ライフサイエンスコーパス: shaft

1 ficking and trap AMPARs inside the dendritic shaft.

2 ells to initiate the formation of a new hair shaft.

3 improved outcomes in the proximal femur and shaft.

4 e synapse on the spine head to the dendritic shaft.

5 e similar to those observed in the dendritic shaft.

6 table stopper is installed at the end of the shaft.

7 ronger antioxidant properties than the white shaft.

8 microtubules (MTs) that splay from the axon shaft.

9 nt enrichment of PSD-95-GFP on the dendritic shaft.

10 nd we propose a model for the GBS PI-1 pilus shaft.

11 cularly in controlling the shape of the hair shaft.

12 ilopodial components localize to the tip and shaft.

13 sprouting axon branches from a primary axon shaft.

14 fusion events in the cell body and dendritic shaft.

15 eficient in tau are present along the axonal shaft.

16 tory synapses made directly on the dendritic shaft.

17 any to underlying growth plate cartilage and shaft.

18 e forces on microtubules (MTs) in the axonal shaft.

19 ion of the urethra, glans/corona, and penile shaft.

20 s to provide a local stimulus along the axon shaft.

21 connected to an uncoated 2-mum-wide central shaft.

22 tion of the outer cortex/cuticle of the hair shaft.

23 nonfluorescent core continuous with the hair shaft.

24 nd well pads, as well as a coal mine venting shaft.

25 1 recruits Ndc80C to the opposite end of the shaft.

26 h compete for control of their shared gamma -shaft.

27 a periodic structure is not observed in the shaft.

28 nal elastic energy of the coiled-coil gamma -shaft.

29 wo globular heads project from a coiled-coil shaft.

30 elate with rotation and coiling of the actin shaft.

31 ive fungal invasion involving the whole hair shaft.

32 n dendritic spines, rather than on dendritic shafts.

33 organization of dendritic Golgi in dendritic shafts.

34 nd colocalizes with PlexinA1 along dendritic shafts.

35 the diffusion constant fourfold in neuritic shafts.

36 l synapses were M1R+ perikarya and dendritic shafts.

37 that is characterized by tightly curled hair shafts.

38 long actin filaments running along dendritic shafts.

39 ing through synapses on dendritic spines and shafts.

40 synapses increased 99% at spines and 167% in shafts.

41 a subset of spines, in addition to dendritic shafts.

42 nals synapsed more frequently with dendritic shafts.

43 ing movements of the neighboring commissural shafts.

44 utons and restricted expression at adjoining shafts.

45 ry synapses mainly on the soma and dendritic shafts.

46 ifugation (30min) to concentrate NMP into MN shafts.

47 ere unlabeled perikarya and M2R(+) dendritic shafts.

48 tmentalization between synapses and neuronal shafts.

49 itatory contacts directly on their dendritic shafts?

50 acted dendritic spines (86.4%) and dendritic shafts (12.1%).

51 l cells, including perikarya (3%), dendritic shafts (47%), and dendritic spines (39%).

52 atory, synapses on dendritic spines (90%) or shafts (8%), with 2% symmetrical, likely inhibitory, syn

53 riking absence of sebaceous glands, and hair shaft abnormalities in KP lesions but not in unaffected

54 opy in vivo that human gray/white scalp hair shafts accumulate hydrogen peroxide (H(2)O(2)) in millim

55 cr1-deficient microglia and abGCs' dendritic shafts, along with increased proportion of microglia-con

56 m the proximal to the distal end of the hair shaft analyzed may indicate a change in the diet due to

57 Axo-shaft and axo-spinous GABAergic synapse numbers in the o

58 spines either by exocytosing in the dendrite shaft and diffusing into spines or through a kinesin to

59 containing vesicles throughout the dendritic shaft and diffusion into spines.

60 EB1-FP is highly mobile along the flagellar shaft and displays a markedly reduced mobility near the

61 P pathogenesis, resulting in downstream hair shaft and epithelial barrier abnormalities.

62 Extracts of the white shaft and green leaves of 30 leek cultivars were investi

63 ticles by (i) capturing along the filopodial shaft and surfing toward the cell body, the most common

64 thin) with BMD at the hip, spine, and radial shaft and the 4-y change in BMD.

