(bs) ) and the CO(2) concentrating

93 When this pathway is blocked, sheath contraction is inhibited, impeding follicle regre

94 Rapid sheath contraction releases a large amount of energy use

95 n-myosin light chain kinase pathway controls sheath contraction.

96 hen initiates a cascade of events leading to sheath contraction; and this contraction converts chemic

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

98 arized by a parahydrogen-based method (SABRE-SHEATH), demonstrating the products' utility as hyperpol

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

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

101 Measurement of optic nerve sheath diameter (ONSD) by point-of-care ultrasound may a

102 c nerve growth curve from normal optic nerve sheath diameter (ONSD) values measured by using B-scan u

103 between point of care and expert optic nerve sheath diameter after enrollment of 50 subjects was poor

104 was to evaluate the accuracy of optic nerve sheath diameter as a noninvasive screening test for the

105 While optic nerve sheath diameter demonstrated a modest, statistically sig

106 Optic nerve sheath diameter greater than 0.72 demonstrated sensitivi

107 The highest axial measurement of optic nerve sheath diameter in either eye is the most predictive of

108 A normal sheath diameter measurement has high sensitivity and a l

109 Optic nerve ultrasonography (optic nerve sheath diameter sonography) has been proposed as a nonin

110 e of the highest expert-measured optic nerve sheath diameter to detect intracranial pressure greater

111 st cutoffs for ultrasound of the optic nerve sheath diameter.

112 The optimal cutoff for optic nerve sheath dilatation on ultrasonography was 5.0 mm.

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

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

115 DMSO replaces the H(2)O in Zn(2+) solvation sheath due to a higher Gutmann donor number (29.8) of DM

116 the typical outward-directed topology of the sheath electric field into a focusing configuration.

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

118 owth from Golgi outposts and controls myelin sheath elongation, linking microtubule cytoarchitecture

119 ar tissue possibly facilitated by the bundle sheath extension.

120 ein networks that allow expression of bundle sheath extensions in some, but not all veins, contrastin

121 e to the propensity for veins to have bundle sheath extensions that exclude stomata from the local ep

122 asured density and area occupation of bundle sheath extensions, density and size of stomata and subsi

123 of septin filaments scaffolds mature myelin sheaths, facilitating rapid nerve conduction in the heal

124 A novel core-sheath fiber loaded with the drug carmustine (BCNU) was

125 mplantation of discs made of compressed core-sheath fibers (NanoMesh) either concurrently with or fiv

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

127 The advantage of sheathed flagella bundles is the high rigidity, making h

128 n the nanometer size range in a high laminar sheath flow of particle-free ambient air and a tunable e

129 ng (e.g., 50 cm) capillary with a conductive sheath flow.

130 tol 4,5-bisphosphate microdomains at nascent sheaths, followed by a filamentous actin network, and re

131 Remyelination is the regeneration of myelin sheaths following demyelination.

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

133 related to the wavy and malformed notochord sheath formation and abnormal axial skeleton segmentatio

134 Ahr gene in mouse impairs optic nerve myelin sheath formation and results in oculomotor deficits shar

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

136 Finally, blocking epidermal sheath formation destabilized dendrite branches and redu

137 ferentiation, neuronal signaling, and myelin sheath formation.

138 PKC epsilon, regulates the number of myelin sheaths formed by individual oligodendrocytes in mouse a

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

140 axial PLGA (50:50) and coaxial PLGA (50:50) (sheath)-gelatin (core) fibers was observed.

141 ously considered controversial, we show that sheath generation by mature oligodendrocytes is not only

142 1% of all light-induced mesophyll and bundle sheath genes were induced only by blue light or only by

143 h Granules Abnormal 1 (SAGA1) because starch sheath granules, or plates, in mutants lacking SAGA1 are

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

145 ets for myelination and regulation of myelin sheath growth are essential for central nervous system (

146 ndrocytes can engage in target selection and sheath growth at the same time and that Neurofascin conc

147 sicular release from neurons promotes myelin sheath growth on axons.

148 odendrocyte Neurofascin, also impairs myelin sheath growth, likely reflecting its association in an a

149 and extracellular adhesion to axons mediate sheath growth.

150 reduces CNS myelination by impairing myelin sheath growth.

151 pave the way to efficient spin-relayed SABRE-SHEATH hyperpolarization of a wide range of imidazole-ba

152 f 3.2 %) by (15) N-(15) N spin-relayed SABRE-SHEATH hyperpolarization technique, relying on simultane

153 In the Drosophila ovary, inner germarial sheath (IGS) cells form a niche for controlling germline

154 Ultrasound measurements of the optic nerve sheath in axial and coronal views either averaged betwee

155 l events leading to disruption of the myelin sheath in MS.

156 as elevated in the dermal papilla and dermal sheath in situ.

157 were associated with thinning of the myelin sheath in the corpus callosum.

158 Destruction of oligodendrocytes and myelin sheaths in cortical gray matter profoundly alters neural

159 The myelin sheath increases the speed of action potential propagati

160 y concentric layers of photosynthetic bundle sheath (inner) and mesophyll (outer) cells.