65 ports the assumption that the type 1 fimbria shaft and the FimH adhesin-receptor interaction are opti

66 the hair follicles and regrowth of the hair shaft and the inner root sheath resulted in subsequent s

67 g the mobility of microtubules in the axonal shaft and the invasion of microtubules into the growth c

68 etics between integrins along the filopodial shaft and the ligands on the surrounding ECM fibers.

69 tase (SrtC2)-dependent polymerization of the shaft and tip fimbrillins, FimA and FimB respectively.

70 ht absorbing carbon, while improved Vertical Shaft and Tunnel kilns were lower emitters.

71 ons were labeled, and about 90% of dendritic shafts and 60% of dendritic spines were M1R+.

72 About 95% of dendritic shafts and 60% of dendritic spines were M2 immunoreactiv

73 ation of glutamatergic synapses on dendritic shafts and a reduction of spontaneous glutamatergic post

74 ubunit (sGluA1) in both spines and dendritic shafts and a small increase in spine size relative to pr

75 exhibit impaired de novo production of hair shafts and all temporary hair cell lineages, owing to a

76 ibited abnormal focal swellings of dendritic shafts and disruptions in axon initial segment (AIS) mor

77 es were complete with sebaceous glands, hair shafts and inner and outer root sheaths.

78 t actin organization and dynamics along axon shafts and presynaptic boutons.

79 t 4EGI-1 depleted polyribosomes in dendritic shafts and selectively prevented their upregulation in s

80 e find that inhibitory synapses on dendritic shafts and spines differ in their distribution across th

81 reactivity was found within apical dendritic shafts and spines of CA1 pyramidal cells.

82 EphA7, localized to dendritic shafts and spines of pyramidal cells, is uniquely expres

83 -immunoreactivity (-IR) within the dendritic shafts and spines of pyramidal neurons in young female r

84 y to produce 3D reconstructions of dendritic shafts and spines to characterize synaptic contacts on M

85 al gradient of type II PKA between dendritic shafts and spines was critical for the regulation of syn

86 s and terminals) and postsynaptic (dendritic shafts and spines) profiles in the stratum radiatum in t

87 symmetrical, likely inhibitory, synapses on shafts and spines.

88 ain postsynaptic targets were M1R+ dendritic shafts and spines.

89 terminals establish synapses with dendritic shafts and spines.

90 0 times higher frequencies of PSDs, on their shafts and spines.

91 report that Shot localizes along microtubule shafts and stabilizes them against pharmacologically ind

92 EphA7 influences protrusions from dendritic shafts and the assembling of synaptic components.

93 dening (about cortical bone--eg, the femoral shaft), and cone-beam artifacts (at joint space surfaces

94 o-terminal tail-attachment domain, a slender shaft, and a carboxyl-terminal domain composed of severa

95 les, which are mostly bundled along the axon shaft, and actin filaments, which are highly enriched in

96 n motor (F(1)), connected by a common rotary shaft, and catalyzes proton flow-driven ATP synthesis an

97 cimens from the coronal sulcus, glans penis, shaft, and scrotum were obtained for the assessment of t

98 ll hair follicle lineages including the hair shaft, and the inner and outer root sheaths in skin reco

99 ne major pilin, GBS80, which forms the pilus shaft, and two secondary pilins, GBS104 and GBS52, which

100 ors and their progeny that generate the hair shaft, and, subsequently, premature induction of the des

101 ical and contacted spines, somata, dendritic shafts, and occasionally other axonal terminals.

102 tic densities (PSDs) of dendritic spines and shafts, and on some astrocytic leaflets, in both hippoca

103 naptic densities were preserved on dendritic shafts, and the strength of excitatory synaptic transmis

104 ove the surface contamination from barbs and shafts, and therefore, it is necessary to develop method

105 analyses reveal that DCV distribution along shafts, and within synapses, follows Poisson statistics,

106 ity coefficient of variation < 1%), the neck-shaft angle (NSA) (P = .017), and the BMD (P = .13).

107 r trend<0.001) and with each extreme of neck shaft angle (P<0.05).

108 ol grip deformity and an abnormally low neck shaft angle in unaffected hips of cases with unilateral

109 ity, wide femoral neck, altered femoral neck-shaft angle, appear to play an important role in the pat

110 of femoral head shape, and the femoral neck shaft angle.

111 ut how the actin filaments in the filopodial shaft are spatially organized to form a bundle with appr

112 Branches that sprout from the axon shaft are termed collateral or interstitial branches.

113 Fimbriae are filamentous structures whose shafts are primarily composed of helically arranged sing

114 tegrity of the sheaths that support the hair shaft, are expressed in the enamel organ and are essenti

115 The second function is to serve as a shaft around which can coil a segment of dsRNA.

116 sed on insertion of dipolar rotator carrying shafts as guests into channels of a host, tris(o-phenyle

117 along microtubular tracks in the proplatelet shafts as shown by confocal observations of proplatelet

118 esional junctions, resulting in twisted hair shafts as well as an unusual deposition of hair cuticle

119 e human hair follicle, inclusive of the hair shaft, as a key element in senile hair graying, which do

120 he catalytic domain and the rotating central shaft, as well as temporal control of substrate binding

121 Furthermore, the pilus shaft assembly in Gram-positive bacteria may require a t

122 ubgroup of atypical fractures of the femoral shaft associated with bisphosphonate use.

123 ch essentially contribute to the microtubule shaft association of Shot.

124 AM-5 expression in dendritic protrusions and shafts at both P14 and P28.

125 ta subunits localize on dendritic spines and shafts at sites extrasynaptic to GABAergic input at pube

126 of upper skin layer exposed keratinized hair shafts at the skin surface.

127 2 anatomical sites (glans/coronal sulcus and shaft) at baseline.

128 esting Ca(2+) concentration along the distal shaft, behind the growing tip.

129 Interestingly, zigzag hair shaft bending depends on noncanonical NF-kappaB signalin

130 tional adjustments, such as length trimming, shaft bending, and bark stripping [4, 6, 7].

131 -bundle stability, is activated at the taper-shaft boundary in a PI(4,5)P(2)-dependent manner, allowi

132 was found in somata and along the dendritic shaft, but FLNa was not detected in dendritic spines.

133 ing loss of Daam1 localization to filopodial shafts, but not tips.

134 hemically isolated from the parent dendritic shaft by their thin neck.

135 focal swelling (beading) along the dendritic shaft by unidentified molecular mechanisms.

136 become localized predominantly to dendritic shafts by P28.

137 nce thought to be restricted to the dendrite shaft, can make excursions into the most distal regions

138 PKA was concentrated in dendritic shafts compared to the soma, axons, and dendritic spines

139 d the mechanisms by which they regulate hair shaft components are poorly understood.

140 A shaft connected to the rotor passes through the peptidog

141 p links, or when tip links, ankle links, and shaft connectors were cut, ruling out these links as the

142 us and ulna made up of elongate, paralleling shafts contacting a series of shorter carpal bones.

143 trophoresis data support the notion that the shaft contains PX-DNA.

144 d ragged and dilapidated cuticle of the hair shaft (CUH, a hair anchoring structure), poor hair ancho

145 tools of distinctive shape, with pronounced shaft curvature and hooks of intermediate depth.

146 rofile of single gene mutations causing hair shaft defects were profound.

147 ecause of strikingly similar defects in hair shaft differentiation and that both mutants suffer from

148 s to prevent inappropriate expression of the shaft differentiation program.

149 s been shown to be essential for proper hair shaft differentiation, as Hoxc13 gene-targeted (Hoxc13(t

150 -3sigma mutation have severe defects in hair shaft differentiation, resulting in destruction of the h

151 nt membrane fusion events into the dendritic shaft domain immediately adjacent to (<300 nm from) the

152 eceptor-binding knob domain, a long flexible shaft domain, and a penton base-attachment tail domain.

153 taper domain forms a sharp boundary with the shaft domain, which contains the plasma membrane Ca(2+)-

154 iation, resulting in destruction of the hair shaft during morphogenesis.

155 ain higher depolarizations than do dendritic shafts during excitatory postsynaptic potentials (EPSPs)

156 wing feathers and broad body contour feather shafts, evolved early in the penguin lineage.