161 pt guideline-directed medical therapy before sheath insertion for PCI, (2) use of transradial primary

162 pt guideline-directed medical therapy before sheath insertion for PCI, transradial primary PCI, and d

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

164 nteraction between the core-intermediate and sheath-intermediate layers of the triaxial fibers contri

165 apoptosis/differentiation in the inner root sheath (IRS) as well as other parts of the hair follicle

166 rystals (LCs) stabilized by an outer polymer sheath is demonstrated.

167 The clearance of damaged myelin sheaths is critical to ensure functional recovery from n

168 50:50 poly (lactic-co-glycolic acid) (PLGA) (sheath layer) and a gelatin (intermediate layer) with a

169 ated by a highly asymmetric, multi-component sheath layer, contrasting with flagellin-only homopolyme

170 malfunction of Schwann cells or their myelin sheaths lead to peripheral neuropathies such as Charcot-

171 n oligodendrocytes cause variable effects on sheath length and number.

172 Here we report that the coleorhiza, a sheath-like organ that surrounds the radicle in grass em

173 The coaxial sheath liquid consisting of 0.2% (v/v) formic acid was a

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

175 r to bridge a hollow tube with a contractile sheath loaded in a metastable state by a baseplate scaff

176 ment sites with variable patterning and most sheaths localize PSD95 with patterning similar to exocyt

177 ferentiation and promotes development of the sheathing maize leaf base.

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

179 ticularly those due to the use of large-bore sheaths, may limit outcomes in these patients.

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

181 Cells were focused with a 1D-sheathing microfluidic device, and fluorescence emission

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

183 Importantly, the sheath model is coupled to component models representing

184 Bundle sheath modulation is associated with higher vein densiti

185 gest a biophysical mechanism by which starch sheath morphology affects pyrenoid number and CO(2)-conc

186 gesting that it may directly regulate starch sheath morphology.

187 and mitochondrial investment in the mestome sheath (MS), where CO(2) is concentrated in C(2) and C(4

188 upper and lower leaf zones, the formation of sheathing/nonsheathing leaf bases and vasculature patter

189 In E- embryos, the collagen sheath notochord markers (col2a1a and col9a2) appeared b

190 glycoprotein, an antigen in the outer myelin sheath of central nervous system neurons, are present.

191 enes known to be expressed in the outer root sheath of hair follicles.

192 lvent component that dominates the solvation sheath of Li(+) .

193 e-shell composite anode, comprising an outer sheath of lithiated liquid metal (Li(x) LM(y) ) and an i

194 that NO(3) (-) participates in the solvation sheath of lithium ions enabling more bis(trifluoromethan

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

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

197 he scalp and are derived from the outer root sheath of the hair follicle.

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

199 In addition, the glass sheath of the Pt tip is thinned to ~150 nm to rarely con

200 tractile actin networks in the myoepithelial sheath of the somatic gonad.

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

202 Purpose To determine the anatomy of tendon sheaths of the forefoot and the relationship between MRI

203 n which the guest that drives actuation is a sheath on a twisted or coiled core that can be an inexpe

204 Dilation of the optic nerve sheath on axial ultrasound of the eye has been correlate

205 ctive characteristics of the inner solvation sheath on electrode surfaces due to their unique solvati

206 These findings reveal how the outer root sheath (ORS) and inner hair follicle layers coordinate h

207 The mean effective sheath outer diameter was 22F (7.3 mm).

208 segments per cell, then spiral around myelin sheaths, penetrating from outer to inner layers.

209 optimal matching from the traditional SABRE-SHEATH picture.

210 nd its interaction with lipids of the myelin sheath plays an important part in the pathology of multi

211 vity was observed in roots, ligules, leaves, sheaths, pollen grains, and surrounding the vascular tis

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

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

214 salt and the solvent in the inner solvation sheath promote their intermolecular proton/charge transf

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

216 Proteomics revealed an increase in dermal sheath proteins in the dermal fibroblast secretome with

217 Distinct sheath proteins localize to the filament inner and outer

218 ation, oligodendrocyte generation and myelin sheath remodeling in the forelimb motor cortex.

219 ated clotting time (ACT) was measured before sheath removal.

220 es alignment transfer to heteronuclei, SABRE-SHEATH) resulted in positive enhancements of up to ~100-

221 This change from guest-filled to sheath-run artificial muscles increases the maximum work

222 A sheath-run electrochemical muscle generates 1.98 watts p

223 dicts the observed performance advantages of sheath-run muscles.

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

225 Plexiform neurofibromas are benign nerve sheath Schwann cell tumors characterized by biallelic mu

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

227 mutation in cmn results in loss of notochord sheath segmentation, altering osteoblast migration to th

228 Sheath shortening is associated with a low frequency of

229 Further innovation to reduce sheath sizes and optimize antithrombotic therapy is nece

230 s was covered with a C-seal, a bioresorbable sheath stapled to the anastomosis.