157 T15(+) stem cell population and produce hair shafts expressing hair-specific keratins.

158 to promoting hair follicle placode and hair shaft fate, beta-catenin signaling actively suppresses e

159 e of distinct adhesive moieties of FimA, the shaft fimbrillin of Actinomyces type 2 fimbriae, which u

160 type 1 fimbria is comprised of the fimbrial shaft FimP and the tip fimbrillin FimQ.

161 parated (13)C NMR markers are present in the shaft for monitoring the degree of insertion.

162 ations of this novel PMS function along axon shafts for axon maintenance and regeneration.

163 iation of hair matrix keratinocytes and hair shaft formation.

164 ctural protein TCHH are all involved in hair shaft formation.

165 o underwent definitive fixation of a femoral shaft fracture at a level I or II trauma center particip

166 ced osteonecrosis and only 1 case of femoral shaft fracture in each group.

167 We prospectively studied patients with femur shaft fracture with RLS evaluation, daily transcranial D

168 Femoral shaft fractures are common in major trauma.

169 was observed in delayed fixation of femoral shaft fractures, which could not be explained by differe

170 the IF-BAR domain of WRP forms a bud on the shaft from which precursors to spines emerge.

171 Hair shafts from AKR/J mice were deficient in these projectio

172 gun proteomic profiling can distinguish hair shafts from different inbred mouse strains.

173 ed by assembly of actin filaments along axon shafts giving rise to filopodia.

174 As a consequence, hair shafts grow longer.

175 atients, P-cadherin silencing inhibited hair shaft growth, prematurely induced HF regression (catagen

176 knob domain associated with a portion of the shaft has been solved by X-ray crystallography, the in s

177 nd small neck that connects to the dendritic shaft, has been shown to facilitate compartmentalization

178 igger de novo spine growth from the dendrite shaft in a location-specific manner.

179 llected with rayon swabs on an aluminum wire shaft in Amies gel with charcoal and those collected wit

180 d by the development of blebs along the hair shaft in mice.

181 of putative inhibitory synapses on dendritic shafts in the right MePD of females in proestrus was hig

182 cation of GluR1 receptors from the dendritic shaft into spines, but it was not required for constitut

183 easingly slowed as they passed from the axon shaft into the growth cone and filopodia.

184 that microtubules polymerize from dendritic shafts into spines and that signaling through synaptic N

185 tide neurotransmitter sensorin from neuritic shafts into synapses.

186 The position of the dumbbell shaft is a function of the site of homology, and its ext

187 Although the hair shaft is derived from the progeny of keratinocyte stem c

188 Transport of proteins in the ciliary shaft is driven by microtubule-dependent motors, kinesin

189 and that Rab11 trafficking along the bristle shaft is mediated by microtubules.

190 hair follicle fate, broadly expressing hair shaft keratins in place of epidermal stratification prot

191 treatment, but not age, increased dendritic shaft labeling.

192 cally interact with each other through their shafts, leading to zippering and unzippering behavior th

193 lar to that of the radius and hyperelongate, shaft-like carpal bones contacting the ulna that are pro

194 In Flailer, neurons show abnormal dendritic shaft localization of PSD-95, stargazin, dynamin3, AMPAR

195 protein is the major component of scalp hair shaft material and it is composed of 21 amino acids.

196 que tip proteins displayed on a common pilus shaft may serve distinct physiological functions.

197 he MNA into the skin, individual microneedle shafts melted away by interstitial fluid from the epider

198 y, despite its strong presence in the axonal shaft, MPS is disrupted in most presynaptic boutons but

199 erous within dermal papillae and around hair shafts (n = 4).

200 assoon-positive clusters along the dendritic shaft of hippocampal interneurons.

201 arious cytosolic proteins in the 250-nm-wide shaft of live primary cilia with a spatiotemporal resolu

202 in axons, spanning nearly the entire axonal shaft of mature neurons.

203 reveal Abeta activates NgRs on the dendritic shaft of neurons, triggering an inhibition of calcium si

204 article components accumulate in the ciliary shaft of ome;crb3a double mutants.

205 Here, we report that the stalk shaft of rat cytoplasmic dynein is an antiparallel alpha

206 The persistence lengths along the shaft of rotary-shadowed smooth and striated muscle trop

207 The flagellar shaft of some bacteria, including several human pathogen

208 f 2 mm in length, and then introduced up the shaft of the 25-gauge trocar.

209 all correlated for the extracts of the white shaft of the 30 leek cultivars.

210 tinct motif looping out from the coiled-coil shaft of the complex, in Saccharomyces cerevisiae.

211 affecting the density of filopodia along the shaft of the extending axon.

212 Swab specimens from the glans and shaft of the penis were collected from men enrolled in a

213 ld light is coupled through a grating at the shaft of the tip, generating plasmons that propagate to

214 The effective shaft of the trocar was then reduced to 2 mm in length.

215 This secures the two sleeves on the shaft of the trocar, such that they act as a spacer.

216 l implications: although the slender feather shafts of Archaeopteryx and Anchiornis make individual f

217 increase occurs on both dendritic spines and shafts of CA1 pyramidal cells and is in response to horm

218 symmetrical) and appositions with spines and shafts of dendrites.

219 s and the labeled apical and basal dendritic shafts of identified CS neurons.

220 pidly from a diffuse distribution within the shafts of neuronal dendrites to a clustered postsynaptic

221 formed mostly large synapses with dendritic shafts of presumed inhibitory neurons in the upper layer

222 A neurons, while 10% contacted the dendritic shafts of presumed interneurons, half of which were CB(+

223 protrude from the microtubule-rich dendritic shafts of principal neurons.

224 f Sema6d results in ectopic placement of the shafts of proprioceptive axons and their associated olig

225 he neuropil, (2) the properties of dendritic shafts of PV-IR interneurons, (3) Type II PV-IR synapses

226 nd efficiently, resulting in diminished hair shaft outgrowth.

227 c side of excitatory synapses onto dendritic shafts, overlapping clusters of PSD-95 and NMDA receptor

228 Here we show that the shaft pilin SpaA harbors a disulfide bond in vivo and al

229 on of the SpaA-type pilus, consisting of the shaft pilin SpaA, tip pilin SpaC and minor pilin SpaB.

230 the delta subunit within dendritic spine and shaft profiles at the onset of puberty.

231 pha4 KO mice have larger dendritic spine and shaft profiles.

232 y upregulated BMP signaling in knockout hair shaft progenitors and demonstrate that Bmp6 inhibits cel

233 Here, we report the identification of hair shaft progenitors in the matrix that are differentiated

234 migration and increased BMP activity of hair shaft progenitors.

235 the migration speed of differentiating hair shaft progenitors.

236 rosion was particularly evident in long bone shafts, progressively increased from Binet stage A to Bi

237 nst CafA inhibits coaggregation, whereas the shaft protein FimA or a polyclonal antibody against FimA

238 To investigate the application of hair-shaft proteomics to the study of such diseases, pelage f

239 For this purpose, analyzing the total hair shaft provided better discrimination than analyzing the

240 Since the hair shaft provides a discrete sampling of the species proteo

241 e lectin-like activity of the polymeric FimA shaft rather than the tip.

242 tergic synapses to be localized on dendritic shafts, rather than on spines as occurs in wild type.

243 evealed that the great majority of dendritic shafts receiving cholinergic inputs were CAMK(+) , indic

244 , and its axial portions function as a drive shaft (rod), a universal joint (hook) and a helical prop

245 Proteomic analysis of hair shaft samples from one of the families revealed no subst

246 r and less precise results were obtained for shaft samples.

247 n the glans penis and coronal sulcus, penile shaft, scrotum, semen, and urine was compared by circumc

248 ver cigarette smoking and infection site(s) (shaft/scrotum and glans/urine vs shaft/scrotum or glans/

249 on site(s) (shaft/scrotum and glans/urine vs shaft/scrotum or glans/urine only) were positively assoc

250 ted with changes in spine size and dendritic shaft sGluA1 intensity following whisker stimulation.

251 ent, which is mostly transient, whereas axon shafts show a more delayed and progressive increase in d

252 es in the growth cone back toward the axonal shaft, significantly decreases the frequency of these wa

253 contact dendritic spines, avoiding dendritic shafts, so spines must play a key role for neurons.