231 ium distachyon In C(4) species, while bundle-sheath strands and whole leaves shared similarity in the

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

233 trolyte components with its unique solvation-sheath structure, where the decompositions of carbonate

234 al spider silk consists of hierarchical core-sheath structured hydrogel fibres, which are reinforced

235 Drug delivery with coaxial core-sheath structures benefits from high drug loading, contr

236 unctional appressoria developed on rice leaf sheath surfaces, but Deltandk1 invasive hyphal growth wa

237 xor tendons crossing MTP joints demonstrated sheaths surrounding tendons.

238 spinal cord inherently produce longer myelin sheaths than those from the cortex(2), and single-cell a

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

240 vision and the production of the hydrophobic sheath that covers Streptomyces aerial hyphae and spores

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

242 cells is evolutionarily conserved, forming a sheath that is anchored to apical junctions and position

243 Here, we identify the dermal sheath that lines the follicle as the key driver of tiss

244 In the nervous system, a myelin sheath that originates from oligodendrocytes or Schwann

245 n increase in the surface area of the starch sheath that surrounds and binds to the liquid-like pyren

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

247 "contraction wave" that propagates along the sheath, the energy that powers the injection machinery,

248 - affecting oligodendrocytes and the myelin sheaths they produce - that plays a crucial role in lear

249 In the proposed treadmilling model, myelin sheath thickness is a dynamic balance between the rates

250 Myelin sheath thickness is precisely regulated and essential fo

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

252 Transplantation of sheath tissues improves tendon repair.

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

254 tems from oligodendroglia, which form myelin sheaths to regulate the conduction of nerve impulses acr

255 TME of cutaneous malignant peripheral nerve sheath tumor (C-MPNST) and spindle cell melanoma (SCM) h

256 Malignant peripheral nerve sheath tumor (MPNST) is an aggressive sarcoma with recur

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

258 ial sarcoma (SS), malignant peripheral nerve sheath tumor (MPNST), and undifferentiated pleomorphic s

259 teristics of lipoma, benign peripheral nerve sheath tumor, and vascular malformation (n = 192) were i

260 enetic drivers of malignant peripheral nerve sheath tumors (MPNST) harboring loss-of-function polycom

261 leiomyosarcomas, malignant peripheral nerve sheath tumors (MPNST), solitary fibrous tumors, synovial

262 n the majority of malignant peripheral nerve sheath tumors (MPNST).

263 d in about 90% of malignant peripheral nerve sheath tumors (MPNST).

264 ons of aggressive malignant peripheral nerve sheath tumors (MPNST).

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

266 Malignant peripheral nerve sheath tumors (MPNSTs) are soft-tissue sarcomas that fre

267 In malignant peripheral nerve sheath tumors (MPNSTs), Polycomb repressive complex 2 (P

268 ogenic driver for malignant peripheral nerve sheath tumors (MPNSTs), which are highly aggressive sarc

269 ANNUBP) and/or to malignant peripheral nerve sheath tumors (MPNSTs).

270 CKGROUNDNeurofibroma/schwannoma hybrid nerve sheath tumors (N/S HNSTs) are neoplasms associated with

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

272 r in a distinct subgroup of peripheral nerve sheath tumors based on genome-wide DNA methylation patte

273 Malignant peripheral nerve sheath tumors often arise in patients with neurofibromat

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

275 se inhibitors against these aggressive nerve sheath tumors.

276 nstream of Ras in malignant peripheral nerve sheath tumors.

277 embedded specimens of human peripheral nerve sheath tumors.

278 d inappropriate), malignant peripheral nerve sheath tumour, non-metastatic and grossly resected derma

279 o chondrosarcoma, malignant peripheral nerve sheath tumour, synovial sarcoma, epithelioid sarcoma and

280 continuum representation of the contractile sheath using elastic constants inferred from atomistic m

281 Sheath-vessel diameter ratio, postprocedure compression

282 An 8 French catheter sheath was inserted into the common carotid artery, and

283 Microscopically, a synovial sheath was present.

284 oncentrations in the seamount-associated or 'sheath'-water than in deep-ocean water unaffected by sea

285 Genomic analyses of flow-sorted, dominant sheath-water bacteria confirm their planktonic origin, w

286 nic origin, whilst proteomic analyses of the sheath-water bacteria, isotopically labelled in situ, in

287 to our radiotracer experiments, it takes the sheath-water bacterioplankton 1.5 years to double their

288 ropose that turbulent mixing of the seamount sheath-water stimulates bacterioplankton growth by incre

289 grow to the 2.4x higher concentration in the sheath-water.

290 etermine whether microglia also prune myelin sheaths, we used zebrafish to visualize and manipulate i

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

292 s were formed in different locations and new sheaths were often established along axon segments previ

293 xed microtubule polarity, and shorter myelin sheaths when cultured on 3-dimensional (3D) microfibers.

294 One candidate, Cadm1b, localizes to myelin sheaths where both PDZ binding and extracellular adhesio

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

296 been observed associated with cell walls or sheaths, which are instead preserved by clay minerals or

297 tubes and poly(epsilon-caprolactone) fibrous sheaths, which improved suture retention strength and en

298 and zebrafish induce formation of epidermal sheaths, which wrap neurites of different types of neuro

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

300 originated from muscle, nerve, and/or tendon sheaths, with frequent invasion into adjacent bone.