254 ression of a mutant Krt75, which causes hair shaft structural defects characterized by the developmen

255 contain SpaA, SpaD, and SpaH, making up the shaft structure.

256 t the "T" domain of gpGT binds to major tail shaft subunit gpV, and present a model for how gpG and g

257 examine otherwise-unidentifiable excitatory shaft synapses in aspiny neurons, such as parvalbumin-po

258 Because spine synapses differ from shaft synapses in their signaling capabilities, the shif

259 lectrical and Ca(2+) signaling in spines and shaft synapses of dopamine neurons.

260 es in betaIII spectrin-depleted neurons make shaft synapses that exhibit increased amplitudes of mini

261 s, or the relative contribution of spine and shaft synapses to excitability.

262 ere less sensitive to hyperpolarization than shaft synapses, suggesting amplification of spine head v

263 immunoreactivity decreased 84% at excitatory shaft synapses.

264 ut result instead in increased axo-dendritic shaft synapses.

265 unstable dendritic protrusions, mislocalized shaft-synapses, and loss of compartmentalization of NMDA

266 eticulum of neuronal perikarya and dendritic shafts, synaptic specializations in dendritic spines, an

267 ogold) was significantly higher in dendritic shafts than in spine heads.

268 ection involves rotation of the gammaepsilon shaft that connects the alpha3beta3 head and the membran

269 les from the head domain and together form a shaft that connects to a predicted outer membrane protei

270 EL2 and the CTD by gripping an alpha-helical shaft that extends from HEL1.

271 incoiffables" is a rare anomaly of the hair shaft that occurs in children and improves with age.

272 h abnormally large swellings and proplatelet shafts that generated giant platelets in culture.

273 like specializations directly onto dendritic shafts, that dendritic protrusions primarily arise indep

274 basal tapers and approximately 1 mum of the shaft, the location of the ankle links, is enriched in t

275 lizes with Syntaxin-4 in the soma, dendritic shaft, the tips of developing hippocampal neurons, and i

276 by actin waves transiently widen the neurite shaft to allow increased microtubule polymerization to d

277 ell can use rotation of the filopodial actin shaft to induce coiling and hence axial shortening of th

278 and by varying the attachment of the axonal shaft to the coverslip, we estimate values for the axial

279 ans for signaling from synapses to dendritic shafts to recruit AMPA receptors into synapses during LT

280 emerge along the proximal region of the axon shaft typically devoid of branches, and they develop int

281 been observed in drill strings inside drill shafts used by the oil-drilling industry, and oil indust

282 The actin shaft was observed to periodically undergo helical coili

283 y straight trajectories of primary dendritic shafts were disrupted, whereas the diameter of higher-or

284 Stalled axon tips and adjacent shafts were intensely immunolabeled with synapse markers

285 n1 has been detected in dendritic spines and shafts where it regulates protein synthesis required to

286 es; the rod is straight and rigid as a drive shaft whereas the hook is flexible in bending as a unive

287 mains are arranged in tandem along the pilus shaft, whereas the respective N1 domain is tilted by app

288 odia emerged from densities in the dendritic shaft, which by electron microscopy contained branched a

289 otein and localizes all along the filopodial shaft, which differs from other formins that localize sp

290 elation to a reference region in the femoral shaft, which represented the bone tracer uptake backgrou

291 e density of labeling decreased in dendritic shaft while increasing in spine heads, implying rapid tr

292 e excitatory inputs cluster at T4's dendrite shafts, while inhibitory inputs localize to the bases.

293 e soma causes calcium currents in the apical shaft whose amplitudes decay with distance from the soma

294 ty of postsynaptic structures were dendritic shafts whose neurons of origin were not identified.

295 n conduction speed that accompanies the axon shaft widening induced by high-frequency AP firing.

296 of axons and were evenly spaced along axonal shafts with a periodicity of ~180 to 190 nanometers.

297 edly dystrophic hair follicles, loss of hair shafts with increased apoptosis, and hyperplastic epider

298 on dendritic spines, and 56.7% on dendritic shafts with KO of the alpha4 subunit, as compared to WT

299 pattern in the rotation of the central gamma-shaft, with a metastable intermediate located-consistent

300 tory synapses on spines and on the dendritic shaft, without affecting the total number of synapses or